<h1><strong>Pharmacist I</strong></h1><p><br></p><h2>Job Description</h2><p>In this role, you will utilize your clinical skills to conduct utilization management reviews, including prior authorizations, coverage exceptions, and quantity limit exceptions. You will work independently within a team of pharmacy professionals to achieve monthly quality and productivity goals. The position is considered for potential long-term employment, with contracts evaluated every six months for extension.</p><p><br></p><h2>Responsibilities</h2><ul><li>Conduct utilization management reviews, including prior authorizations, coverage exceptions, and quantity limit exceptions.</li><li>Work independently among a team of pharmacy professionals.</li><li>Meet monthly quality and productivity goals.</li></ul><h2>Essential Skills</h2><ul><li>Two years of experience in retail, managed care, or clinical pharmacy.</li><li>Doctor of Pharmacy (PharmD) or Bachelor of Science Pharmacy degree.</li><li>Current pharmacist license in good standing with the State Board of Pharmacy where the position is located.</li><li>Ability to prioritize tasks and manage multiple projects simultaneously.</li><li>Drive to deliver results orientation.</li><li>Motivated self-starter who does not need constant direction or feedback.</li><li>Ability to make clinical decisions independently.</li><li>Flexibility to change and resourcefulness.</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>Previous Pharmacy Benefits Management (PBM) or Case/Care Management experience preferred.</li><li>Retail experience highly preferred over hospital experience.</li><li>Proficient with learning new computer systems and basic IT troubleshooting.</li><li>Proficiency in Word and Excel.</li><li>Ability to type 35+ WPM.</li></ul><h2>Work Environment</h2><p>This is a fully remote work-from-home position, available in any state except California, Hawaii, or Virginia. Core business hours are Monday through Friday, with newer employees typically starting between 9-9:30 AM CST. Candidates should plan for a full-time schedule plus overtime during peak seasons, typically December through April. Training is conducted Monday through Friday, 8:00 AM to 4:30 PM CST, over 10-12 weeks, and consists of instructor-led sessions, videos, worksheets, and practice cases.</p>

public

Clinical Review Pharmacist - Remote

<h1 style="font-weight: 700;">Job Title: Site Start Up Specialist</h1><br><h2>Job Description</h2><p>As a Clinical Site Start Up Specialist, you will be responsible for developing awareness of regulatory legislation, guidance, and practices in assigned countries with the support of <span style="color: rgb(8, 7, 7); background-color: none;"><span style="color: rgb(8, 7, 7); background-color: none;"><span style="color: rgb(8, 7, 7); background-color: none;"><span style="color: rgb(8, 7, 7); background-color: none;">senior</span></span></span></span> staff. You will assist in compiling, preparing, submitting and obtaining approval of submission documents to IRB/IEC/Third body/Regulatory Authority in accordance with local requirements. Your job will also include liaising with internal and external vendors in the generation of Regulatory Authority submissions. You will perform reviews of final submission documents, organize communication related to the submissions/outcomes within our organization, and escalate study issues appropriately and timely. You will also serve as a primary contact for investigative sites and ensure all necessary documents are collected in a timely manner. The role includes ensuring that all assigned maintenance and Start-up activities are on track and in accordance with client expectations, ICH/GCP, SOPs, budget, quality and applicable laws and guidelines. You will also be responsible for updating study documents when there are changes in study personnel/study amendments and ensuring high quality documents are filed and systems are updated on an ongoing and timely basis. With guidance from the line manager and experienced colleagues, you&#39;ll adapt Informed Consent Forms and other patient facing material to country-specific requirements. The role may also involve supporting/assisting the contract negotiation process under the supervision of an experienced colleague or line manager.</p><br><h2>Responsibilities</h2><ul><li>Develop awareness of regulatory legislation, guidance, and practices in assigned countries.</li><li>Assist in compiling, preparing, submitting, and obtaining approval of submission documents to IRB/IEC/Third body/Regulatory Authority.</li><li>Liaise with internal and external vendors for the generation of Regulatory Authority submissions.</li><li>Perform reviews of final submission documents and organize communication related to the submissions/outcomes.</li><li>Escalate study issues appropriately and timely.</li><li>Serve as a primary contact for investigative sites and ensure timely collection of necessary documents.</li><li>Ensure that all assigned maintenance and start-up activities are on track and in accordance with client expectations, ICH/GCP, SOPs, budget, quality, and applicable laws and guidelines.</li><li>Update study documents when there are changes in study personnel/study amendments.</li><li>Adapt Informed Consent Forms and other patient-facing material to country-specific requirements.</li><li>Support/assist the contract negotiation process under supervision.</li></ul><h2>Essential Skills</h2><ul><li>Contracts and negotiation of budgets and contracts.</li><li>Regulatory review and start-up processes.</li><li>Experience with IRB, TMF, and clinical research.</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>Strong communication skills.</li><li>Problem-solving abilities.</li><li>Attention to detail.</li><li>Proactive approach.</li></ul><h2>Work Environment</h2><p>This is a 100% Work From Home position. The successful candidate must be able to work on East Coast timezone hours (Monday - Friday) 8-5PM EST. The role is fully remote and can be based anywhere in the USA.</p><br>

Clinical Start Up Specialist

<h1><strong>Clinical Supply Chain Manager</strong></h1><p><br></p><h2>Job Description</h2><p>The Clinical Supply Chain Manager will ensure the effective management of drug manufacturing and the clinical supply chain, ensuring seamless provision of drug and ancillary supplies across the clinical portfolio. This role requires collaboration with internal clinical supply chain, clinical operation, regulatory, and manufacturing colleagues to assist in the delivery of clinical supplies in line with regulatory requirements and internal quality processes.</p><p><br></p><h2>Responsibilities</h2><ul><li>Lead and provide direction around Supply Chain discussions in team meetings, maintaining effective communication with customers and partners.</li><li>Set up the clinical supply chain strategy for studies and/or clinical portfolio of studies.</li><li>Design and implement labeling, packaging, and supply strategies that meet study design, clinical study sites, and regulatory authority requirements, while maximizing supply efficiency.</li><li>Manage, with input from CMC and Regulatory groups, the generation and approval of label texts, translations (where required), and label proof.</li><li>Produce a clinical supply agreement document detailing the design, setup, and operation of the supply chain for responsible studies or groups of studies.</li></ul><h2>Essential Skills</h2><ul><li>Experience in supply chain management and clinical supplies.</li><li>Knowledge of IRT, Cold Chain, GxP, GmP, and regulatory compliance.</li><li>Vendor management and pharmaceutical forecasting expertise.</li><li>Proficiency in budget management, labeling, and shipping processes.</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>Degree or higher in a relevant scientific subject or business management, or equivalent industry experience.</li><li>Masters or PhD in a relevant scientific subject is desirable.</li><li>Demonstrated computer skills with a functional knowledge of Microsoft packages (MS Word, Excel, Power Point, Outlook, MS Project, SharePoint).</li></ul><h2>Work Environment</h2><p>This role requires a presence on-site three to four days a week, either in Conshohocken, PA or Gaithersburg, MD. Join a leading T-Cell Oncology biotech company with a strong pipeline, offering opportunities for long-term growth into <span style="color: rgb(8, 7, 7); background-color: none;"><span style="color: rgb(8, 7, 7); background-color: none;">senior</span></span> positions.</p>

Clinical Supply Chain Manager (Hybrid)

<h1><strong>Clinical Supply Chain Manager</strong></h1><p><br></p><h2>Job Description</h2><p>The Clinical Supply Chain Manager will ensure the effective management of drug manufacturing and the clinical supply chain, ensuring seamless provision of drug and ancillary supplies across the clinical portfolio. This role requires collaboration with internal clinical supply chain, clinical operation, regulatory, and manufacturing colleagues to assist in the delivery of clinical supplies in line with regulatory requirements and internal quality processes.</p><p><br></p><h2>Responsibilities</h2><ul><li>Lead and provide direction around Supply Chain discussions in team meetings, maintaining effective communication with customers and partners.</li><li>Set up the clinical supply chain strategy for studies and/or clinical portfolio of studies.</li><li>Design and implement labeling, packaging, and supply strategies that meet study design, clinical study sites, and regulatory authority requirements, while maximizing supply efficiency.</li><li>Manage, with input from CMC and Regulatory groups, the generation and approval of label texts, translations (where required), and label proof.</li><li>Produce a clinical supply agreement document detailing the design, setup, and operation of the supply chain for responsible studies or groups of studies.</li></ul><h2>Essential Skills</h2><ul><li>Experience in supply chain management and clinical supplies.</li><li>Knowledge of IRT, Cold Chain, GxP, GmP, and regulatory compliance.</li><li>Vendor management and pharmaceutical forecasting expertise.</li><li>Proficiency in budget management, labeling, and shipping processes.</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>Degree or higher in a relevant scientific subject or business management, or equivalent industry experience.</li><li>Masters or PhD in a relevant scientific subject is desirable.</li><li>Demonstrated computer skills with a functional knowledge of Microsoft packages (MS Word, Excel, Power Point, Outlook, MS Project, SharePoint).</li></ul><h2>Work Environment</h2><p>This role requires a presence on-site three to four days a week, either in Conshohocken, PA or Gaithersburg, MD. Join a leading T-Cell Oncology biotech company with a strong pipeline, offering opportunities for long-term growth into <span style="color: rgb(8, 7, 7); background-color: none;">senior</span> positions.</p>

<h1 style="font-weight: 700;">Job Title: Clinical Trial Assistant</h1><br><h2>Job Description</h2><p>We are seeking a highly organized and detail-oriented Clinical Trial Assistant to join our clinical operations team in Rockville, MD. The Clinical Trial Assistant will play a pivotal role in supporting clinical trial activities, including supply tracking, trial master file maintenance, site invoice processing, query reporting, and subject tracking.</p><br><h2>Responsibilities</h2><ul><li>Support site initiation, monitoring, and close-out visits as needed.</li><li>Maintain effective communication with clinical sites to resolve operational issues.</li><li>Support subject enrollment and tracking activities across all trial sites.</li><li>Assist with investigator and site staff training materials and logistics.</li><li>Track and manage study supplies to ensure timely availability across clinical sites.</li><li>Assist in the preparation, submission, and tracking of IRB/EC submissions and approvals.</li><li>Maintain and update the Trial Master File (TMF) in compliance with regulatory requirements.</li><li>Support audits and inspections by preparing documentation and responding to findings.</li><li>Monitor data entry timelines and assist in resolving data discrepancies.</li><li>Liaise with CROs, labs, and other third-party vendors.</li><li>Collaborate with cross-functional teams to ensure efficient trial execution.</li><li>Process clinical site invoices and assist with budget tracking.</li><li>Organize internal and external study meetings, such as investigator meetings and DMC.</li><li>Draft meeting agendas and take minutes to track action items.</li></ul><h2>Essential Skills</h2><ul><li>Solid understanding of Good Clinical Practice (GCP), ICH guidelines, and applicable FDA regulations.</li><li>Strong attention to detail and organizational skills.</li><li>Excellent verbal and written communication skills.</li><li>Ability to manage multiple priorities and meet deadlines.</li><li>Comfortable collaborating across cross-functional teams and with external partners.</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>Bachelor’s degree in a relevant field (e.g., Life Sciences, Nursing, Public Health, Pharmacy).</li><li>Experience working in a healthcare or biotechnology setting.</li><li>Familiarity with electronic data capture systems; experience with specific systems is a plus.</li><li>Proficiency with Microsoft Office Suite (Excel, Word, Outlook, PowerPoint).</li><li>Understanding of Trial Master File (TMF) maintenance and clinical trial documentation practices.</li></ul><h2>Work Environment</h2><p>This position operates in an office environment. The team is small and collaborative, focusing on advanced oral drug delivery using precision immunotherapy. The new technology allows for delivering medicine through capsules, offering convenience for patients by avoiding IV infusion centers, particularly for the treatment of autoimmunity and cancer.</p><br>

Clinical Trial Assistant

<h1 style="font-weight: 700;">Job Title: <span style="color: rgb(8, 7, 7); background-color: none;"><span style="color: rgb(8, 7, 7); background-color: none;"><span style="color: rgb(8, 7, 7); background-color: none;"><span style="color: rgb(8, 7, 7); background-color: none;"><span style="color: rgb(8, 7, 7); background-color: none;"><span style="color: rgb(8, 7, 7); background-color: none;"><span style="color: rgb(8, 7, 7); background-color: none;"><span style="color: rgb(8, 7, 7); background-color: none;"><span style="color: rgb(8, 7, 7); background-color: none;">Senior</span></span></span></span></span></span></span></span></span> Clinical Project Manager</h1><br><h2>Job Description</h2><p>We are seeking a dedicated <span style="color: rgb(8, 7, 7); background-color: none;"><span style="color: rgb(8, 7, 7); background-color: none;"><span style="color: rgb(8, 7, 7); background-color: none;"><span style="color: rgb(8, 7, 7); background-color: none;"><span style="color: rgb(8, 7, 7); background-color: none;"><span style="color: rgb(8, 7, 7); background-color: none;"><span style="color: rgb(8, 7, 7); background-color: none;"><span style="color: rgb(8, 7, 7); background-color: none;"><span style="color: rgb(8, 7, 7); background-color: none;">Senior</span></span></span></span></span></span></span></span></span> Clinical Project Manager responsible for overseeing the planning, execution, and management of clinical trials across multiple phases. This role ensures compliance with regulatory requirements, timelines, and budget constraints while driving operational excellence in clinical trial execution.</p><br><h2>Responsibilities</h2><ul><li>Lead end-to-end clinical trial management from protocol development to study closeout.</li><li>Develop and maintain detailed project plans, timelines, and budgets.</li><li>Collaborate with regulatory teams for submissions, amendments, and compliance-related documentation.</li><li>Address protocol deviations, audit findings, and inspection readiness.</li><li>Select, negotiate, and manage relationships with CROs, central labs, and other external vendors.</li><li>Track performance metrics and ensure service level agreements are met.</li><li>Proactively identify study risks and develop mitigation strategies.</li><li>Address operational challenges, protocol deviations, and recruitment/retention issues.</li><li>Ensure efficient resource allocation to optimize study costs.</li><li>Monitor trial-related invoices and payments in collaboration with finance teams.</li><li>Act as the primary point of contact for all internal and external stakeholders.</li><li>Provide leadership and mentorship to junior project managers, CRAs, and study coordinators.</li><li>Facilitate collaboration among cross-functional teams including Clinical Operations, Data Management, Medical Writing, Quality Assurance, and other departments.</li><li>Ensure high-quality data collection and adherence to data integrity standards.</li><li>Work closely with data management and biostatistics teams to ensure timely database locks.</li><li>Provide regular study updates to <span style="color: rgb(8, 7, 7); background-color: none;"><span style="color: rgb(8, 7, 7); background-color: none;"><span style="color: rgb(8, 7, 7); background-color: none;"><span style="color: rgb(8, 7, 7); background-color: none;"><span style="color: rgb(8, 7, 7); background-color: none;"><span style="color: rgb(8, 7, 7); background-color: none;"><span style="color: rgb(8, 7, 7); background-color: none;"><span style="color: rgb(8, 7, 7); background-color: none;"><span style="color: rgb(8, 7, 7); background-color: none;">senior</span></span></span></span></span></span></span></span></span> leadership and stakeholders.</li><li>Develop strategies to optimize patient recruitment and retention.</li><li>Oversee site relationships, investigator engagement, and performance metrics.</li><li>Support protocol development and feasibility assessments.</li><li>Contribute to clinical development plans, study endpoints, and operational feasibility considerations.</li><li>Develop organizational systems including SOPs, document management systems, and project finance management.</li><li>Ensure compliance with regulatory requirements and standard operating procedures.</li><li>Perform any other duties as assigned by the supervisor.</li></ul><h2>Essential Skills</h2><ul><li>Strong leadership, communication, and negotiation skills.</li><li>Ability to work in a fast-paced environment and manage multiple priorities.</li><li>Proficiency in clinical trial management systems (CTMS) and regulatory submission platforms.</li><li>Excellent problem-solving and risk management abilities.</li><li>Financial acumen for budget forecasting and cost control.</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>Bachelor’s degree in life sciences, pharmacy, nursing, or a related field (Master’s or PhD preferred).</li><li>7+ years of experience in clinical trial management within the pharmaceutical, biotech, or CRO industry.</li><li>Proven experience in leading Phase I-IV clinical trials.</li><li>Strong understanding of GCP, ICH guidelines, FDA, EMA, and other regulatory requirements.</li><li>Experience managing CROs, vendors, and multi-site global trials.</li><li>Prior experience in neurology and rare diseases is a plus.</li><li>Experience working in an FDA-regulated and/or EMA-regulated environment.</li><li>Knowledge of adaptive trial designs and decentralized clinical trials is an advantage.</li></ul><h2>Work Environment</h2><p>This position will require domestic and international travel (10%). The work environment is dynamic and performance-driven, offering high visibility in a smaller company setting. The company provides a supportive culture with a rewards program, cellphone reimbursement, tuition reimbursement, 401K matching, and excellent benefits. Employees are encouraged to take ownership of tasks and proactively seek solutions, working in a collaborative and goal-oriented environment.</p><br>

Clinical Trial Manager

<h1 style="font-weight: 700;">Job Title: <span style="color: rgb(8, 7, 7); background-color: none;"><span style="color: rgb(8, 7, 7); background-color: none;"><span style="color: rgb(8, 7, 7); background-color: none;"><span style="color: rgb(8, 7, 7); background-color: none;"><span style="color: rgb(8, 7, 7); background-color: none;"><span style="color: rgb(8, 7, 7); background-color: none;"><span style="color: rgb(8, 7, 7); background-color: none;"><span style="color: rgb(8, 7, 7); background-color: none;">Senior</span></span></span></span></span></span></span></span> Clinical Project Manager</h1><br><h2>Job Description</h2><p>We are seeking a dedicated <span style="color: rgb(8, 7, 7); background-color: none;"><span style="color: rgb(8, 7, 7); background-color: none;"><span style="color: rgb(8, 7, 7); background-color: none;"><span style="color: rgb(8, 7, 7); background-color: none;"><span style="color: rgb(8, 7, 7); background-color: none;"><span style="color: rgb(8, 7, 7); background-color: none;"><span style="color: rgb(8, 7, 7); background-color: none;"><span style="color: rgb(8, 7, 7); background-color: none;">Senior</span></span></span></span></span></span></span></span> Clinical Project Manager responsible for overseeing the planning, execution, and management of clinical trials across multiple phases. This role ensures compliance with regulatory requirements, timelines, and budget constraints while driving operational excellence in clinical trial execution.</p><br><h2>Responsibilities</h2><ul><li>Lead end-to-end clinical trial management from protocol development to study closeout.</li><li>Develop and maintain detailed project plans, timelines, and budgets.</li><li>Collaborate with regulatory teams for submissions, amendments, and compliance-related documentation.</li><li>Address protocol deviations, audit findings, and inspection readiness.</li><li>Select, negotiate, and manage relationships with CROs, central labs, and other external vendors.</li><li>Track performance metrics and ensure service level agreements are met.</li><li>Proactively identify study risks and develop mitigation strategies.</li><li>Address operational challenges, protocol deviations, and recruitment/retention issues.</li><li>Ensure efficient resource allocation to optimize study costs.</li><li>Monitor trial-related invoices and payments in collaboration with finance teams.</li><li>Act as the primary point of contact for all internal and external stakeholders.</li><li>Provide leadership and mentorship to junior project managers, CRAs, and study coordinators.</li><li>Facilitate collaboration among cross-functional teams including Clinical Operations, Data Management, Medical Writing, Quality Assurance, and other departments.</li><li>Ensure high-quality data collection and adherence to data integrity standards.</li><li>Work closely with data management and biostatistics teams to ensure timely database locks.</li><li>Provide regular study updates to <span style="color: rgb(8, 7, 7); background-color: none;"><span style="color: rgb(8, 7, 7); background-color: none;"><span style="color: rgb(8, 7, 7); background-color: none;"><span style="color: rgb(8, 7, 7); background-color: none;"><span style="color: rgb(8, 7, 7); background-color: none;"><span style="color: rgb(8, 7, 7); background-color: none;"><span style="color: rgb(8, 7, 7); background-color: none;"><span style="color: rgb(8, 7, 7); background-color: none;">senior</span></span></span></span></span></span></span></span> leadership and stakeholders.</li><li>Develop strategies to optimize patient recruitment and retention.</li><li>Oversee site relationships, investigator engagement, and performance metrics.</li><li>Support protocol development and feasibility assessments.</li><li>Contribute to clinical development plans, study endpoints, and operational feasibility considerations.</li><li>Develop organizational systems including SOPs, document management systems, and project finance management.</li><li>Ensure compliance with regulatory requirements and standard operating procedures.</li><li>Perform any other duties as assigned by the supervisor.</li></ul><h2>Essential Skills</h2><ul><li>Strong leadership, communication, and negotiation skills.</li><li>Ability to work in a fast-paced environment and manage multiple priorities.</li><li>Proficiency in clinical trial management systems (CTMS) and regulatory submission platforms.</li><li>Excellent problem-solving and risk management abilities.</li><li>Financial acumen for budget forecasting and cost control.</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>Bachelor’s degree in life sciences, pharmacy, nursing, or a related field (Master’s or PhD preferred).</li><li>7+ years of experience in clinical trial management within the pharmaceutical, biotech, or CRO industry.</li><li>Proven experience in leading Phase I-IV clinical trials.</li><li>Strong understanding of GCP, ICH guidelines, FDA, EMA, and other regulatory requirements.</li><li>Experience managing CROs, vendors, and multi-site global trials.</li><li>Prior experience in neurology and rare diseases is a plus.</li><li>Experience working in an FDA-regulated and/or EMA-regulated environment.</li><li>Knowledge of adaptive trial designs and decentralized clinical trials is an advantage.</li></ul><h2>Work Environment</h2><p>This position will require domestic and international travel (10%). The work environment is dynamic and performance-driven, offering high visibility in a smaller company setting. The company provides a supportive culture with a rewards program, cellphone reimbursement, tuition reimbursement, 401K matching, and excellent benefits. Employees are encouraged to take ownership of tasks and proactively seek solutions, working in a collaborative and goal-oriented environment.</p><br>

<h1><strong>IMMEDIATE: CMM Programmer</strong></h1><h2>Job Description</h2><p>We are seeking an experienced CMM Programmer with expertise in using PC-DMIS software. The ideal candidate will have a comprehensive understanding of GD&amp;T, be adept at programming complex parts, and possess machining experience to thrive in a machine shop environment.</p><p><br></p><h2>Responsibilities</h2><ul><li>Interpret engineering drawings, specifications, and GD&amp;T requirements to create effective and efficient CMM programs.</li><li>Develop, modify, and optimize CMM programs using PC-DMIS software.</li><li>Design and develop CMM fixturing and tooling to streamline setups.</li><li>Execute CMM programs and analyze results to ensure compliance with quality standards.</li><li>Conduct first-article and in-process inspections.</li><li>Mark parts effectively with machining moves to meet customer specifications.</li><li>Collaborate with engineering and production teams to troubleshoot measurement issues and implement corrective actions.</li><li>Train and mentor staff on CMM programming and measurement techniques as needed.</li><li>Participate in continuous improvement initiatives to enhance measurement processes and efficiency.</li><li>Complete 100% dimensional layouts for PPAP as required.</li><li>Operate multiple CMMs simultaneously to support production checks during the shift.</li><li>Perform routine maintenance and calibration of CMM equipment to ensure accuracy and reliability.</li><li>Stay updated with advances in CMM technologies and measurement techniques.</li></ul><h2>Essential Skills</h2><ul><li>Degree in Manufacturing Engineering, Quality Assurance, or a related field, or equivalent work experience.</li><li>Proven experience as a CMM programmer using PC-DMIS software for complex parts.</li><li>Strong understanding of geometric dimensioning and tolerancing (GD&amp;T) principles.</li><li>Familiarity with CAD software and the ability to read technical drawings.</li><li>Excellent analytical and problem-solving skills.</li><li>Attention to detail and commitment to quality standards.</li><li>Effective communication skills and ability to work collaboratively in a team setting.</li><li>Knowledge of statistical process control (SPC) methodologies.</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>Certification in metrology or quality control (ASQ, Six Sigma, etc.) is a plus.</li><li>Experience with different types of measuring equipment, such as laser scanners and optical comparators, is desirable.</li><li>Knowledge of casting and machining is preferred.</li></ul><h2>Work Environment</h2><p>The work environment includes a quality lab equipped with four CMMs, where 90% of the workday will be spent. The lab is air-conditioned and clean, while the shop floor is a CNC machine shop with multiple buildings inside the main building. The plant is air-conditioned and well-lit, except for the shipping dock. The position involves working five days a week with flexible hours, including options such as 5am-1:30pm, 6am-2:30pm, or 7am-3:30pm. No overtime is required, and an unpaid lunch break is included. A CMM Operator will assist in this role. </p>

Cmm Programmer

<p><strong>CMM Programmer – PC-DMIS</strong></p><p><strong>Location:</strong> Southeastern Wisconsin</p><p><strong>Schedule:</strong> Monday–Friday | Flexible shifts: 5:00am–1:30pm, 6:00am–2:30pm, or 7:00am–3:30pm</p><p><strong>Environment:</strong> Air-conditioned quality lab and CNC machine shop</p><p><strong>Reports to: </strong>Quality Manager</p><p><br></p><p><strong>Position Overview</strong></p><p>A precision manufacturing facility is seeking a skilled and detail-oriented CMM Programmer with hands-on experience using PC-DMIS software. This role is ideal for someone with a strong <span style="color: rgb(8, 7, 7); background-color: none;">background</span> in dimensional inspecting, and machining, who thrives in a fast-paced, low-volume/high-mix production environment.</p><p>Key Responsibilities</p><ul><li>Program, operate, and optimize CMMs using PC-DMIS to inspect complex machined parts</li><li>Interpret engineering drawings and GD&amp;T to develop accurate inspection routines</li><li>Perform first-article, in-process, and final inspections to ensure compliance with specifications</li><li>Create and maintain CMM fixturing and tooling to improve efficiency and repeatability</li><li>Conduct 100% dimensional layouts for PPAP submissions</li><li>Collaborate with engineering and production teams to resolve measurement discrepancies and implement corrective actions</li><li>Train and support CMM Operators and other team members on inspection techniques</li><li>Maintain and calibrate CMM equipment to ensure accuracy and reliability</li><li>Stay current with advancements in metrology and inspection technologies</li></ul><p><strong>Required Qualifications</strong></p><ul><li>Degree in Manufacturing Engineering, Quality Assurance, or equivalent work experience</li><li>Proven experience programming CMMs using PC-DMIS for complex geometries</li><li>Strong knowledge of GD&amp;T and ability to interpret technical drawings</li><li>Familiarity with CAD software and 3D models</li><li>Excellent attention to detail and commitment to quality</li><li>Strong communication and collaboration skills</li><li>Ability to operate multiple CMMs during a shift</li></ul><p><strong>Preferred Qualifications</strong></p><ul><li>Certification in Metrology, ASQ, or Six Sigma methodologies</li><li>Experience with laser scanners, optical comparators, or other advanced metrology tools</li><li><span style="color: rgb(8, 7, 7); background-color: none;">Background</span> in casting and machining environments</li><li>Knowledge of SPC and data-driven quality control practices</li></ul><p><strong>Work Environment</strong></p><p>90% of work is performed in a clean, air-conditioned quality lab equipped with multiple CMMs</p><p>CNC machine shop environment with multiple departments under one roof</p><p>No mandatory overtime; unpaid lunch break included</p><h1><br></h1>

<p><strong>Description</strong></p>
					<p>We are seeking an experienced CNC Programmer with expertise in MazaCAM programming for Mazak QTE-300M SG and Mazak QT-450M machines. The ideal candidate will have strong programming skills, hands-on machining experience, and the ability to optimize processes for efficiency and precision.</p>
					<p><strong>Skills</strong></p>
					<p>cnc programming, cnc machining, lathe setup, lathe programming, lathe operation, mazak lathe, cad/cam</p>
					<p><strong>Top Skills Details</strong></p>
					<p>cnc programming,cnc machining,lathe setup,lathe programming,lathe operation,mazak lathe,cad/cam</p>
					<p><strong>Additional Skills &amp; Qualifications</strong></p>
					<p>•	Proven experience in CNC programming with MazaCAM for Mazak QTE-300M SG and Mazak QT-450M.
•	Strong knowledge of GD&amp;T.
•	Strong knowledge of Mazak controls, tooling, and machining best practices.
•	Ability to read and interpret blueprints, GD&amp;T, and technical drawings.
•	Experience with CNC lathe setup, troubleshooting, and process optimization.
•	Willingness and ability to travel to Italy one week per month.
•	Strong problem-solving skills and attention to detail.
•	Ability to work independently and within a team environment.</p>
					<p><strong>Experience Level</strong></p>
					<p>Intermediate Level</p>

Cnc Machinist And Programmer

<h1 style="font-weight: 700;">Job Title: Programmer</h1><br><h2>Job Description</h2><p>We are seeking a skilled programmer proficient in utilizing the latest SolidWorks 3D solid modeling software for fixture and tooling design. The ideal candidate will have a foundational understanding of GD &amp; T and the ability to create or modify CNC programs for manufacturing purposes. This role involves supporting the development and introduction of new products into manufacturing, developing routings using the current ERP system, and designing work holding and cutting tool technology to enhance machine performance.</p><br><h2>Responsibilities</h2><ul><li>Utilize SolidWorks 3D solid modeling software for fixture and tooling design.</li><li>Create or modify CNC programs for manufacturing processes.</li><li>Support the development and introduction of new products into manufacturing.</li><li>Develop routings using the current ERP system.</li><li>Design work holding and cutting tool technology to improve machine performance.</li><li>Provide support in developing new CNC machine tool requirements.</li><li>Work closely with operators and engineers to troubleshoot CNC programs and machining operations.</li><li>Support new capital projects.</li></ul><h2>Essential Skills</h2><ul><li>Proficiency in SolidWorks and/or MasterCAM.</li><li>Experience in machining and fabrication.</li><li>2+ years of experience with a 2-year degree in Engineering or similar, or 5+ years with no degree.</li><li>Ability to utilize Microsoft Office programs such as Word and Excel.</li><li>Proficiency with the latest Mastercam CAM software for CNC program creation and verification.</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>Self-starter with the ability and desire to continuously improve skills.</li></ul><h2>Work Environment</h2><p>This position is for the 2nd shift with working hours from 3 PM to 1 AM or 1 PM to 11 PM, Monday through Thursday. The role reports to the ME and Engineering Manager.</p><br>

Cnc Programmer

<h1><strong>Job Title: Sheet Metal Machine Programmer - CNC Programmer</strong></h1><p><strong>Irving, TX</strong></p><p><br></p><h2>Job Description</h2><p>We are seeking an experienced Sheet Metal Machine Programmer to become an integral part of our fabrication team. This role is centered around creating precise CNC programs for laser cutting, punching, tube laser, and bending machines using Trumpf TruTops Boost. The ideal candidate will excel in reading engineering drawings, selecting appropriate tooling, and determining optimal bend sequences. A comprehensive understanding of sheet metal fabrication processes and material optimization is crucial. You will collaborate closely with engineers and operators to troubleshoot issues, enhance workflow, and support production efficiency in a dynamic environment.</p><p><br></p><h2>Responsibilities</h2><ul><li>Utilize Trumpf TruTops Boost to calculate bend deductions and create flat patterns for accurate preparation of parts for punch, lasers, and press brakes.</li><li>Develop CNC programs for laser cutting, punching, tube laser, and bending machines using Trumpf TruTops Boost.</li><li>Select appropriate tooling based on material type and thickness.</li><li>Determine proper brake tooling and bend sequences.</li><li>Read and interpret engineering drawings and work orders.</li><li>Collaborate with team members to optimize productivity.</li><li>Demonstrate strong attention to detail and ability to follow instructions accurately.</li><li>Troubleshoot issues related to CAD/CAM outputs, nesting errors, and machine compatibility.</li><li>Complete work accurately and in a timely manner with attention to detail.</li></ul><h2>Essential Skills</h2><ul><li>5+ years experience in sheet metal fabrication operations such as experience in Punch, Laser, Panel Bender, Tube Laser, Brake Press.</li><li>3+ years of experience with programming sheet metal fabrication machines using Trumpf TruTops Boost software (preferred) or similar CNC software.</li><li>Familiarity with MRP/ERP software for fabrication workflows.</li><li>Demonstrated ability to read blueprints and develop optimal tool paths and setups with high accuracy and attention to maximum material utilization.</li><li>Excellent oral and written communication skills.</li><li>Ability to multi-task in a fast-paced team-oriented manufacturing environment.</li><li>Strong problem-solving skills.</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>Nesting experience is a plus.</li></ul><h2>Work Environment</h2><p>The position is based in an office environment with scheduled time on the factory floor for collaboration meetings. The role is expected to work 40 hours per week, with flexible start time schedules available.</p>

<h1><strong>Job Title: CNC Programmer</strong></h1><p><strong>Irving, TX</strong></p><p><br></p><h2>Job Description</h2><p>We are seeking an experienced CNC Programmer to become an integral part of our fabrication team. This role is centered around creating precise CNC programs for laser cutting, punching, tube laser, and bending machines using Trumpf TruTops Boost. The ideal candidate will excel in reading engineering drawings, selecting appropriate tooling, and determining optimal bend sequences. A comprehensive understanding of sheet metal fabrication processes and material optimization is crucial. You will collaborate closely with engineers and operators to troubleshoot issues, enhance workflow, and support production efficiency in a dynamic environment.</p><p><br></p><h2>Responsibilities</h2><ul><li>Utilize Trumpf TruTops Boost to calculate bend deductions and create flat patterns for accurate preparation of parts for punch, lasers, and press brakes.</li><li>Develop CNC programs for laser cutting, punching, tube laser, and bending machines using Trumpf TruTops Boost.</li><li>Select appropriate tooling based on material type and thickness.</li><li>Determine proper brake tooling and bend sequences.</li><li>Read and interpret engineering drawings and work orders.</li><li>Collaborate with team members to optimize productivity.</li><li>Demonstrate strong attention to detail and ability to follow instructions accurately.</li><li>Troubleshoot issues related to CAD/CAM outputs, nesting errors, and machine compatibility.</li><li>Complete work accurately and in a timely manner with attention to detail.</li></ul><h2>Essential Skills</h2><ul><li>5+ years experience in sheet metal fabrication operations such as experience in Punch, Laser, Panel Bender, Tube Laser, Brake Press.</li><li>3+ years of experience with programming sheet metal fabrication machines using Trumpf TruTops Boost software (preferred) or similar CNC software.</li><li>Familiarity with MRP/ERP software for fabrication workflows.</li><li>Demonstrated ability to read blueprints and develop optimal tool paths and setups with high accuracy and attention to maximum material utilization.</li><li>Excellent oral and written communication skills.</li><li>Ability to multi-task in a fast-paced team-oriented manufacturing environment.</li><li>Strong problem-solving skills.</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>Nesting experience is a plus.</li></ul><h2>Work Environment</h2><p>The position is based in an office environment with scheduled time on the factory floor for collaboration meetings. The role is expected to work 40 hours per week, with flexible start time schedules available.</p>

<h1><strong>Job Title: CNC Programmer</strong></h1><p><br></p><h2>Job Description</h2><p>We are seeking an experienced CNC Programmer with a deep understanding of Makino’s Modular Machining Complex (MMC2) technology and modular automated material handling systems. The ideal candidate should possess knowledge of Fanuc Macros and be adept at using machine variables in NC Programs. A full understanding of advanced CNC editing and programming, including CAM programming with software such as Surf cam, UG/NX, and Mastercam, is essential.</p><p><br></p><h2>Responsibilities</h2><ul><li>Coordinate schedules and set up CNC machines and manufacturing cells to meet production demands.</li><li>Document setups and train personnel on the proper setup and operation of jobs.</li><li>Maintain heightened awareness of project schedules and ensure jobs are set up and run according to project deadlines and budget performance.</li><li>Anticipate and mitigate obstacles in the setup and operation of jobs.</li></ul><h2>Essential Skills</h2><ul><li>Minimum of 5 years of programming and setting up horizontal and vertical CNC machines.</li><li>Strong knowledge of shop skills and shop environment.</li><li>Ability to work with minimal supervision and follow-up.</li><li>Strong math skills.</li><li>Understanding of ISO Quality Policies and ability to operate within its framework.</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>Knowledge of automotive aftermarket products.</li><li>Proficiency in Renishaw probing routines.</li><li>Lean manufacturing skills.</li><li>Experience with shop floor inspection tools.</li><li>Good communication skills and team-oriented mindset.</li><li>Experience in investigating and analyzing non-conformances.</li><li>Commitment to pursuing zero defects.</li></ul><h2>Work Environment</h2><p>The work environment is a shop setting where the candidate will be expected to demonstrate strong shop skills. The position requires good attendance and punctuality, as well as the ability to work well with others to maximize productivity. The candidate must be self-starting, motivated, and able to work with minimal supervision. A proactive approach to tasks and a focus on maintaining project schedules and deadlines are crucia</p>

<h1><strong>Job Title: Sheet Metal Machine Programmer - CNC Programmer</strong></h1><p><strong><u>Dallas or Midland, Texas</u></strong></p><p><br></p><h2>Job Description</h2><p>We are seeking an experienced Sheet Metal Machine Programmer to become an integral part of our fabrication team. This role is centered around creating precise CNC programs for laser cutting, punching, tube laser, and bending machines using Trumpf TruTops Boost. The ideal candidate will excel in reading engineering drawings, selecting appropriate tooling, and determining optimal bend sequences. A comprehensive understanding of sheet metal fabrication processes and material optimization is crucial. You will collaborate closely with engineers and operators to troubleshoot issues, enhance workflow, and support production efficiency in a dynamic environment.</p><p><br></p><h2>Responsibilities</h2><ul><li>Utilize Trumpf TruTops Boost to calculate bend deductions and create flat patterns for accurate preparation of parts for punch, lasers, and press brakes.</li><li>Develop CNC programs for laser cutting, punching, tube laser, and bending machines using Trumpf TruTops Boost.</li><li>Select appropriate tooling based on material type and thickness.</li><li>Determine proper brake tooling and bend sequences.</li><li>Read and interpret engineering drawings and work orders.</li><li>Collaborate with team members to optimize productivity.</li><li>Demonstrate strong attention to detail and ability to follow instructions accurately.</li><li>Troubleshoot issues related to CAD/CAM outputs, nesting errors, and machine compatibility.</li><li>Complete work accurately and in a timely manner with attention to detail.</li></ul><h2>Essential Skills</h2><ul><li>5+ years experience in sheet metal fabrication operations such as experience in Punch, Laser, Panel Bender, Tube Laser, Brake Press.</li><li>3+ years of experience with programming sheet metal fabrication machines using Trumpf TruTops Boost software (preferred) or similar CNC software.</li><li>Familiarity with MRP/ERP software for fabrication workflows.</li><li>Demonstrated ability to read blueprints and develop optimal tool paths and setups with high accuracy and attention to maximum material utilization.</li><li>Excellent oral and written communication skills.</li><li>Ability to multi-task in a fast-paced team-oriented manufacturing environment.</li><li>Strong problem-solving skills.</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>Nesting experience is a plus.</li></ul><h2>Work Environment</h2><p>The position is based in an office environment with scheduled time on the factory floor for collaboration meetings. The role is expected to work 40 hours per week, with flexible start time schedules available.</p>

<h1 style="font-weight: 700;">Job Title: Color Laboratory Technician</h1><br><h2>Job Description</h2><p>We are seeking a skilled Color Laboratory Technician to join our team. This role requires expertise in color matching, formulating, and designing various resins, including olefins, engineering resins, glass-filled, and high-heat resins. The ideal candidate will have prior experience in a color house, with a preference for those with pellet master batch formulation experience. Candidates with liquid color formulation experience may also be considered with additional training.</p><br><h2>Responsibilities</h2><ul><li>Match colors accurately and formulate designs for various resins.</li><li>Perform quality control and quality assurance tasks.</li><li>Conduct laboratory tests and inspections to ensure high standards.</li><li>Collaborate with production, sales, and customer service teams.</li><li>Operate small-scale molding machines and weigh small amounts of pigments.</li><li>Work independently while effectively contributing to team efforts.</li></ul><h2>Essential Skills</h2><ul><li>Expertise in color matching and chemistry.</li><li>Basic math skills.</li><li>Ability to pass a color test.</li><li>Operation of small-scale molding machines.</li><li>Quality control and quality assurance experience.</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>College-level education in polymer science and color theory is preferred.</li><li>Minimum of 2 years of experience, but 1 year may be considered for a strong candidate.</li><li>Experience in extrusion and screen printing is beneficial.</li></ul><h2>Work Environment</h2><p>The position is based in a laboratory setting. The working hours are from 6 AM to 4:30 PM, Monday through Friday, with occasional overtime as needed.</p><br>

Color Laboratory Technician

<h1><strong>Quality Control - Roof Observer</strong></h1><p><br></p><h2>Job Description</h2><p>The Roof Observer will maintain a presence at the construction site to ensure and confirm that the roofing contractor is compliant with the contract documents, approved submittals, schedule, and safety procedures. The Roof Observer is responsible for completing daily quality and safety reports among other submittals throughout the week.</p><p><br></p><h2>Responsibilities</h2><ul><li>Maintain a presence at the construction site and interact daily with roofing contractors and client representatives, coordinating site requirements per job specifications.</li><li>Take photographs of job-site progress and provide daily documentation and reporting.</li><li>Ensure the roofing contractor&#39;s compliance with the contract documents.</li><li>Complete and submit daily quality and safety reports.</li><li>Inform the Interstate Project Manager of quality issues and safety violations by the contractor.</li><li>Ensure incomplete work is finished prior to the final inspection.</li></ul><h2>Essential Skills</h2><ul><li>Proficiency in Excel and Microsoft Office.</li><li>Experience in Roofing Inspection and Quality Control.</li><li>Ability to coordinate projects efficiently.</li><li>Minimum of 2 years experience with residential or commercial roofing, including demo, inspection, or shingling.</li><li>At least 1 year experience using an iPad.</li></ul><h2><br></h2>

Commercial Roofer

<h1><strong>Job Title: Commercial Construction Superintendent</strong></h1><p><br></p><h2>Job Description</h2><p>We are seeking an experienced Superintendent to join our team for several basebuild projects this summer, with project sizes ranging from $4-10 million including site-work packages. The ideal candidate will have experience with public infrastructure projects such as police and fire stations, libraries, schools, and government offices.</p><p><br></p><h2>Responsibilities</h2><ul><li>Plan, organize, and direct activities related to the construction and maintenance of structures, facilities, and systems.</li><li>Study job specifications to determine appropriate construction methods, time, and costs.</li><li>Prepare contracts and negotiate revisions, changes, and additions to contractual agreements with architects, consultants, clients, subcontractors, and suppliers.</li><li>Obtain all necessary permits and licenses.</li><li>Schedule projects in logical steps and budget time required to meet deadlines.</li><li>Explain plans and contract terms to field personnel, administrative staff, and other Superintendents, Laborers, and Carpenters.</li><li>Inspect and review projects to monitor compliance with building and safety codes and other regulations.</li><li>Confer with supervisory personnel, owners, contractors, and design professionals to discuss and resolve complaints and problems as necessary.</li><li>Plan long-term project goals and verify that schedules are met and quality control is maintained.</li><li>Assist co-workers in any additional tasks to help meet the company&#39;s overall business objectives.</li><li>Apply knowledge of company policies, standards, and procedures.</li><li>Utilize company equipment, applications, and resources effectively.</li><li>Understand the AIA 17 division breakdown.</li><li>Apply principles of strategic planning, resource allocation, and leadership in business and management.</li></ul><h2>Essential Skills</h2><ul><li>10+ years of experience in the construction field with at least 6 years in a Superintendent role.</li><li>Experience managing both large and small projects averaging $3-5 million.</li><li>Experience with ground-up construction and commercial construction.</li><li>Proficiency in reading and interpreting blueprints.</li><li>Ability to manage multiple projects ranging from 2 to 14 projects at one time depending on size.</li><li>Strong scheduling and project management skills.</li><li>Experience working with subcontractors and handling change orders.</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>Knowledge of building and safety codes.</li><li>Ability to resolve complaints and problems.</li><li>Experience with strategic planning and resource allocation.</li><li>Strong leadership and team management skills.</li></ul><h2>Work Environment</h2><p>The Superintendent will manage on-site projects and oversee other team members. The role involves direct management of project activities and ensuring compliance with all relevant codes and standards. The work environment is collaborative with a strong office culture and support team. This role offers a great opportunity for advancement within the team, working on local projects with long-term client relationships.</p>

Commerical Construction Superintendent

<p><strong>Description</strong></p>
					<p>This Client is seeking commissioning engineer with a mechanical <span style="color: rgb(8, 7, 7); background-color: none;"><span style="color: rgb(8, 7, 7); background-color: none;"><span style="color: rgb(8, 7, 7); background-color: none;"><span style="color: rgb(8, 7, 7); background-color: none;"><span style="color: rgb(8, 7, 7); background-color: none;"><span style="color: rgb(8, 7, 7); background-color: none;"><span style="color: rgb(8, 7, 7); background-color: none;"><span style="color: rgb(8, 7, 7); background-color: none;"><span style="color: rgb(8, 7, 7); background-color: none;"><span style="color: rgb(8, 7, 7); background-color: none;"><span style="color: rgb(8, 7, 7); background-color: none;"><span style="color: rgb(8, 7, 7); background-color: none;"><span style="color: rgb(8, 7, 7); background-color: none;"><span style="color: rgb(8, 7, 7); background-color: none;">background</span></span></span></span></span></span></span></span></span></span></span></span></span></span> that has experience within datacenters markets and able to help carry out project assignments.
  Experience working within the following vertical markets:  Hospitals, Large / Complex Facilities and Mission Critical Facilities (data centers, telecommunications, or disaster recovery sites)
  Participate in daily commissioning activity meetings which services include:
•       Equipment pre-start-up procedures; Development of standard operating procedures (SOP&#39;s) and Methods of Procedures (MOPs); Comprehensive Commissioning documentation;
•       Prepare commissioning test procedures and reports
•       Develop and maintain commissioning logs, equipment checklist, and other tools to track commissioning projects
•       Write comprehensive reports which include the following sections: recommendations for optimizing building operations, functional checklists, list of deficiencies, equipment operation and maintenance manuals
•       Review design criteria, specifications, drawings, equipment submittals, and other documentation pertinent to commissioning
•       Develop and administer functional tests for various systems, such as mechanical central chilled water plants, packaged rooftop units, boilers, chillers, computer room air conditioning units, fire protection systems, etc. 
•       Integrated system testing; Building management system testing; Compilation of all testing procedure results</p>
					<p><strong>Skills</strong></p>
					<p>Construction, Commissioning, Control system, Engineering, mechanical design, mechanical engineering, mechanical equipment</p>
					<p><strong>Top Skills Details</strong></p>
					<p>Construction,Commissioning</p>
					<p><strong>Additional Skills &amp; Qualifications</strong></p>
					<p>  Minimum 10 years’ experience in the Electrical Mission Critical Field
  Bachelor&#39;s / Associates Degree as an Mechanical Engineer a plus
  A/E experience working in complex facilities or mission-critical projects a big plus
  Good communication skills, Interface with clients, contractors, equipment vendors, and owners agents as needed; Execute project assignments; Interface with project contractors, vendors, and testing technicians; Interact with all facets of the company: engineering, design, etc
  Experience with IEEE procedures and protocols a plus
  Possess basic knowledge of system design
  Commissioning certification or PE
  OSHA 10/30 certification a plus</p>
					<p><strong>Experience Level</strong></p>
					<p>Intermediate Level</p>

Commissioning Engineer

<h1><strong>Job Title: Commissioning Engineering Technician</strong></h1><p><br></p><h2>Job Description</h2><p>As a Commissioning Engineering Technician, you will work both individually and collaboratively within teams to support capital projects and implement solutions. Your role will be pivotal in helping clients make critical changes to enhance performance and achieve their most significant goals. You will coordinate schedules, manage commissioning constraints, integrate construction schedules, and provide comprehensive reports and updates.</p><p><br></p><h2>Responsibilities</h2><ul><li>Coordinate operations technicians&#39; work schedules and manpower forecasts.</li><li>Manage and track commissioning constraints and deficiencies related to schedule or quality of Basebuild utility systems post-construction.</li><li>Integrate construction and design schedules with commissioning activities.</li><li>Provide reports and updates on schedule and quality metrics.</li><li>Conduct system and facility engineering assessments.</li><li>Troubleshoot and perform root cause failure analysis on assigned projects.</li><li>Train suppliers in commissioning software systems.</li><li>Provide and manage supplier access to commissioning software systems.</li><li>Interface smoothly with engineering design team members and client representatives.</li></ul><h2>Essential Skills</h2><ul><li>2+ years of experience in commissioning or construction for I&amp;C or Electrical Basebuild systems in the Advanced Technology sector.</li><li>Experience with Rockwell Automation, PLC5, and Control Logix hardware and software.</li><li>Experience with multi-discipline large capital projects involving Owners, General Contractors, Contractors, and System Integrators.</li><li>Understanding of Design/Build (Engineering and Construction).</li><li>Understanding of complex process systems architecture and design, Instrumentation, Device Selection, Networking, PLC &amp; I/O architectures, P&amp;IDs, data sheets, and SCADA.</li><li>Working knowledge of environments common in large industrial applications such as Dry/Wet Mechanical, AWN, Gas/Chem Distribution, HVAC, and Clean Room environmental control.</li><li>Proficiency in control systems programming and configuration.</li><li>Strong understanding of HVAC, electrical, and building automation systems.</li><li>Ability to read and interpret technical drawings and schematics.</li><li>Experience conducting I/O checkouts.</li><li>Minimum of 3 years of experience working with control systems in a data center or similar environment.</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>Bachelor’s degree in electrical, mechanical, chemical engineering, or similar technical field preferred.</li><li>Associate&#39;s degree or technical certification in electrical, mechanical, or control systems engineering or a related field. Direct experience will be considered in lieu of degree.</li><li>Familiarity with various control system platforms; BMS (Building Management Systems) or SCADA is a plus.</li><li>Excellent problem-solving and analytical skills.</li><li>Strong communication and teamwork abilities.</li><li>Attention to detail and a proactive approach to work.</li></ul><h2>Work Environment</h2><p>The role is based onsite in Reno,  with a work schedule of 50 hours per week. Per diem is included for onsite work.</p>

Commissioning Engineering Technician

<h1><strong>Job Title: Commissioning Engineering Technician</strong></h1><p><br></p><h2>Job Description</h2><p>As a Commissioning Engineering Technician, you will work both individually and collaboratively within teams to support capital projects and implement solutions. Your role will be pivotal in helping clients make critical changes to enhance performance and achieve their most significant goals. You will coordinate schedules, manage commissioning constraints, integrate construction schedules, and provide comprehensive reports and updates.</p><p><br></p><h2>Responsibilities</h2><ul><li>Coordinate operations technicians&#39; work schedules and manpower forecasts.</li><li>Manage and track commissioning constraints and deficiencies related to schedule or quality of Basebuild utility systems post-construction.</li><li>Integrate construction and design schedules with commissioning activities.</li><li>Provide reports and updates on schedule and quality metrics.</li><li>Conduct system and facility engineering assessments.</li><li>Troubleshoot and perform root cause failure analysis on assigned projects.</li><li>Train suppliers in commissioning software systems.</li><li>Provide and manage supplier access to commissioning software systems.</li><li>Interface smoothly with engineering design team members and client representatives.</li></ul><h2>Essential Skills</h2><ul><li>2+ years of experience in commissioning or construction for I&amp;C or Electrical Basebuild systems in the Advanced Technology sector.</li><li>Experience with Rockwell Automation, PLC5, and Control Logix hardware and software.</li><li>Experience with multi-discipline large capital projects involving Owners, General Contractors, Contractors, and System Integrators.</li><li>Understanding of Design/Build (Engineering and Construction).</li><li>Understanding of complex process systems architecture and design, Instrumentation, Device Selection, Networking, PLC &amp; I/O architectures, P&amp;IDs, data sheets, and SCADA.</li><li>Working knowledge of environments common in large industrial applications such as Dry/Wet Mechanical, AWN, Gas/Chem Distribution, HVAC, and Clean Room environmental control.</li><li>Proficiency in control systems programming and configuration.</li><li>Strong understanding of HVAC, electrical, and building automation systems.</li><li>Ability to read and interpret technical drawings and schematics.</li><li>Experience conducting I/O checkouts.</li><li>Minimum of 3 years of experience working with control systems in a data center or similar environment.</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>Bachelor’s degree in electrical, mechanical, chemical engineering, or similar technical field preferred.</li><li>Associate&#39;s degree or technical certification in electrical, mechanical, or control systems engineering or a related field. Direct experience will be considered in lieu of degree.</li><li>Familiarity with various control system platforms; BMS (Building Management Systems) or SCADA is a plus.</li><li>Excellent problem-solving and analytical skills.</li><li>Strong communication and teamwork abilities.</li><li>Attention to detail and a proactive approach to work.</li></ul><h2>Work Environment</h2><p>The role is based onsite in Abilene,  with a work schedule of 50 hours per week. Per diem is included for onsite work.</p>

<hr><h2><strong>&#128640; Job Opening: PLC Commissioning Engineering Technician</strong></h2><h2><strong>&#128205;<em>Location: Abilene, TX</em></strong></h2><p><strong>&#128295;<em>Industry: Advanced Technology | Automation | Controls</em></strong></p><p><strong><em>     Shift: 10 days on, 4 days off with opportunity for overtime</em></strong></p><p><strong>     <em>Per Diem offered </em></strong></p><hr><h3>About the Role</h3><p>Are you passionate about automation, innovation, and solving complex technical challenges? As a PLC Commissioning Engineering Technician, you’ll be at the forefront of cutting-edge capital projects—working hands-on with advanced control systems to help clients optimize performance and achieve mission-critical goals. You’ll collaborate with cross-functional teams, troubleshoot real-world issues, and bring high-tech systems to life. If you thrive in fast-paced environments and love turning plans into reality, this role is for you.</p><hr><h3>What You’ll Do</h3><ul><li>&#128467;️ Coordinate work schedules and manpower forecasts for operations teams.</li><li>&#128736;️ Manage commissioning constraints and resolve post-installation issues in Basebuild utility systems.</li><li>&#128260; Integrate construction and design timelines with commissioning milestones.</li><li>&#128202; Deliver clear reports and updates on schedule and quality metrics.</li><li>&#128119; Conduct on-site system and facility assessments.</li><li>&#128269; Perform root cause analysis and troubleshoot system failures.</li><li>&#129504; Train suppliers on commissioning software and manage access.</li><li>&#129309; Collaborate with engineering teams and client stakeholders.</li></ul><hr><h3>What You Bring</h3><ul><li>✅ 2+ years of hands-on experience in commissioning or construction for Instrumentation &amp; Control (I&amp;C) or Electrical Basebuild systems.</li><li>&#129520; Proficiency with Rockwell Automation, PLC5, and ControlLogix platforms.</li><li>&#127959;️ Experience with large-scale capital projects involving multiple stakeholders.</li><li>&#129504; Strong grasp of Design/Build processes and complex process system architecture.</li><li>&#128208; Deep understanding of P&amp;IDs, device selection, SCADA, and I/O architectures.</li><li>&#127777;️ Familiarity with industrial environments: HVAC, gas/chemical distribution, clean rooms, and more.</li><li>&#128483;️ Excellent communication skills—both written and verbal.</li></ul><hr><h3>Preferred Qualifications</h3><ul><li>&#127891; Bachelor’s degree in Electrical, Mechanical, or Chemical Engineering (or related field).</li><li>&#127891; Associate’s degree or technical certification in control systems or electrical/mechanical engineering.</li><li>&#128421;️ 3+ years working with control systems in data centers or similar environments.</li><li>&#128161; Experience with BMS, SCADA, and conducting I/O checkouts.</li><li>&#129513; Strong analytical and problem-solving skills.</li><li>&#129309; Team player with a proactive mindset and attention to detail.</li></ul><hr><h3>Why Join Us?</h3><h1>You’ll be part of a forward-thinking team that values innovation, precision, and collaboration. This is more than a job—it’s a chance to shape the future of automation and technology.</h1>

<p style="text-align: center;"><strong>*If interested in this role, please contact Kyle McLean at kymclean@actalentservices.com*</strong></p><p style="text-align: center;"><br></p><h2><strong>Commissioning Controls Technician - Abilene TX (If you are not local, per diem is included)</strong></h2><p>Overview:</p><h3>Seeking a detail-oriented Commissioning Engineer to support scheduling, quality assurance, and system integration for Basebuild utility systems. This role involves coordinating commissioning activities, troubleshooting system issues, and interfacing with design and construction teams.</h3><h3>Key Responsibilities:</h3><ul><li>Coordinate technician schedules and manpower forecasts</li><li>Track and resolve commissioning constraints and deficiencies</li><li>Integrate construction/design schedules with commissioning timelines</li><li>Conduct system walkdowns and root cause failure analysis</li><li>Train and manage supplier access in commissioning software</li><li>Generate reports on schedule and quality metrics</li><li>Collaborate with engineering teams and client representatives</li></ul><hr><h3>Qualifications:</h3><ul><li>2+ years in commissioning or construction (I&amp;C or Electrical systems)</li><li>Experience with Rockwell Automation, PLC5, and Control Logix</li><li>Familiarity with large capital projects and multi-discipline teams</li><li>Strong understanding of process systems, P&amp;IDs, SCADA, and BMS</li><li>Proficient in reading technical drawings and conducting I/O checkouts</li><li>Excellent communication, problem-solving, and teamwork skills</li></ul><hr><h3>Preferred:</h3><ul><li>Bachelor’s or Associate’s degree in engineering or related field</li><li>3+ years working with control systems in data centers or similar environments</li></ul><p> </p>

Commissioning Engineering Techs

<hr><h3>&#128640; Job Opening: PLC Commissioning Engineering Technician</h3><p>&#128205;<em>Location: Abilene, TX</em></p><p>&#128295;<em>Industry: Advanced Technology | Automation | Controls</em></p><p><em>     Shift: 10 days on, 4 days off with opportunity for overtime</em></p><p>Must have OSHA Cert</p><p>Per Diem offered </p><hr><h3>About the Role</h3><p>Are you passionate about automation, innovation, and solving complex technical challenges? As a PLC Commissioning Engineering Technician, you’ll be at the forefront of cutting-edge capital projects—working hands-on with advanced control systems to help clients optimize performance and achieve mission-critical goals.</p><p>You’ll collaborate with cross-functional teams, troubleshoot real-world issues, and bring high-tech systems to life. If you thrive in fast-paced environments and love turning plans into reality, this role is for you.</p><hr><h3>What You’ll Do</h3><ul><li>&#128467;️ Coordinate work schedules and manpower forecasts for operations teams.</li><li>&#128736;️ Manage commissioning constraints and resolve post-installation issues in Basebuild utility systems.</li><li>&#128260; Integrate construction and design timelines with commissioning milestones.</li><li>&#128202; Deliver clear reports and updates on schedule and quality metrics.</li><li>&#128119; Conduct on-site system and facility assessments.</li><li>&#128269; Perform root cause analysis and troubleshoot system failures.</li><li>&#129504; Train suppliers on commissioning software and manage access.</li><li>&#129309; Collaborate with engineering teams and client stakeholders.</li></ul><hr><h3>What You Bring</h3><ul><li>✅ 2+ years of hands-on experience in commissioning or construction for Instrumentation &amp; Control (I&amp;C)or Electrical Basebuild systems.</li><li>&#129520; Proficiency with Rockwell Automation,PLC5, and ControlLogix platforms.</li><li>&#127959;️ Experience with large-scale capital projects involving multiple stakeholders.</li><li>&#129504; Strong grasp of Design/Build processes and complex process system architecture.</li><li>&#128208; Deep understanding of P&amp;IDs, device selection, SCADA, and I/O architectures.</li><li>&#127777;️ Familiarity with industrial environments: HVAC, gas/chemical distribution, clean rooms, and more.</li><li>&#128483;️ Excellent communication skills—both written and verbal.</li></ul><hr><h3>Preferred Qualifications</h3><ul><li>&#127891; Bachelor’s degree in Electrical, Mechanical, or Chemical Engineering (or related field).</li><li>&#127891; Associate’s degree or technical certification in control systems or electrical/mechanical engineering.</li><li>&#128421;️ 3+ years working with control systems in data centers or similar environments.</li><li>&#128161; Experience with BMS, SCADA, and conducting I/O checkouts.</li><li>&#129513; Strong analytical and problem-solving skills.</li><li>&#129309; Team player with a proactive mindset and attention to detail.</li></ul><hr><h3>Why Join Us?</h3><h1>You’ll be part of a forward-thinking team that values innovation, precision, and collaboration. This is more than a job—it’s a chance to shape the future of automation and technology.</h1>

<hr><h3>&#128640; Job Opening: PLC Commissioning Engineering Technician</h3><p>&#128205;<em>Location: Abilene, TX</em></p><p>&#128295;<em>Industry: Advanced Technology | Automation | Controls</em></p><p><em>     Shift: 10 days on, 4 days off with opportunity for overtime</em></p><p>Per Diem offered </p><hr><h3>About the Role</h3><p>Are you passionate about automation, innovation, and solving complex technical challenges? As a PLC Commissioning Engineering Technician, you’ll be at the forefront of cutting-edge capital projects—working hands-on with advanced control systems to help clients optimize performance and achieve mission-critical goals.</p><p>You’ll collaborate with cross-functional teams, troubleshoot real-world issues, and bring high-tech systems to life. If you thrive in fast-paced environments and love turning plans into reality, this role is for you.</p><hr><h3>What You’ll Do</h3><ul><li>&#128467;️ Coordinate work schedules and manpower forecasts for operations teams.</li><li>&#128736;️ Manage commissioning constraints and resolve post-installation issues in Basebuild utility systems.</li><li>&#128260; Integrate construction and design timelines with commissioning milestones.</li><li>&#128202; Deliver clear reports and updates on schedule and quality metrics.</li><li>&#128119; Conduct on-site system and facility assessments.</li><li>&#128269; Perform root cause analysis and troubleshoot system failures.</li><li>&#129504; Train suppliers on commissioning software and manage access.</li><li>&#129309; Collaborate with engineering teams and client stakeholders.</li></ul><hr><h3>What You Bring</h3><ul><li>✅ 2+ years of hands-on experience in commissioning or construction for Instrumentation &amp; Control (I&amp;C)or Electrical Basebuild systems.</li><li>&#129520; Proficiency with Rockwell Automation,PLC5, and ControlLogix platforms.</li><li>&#127959;️ Experience with large-scale capital projects involving multiple stakeholders.</li><li>&#129504; Strong grasp of Design/Build processes and complex process system architecture.</li><li>&#128208; Deep understanding of P&amp;IDs, device selection, SCADA, and I/O architectures.</li><li>&#127777;️ Familiarity with industrial environments: HVAC, gas/chemical distribution, clean rooms, and more.</li><li>&#128483;️ Excellent communication skills—both written and verbal.</li></ul><hr><h3>Preferred Qualifications</h3><ul><li>&#127891; Bachelor’s degree in Electrical, Mechanical, or Chemical Engineering (or related field).</li><li>&#127891; Associate’s degree or technical certification in control systems or electrical/mechanical engineering.</li><li>&#128421;️ 3+ years working with control systems in data centers or similar environments.</li><li>&#128161; Experience with BMS, SCADA, and conducting I/O checkouts.</li><li>&#129513; Strong analytical and problem-solving skills.</li><li>&#129309; Team player with a proactive mindset and attention to detail.</li></ul><hr><h3>Why Join Us?</h3><h1>You’ll be part of a forward-thinking team that values innovation, precision, and collaboration. This is more than a job—it’s a chance to shape the future of automation and technology.</h1>

<h1 style="font-weight: 700;">Job Title: Commissioning Manager</h1><br><h2>Job Description</h2><p>This role requires 100% travel and commitment to one site, primarily new build data centers located mostly in the Southeast. The position involves managing electrical and specialty systems QAQC and commissioning scopes of work, as well as overseeing commissioning and startup schedules.</p><br><h2>Responsibilities</h2><ul><li>Develop and manage QAQC and commissioning scopes, schedules, and budgets.</li><li>Review outgoing QAQC and commissioning estimates with the Estimating Department for accuracy.</li><li>Utilize internal functional groups and monitor progress of project deliverables.</li><li>Develop and implement QAQC and commissioning safety plans in collaboration with internal safety departments.</li><li>Ensure startup and operational procedures are executed safely and comply with client specifications.</li><li>Coordinate daily, weekly, and monthly meetings related to QAQC, commissioning, equipment, coordination, scheduling, staffing, and project management.</li><li>Manage QAQC and commissioning issues logs and coordinate with affected parties to resolve issues.</li><li>Work with third-party testing and commissioning agencies to ensure proper coverage during procedures.</li><li>Collaborate with Human Resources on recruiting, selection, and employee relations.</li><li>Coach and develop managerial talent and effectively select and train individuals.</li><li>Create a supportive environment that encourages learning from mistakes and provides constructive feedback.</li></ul><h2>Essential Skills</h2><ul><li>Proficiency in Microsoft Office Suite and Google G-Suite.</li><li>Knowledge of the electrical construction trade.</li><li>Experience in industrial or data center commissioning.</li><li>Bachelor’s Degree in Engineering, Construction Management, or equivalent technical training/experience.</li><li>5 years of experience in Project Management, Construction Management, Project Engineering, or Commissioning Management.</li><li>8 years of experience in commissioning/start-up for electrical and/or mechanical systems.</li><li>Experience leading commissioning/start-up activities for projects exceeding $25MM in contract value.</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>Experience in Mission Critical, Industrial, and Commercial sectors.</li><li>Experience as an electrician, engineer, technician, or similar role in oil and gas industry.</li></ul><h2>Work Environment</h2><p>The position requires extensive travel and commitment to project sites. A car allowance or rental car/flights are provided. The role involves working with a commissioning team on new build data center projects scattered across various locations, primarily in the Southeast.</p><br>

Commissioning Manager

<p><strong>Job Title: </strong>Technical Writer – Compliance</p><p><strong>Location: </strong>Parsippany, NJ </p><p><strong>Employment Type: </strong><em>12-Month Contract </em></p><p><strong>Industry: </strong>Pharmaceuticals / Biotechnology</p><hr><h3><strong>About the Role</strong></h3><p>We are seeking a detail-oriented and experienced Technical Writer – Compliance to join our Quality or Manufacturing team. In this role, you will be responsible for authoring, reviewing, and managing investigations and deviations from both compliance and operational perspectives. You will play a key role in ensuring adherence to GMP standards, driving root cause analysis, and supporting continuous improvement initiatives across manufacturing operations.</p><p>This position requires strong technical writing skills, a solid understanding of GMP regulations, and the ability to collaborate effectively with cross-functional teams, including manufacturing personnel and external vendors.</p><hr><h3><strong>Key Responsibilities</strong></h3><ul><li>Lead and author investigations for Deviations, Non-Conformances, OOS/OOT results, field complaints, and environmental excursions.</li><li>Conduct thorough root cause analyses using industry-standard tools and methodologies.</li><li>Develop and implement effective Corrective and Preventive Actions (CAPAs) to prevent recurrence.</li><li>Manage multiple investigations simultaneously, ensuring timely closure in alignment with compliance deadlines and product release schedules.</li><li>Collaborate with cross-functional teams to develop, track, and communicate CAPA plans.</li><li>Identify trends and establish rules to proactively trigger corrective actions.</li><li>Analyze process data to identify opportunities for operational and quality improvements.</li><li>Apply change management principles to support continuous improvement.</li><li>Create and deliver training materials on investigation writing and root cause analysis techniques.</li><li>Serve as a CAPA champion, ensuring timely and effective implementation.</li><li>Maintain clear communication with stakeholders regarding ongoing investigations and CAPAs.</li><li>Ensure all documentation complies with internal quality standards and regulatory requirements.</li></ul><hr><h3><strong>Required Qualifications</strong></h3><ul><li>Bachelor’s degree in a scientific or technical discipline (e.g., Biology, Chemistry, Engineering).</li><li>3–5 years of experience writing and reviewing deviations, investigations, and CAPAs in a GMP-regulated environment.</li><li>Proven experience supporting manufacturing operations in the pharmaceutical, biotechnology, or cell and gene therapy sectors.</li><li>Strong knowledge of aseptic techniques and GMP compliance.</li><li>Proficiency in root cause analysis tools (e.g., 5 Whys, Fishbone, FMEA).</li><li>Excellent technical writing and communication skills.</li><li>Experience working with e-Quality Management Systems (eQMS).</li></ul><hr><h3><strong>Preferred Qualifications</strong></h3><ul><li>Prior experience in Quality Assurance or Compliance roles.</li><li>Familiarity with FDA-regulated operations and regulatory expectations.</li><li>Experience with biologics, cell and gene therapies, or advanced therapy medicinal products (ATMPs).</li><li>Proficiency with Microsoft Office Suite, including Excel, Visio, and Project.</li></ul><hr><h3><strong>Why Join Us?</strong></h3><ul><li>Be part of a mission-driven organization advancing life-saving therapies.</li><li>Collaborate with a passionate and innovative team.</li><li>Opportunity to grow your career in a cutting-edge, fast-paced environment.</li></ul><h1><br></h1>

Compliance Investigator

<h1><strong>Job Title: Technical Writer Compliance</strong></h1><p><br></p><h2>Job Description</h2><p>We are seeking a skilled Technical Writer Compliance professional who will be responsible for writing and completing investigations and deviations from both compliance and operations perspectives. The role involves reviewing investigations and deviations to ensure manufacturing and GMP compliance, conducting root cause analysis, and managing the entire lifecycle of an investigation independently. This position requires excellent technical writing skills and effective communication as you will be interviewing manufacturing personnel and speaking with vendors regarding investigations.</p><p><br></p><h2>Responsibilities</h2><ul><li>Determine the causes and preventative actions for Deviations, Non-Conformances, OOS, OOT, field complaints, and environmental excursion investigations.</li><li>Drive investigations to true root cause using appropriate tools and benchmark industry standards.</li><li>Define and implement effective preventative actions to prevent recurrence.</li><li>Manage multiple investigations in different stages to meet compliance deadlines and product release dates.</li><li>Collaborate with cross-functional teams to develop and track CAPA plans.</li><li>Identify and create trending rules that trigger corrective actions.</li><li>Analyze process data and evaluate trends to identify major improvement opportunities.</li><li>Utilize change management approaches effectively.</li><li>Develop training materials for personnel on writing problem statements and using root cause analysis tools.</li><li>Champion CAPA plans and implementation.</li><li>Provide communication plans for ongoing deviations and CAPAs.</li><li>Create and communicate CAPA plans to responsible parties.</li><li>Oversee timely completion of deviations, CAPAs, and Change Controls as necessary.</li><li>Abide by quality standards.</li></ul><h2>Essential Skills</h2><ul><li>Compliance expertise</li><li>Aseptic technique knowledge</li><li>Root cause analysis proficiency</li><li>Strong technical writing skills</li><li>Experience in writing deviations and CAPAs</li><li>3-5 years of experience in writing and reviewing deviations and investigations</li><li>3-5 years of experience in a pharma company supporting manufacturing</li><li>Previous quality assurance team experience</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>Bachelor&#39;s degree in a related scientific field</li><li>Experience in GMP Operations or Quality Assurance in Cell Therapies, Biotechnology, or Bio-Pharma</li><li>Preferred experience in pharmaceutical or FDA regulated operations</li><li>Experience using e-Quality Management Systems</li><li>Proficiency with IT skills, including Visio, Microsoft Project, and Excel</li><li>CAPA experience</li><li>Previous experience with cell and gene or biologics</li></ul><p><br></p>

Compliance Specialist

<h1 style="font-weight: 700;">Job Title: Pharmaceutical Compounder</h1><br><h2>Job Description</h2><p>We are seeking a dedicated Pharmaceutical Compounder to join our dynamic Production Department. This role involves working in various areas such as Granulation, Blending, Compression, Coating, Dispensing, or Technical Service, based on project needs and management discretion. Comprehensive training will be provided to ensure proficiency in all assigned tasks.</p><br><h2>Responsibilities</h2><ul><li>Follow all procedures and policies in the manufacturing facility.</li><li>Stay updated with the latest versions of SOPs and document training records.</li><li>Clean, set up, and operate all related equipment in the manufacturing facility.</li><li>Produce pharmaceutical products according to cGMP standards.</li><li>Adhere to Good Documentation Practices.</li><li>Coordinate with the Quality Assurance Department for line clearance after cleaning.</li><li>Work with the Engineering Department or Production Supervisor for equipment or facility breakdowns.</li><li>Train new employees and operators on processing equipment.</li><li>Perform additional tasks as assigned by the Production Supervisor.</li></ul><h2>Essential Skills</h2><ul><li>Experience in Pharmaceutical Compounding, Mixing, Blending, and Compression.</li><li>Pharma GMP experience.</li><li>Proficiency in documentation practices.</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>High School Graduate or equivalent experience within a pharmaceutical facility.</li><li>Qualified in operating oral solids pharmaceutical manufacturing equipment.</li><li>Basic computer skills, with knowledge of MS Word and Excel being an advantage.</li><li>Strong communication skills for department and inter-departmental coordination.</li><li>Ability to perform basic math and handle stress effectively.</li></ul><h2>Work Environment</h2><p>Join a growing manufacturing department in a new location with stable finances and a family-like environment. Work hours are typically 8-4 or 9-5, with the option to work four 10-hour days. Opportunities for overtime are available during the week or weekends. The role requires accessibility to all areas, safe ladder climbing, wearing required PPE, and the ability to lift up to 100 lbs. You&#39;ll need specific vision capabilities for reading documents and computer use, and the ability to sit, stand, or walk for prolonged periods.</p><br>

Compounder

<p><strong>Pharmacist </strong></p><p>We are seeking a fulltime staff Pharmacist with a focus on compounding. This role involves preparing customized medication formulations tailored to individual patient needs, ensuring high standards of safety and quality, and providing expert consultation.</p><p><br></p><p>Key Responsibilities:</p><ul><li>Prepare and compound medications based on specific prescriptions.</li><li>Consult with healthcare providers and patients to ensure optimal therapeutic outcomes.</li><li>Maintain compliance with all regulatory and safety standards.</li><li>Oversee pharmacy technicians and support staff in compounding processes.</li><li>Stay updated on compounding techniques and pharmaceutical best practices.</li></ul><p><br></p><p><strong>Skills &amp; Qualifications</strong></p><ul><li>WI Pharmacist License</li><li>2+ years of compounding experience</li></ul><p><strong>Additional Information</strong></p><p>This role is fulltime onsite Monday-Friday. This individual would work 9am - 5pm. This role is a permanent position that also offers full benefits. </p>

Compounding Pharmacist

<h2>Job Description</h2><p>The IV Compounding Pharmacy Technician is responsible for mixing intravenous and other pharmaceutical preparations using proper sterile compounding techniques. This role requires adherence to all documented instructions, warnings, procedures, and best practices to ensure safe and effective drug preparation. The technician performs environmental monitoring, sanitation, testing, and other activities as required by federal and state pharmacy regulations and USP-797 standards.</p><p><br></p><h2>Responsibilities</h2><ul><li>Maintain accurate drug inventory through purchasing, receiving, stocking, pulling, counting, and tracking drug items in accordance with established policies and procedures.</li><li>Enter home medication lists and lab results into CPR+ for the patient&#39;s profile when available.</li><li>Clean ante-room and clean room according to USP-797 standards and maintain clean room logs.</li><li>Verify lot numbers and perform periodic checks in inventory.</li><li>Successfully complete a competency verification plan upon hire and annually thereafter to ensure compliance with company policies and procedures, as well as federal, state, and regulatory standards.</li><li>Maintain confidentiality concerning company proprietary information and patient/client care in compliance with federal and state laws regarding protected health information (PHI) and electronic protected health information (EPHI) following HIPAA guidelines.</li></ul><h2>Qualifications</h2><ul><li>Must have compounding experience of some kind</li><li>Must be certified</li></ul>

Compounding Pharmacy Technician

<h2>Sterile Compounding Pharmacy Technician</h2><p>Location: Fairfield, OH</p><p>Job Type: Full-Time | Multiple Shifts Available</p><hr><h3>About the Role</h3><p>Are you a detail-driven pharmacy technician with a passion for precision and patient safety? We’re seeking a Sterile Compounding Certified Pharmacy Technician to join our growing team in Fairfield, OH. In this critical role, you’ll work in a state-of-the-art cleanroom environment, preparing sterile medications that directly impact patient care.</p><p>We offer competitive wages, excellent benefits, and the stability of a well-established company committed to professional growth and operational excellence.</p><hr><h3>Key Responsibilities</h3><ul><li>Prepare sterile compounded medications under pharmacist supervision</li><li>Accurately draw and label pre-filled syringes with precise volume and air-free contents</li><li>Maintain sterility in ISO-classified environments, including laminar flow hoods and cleanrooms</li><li>Follow strict gowning, hygiene, and USP &lt;797&gt;/&lt;800&gt; compliance protocols</li><li>Monitor environmental conditions and document compounding activities</li><li>Operate and maintain sterile compounding equipment (IV pumps, mixers, filtration systems)</li><li>Track inventory, manage stock rotation, and assist with procurement</li><li>Support quality assurance and participate in audits and training initiatives</li></ul><hr><h3>What You Bring</h3><ul><li>Must be registered with the Ohio Board of Pharmacy as a Registered or Certified Technician</li><li>Completion of a sterile compounding training program or certification</li><li>PTCB Sterile Compounding Certification preferred</li><li>Previous experience in sterile compounding (hospital or specialty pharmacy setting ideal)</li><li>Strong attention to detail, documentation, and compliance standards</li><li>High school diploma or equivalent required</li></ul><hr><h3>Why Join Us?</h3><ul><li>Competitive pay and shift differentials</li><li>Comprehensive benefits including health, dental, vision, and retirement plans</li><li>Company stability with a strong reputation in the healthcare industry</li><li>Opportunities for advancement and ongoing professional development</li><li>A clean, modern, and compliant work environment that values safety and teamwork</li></ul><hr><h3>Work Environment</h3><p>This role involves working in ISO-classified cleanrooms with strict gowning procedures. Technicians must be comfortable standing for extended periods, handling sterile equipment, and adhering to USP and state regulatory standards.</p><hr><h1>Ready to take your pharmacy career to the next level? Apply today and become part of a team that’s making a difference—one sterile preparation at a time.</h1>

<h2>Sterile Compounding Pharmacy Technician</h2><p>Location: Fairfield, OH</p><p>Job Type: Full-Time | Multiple Shifts Available</p><hr><h3>About the Role</h3><p>Are you a detail-driven pharmacy technician with a passion for precision and patient safety? We’re seeking a Sterile Compounding Certified Pharmacy Technician to join our growing team in Fairfield, OH. In this critical role, you’ll work in a state-of-the-art cleanroom environment, preparing sterile medications that directly impact patient care.</p><p>We offer competitive wages, excellent benefits, and the stability of a well-established company committed to professional growth and operational excellence.</p><hr><h3>Key Responsibilities</h3><ul><li>Prepare sterile compounded medications under pharmacist supervision</li><li>Accurately draw and label pre-filled syringes with precise volume and air-free contents</li><li>Maintain sterility in ISO-classified environments, including laminar flow hoods and cleanrooms</li><li>Follow strict gowning, hygiene, and USP &lt;797&gt;/&lt;800&gt; compliance protocols</li><li>Monitor environmental conditions and document compounding activities</li><li>Operate and maintain sterile compounding equipment (IV pumps, mixers, filtration systems)</li><li>Track inventory, manage stock rotation, and assist with procurement</li><li>Support quality assurance and participate in audits and training initiatives</li></ul><hr><h3>What You Bring</h3><ul><li>Must be registered with the Ohio Board of Pharmacy as a Registered or Certified Technician</li><li>Completion of a sterile compounding training program or certification</li><li>PTCB Sterile Compounding Certification preferred</li><li>Previous experience in sterile compounding (hospital or specialty pharmacy setting ideal)</li><li>Strong attention to detail, documentation, and compliance standards</li><li>High school diploma or equivalent required</li></ul><hr><h3>Why Join Us?</h3><ul><li>Competitive pay and shift differentials</li><li>Comprehensive benefits including health, dental, vision, and retirement plans</li><li>Company stability with a strong reputation in the healthcare industry</li><li>Opportunities for advancement and ongoing professional development</li><li>A clean, modern, and compliant work environment that values safety and teamwork</li></ul><hr><h3>Work Environment</h3><p>This role involves working in ISO-classified cleanrooms with strict gowning procedures. Technicians must be comfortable standing for extended periods, handling sterile equipment, and adhering to USP and state regulatory standards.</p><h1><br></h1>

<h1><strong>Job Title: Compounding Pharmacy Technician</strong></h1><p><em>IF INTERESTED PLEASE SEND UPDATED RESUMES TO BROWOODRUFF @ACTALENTSERVICES.COM</em></p><p><br></p><h2>Job Description</h2><p>The Compounding Pharmacy Technician plays a crucial role in the preparation and handling of sterile medications, ensuring precision and compliance with regulatory standards. This position requires a strong commitment to sterile technique and inventory oversight, as well as ongoing professional development to maintain the highest standards of patient safety and operational efficiency.</p><p><br></p><h2>Responsibilities</h2><ul><li>Accurately draw and label pre-filled syringes, ensuring precise volume and air-free contents.</li><li>Compound sterile preparations based on prescription requirements under pharmacist supervision.</li><li>Measure and mix ingredients with precision to achieve correct dosages and concentrations.</li><li>Maintain sterility within ISO-classified environments, including laminar flow hoods and cleanrooms.</li><li>Follow strict gowning and hygiene procedures to prevent contamination.</li><li>Monitor and document environmental conditions to ensure compliance with sterile standards.</li><li>Inspect compounded products for clarity, consistency, and absence of particulates.</li><li>Maintain detailed records of compounding activities, including lot numbers and expiration dates.</li><li>Assist in compiling batch records and logs for regulatory and internal audits.</li><li>Operate sterile compounding tools such as filtration systems, IV pumps, and automated mixers.</li><li>Perform routine cleaning, calibration, and troubleshooting of equipment.</li><li>Coordinate with technical teams for equipment servicing when needed.</li><li>Track inventory levels of sterile supplies and medications.</li><li>Work with procurement to ensure timely restocking and avoid shortages.</li><li>Conduct regular audits and manage stock rotation to minimize waste and ensure compliance.</li><li>Adhere to all applicable guidelines including USP &lt;797&gt;, USP &lt;800&gt;, and state regulations.</li><li>Participate in ongoing training to stay current with best practices and regulatory updates.</li><li>Support quality improvement initiatives aimed at enhancing patient safety and operational efficiency.</li></ul><h2>Essential Skills</h2><ul><li>Proficiency in pharmacy and compounding techniques.</li><li>Completion of a sterile compounding training program or certification.</li><li>Registration with the Ohio Board of Pharmacy as a Registered Technician or Certified Technician.</li><li>Previous experience in sterile compounding, preferably in a hospital or specialty pharmacy setting.</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>High school diploma or equivalent.</li><li>Pharmacy Technician Certification Board (PTCB) Sterile Compounding Certification is preferred.</li></ul><h2>Work Environment</h2><p>The work environment includes maintaining sterility within ISO-classified cleanrooms, and handling sterile compounding tools such as filtration systems, IV pumps, and automated mixers. Employees must adhere to strict gowning and hygiene procedures to prevent contamination, while also ensuring compliance with USP guidelines and state regulations.</p>

<h1 style="font-weight: 700;">Job Title: Compounding Pharmacy Technician</h1><br><h2>Job Description</h2><p>The Compounding Pharmacy Technician plays a crucial role in the preparation and handling of sterile medications, ensuring precision and compliance with regulatory standards. This position requires a strong commitment to sterile technique and inventory oversight, as well as ongoing professional development to maintain the highest standards of patient safety and operational efficiency.</p><br><h2>Responsibilities</h2><ul><li>Accurately draw and label pre-filled syringes, ensuring precise volume and air-free contents.</li><li>Compound sterile preparations based on prescription requirements under pharmacist supervision.</li><li>Measure and mix ingredients with precision to achieve correct dosages and concentrations.</li><li>Maintain sterility within ISO-classified environments, including laminar flow hoods and cleanrooms.</li><li>Follow strict gowning and hygiene procedures to prevent contamination.</li><li>Monitor and document environmental conditions to ensure compliance with sterile standards.</li><li>Inspect compounded products for clarity, consistency, and absence of particulates.</li><li>Maintain detailed records of compounding activities, including lot numbers and expiration dates.</li><li>Assist in compiling batch records and logs for regulatory and internal audits.</li><li>Operate sterile compounding tools such as filtration systems, IV pumps, and automated mixers.</li><li>Perform routine cleaning, calibration, and troubleshooting of equipment.</li><li>Coordinate with technical teams for equipment servicing when needed.</li><li>Track inventory levels of sterile supplies and medications.</li><li>Work with procurement to ensure timely restocking and avoid shortages.</li><li>Conduct regular audits and manage stock rotation to minimize waste and ensure compliance.</li><li>Adhere to all applicable guidelines including USP , USP , and state regulations.</li><li>Participate in ongoing training to stay current with best practices and regulatory updates.</li><li>Support quality improvement initiatives aimed at enhancing patient safety and operational efficiency.</li></ul><h2>Essential Skills</h2><ul><li>Proficiency in pharmacy and compounding techniques.</li><li>Completion of a sterile compounding training program or certification.</li><li>Registration with the Ohio Board of Pharmacy as a Registered Technician or Certified Technician.</li><li>Previous experience in sterile compounding, preferably in a hospital or specialty pharmacy setting.</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>High school diploma or equivalent.</li><li>Pharmacy Technician Certification Board (PTCB) Sterile Compounding Certification is preferred.</li></ul><h2>Work Environment</h2><p>The work environment includes maintaining sterility within ISO-classified cleanrooms, and handling sterile compounding tools such as filtration systems, IV pumps, and automated mixers. Employees must adhere to strict gowning and hygiene procedures to prevent contamination, while also ensuring compliance with USP guidelines and state regulations.</p><br>

<p style="text-align: center;"><strong><u>Urgent hiring for &quot;Compounding Pharmacy Technician&quot; in Fairfield, OH !</u></strong></p><p style="text-align: center;"><strong><u>﻿*Must be located closer to Fairfield, OH*</u></strong></p><p style="text-align: center;"><br></p><p><strong><u>Job Description:</u></strong></p><ul><li>Measure and mix ingredients with precision to achieve correct dosages and concentrations.</li><li>Monitor and document environmental conditions to ensure compliance with sterile standards.</li><li>Inspect compounded products for clarity, consistency, and absence of particulates.</li><li>Operate sterile compounding tools such as filtration systems, IV pumps, and automated mixers.</li><li>Track inventory levels of sterile supplies and medications.</li></ul><p><strong><u>Qualifications:</u></strong></p><ul><li><strong>Must Hold Pharmacy License from state of OH is Mandatory</strong></li><li><strong>2+ yeard of Exp working with sterile compounding, preferably in a hospital or specialty pharmacy setting.is Mandatory</strong></li><li><strong>Pharmacy Technician Certification Board (PTCB) Sterile Compounding Certification is Mandatory</strong></li></ul><p><br></p><p style="text-align: center;"><strong><u>If you are Interested , Kindly give a call : (726) 216-6069</u></strong></p><p style="text-align: center;"><br></p>

<h1 style="font-weight: 700;">Job Title: Computer Vision Engineer</h1><br><h2>Job Description</h2><p>As a Computer Vision Engineer, you will be responsible for developing and optimizing computer vision algorithms and solutions to enable autonomous vehicles to interpret and understand visual data. You will work on a variety of challenging projects, including image recognition, object detection, video analysis, and deep learning applications. The ideal candidate will have a strong foundation in computer vision techniques, machine learning, and programming, along with experience in deploying real-world applications.</p><br><h2>Responsibilities</h2><ul><li>Develop and optimize computer vision pipelines for real-time and scalable performance in production environments.</li><li>Design, develop, and implement computer vision algorithms for applications such as image classification, object detection, and segmentation.</li><li>Train and fine-tune deep learning models (e.g., CNNs, RNNs) for visual data analysis, ensuring high accuracy and performance.</li><li>Perform data preprocessing, augmentation, and develop annotation tools for large-scale image and video datasets.</li><li>Collaborate with cross-functional teams, including software engineers and hardware engineers, to integrate vision systems into products.</li><li>Conduct experiments and evaluations to measure the performance and efficiency of vision algorithms.</li><li>Implement and test solutions on various hardware platforms (e.g., GPUs, embedded systems, edge devices).</li><li>Stay up to date with the latest research, trends, and advancements in computer vision and machine learning.</li><li>Troubleshoot and resolve issues related to model accuracy, performance, and system integration.</li><li>Provide technical documentation and support for computer vision solutions and algorithms.</li><li>Ensure the deployment of robust and maintainable vision-based systems in real-world applications.</li><li>Optimize algorithms for computational efficiency, including memory and processing time constraints.</li><li>Maintain integrity of customer, company standards, and requirements during development activities.</li></ul><h2>Essential Skills</h2><ul><li>Strong foundation in computer vision techniques, machine learning, and programming.</li><li>Proficiency in computer vision algorithms and feature extraction methods (e.g., SIFT, HOG).</li><li>Mastery of deep learning models and classical machine learning principles.</li><li>Experience with linear and logistic regression, SVMs, decision trees (Random Forests and boosting), k-Nearest Neighbors, and probabilistic classifiers.</li><li>Competence in programming languages such as Python and C++.</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>Bachelor&#39;s degree in Computer Science, Electrical Engineering, Robotics, Mathematics, or a related field.</li><li>Experience in deploying real-world applications.</li><li>Knowledge of CNNs and RNNs for visual data analysis.</li><li>Familiarity with YOLO and unmanned systems.</li></ul><h2>Work Environment</h2><p>The work environment includes office settings, research and development facilities, and manufacturing areas. The position requires the candidate to be at the assigned worksite during designated hours, with exceptions for PTO, FML/STD/LTD. The role involves working with technologies such as GPUs, embedded systems, and edge devices.</p><br>

Computer Vision Engineer

<p><strong>Description</strong></p>
					<p>Seeking an ICC special inspector with 2+ years of experience and a reinforced concrete certification . Ideal candidates will have prior experience for a geotechnical engineering or materials testing company. Perform testing, inspection, and field observations during construction. 
- Perform testing on materials including, soils, reinforcing steel, concrete, masonry, structural steel, fireproofing, metal decking, roofing and asphalt paving
-Inspect and review construction sites for compliance
-Coordinate and interact with contractors in field
- Write Daily Field Reports documenting work performed by the various contractors and indicating compliance/non-compliance with contract documents
- Coordinate with the department manager about progress of projects.
-Ability to lift up to 50lbs to transport material samples, and move nuclear densometer.
-Will be expected to carry nuclear densometer (25lbs) short distances. 
-ACI OR ICC cert 
-Experience with reinforced concrete preferred</p>
					<p><strong>Skills</strong></p>
					<p>concrete, material testing, aci certification, aci certified, structural masonry, concrete testing, concrete inspection, materials testing, inspection, aci, reinforced concrete, construction, construction inspection, welding inspection, steel inspection, ndt</p>
					<p><strong>Top Skills Details</strong></p>
					<p>concrete,material testing,aci certification,aci certified,structural masonry,concrete testing,concrete inspection,materials testing,inspection,aci,reinforced concrete,construction</p>
					<p><strong>Additional Skills &amp; Qualifications</strong></p>
					<p>2 years experience in  construction inspection.
Experience with 1 of the following:
- Concrete testing, 
- reinforced concrete. 
- OBOA or WABO certification or able to get it within a few months.
- Nuclear Density Gauge training and certification a plus
- valid driver&#39;s license

Must have 1 of the following certificates: 
- American Concrete Institute (ACI):  Concrete Field Testing Technician Grade I

And ONE of the following ICC Certifications
•	Reinforced Concrete
•	Structural Masonry
•	Pre-stressed/Post-tensioned Concrete
•	Structural Steel Bolting
•	Structural Steel Welding

OR one of the following AWS-CWI Welding with construction inspection experience A PLUS
OBOA (Oregon Building Officials Association), WABO (WA Association of Building Officials), ODOT Certifications A PLUS</p>
					<p><strong>Experience Level</strong></p>
					<p>Entry Level</p>

Concrete Inspector

<p><strong style="font-size: 18px;"><em>IF INTERESTED, PLEASE EMAIL YOUR RESUME TO AGATES@ACTALENTSERVICES. COM</em></strong></p><p><strong>Description</strong></p><p>Seeking an ICC special inspector with 2+ years of experience and a reinforced concrete certification . Ideal candidates will have prior experience for a geotechnical engineering or materials testing company. Perform testing, inspection, and field observations during construction. </p><p>- Perform testing on materials including, soils, reinforcing steel, concrete, masonry, structural steel, fireproofing, metal decking, roofing and asphalt paving</p><p>-Inspect and review construction sites for compliance</p><p>-Coordinate and interact with contractors in field</p><p>- Write Daily Field Reports documenting work performed by the various contractors and indicating compliance/non-compliance with contract documents</p><p>- Coordinate with the department manager about progress of projects.</p><p>-Ability to lift up to 50lbs to transport material samples, and move nuclear densometer.</p><p>-Will be expected to carry nuclear densometer (25lbs) short distances. </p><p>-ACI OR ICC cert </p><p>-Experience with reinforced concrete preferred</p><p><strong>Skills</strong></p><p>concrete, material testing, aci certification, aci certified, structural masonry, concrete testing, concrete inspection, materials testing, inspection, aci, reinforced concrete, construction, construction inspection, welding inspection, steel inspection, ndt</p><p><strong>Top Skills Details</strong></p><p>concrete,material testing,aci certification,aci certified,structural masonry,concrete testing,concrete inspection,materials testing,inspection,aci,reinforced concrete,construction</p><p><strong>Additional Skills &amp; Qualifications</strong></p><p>2 years experience in  construction inspection.</p><p>Experience with 1 of the following:</p><p>- Concrete testing, </p><p>- reinforced concrete. </p><p>- OBOA or WABO certification or able to get it within a few months.</p><p>- Nuclear Density Gauge training and certification a plus</p><p>- valid driver&#39;s license</p><p><br></p><p>Must have 1 of the following certificates: </p><p>- American Concrete Institute (ACI):  Concrete Field Testing Technician Grade I</p><p><br></p><p>And ONE of the following ICC Certifications</p><p>•	Reinforced Concrete</p><p>•	Structural Masonry</p><p>•	Pre-stressed/Post-tensioned Concrete</p><p>•	Structural Steel Bolting</p><p>•	Structural Steel Welding</p><p><br></p><p>OR one of the following AWS-CWI Welding with construction inspection experience A PLUS</p><p>OBOA (Oregon Building Officials Association), WABO (WA Association of Building Officials), ODOT Certifications A PLUS</p><p><strong>Experience Level</strong></p><p>Entry Level</p>

<h3><strong>Job Title: ICC Special Inspector </strong></h3><p><strong>Description:</strong></p><p><strong>We are seeking an ICC Special Inspector</strong> with at least <strong>2 years of experience</strong> and a valid <strong>Reinforced Concrete certification</strong>. The ideal candidate will have prior experience working with a geotechnical engineering or materials testing firm. This role involves performing field inspections, testing, and observations during construction to ensure compliance with project specifications and industry standards.</p><p><strong>Key Responsibilities:</strong></p><ul><li>Conduct field testing and inspections on materials such as:<ul><li>Soils</li><li>Reinforcing steel</li><li>Concrete</li><li>Masonry</li><li>Structural steel</li><li>Fireproofing</li><li>Metal decking</li><li>Roofing</li><li>Asphalt paving</li></ul></li><li>Review construction sites for code and specification compliance.</li><li>Coordinate with contractors and field personnel.</li><li>Prepare detailed Daily Field Reports documenting contractor activities and compliance status.</li><li>Communicate project progress with the department manager.</li><li>Transport material samples and equipment (up to 50 lbs), including a nuclear densometer (25 lbs).</li></ul><p><strong>Required Certifications (must have one of each):</strong></p><ul><li><strong>ACI Certification</strong>:<ul><li><em>Concrete Field Testing Technician – Grade I</em></li></ul></li></ul><p><strong>AND one of the following ICC Certifications</strong>:</p><ul><li>Reinforced Concrete</li><li>Structural Masonry</li><li>Pre-stressed/Post-tensioned Concrete</li><li>Structural Steel Bolting</li><li>Structural Steel Welding</li></ul><p><strong>Preferred Certifications (a plus):</strong></p><ul><li>AWS-CWI (Certified Welding Inspector) with construction inspection experience</li><li>OBOA (Oregon Building Officials Association)</li><li>WABO (Washington Association of Building Officials)</li><li>ODOT Certifications</li><li>Nuclear Density Gauge training and certification</li></ul><p><strong>Qualifications:</strong></p><ul><li>Minimum <strong>2 years of construction inspection or materials testing experience</strong></li><li><strong>Experience in at least one of the following:</strong><ul><li><strong>Concrete testing</strong></li><li>Reinforced concrete inspection</li></ul></li><li>Strong communication and documentation skills</li><li>Valid driver’s license</li><li>Ability to work independently and manage time effectively</li></ul><p><strong>Skills:</strong></p><ul><li>Concrete and materials testing</li><li>ACI/ICC certifications</li><li>Structural masonry and concrete inspection</li><li>Construction site compliance</li><li>Welding and steel inspection (preferred)</li><li>Familiarity with NDT (non-destructive testing) methods</li></ul><p><br></p>

<h1 style="font-weight: 700;">Job Title: Concrete Project Manager</h1><br><h2>Job Description</h2><p>We are seeking an experienced Civil (Industrial Concrete) Project Manager to lead client development and project delivery while ensuring efficient and safe work environments in Raleigh, NC. The ideal candidate should possess substantial experience in managing large civil projects, particularly within the industrial sector, including manufacturing, distribution centers, hospitals, chemical, and biopharma facilities.</p><br><h2>Responsibilities</h2><ul><li>Collaborate closely with clients, other project managers, and supervisory teams to prepare, plan, develop, and oversee site projects.</li><li>Establish priorities and allocate resources or capital effectively.</li><li>Manage all aspects of cost management, including estimating, funding, budgeting, forecasting, controlling, and reporting.</li><li>Utilize extensive knowledge of project scheduling, bids, take-offs, change orders, and contracts to identify and process scope changes, address issues, and communicate regarding project milestones.</li><li>Continuously develop relationships to identify and cultivate new opportunities.</li><li>Plan and schedule resources to meet project demands.</li><li>Devise innovative approaches to problems and prepare or modify drawings, specifications, calculations, charts, and graphs.</li><li>Monitor work for compliance with applicable codes and accepted engineering practices.</li><li>Ensure that all equipment, tools, and employees assigned to projects operate in accordance with SIC policy, government regulations, and customer requirements.</li><li>Champion a Safety First mentality by monitoring the execution of the SIC safety program and the performance of work by internal staff and external vendors.</li><li>Provide regular updates on project statuses to <span style="color: rgb(8, 7, 7); background-color: none;"><span style="color: rgb(8, 7, 7); background-color: none;">Senior</span></span> Management.</li><li>Travel regularly to job sites to oversee projects.</li></ul><h2>Essential Skills</h2><ul><li>Project management</li><li>Construction management</li><li>Concrete project management</li><li>Industrial project management</li><li>Healthcare construction</li><li>Industrial construction</li><li>Construction project management</li><li>Blueprint reading</li><li>Safety</li><li>OSHA regulations</li><li>Industrial retrofit</li><li>Rigging</li><li>MEP systems</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>10-15 years of experience in manufacturing, power, and chemical markets managing projects up to $1M with high complexity.</li><li>Proven success in team leadership, process adherence, ownership/commitment, learning agility, and risk management capabilities.</li><li>Strategic thinker capable of establishing and managing plans while building and fostering relationships.</li><li>Proficient in PC skills, including Microsoft Office Suite and project management scheduling software.</li></ul><h2>Work Environment</h2><p>This role is based in the Raleigh office with regular travel to project sites. The position involves working closely with various stakeholders and requires adherence to safety standards and regulations.</p><br>

Concrete Project Manager

<h1><strong>Job Title: Concrete Project Manager</strong></h1><p><br></p><h2>Job Description</h2><p>We are seeking an experienced Civil (Industrial Concrete) Project Manager to lead client development and project delivery while ensuring efficient and safe work environments in Raleigh, NC. The ideal candidate should possess substantial experience in managing large civil projects, particularly within the industrial sector, including manufacturing, distribution centers, hospitals, chemical, and biopharma facilities.</p><p><br></p><h2>Responsibilities</h2><ul><li>Collaborate closely with clients, other project managers, and supervisory teams to prepare, plan, develop, and oversee site projects.</li><li>Establish priorities and allocate resources or capital effectively.</li><li>Manage all aspects of cost management, including estimating, funding, budgeting, forecasting, controlling, and reporting.</li><li>Utilize extensive knowledge of project scheduling, bids, take-offs, change orders, and contracts to identify and process scope changes, address issues, and communicate regarding project milestones.</li><li>Continuously develop relationships to identify and cultivate new opportunities.</li><li>Plan and schedule resources to meet project demands.</li><li>Devise innovative approaches to problems and prepare or modify drawings, specifications, calculations, charts, and graphs.</li><li>Monitor work for compliance with applicable codes and accepted engineering practices.</li><li>Ensure that all equipment, tools, and employees assigned to projects operate in accordance with SIC policy, government regulations, and customer requirements.</li><li>Champion a Safety First mentality by monitoring the execution of the SIC safety program and the performance of work by internal staff and external vendors.</li><li>Provide regular updates on project statuses to <span style="color: rgb(8, 7, 7); background-color: none;">Senior</span> Management.</li><li>Travel regularly to job sites to oversee projects.</li></ul><h2>Essential Skills</h2><ul><li>Project management</li><li>Construction management</li><li>Concrete project management</li><li>Industrial project management</li><li>Healthcare construction</li><li>Industrial construction</li><li>Construction project management</li><li>Blueprint reading</li><li>Safety</li><li>OSHA regulations</li><li>Industrial retrofit</li><li>Rigging</li><li>MEP systems</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>10-15 years of experience in manufacturing, power, and chemical markets managing projects up to $1M with high complexity.</li><li>Proven success in team leadership, process adherence, ownership/commitment, learning agility, and risk management capabilities.</li><li>Strategic thinker capable of establishing and managing plans while building and fostering relationships.</li><li>Proficient in PC skills, including Microsoft Office Suite and project management scheduling software.</li></ul><h2>Work Environment</h2><p>This role is based in the Raleigh office with regular travel to project sites. The position involves working closely with various stakeholders and requires adherence to safety standards and regulations.</p>

<h1 style="font-weight: 700;">Job Title: Configuration Engineer</h1><br><h2>Job Description</h2><p>As a Configuration Engineer, you will provide hands-on technical support to configure and troubleshoot networked IT and voice systems for the air traffic control network. You will be responsible for preparing, configuring, and testing computing, network equipment, and communications hardware in an assembly environment.</p><br><h2>Responsibilities</h2><ul><li>Review requirements and work orders to evaluate current configuration needs.</li><li>Follow installation documentation, drawings, and implementation schedules.</li><li>Install, configure, and test workstations, printers, network connections, teleconferencing devices, and peripheral hardware as specified.</li><li>Troubleshoot computers, networks, and telecommunications equipment for installation or application configuration issues.</li><li>Attend user training on hardware functionality and best practices.</li><li>Document all configuration changes and test activities.</li><li>Perform physical labor, including lifting equipment up to 50 lbs.</li></ul><h2>Essential Skills</h2><ul><li>Proficient in Linux and Windows operating systems.</li><li>Proficient in troubleshooting and repairing hardware and peripherals.</li><li>Experience installing and configuring operating systems and software applications.</li><li>Knowledge of antivirus software, patch management, and basic networking.</li><li>Ability to interpret technical manuals and schematics.</li><li>Strong skills in Microsoft Office Suite (Word, Excel, PowerPoint, Access).</li><li>Familiarity with Active Directory policies and security.</li><li>Excellent time management, communication, and customer service skills.</li><li>Capable of working independently with minimal supervision.</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>High school diploma or GED with 2–4 years of relevant technical experience.</li><li>Associate or bachelor’s degree in a technical field with relevant technical experience is preferred.</li></ul><h2>Work Environment</h2><p>The position is located in Coppell, TX, where teams of configuration and test engineers work in parallel to assemble, configure, and perform validation testing of communications equipment. The work environment includes both office settings and assembly floor conditions.</p><br>

Configuration Engineer

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