<p><strong>Description</strong></p><p>- Must have Oncology nursing experience and electronic medical abstraction experience. </p><p> - Accurately and efficiently conduct electronic medical record abstraction services. </p><p> - Accurately abstract information from the electronic medical record into the electronic data capture tool. </p><p>-  Complete quality and accuracy testing as requested in a timely manner </p><p> - Abide by all HIPAA and associated patient confidentiality requirements </p><p>-  Fully Remote </p><p>- Schedule : Monday - Friday 8-5 (flexible with schedule)</p><p><br></p><p><strong>Skills</strong></p><p>medical record, oncology, oncology nursing, charting, EMR, chart abstraction, EHR, HIPPA, Database</p><p><br></p><p><strong>Top Skills Details</strong></p><p>medical record,oncology,oncology nursing,charting,EMR,chart abstraction,EHR,HIPPA,Database</p><p><br></p><p><strong>Additional Skills &amp; Qualifications</strong></p><p>-  Should be comfortable working independently in a remote environment with minimal guidance from management </p><p> - Must have Oncology RN experience </p><p> - Must have Electronic Medical Chart abstraction experience </p><p> - Must be proficient in navigating through EHR databases. </p><p> - Clinical experience/pharmaceutical experience prefer experience in performing chart abstractions in an oncology setting academic or research experience helpful. </p><p> - Previous data analysis experience is a plus. </p><p> </p><p>Specialized Knowledge/Skills </p><p> - Excellent verbal and written skills. </p><p> - Detail oriented. </p><p> - Team work oriented. </p><p> - Ability to multi-task and meet deadlines. </p><p> - Excellent computer skills including: MS Word MS PowerPoint MS Excel MS Outlook </p><p> - Must have high speed internet access </p><p> - Utilized TEAMs platform</p><p><br></p>

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Registered Nurse Data Abstractor

<p style="text-align: center;"><strong>Actalent is urgently hiring for an Assistant Director of Patient Services! </strong></p><h4>Overview:</h4><p>We are seeking a dedicated and experienced Registered Nurse (RN) to join our leadership team as an Assistant Director of Patient Services. This role is ideal for a compassionate and detail-oriented RN with a strong history in home care and supervisory responsibilities. The successful candidate will play a key role in ensuring high-quality patient care, regulatory compliance, and operational excellence.</p><h4>Qualifications:</h4><ul><li>Current RN license in good standing (New York State)</li><li>Minimum 3 years of nursing experience, preferably in home care or community health</li><li>Proven supervisory or leadership experience</li><li>Proficiency in UAS-NY assessments and home care evaluations</li><li>Strong organizational and communication skills</li><li>Experience with chart audits and regulatory preparedness is a plus</li></ul><h4>Key Responsibilities:</h4><ul><li>Conduct initial assessments for new home care cases</li><li>Oversee and review documentation submitted by field nurses to ensure accuracy and compliance</li><li>Prepare for audits by maintaining up-to-date and compliant patient records</li><li>Perform chart audits and implement quality improvement measures</li><li>Collaborate with the Director of Patient Services to support staff development and operational goals</li><li>Serve as a clinical resource and mentor to nursing staff</li></ul><h4>Why Join Us?</h4><ul><li>Supportive and collaborative team environment</li><li>Opportunities for professional growth and leadership development</li><li>Make a meaningful impact on patient care and community health</li></ul><p><br></p><p><br></p><p style="text-align: center;"><strong>Please apply directly for immediate consideration! </strong></p><p style="text-align: center;"><br></p><p style="text-align: center;"><br></p><p>#lpn25</p>

Registered Nurse Supervisor - Homecare

<p style="text-align: center;"><strong>﻿<u>Immediate Hiring for &quot;Registered Nurse&quot; in Tulsa, OK!</u></strong></p><p style="text-align: center;"><strong><u>﻿*Must be located closer to Tulsa, OK*</u></strong></p><p><br></p><p><strong>Job Description</strong></p><p>Individuals within this job classification are accountable for assessing, planning, implementing, evaluating and documenting care activities in accordance with HHS standards to deliver efficient, effective, and quality patient care. The Registered Nurse (RN) must demonstrate the knowledge and skills necessary to provide care appropriate to the age of the patients served on the assigned unit. Additionally, the RN must demonstrate knowledge of contrast media injections and reactions and possess the ability to assess data reflective of the patient’s status, interpreting the appropriate information needed to identify each patient&#39;s requirements relative to their age-specific needs. The RN is responsible for planning the provision of patient care, including the development, modification, and implementation of the plan of care in accordance with HHS standards, as described in the Patient Care policies and procedures. Adherence to the Oklahoma Nursing Practice Act is expected. Participation in performance improvement initiatives and assisting with other day-to-day departmental activities is required. Must be available for 24-hour call back with a 60-minute response time.</p><p><br></p><h2><strong>Responsibilities</strong></h2><ul><li>Assess, plan, implement, evaluate, and document care activities in accordance with HHS standards.</li><li>Provide care appropriate to the age of the patients served on the assigned unit.</li><li>Demonstrate knowledge of contrast media injections and reactions.</li><li>Assess data reflective of the patient’s status and interpret appropriate information to identify each patient&#39;s requirements relative to their age-specific needs.</li><li>Plan for the provision of patient care, including the development, modification, and implementation of the plan of care.</li><li>Adhere to the rules and regulations set forth by the Oklahoma Nursing Practice Act.</li><li>Participate in performance improvement initiatives.</li><li>Assist with other activities necessary for the day-to-day operation of the department.</li><li>Must be available for 24-hour call back with a 60-minute response time.</li></ul><h2><strong>Essential Skills</strong></h2><ul><li>Bachelor of Science in Nursing (BSN)</li><li>Current Oklahoma Nursing License</li><li>Basic Life Support (BLS) Certification</li><li>Advanced Cardiac Life Support (ACLS) Certification</li><li>1 year of ICU experience</li><li>Procedure experience</li></ul><h2><strong>Additional Skills &amp; Qualifications</strong></h2><ul><li>Pediatric Advanced Life Support (PALS) Certification</li><li>Experience with post-operative patient care</li><li>Experience with invasive radiology procedures</li></ul><h2><strong>Work Environment</strong></h2><ul><li>The work environment consists of Monday through Friday shifts from either 7:30 AM to 4:00 PM or 8:00 AM to 4:30 PM. Rotating weekend call will occur every 8th to 10th weekend, and weekday call rotation will also follow a similar schedule. RNs will cover 3 labs, 5 holding bays for pre- and post-procedure patients, CT invasive procedures averaging 5 per day, ultrasound invasive procedures averaging 10 per day, and MRI anesthesia and pacemaker cases averaging 3 per day. The team environment is friendly and accommodating, with a focus on collaboration and support. Additionally, the organization offers an excellent retirement plan with quick vestment. The culture emphasizes teamwork and support, ensuring a positive experience for both staff and patients.</li></ul><p><br></p><p style="text-align: center;"><br></p><p style="text-align: center;"><br></p>

Registered Nurse- OR And L&D

<h1 style="text-align: center;"><strong><u>Regulatory Affairs Director</u></strong></h1><p><strong><u>Job Description</u></strong></p><p>As a Regulatory Affairs Director, you will develop, implement, and coordinate compliance with federal, state, local, and international regulatory requirements applicable to institution cleaning chemicals, equipment, water-based coatings, and bacillus species. You will be responsible for providing analysis and support for the company’s compliance activities, managing day-to-day administration of regulatory matters, and promoting sound product stewardship. This role requires providing technical advice concerning regulatory affairs to internal team members and customers, as well as organizing and maintaining proper documentation regarding regulatory compliance.</p><p><br></p><p><strong><u>Responsibilities</u></strong></p><ul><li>Proof all labels for chemical and equipment, Basic Coatings, and Bio-Systems, including accompanying literature, training materials, or other written or digital materials for compliance with OSHA, FIFRA, CPSC, OAQPS, FDA, DOT, EPA, USDA, CDC, VOC, and other applicable federal, state, or local requirements.</li><li>Ensure accuracy of warning statements and first aid statements on labels, and compliance on labels and (M)SDS’s according to US and International requirements.</li><li>Monitor activities at federal, state, and regional regulatory agencies to find opportunities for new product development and present findings.</li><li>Analyze, interpret, and present information to management concerning regulatory affairs related to current and potential future products.</li><li>Lead the implementation of regulatory requirements to ensure compliance.</li><li>Maintain and ensure accuracy of OSHA SDS generation Sphera, raw material SDS database, and assignment of proper BOL codes to products.</li><li>Ensure communication and compliance with OSHA, FIFRA, CPSC, OAQPS, FDA, DOT, EPA, USDA, CDC, VOC, and other applicable federal, state, or regional requirements.</li><li>Handle DOT UN approved container testing, NAFTA classification of chemicals and equipment parts, EU REACH regulations, Canadian compliance for DIN, CFIA, CEPA, and Nonylphenol phase-out regulations.</li><li>Manage California Mill assessments for EPA products, sub-registrant relationships, and coordination with vendors.</li><li>Prepare letters of guarantee for food establishments, state and regional compliance in formulation and labeling for Phosphate, and annual EPA state registration.</li><li>Accountable for monthly, quarterly, and annual regulatory reporting and fees.</li><li>Communicate with internal/external customers regarding questions and requests for documentation related to regulatory activities.</li><li>Complete jurisdictional and company-specific safety paperwork on behalf of customers as requested.</li><li>Advise on storage, handling, and spill clean-up.</li><li>Attend seminars, conferences, and workshops to track new trends in regulatory activities and interact with trade associations and other regulatory professionals.</li><li>Prepare annual regulatory affairs budget.</li><li>Manage direct reports to support overall regulatory needs and provide regulatory support for affairs.</li></ul><p><strong><u>Essential Skills</u></strong></p><ul><li>7-10 years of regulatory experience in a chemical/product manufacturing environment.</li><li>4-year college degree in Chemistry, Biology, or Environmental Science.</li><li>Knowledge of law and regulations.</li><li>Proficiency in Microsoft Office.</li><li>Time management skills.</li><li>Ability to work independently and with minimal supervision.</li></ul><p><strong><u>Additional Skills &amp; Qualifications</u></strong></p><ul><li>Law degree is desirable.</li><li>Minimum of 1 year of college-level math.</li></ul><p><strong><u>Work Environment</u></strong></p><p>The role will involve collaboration with lab, field, and manufacturing teams. The physical requirements include standing for long periods and lifting up to 50 pounds.R</p>

Regulatory Affairs Director

<p>&#128680;NOW HIRING: Regulatory Affairs Director</p><p>&#128205; On-Site | &#129514; Chemical &amp; Product Manufacturing | &#128188; Leadership Role | &#127757; Global Compliance</p><p>Are you a regulatory power house with a sharp eye for detail and a passion for keeping innovation compliant?</p><p>We’re looking for a Regulatory Affairs Director who’s ready to lead from the front—someone who thrives at the intersection of science, strategy, and safety. If you know your way around OSHA, EPA, FDA, DOT, REACH, and more, and you’re ready to make a real impact in a dynamic, fast-paced environment, this is your moment.</p><hr><p>&#128269; What You’ll Own:</p><ul><li>Lead regulatory compliance for a diverse portfolio: cleaning chemicals, coatings, equipment, and biologicals</li><li>Review and approve labels, SDSs, and documentation across U.S. and international standards</li><li>Monitor regulatory changes and turn them into opportunities for innovation</li><li>Advise internal teams and customers with confidence and clarity</li><li>Oversee audits, reporting, and documentation with precision</li><li>Manage a small but mighty team of regulatory professionals</li></ul><hr><p>&#127919; What You Bring:</p><ul><li>7–10 years of regulatory experience in chemical/product manufacturing</li><li>Degree in Chemistry, Biology, or Environmental Science (Law degree = a big plus)</li><li>Deep knowledge of federal, state, and international regulations</li><li>Strong leadership, communication, and time management skills</li><li>Proficiency in Microsoft Office and regulatory systems</li></ul><hr><p>&#128161; Bonus Points For:</p><ul><li>Experience with Sphera SDS systems</li><li>Familiarity with Canadian, EU, and California-specific compliance</li><li>A strategic mindset with a hands-on approach</li></ul><hr><p>&#127775; Why Join Us?</p><ul><li>Be the go-to expert in a company that values your voice</li><li>Collaborate with R&amp;D, manufacturing, and field teams</li><li>Competitive compensation and benefits</li><li>A culture that respects work-life balance and professional growth</li></ul><hr><p>&#128233;Ready to lead with purpose and precision?</p><p>Let’s connect. This isn’t just a job—it’s a chance to shape the future of safe, sustainable innovation.</p><p>#RegulatoryAffairs #DirectorRole #ChemicalIndustryJobs #ComplianceLeadership #NowHiring #EnvironmentalHealth #ProductStewardship #CareerOpportunity</p><h1><br></h1>

<h1><strong>Job Title: Regulatory Affairs Project Manager</strong></h1><h2><strong>MUST HAVE </strong></h2><ul><li><strong><em>Project management expertise with 6-8+ years of experience.</em></strong></li><li><strong><em>Experience in medical device industry.</em></strong></li><li><strong><em>PMP certification or equivalent preferred.</em></strong></li><li><strong><em>Strong skills in stakeholder alignment and resource prioritization.</em></strong></li><li><strong><em>Experience with EU MDR and labeling.</em></strong></li><li><strong><em>Bachelor&#39;s Degree in Engineering.</em></strong></li><li><strong><em>6+ years of post-graduate work experience.</em></strong></li><li><strong><em>Experience in new product introduction.</em></strong></li></ul><h2>Job Description</h2><p>Lead and manage projects for implementing manufacturing strategies for new neurovascular products, focusing on venous thromboembolism clot removal. This role requires accountability for all design transfer activities to deliver the product on time, within scope, maintaining quality, and adhering to budget constraints.</p><p><br></p><h2>Responsibilities</h2><ul><li>Manage project and product costs while proactively identifying and mitigating project risks.</li><li>Activate and motivate the project team to drive project success and achieve goals on time.</li><li>Collaborate closely with R&amp;D, production, and suppliers to understand end-customer needs and ensure successful project implementation.</li><li>Innovate and improve current project management tools and PMO governance.</li><li>Ensure stakeholder alignment and resource prioritization.</li><li>Escalate employee performance and any workflow issues.</li><li>Review deliverables and perform spot checks.</li></ul><h2>Work Environment</h2><p>This position is onsite in Irvine, CA. The role offers 2 weeks of PTO (burdened) and 10 client-paid holidays. The work environment emphasizes collaboration with cross-functional teams and focuses on innovation in project management processes.</p>

Regulatory Affairs Project Manager

<p><strong>Regulatory Affairs Specialist needed in Grand Prairie, Texas!</strong></p><p><strong>Description/Job Duties:</strong></p><ul><li>Ensure lab practices align with FDA, Health Canada, and international regulatory standards</li><li>Maintain and review documentation for product testing, adverse event reporting, and compliance</li><li>Support audits and regulatory submissions for personal care and OTC products</li><li>Collaborate with QA and R&amp;D to ensure product safety and regulatory readiness</li><li>Monitor regulatory updates and implement changes in lab protocols accordingly</li></ul><p><strong>Pay: </strong>60,000-80,000 USD Yearly</p><p><strong>Education: </strong>College degree required</p><p><strong>Experience:</strong> 2-5 years experience in Regulatory Affairs in the Over-the-Counter Drug, Cosmetic, and/or Food Industry</p>

Regulatory Affairs Specialist

<h1><strong>Job Title: Regulatory Specialist</strong></h1><p><br></p><h2>Job Description</h2><p>We are seeking a global regulatory specialist based in Chicago, IL. The role involves creating ingredient statements and nutrition fact panels while reviewing and approving raw materials and formulas for compliance with FDA regulations and standards.</p><p><br></p><h2>Responsibilities</h2><ul><li>Independently create and validate technical lab copy through application of global regulations such as Codex, FDA, CFIA, FSANZ, FSA, CFDA, COFEPRIS, and standards of nutrition and food science.</li><li>Provide ingredient, formula, claim, labeling, and regulatory guidance to cross-functional teams on commercialization projects, including formula renovations, ingredient supply chain continuity, and formula line extensions.</li><li>Offer proactive and risk-based regulatory recommendations on ingredient, formula, claim, and labeling to cross-functional stakeholders on complex commercialization projects.</li><li>Review, register, and certify raw materials and finished goods with third-party certification bodies such as Kosher, Organic, Gluten-Free, and non-GMO.</li><li>Collaborate cross-functionally to review label content and ensure regulatory standards are met.</li><li>Work within SAP PLM to review and approve ingredients, formulas, and graphics.</li><li>Research information and stay informed about upcoming regulatory changes, and identify and assess regulatory risks in commercialization projects.</li><li>Partner with external regulatory experts to build internal expertise.</li><li>Develop SOPs and related trainings.</li><li>Co-lead third-party certification audits.</li></ul><h2>Essential Skills</h2><ul><li>3+ years experience in a regulatory position with a food company following US and global regulations.</li><li>Proficiency in CFR21, FDA, SAP, food regulatory processes, nutrition fact panels, ingredient statements, and EU regulations.</li><li>Experience with EU, Asia, or South American food regulations.</li><li>Proficiency in writing ingredient statements and nutrition fact panels.</li><li>Experience reviewing ingredients, formulas, and graphics.</li><li>Knowledge of PLM or SAP systems.</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>Experience with cross-functional teams.</li><li>Strong communication skills, both verbal and written.</li><li>Adaptability and flexibility to change.</li><li>Strong prioritization and time management skills.</li></ul><h2><br></h2>

Regulatory Specialist

<h1 style="text-align: center;"><strong>Job Title: Reliability Engineer</strong></h1><p><br></p><h2>Job Description</h2><p>We are seeking a highly skilled and proactive Electrical Reliability Engineer to join our dynamic team. This role is critical in ensuring the safe, efficient, and reliable operation of our plant’s electrical infrastructure, instrumentation systems, and combustion burner technologies. The ideal candidate will bring a strong foundation in electrical engineering, a passion for continuous improvement, and a commitment to operational excellence.</p><p><br></p><h2>Responsibilities</h2><ul><li>Maximize Overall Equipment Effectiveness (OEE) through systematic evaluation and improvement initiatives utilizing established electrical maintenance, reliability, and engineering best practices and processes.</li><li>Champion and drive optimization of the CMMS to continually improve efficiency and effectiveness of maintenance programs.</li><li>Identify, develop and leverage internal and external subject matter expertise to drive improvements in maintenance and reliability execution.</li><li>Develop engineering solutions to repetitive failures and all other problems that adversely affect plant operations, including capacity, quality, cost, or regulatory compliance issues.</li><li>Apply Reliability modeling and prediction, Root Cause Analysis (RCA), Failure Mode and Effects Analysis (FMEA), and Asset criticality assessments.</li><li>Oversee calibration, maintenance, and reliability of process instrumentation such as pressure, temperature, flow, and level.</li><li>Support maintenance team by advising on critical spare instrumentation parts, rebuild kits, and instruments.</li><li>Lead instrumentation upgrades and support commissioning of new equipment.</li><li>Develop documentation and standard operating procedures (SOPs) for instrumentation systems.</li><li>Monitor and optimize performance of combustion systems used in smelting and refining processes.</li><li>Ensure burner systems meet environmental and safety regulations, including emissions and flame safety.</li><li>Troubleshoot burner control systems, including flame scanners, actuators, and fuel delivery systems.</li><li>Collaborate with process engineers to improve thermal efficiency and reduce fuel consumption.</li></ul><h2>Essential Skills</h2><ul><li>Bachelor’s degree in Electrical Engineering or related field.</li><li>5+ years of experience in industrial electrical engineering, preferably in metals, recycling, or heavy manufacturing.</li><li>Strong knowledge of electrical codes, instrumentation, and combustion systems.</li><li>Familiarity with electrical design software (e.g., AutoCAD Electrical, ETAP) and control systems (e.g., Allen-Bradley, Siemens).</li><li>Strong knowledge of electrical equipment found in low voltage electrical distribution systems, including transformers, switch gear, power circuit breakers, and grounding systems.</li><li>Experience with motor control centers, motor control circuits, VFDs, soft starters, electrical protection systems, smart MCCs, and relays.</li><li>Industrial instrumentation design, specification, and maintenance support.</li><li>Process instrumentation familiarity for flowmeters, level transmitters, temperature transmitters, analyzers, and weighing systems.</li><li>Familiarity with regulatory requirements and safety standards in a heavy industrial plant setting.</li><li>Knowledge of electrical codes and standards (IEEE, ISA, NFPA, CSA).</li><li>Experience managing small capital projects in coordination with site maintenance, operations teams, and capital project group.</li><li>Demonstrated ability to revise procedures relating to inspection, repair, and maintenance as required.</li><li>Experience working with third-party engineering consulting firms specializing in engineering evaluations.</li><li>Solid experience in facilitating Root-cause Analysis and corrective actions.</li><li>Excellent problem-solving, project management, and communication skills.</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>Ability to work in a fast-paced, industrial environment.</li><li>Knowledge of HART communication protocols for transmitter configuration.</li></ul><h2>Work Environment</h2><p>The role requires working onsite from Monday to Friday, 7 AM to 4 PM. Candidates must have the ability to move about the plant and work in hot production areas, as well as wear necessary equipment in designated areas.</p>

Reliability Engineer

<h1 style="font-weight: 700;">Job Title: Reliability Engineer</h1><br><h2>Job Description</h2><p>As a Reliability Engineer, you will play a crucial role in ensuring that plant maintenance activities are executed and coordinated in a cost-effective manner by reducing waste and improving wrench time. You will conduct analyses of usage rates and equipment criticality to support a comprehensive parts inventory management plan, while scoping and evaluating the full extent of maintenance work needed to support reliable performance of production processes. Your efforts will drive the continuous improvement of maintenance systems through the establishment of performance objectives, execution of projects, and sharing of best practices.</p><br><h2>Responsibilities</h2><ul><li>Ensure plant maintenance activities are executed and coordinated cost-effectively.</li><li>Conduct analyses of usage rates and equipment criticality for parts inventory management.</li><li>Evaluate maintenance work needed for reliable production performance.</li><li>Drive continuous improvement of maintenance systems.</li><li>Resolve day-to-day maintenance issues while balancing projects across departments.</li><li>Understand and apply baseline knowledge of unit operations in maintenance functions.</li><li>Design, plan, and execute simple projects.</li><li>Recognize and implement opportunities for improvement.</li></ul><h2>Essential Skills</h2><ul><li>Mechanical engineering expertise.</li><li>Experience in preventive maintenance.</li><li>Proficiency in root cause analysis.</li><li>Continuous improvement capabilities.</li><li>SAP knowledge.</li><li>Reliability engineering experience.</li><li>Mechanical aptitude.</li><li>Mechanical design skills.</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>Bachelor&#39;s degree in Engineering; mechanical or electrical required.</li><li>Experience with high-speed rotating equipment.</li><li>Knowledge of non-destructive testing.</li><li>Utilities maintenance experience.</li><li>Project management skills.</li></ul><h2>Work Environment</h2><p>This role involves spending 70% of the time in the office doing analysis and planning, and 30% on the floor performing tasks. You will be the only reliability engineer on the team, supported by a range of maintenance technicians. The position requires less than 5% travel.</p><br>

<h1 style="font-weight: 700;">Job Title: Reliability Engineer</h1><br><h2>Job Description</h2><p>We are seeking a highly skilled and proactive Electrical Reliability Engineer to join our dynamic team. This role is critical in ensuring the safe, efficient, and reliable operation of our plant’s electrical infrastructure, instrumentation systems, and combustion burner technologies. The ideal candidate will bring a strong foundation in electrical engineering, a passion for continuous improvement, and a commitment to operational excellence.</p><br><h2>Responsibilities</h2><ul><li>Maximize Overall Equipment Effectiveness (OEE) through systematic evaluation and improvement initiatives utilizing established electrical maintenance, reliability, and engineering best practices and processes.</li><li>Champion and drive optimization of the CMMS to continually improve efficiency and effectiveness of maintenance programs.</li><li>Identify, develop and leverage internal and external subject matter expertise to drive improvements in maintenance and reliability execution.</li><li>Develop engineering solutions to repetitive failures and all other problems that adversely affect plant operations, including capacity, quality, cost, or regulatory compliance issues.</li><li>Apply Reliability modeling and prediction, Root Cause Analysis (RCA), Failure Mode and Effects Analysis (FMEA), and Asset criticality assessments.</li><li>Oversee calibration, maintenance, and reliability of process instrumentation such as pressure, temperature, flow, and level.</li><li>Support maintenance team by advising on critical spare instrumentation parts, rebuild kits, and instruments.</li><li>Lead instrumentation upgrades and support commissioning of new equipment.</li><li>Develop documentation and standard operating procedures (SOPs) for instrumentation systems.</li><li>Monitor and optimize performance of combustion systems used in smelting and refining processes.</li><li>Ensure burner systems meet environmental and safety regulations, including emissions and flame safety.</li><li>Troubleshoot burner control systems, including flame scanners, actuators, and fuel delivery systems.</li><li>Collaborate with process engineers to improve thermal efficiency and reduce fuel consumption.</li></ul><h2>Essential Skills</h2><ul><li>Bachelor’s degree in Electrical Engineering or related field.</li><li>5+ years of experience in industrial electrical engineering, preferably in metals, recycling, or heavy manufacturing.</li><li>Strong knowledge of electrical codes, instrumentation, and combustion systems.</li><li>Familiarity with electrical design software (e.g., AutoCAD Electrical, ETAP) and control systems (e.g., Allen-Bradley, Siemens).</li><li>Strong knowledge of electrical equipment found in low voltage electrical distribution systems, including transformers, switch gear, power circuit breakers, and grounding systems.</li><li>Experience with motor control centers, motor control circuits, VFDs, soft starters, electrical protection systems, smart MCCs, and relays.</li><li>Industrial instrumentation design, specification, and maintenance support.</li><li>Process instrumentation familiarity for flowmeters, level transmitters, temperature transmitters, analyzers, and weighing systems.</li><li>Familiarity with regulatory requirements and safety standards in a heavy industrial plant setting.</li><li>Knowledge of electrical codes and standards (IEEE, ISA, NFPA, CSA).</li><li>Experience managing small capital projects in coordination with site maintenance, operations teams, and capital project group.</li><li>Demonstrated ability to revise procedures relating to inspection, repair, and maintenance as required.</li><li>Experience working with third-party engineering consulting firms specializing in engineering evaluations.</li><li>Solid experience in facilitating Root-cause Analysis and corrective actions.</li><li>Excellent problem-solving, project management, and communication skills.</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>Ability to work in a fast-paced, safety-conscious industrial environment.</li><li>Knowledge of HART communication protocols for transmitter configuration.</li></ul><h2>Work Environment</h2><p>The role requires working onsite from Monday to Friday, 7 AM to 4 PM. Candidates must have the ability to move about the plant and work in hot production areas, as well as wear necessary equipment in designated areas.</p><br>

<h1><strong>Job Title: Reliability Engineer</strong></h1><p><br></p><h2>Responsibilities</h2><ul><li>Coach the team on evaluating and improving the reliability of an electromechanical hand piece.</li><li>Help the team understand and apply concepts like Mean Time Between Failures (MTBF), Mean Time to Failure (MTTF), and Bathtub Curve analysis.</li><li>Assess whether the team has the right data, what additional data is needed, and whether accelerated testing is required.</li><li>Recommend medium-level design changes to improve reliability, avoiding full redesigns.</li><li>Guide Return on Investment (ROI) analysis for potential design improvements.</li></ul>

<h1 style="font-weight: 700;">Job Title: Pharmacy Technician</h1><br><h2>Job Description</h2><p>We are seeking dedicated pharmacy technicians to join a dynamic team in the EST timezone. Technicians will be responsible for reviewing Prior Authorizations for coverage determination as part of a Pharmacy Services department within a large healthcare insurance company. The role involves approving or denying requests, which are then sent to a Pharmacist for final review. This position involves handling various health plans and medication types, with minimal phone work primarily involving outbound calls.</p><br><h2>Responsibilities</h2><ul><li>Track coverage determination requests and obtain verbal authorizations.</li><li>Approve requests based on established criteria and enter decisions into the PBM system.</li><li>Notify providers and members of approval or denial outcomes.</li><li>Respond to client inquiries and refer requests for specialty drugs.</li><li>Contact providers for additional information and notify stakeholders of decision outcomes.</li><li>Request detailed clinical information from prescribers.</li><li>Assist with inbound and/or outbound patient or physician calls, if necessary.</li></ul><h2>Essential Skills</h2><ul><li>High School diploma or equivalent.</li><li>Current Pharmacy Registration and Certification as required by state of operation.</li><li>Basic computer skills.</li><li>Strong proficiency in Microsoft Office and Outlook.</li><li>Pharmacy technician license.</li><li>Certified Pharmacy Technician (CPhT).</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>National certification such as PTCB or NHA.</li><li>Experience with prior authorization processes.</li><li>Experience in retail pharmacy, call center, hospital, or specialty pharmacy settings.</li><li>Familiarity with Medicare and Medicaid prescription benefits.</li></ul><h2>Work Environment</h2><p>This is a professional remote work environment requiring strong WiFi and a private office space with a closed door. You will be working on multiple screens and systems. The schedule requires availability Monday through Friday, 8 am to 8 pm in your local timezone, with rotating weekends every 4-6 weeks and some holidays. Training is from 10 am to 6:30 pm EST, followed by a regular shift. Schedules are provided three months in advance. The company offers flexibility for those who meet metrics and have tenure. Equipment provided includes a computer, monitor, and headset.</p><br>

Remote  Pharmacy Technician

<p style="text-align: center;"><strong><u>Quick Hiring for Remote Pharmacy Technician</u></strong></p><p style="text-align: center;"><br></p><p><strong><u>Job Description:</u></strong></p><ul><li>Order Entry for new/refill medications.</li><li>Respond to customer inquiries as necessary.</li><li>Assist in other phases of computer operations including billing procedures</li><li>Prior Authorizations</li><li>Insurance Verifications</li></ul><p><strong><u>Qualifications:</u></strong></p><ul><li><strong>2+ year of Prior Authorization pharmacy experience is Mandatory</strong></li><li><strong>Pharmacy Tech State Certification is Mandatory AND PTCB 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>

Remote - Prior Authorization Pharmacy Technician

<p style="text-align: center;"><strong><u>Immediate Hiring for Remote Pharmacy Technician</u></strong></p><p style="text-align: center;"><br></p><p><strong><u>Job Description:</u></strong></p><ul><li>Order Entry for new/refill medications.</li><li>Respond to customer inquiries as necessary.</li><li>Assist in other phases of computer operations including billing procedures</li><li>Prior Authorizations</li><li>Insurance Verifications</li></ul><p><strong><u>Qualifications:</u></strong></p><ul><li><strong>2+ year of Prior Authorization pharmacy experience is Mandatory</strong></li><li><strong>Pharmacy Tech State Certification is Mandatory AND PTCB 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>

<h1 style="font-weight: 700;">Job Title: BIM Designer</h1><br><h2>Job Description</h2><p>We are seeking a talented BIM Designer to assist in producing technology construction drawings using Revit. You will play a pivotal role in modeling construction plans, details, smart schedules, and parametric Revit families ranging from LOD 200 to 400.</p><br><h2>Responsibilities</h2><ul><li>Produce technology construction drawings using Revit.</li><li>Model construction plans, details, smart schedules, and parametric Revit families (LOD 200-400).</li><li>Support low voltage design work.</li><li>Design physical security systems using Revit, BIM, AutoCAD, Navisworks, and construction documentation.</li><li>Complete redlines handed off in Revit.</li><li>Place physical security systems within drawing sets.</li></ul><h2>Essential Skills</h2><ul><li>Proficiency in Revit.</li><li>Experience supporting low voltage design work.</li><li>Experience designing physical security systems in Revit.</li><li>Experience with construction documentation.</li><li>1-2 years minimum of Revit experience.</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>Experience with data center projects is a plus.</li><li>Experience working with low-voltage systems.</li></ul><h2>Work Environment</h2><p>This is a fully remote role with an 8-12 month assignment and the possibility for extension. The position is part-time, requiring 15-20 hours that can be completed off hours. Ideally, candidates should be available for 1 hour every day for coordination with the team, with touchpoints every 2-3 days. Independent work is expected, and candidates do not need to be local to Chicago. Candidates will connect remotely using their own laptops with Revit and Bluebeam systems, as equipment will not be provided. Training during the first week will be conducted to familiarize you with the Revit systems and families.</p><br>

Remote BIM Designer

<h1><strong>Job Title: Remote Technical Writer (Active Secret Clearance)</strong></h1><p><br></p><h2><strong>Job Description</strong></h2><p>Join a high-performing team dedicated to developing technical documentation for advanced military systems, including radars for F-22, F-35, Joint Strike Fighter, F-16, B-1B, MESA, G/ATOR, VADER, and other UAV systems.</p><p><br></p><h2><strong>Responsibilities</strong></h2><ul><li>Write, rewrite, and edit technical documents such as technical procedure manuals, user manuals, programming manuals, service manuals, operational specifications, and related technical publications to communicate technical information clearly and effectively to a diverse audience.</li><li>Oversee the preparation of illustrative materials, selecting drawings, sketches, diagrams, and charts.</li><li>Conduct quality reviews of materials.</li><li>Publish materials in various formats, including page-based, electronic (basic and interactive), and structured (HTML, XML, and SGML).</li><li>Collaborate with task leads, writers, engineers, and instructors to develop and deliver sensor/system technical manuals in varying levels of detail and delivery formats.</li><li>Perform Desktop Publishing tasks for program/project reports, whitepapers, articles, and other documents.</li><li>Research and compile information from program documents and engineering sources to develop manual outlines and adhere to military/civilian specifications and standards of technical writing.</li><li>Perform other duties as assigned.</li></ul><h2><strong>Essential Skills</strong></h2><ul><li>Bachelor’s Degree in STEM discipline or related field, or military operations and maintenance experience with radar, communications, electro-optics, networks, and information technology-based sensors/systems.</li><li>Expert knowledge of MS Office Products.</li><li>Minimum of 2 years’ experience with structured authoring applications such as MadCap, FrameMaker, or Arbortext.</li><li>Proven ability to manage several tasks simultaneously.</li><li>Excellent attention to detail.</li><li>Possess and maintain Department of Defense (DoD) Secret clearance.</li><li>Self-starter and engaged team member.</li></ul><h2><strong>Additional Skills &amp; Qualifications </strong><em>(Preferred)</em></h2><ul><li>Minimum of 5 years’ technical writing experience.</li><li>Knowledge of standard content management strategies.</li><li>Knowledge of Simplified Technical English (ASD-STE 100).</li><li>Knowledge of standards – XML, SGML, HTML, S1000 – for structured content.</li><li>Possess and maintain DoD Secret or Top Secret/Sensitive Compartmented Information (TS/SCI).</li></ul>

Remote Cleared Technical Writer

<p><strong>A design and installation company for HVAC and refrigeration projects is looking to add an Electrical Engineer to their team! While this position is remote, individuals must be located in either Eastern or Central Time Zones. </strong></p><p><br></p><p><strong><u>Job Description</u>:</strong></p><ul><li>Design and specify (medium and low voltage) power systems for large scale capital HVAC replacement and one-off complex projects</li><li>Efforts include but are not limited to project/peak load calculations, one-line diagrams, equipment sizing and selection, equipment layouts, and associated system controls as part of project planning, development and construction/permit drawing design</li><li>Interact with a multi-disciplinary engineering team to review, define and design to meet customer requirements</li><li>Candidate needs to be motivated, highly self-directed and capable of organizing/planning/running multiple concurrent projects with minimal direction meeting deadlines with high quality deliverables</li><li>Coordinate and develop client relationships</li></ul><p><strong><u>Qualifications</u>:</strong></p><ul><li>Bachelors or Masters Degree in Structural Engineering</li><li>Professional Engineering (PE/SE) License or actively pursuing this</li><li>7+ years professional experience</li><li>Experience working directly with clients</li><li>Proficiency in Revit, AutoCAD, Microsoft Suite applications</li><li>Ability to work in a fast-paced environment on a multi-disciplinary team</li><li>Knowledge of building and energy codes</li><li>Must be located in Eastern or Central Time Zones</li></ul>

Remote Electrical Engineer

<p><strong><em>Overview:</em></strong></p><p>We are seeking experienced Marine Designers to help support a project designing and creating new vessels for the US Special Forces. </p><p><br></p><p><strong><em>Description:</em></strong></p><ul><li>Drafting &amp; Designing vessels and components.</li><li>Working with team to create the most efficient processes.</li></ul><p><strong><em>Qualifications:</em></strong></p><ul><li>3+ years of marine design experience. </li><li>Experience with Solidworks.</li><li>Marine Design disciplines seeking: structural, mechanical, piping, HVAC. (Possibly electrical)</li></ul>

Remote Marine Designer

<p><strong>Description</strong></p><p>3 month++ contract (will likely be longer) supporting a large client. </p><p><br></p><p>Client is chasing a project in MD that involves the design of a blending system for a vinyl siding and exterior trim extrusion plant.  when they get the project, design will begin in August and continue through November. The engineer does not have to relocate but occasional travel to the customer in MD will be required.</p><p> </p><p>The engineer will need the following skills/capabilities</p><p>High Level</p><p>Pneumatic conveying- dilute and dense phase</p><p>Dust collection</p><p>Weigh hoppers- load cells</p><p>Bulk bag unloaders</p><p> </p><p>Medium Level</p><p>Structural supports for equipment</p><p> </p><p>Coordinate with others</p><p>PLC controls</p><p>Weight controls</p><p>Power and control wiring</p><p> </p><p>Scope will be to specify equipment, develop design documents, work with customer staff on approvals, assist with operating manual development</p><p><strong>Skills</strong></p><p>Mechanical Engineering, Material handling system design, AutoCAD OR Solidworks, Social skills</p><p><strong>Top Skills Details</strong></p><p>Mechanical Engineering, Material handling system design, AutoCAD OR Solidworks</p><p><strong>Additional Skills &amp; Qualifications</strong></p><p>Material handling system design</p><p>Mechanical engineering experience</p><p>AutoCAD OR Solidworks experience</p><p><strong>Experience Level</strong></p><p>Intermediate Level</p>

Remote Mechanical Design Engineer

<h2><strong>Structural Engineer (100% Remote)</strong></h2><p>One of the top nuclear engineering firms in the United States is looking to add a <strong>Structural Engineer</strong> to their team! If you have expertise in structural analysis and design for nuclear power plants, industrial facilities, or similar environments, we want to hear from you.</p><h3><br></h3><h3><strong>﻿Job Description:</strong></h3><p>As a Structural Engineer, you will be responsible for:</p><ul><li>Performing structural analysis (static or response spectra) for seismic and other load combinations per plant criteria</li><li>Designing equipment and piping supports, building structural frames, and foundations</li><li>Conducting piping or pipe support analysis per ASME Section III or B31.1 design requirements</li><li>Developing lifting assembly, rigging, or crane designs</li><li>Applying AISC steel and ACI concrete design codes</li><li>Conducting component stress analysis (GTSTRUDL or ANSYS)</li><li>Performing plant impact reviews and evaluations</li><li>Assessing existing structures and developing retrofit designs</li></ul><h3><strong>Qualifications:</strong></h3><ul><li>Bachelor’s Degree in Civil and/or Structural Engineering from an accredited U.S. college</li><li>Experience working with <strong>nuclear power plants, industrial facilities, power plants, <u>or </u>relevant project types</strong></li><li>Strong understanding of structural engineering principles and seismic analysis</li><li>Must be based in <strong>Central or Eastern time zones</strong></li></ul><h3><strong>Why Join Us?</strong></h3><ul><li><strong>100% remote work</strong></li><li>Competitive compensation and benefits package</li><li>Work with an industry-leading nuclear engineering firm</li><li>Collaborate with highly skilled professionals on challenging and meaningful projects</li></ul><h1><br></h1>

Remote Nuclear Structural Engineer

<h3 style="text-align: center;"><strong>Pharmacist (Fully Remote)</strong></h3><p style="text-align: center;">Location: Remote (U.S. only; excluding CA, HI, VA)</p><p style="text-align: center;">Schedule: Full-time, M–F, with possible overtime during peak season</p><p style="text-align: center;">Training: 10–12 weeks, M–F, 8:00 AM–4:30 PM CST (No time off during training)</p><hr><h3>Overview</h3><p>Join a remote team conducting utilization management reviews (e.g., prior authorizations, coverage exceptions). Work independently within a collaborative pharmacy team. Performance is measured by monthly quality and productivity goals.</p><hr><h3>Key Qualifications</h3><ul><li>PharmD or BS in Pharmacy</li><li>2+ years in retail, managed care, or clinical pharmacy</li><li>Active U.S. pharmacist license in good standing</li><li>Strong decision-making and multitasking skills</li><li>Self-motivated and results-driven</li></ul><hr><h3>Preferred Skills</h3><ul><li>PBM or Case/Care Management experience</li><li>Retail pharmacy <span style="color: rgb(8, 7, 7); background-color: none;">background</span> preferred</li><li>Proficient in Word, Excel, and basic IT troubleshooting</li><li>Typing speed of 35+ WPM</li></ul><hr><h3>Work Environment</h3><ul><li>100% remote (must reside outside CA, HI, VA)</li><li>Licensure can be from any U.S. state</li><li>Shifts typically start between 9–10 AM CST</li><li>Weekend and holiday rotations based on seniority</li><li>Peak season: Nov–May (overtime may be required)</li><li>Annual unpaid time off: 80–120 hours (post-training)</li></ul><hr><h3>Why Apply?</h3><p>Ideal for pharmacists seeking a remote role outside retail. Potential for cross-training in specialized areas and long-term employment. Competitive benefits available upon conversion.</p><h1 style="text-align: center;"><br></h1><h3><br></h3>

Remote Pharmacist

<p><br></p><h1 style="text-align: center;"><strong>Remote Pharmacist (100% remote; Entry Level, PBM)</strong></h1><p style="text-align: center;"><strong>Long-Term Opportunity | Offers Benefits | Pay: $55/hr. | Growth Opportunities</strong></p><p><br></p><h2><strong>Job Description</strong></h2><p>Your main role will be utilizing your clinical skills to complete utilization management reviews, including prior authorizations, coverage exceptions, and quantity limit exceptions. You will perform these reviews independently within a team of your peers and other pharmacy professionals.</p><p><br></p><h2><strong>Responsibilities</strong></h2><ul><li>Conduct utilization management reviews independently.</li><li>Participate in a team of pharmacy professionals to ensure high-quality service.</li><li>Meet monthly quality and productivity goals.</li><li>Assist in cross-department training opportunities, such as Medication Therapy Management or Call Center Counseling, if available.</li></ul><h2><strong>Essential Skills</strong></h2><ul><li>Doctor of Pharmacy (PharmD) or Bachelor of Science Pharmacy degree.</li><li>2 years of work experience in retail, managed care, or clinical pharmacy.</li><li>Current pharmacist license in good standing with the State Board of Pharmacy.</li></ul><h2><strong>Additional Skills &amp; Qualifications</strong></h2><ul><li>Previous Pharmacy Benefits Management or Case/Care Management experience preferred.</li><li>Retail experience, such as CVS or Walgreens, is highly preferred over hospital experience.</li></ul><h2><strong>Work Environment</strong></h2><ul><li>This is a fully remote work-from-home position, open to candidates located in any state except California, Hawaii, or Virginia.</li><li>Candidates can be licensed in any U.S. state but cannot reside in California, Hawaii, or Virginia.</li><li>Shifts typically start between 9-10 am CST and are determined by team bid based on seniority.</li><li>Candidates should expect full-time schedules with potential overtime during peak seasons, typically November through May.</li><li>The team rotates weekend shifts, with holidays determined by a team bid.</li><li>Training is mandatory and lasts approximately 10-12 weeks, with hours from 8 am to 4:30 pm CST, Monday through Friday. Time off during training is limited, and any required time off must be discussed during the interview for consideration.</li></ul><h3><br></h3>

Remote Pharmacist - Entry Level

<p><strong>Job Title: Remote Pharmacy Technician</strong></p><p><br></p><p><strong><u>Job Description:</u></strong></p><p>As a Remote Pharmacy Technician, you will play a crucial role in managing coverage determination requests and ensuring efficient communication between providers, members, and the pharmacy benefit management (PBM) system. Your key duties will include:</p><p><br></p><ul><li>Monitoring and prioritizing coverage determination requests submitted by providers.</li><li>Approving coverage determination requests based on defined criteria and entering decisions into the PBM system.</li><li>Notifying physicians, providers, and members of coverage determination request decisions.</li><li>Responding to client inquiries regarding authorization approvals and PBM online applications.</li><li>Referring coverage determination requests for specialty drugs to delegated vendors or clients for processing.</li><li>Contacting providers for additional information to facilitate coverage determination reviews.</li><li>Maintaining accurate records of all coverage determination requests and decisions.</li><li>Building a culture of care, engagement, and recognition with clear outcomes.</li></ul><p><strong><u>Hard Skills:</u></strong></p><ul><li>Registered Pharmacy Technician license.</li><li>Strong computer skills, including proficiency in Microsoft Suite.</li><li>Attention to detail and excellent organizational skills.</li><li>Strong communication and interpersonal skills.</li><li>Ability to work independently in a remote setting.</li></ul><p><strong><u>Preferred Qualifications:</u></strong></p><ul><li>Previous experience in a retail pharmacy setting.</li><li>Prior authorization experience.</li><li>Familiarity with third-party claims processing.</li><li>Certified Pharmacy Technician (PTCB or NHA).</li></ul><p><strong><u>Work Environment:</u></strong></p><ul><li>This is a fully remote position.</li><li>Must have a dedicated workspace with reliable high-speed internet.</li><li>Flexible scheduling, including availability for weeknights and weekends.</li></ul>

Remote Pharmacy Technician

<h1 style="text-align: center;"><strong> Remote Pharmacy Technician</strong></h1><p><strong>Job Description</strong></p><p>We are seeking a dedicated Remote Pharmacy Technician to join our team working in the<strong>EST time zone</strong>. As a Pharmacy Technician, you will be responsible for reviewing Prior Authorizations for coverage determination for a Pharmacy Services department within a large healthcare insurance company. You will make initial approval or denial decisions before passing them to Pharmacists for final review.</p><p><strong>Responsibilities</strong></p><ul><li>Track coverage determination requests</li><li>Obtain verbal authorizations</li><li>Approve requests based on criteria</li><li>Enter decisions into the PBM system</li><li>Notify providers and members of decisions</li><li>Respond to client inquiries</li><li>Refer requests for specialty drugs</li><li>Contact providers for additional information</li><li>Notify stakeholders of decision outcomes</li><li>Obtain detailed clinical information from prescribers</li><li>Assist with inbound and/or outbound patient or physician calls if needed</li></ul><p><strong>Requirements</strong></p><ul><li>High School diploma or GED</li><li><strong>State Registration AND National Certification</strong></li><li>Basic computer skills</li><li>Experience with Prior Authorization processes</li><li>Proficiency in Microsoft Office and Outlook</li><li>Data entry skills</li></ul>

<h1><strong>Job Title: Power Generation Designer</strong></h1><p><br></p><h2>Job Description</h2><p>As a Power Generation Designer, you will be involved in designing conventional power generation systems, including simple cycle, combined cycle.</p><p><br></p><h2>Responsibilities</h2><ul><li>Design conventional power generation systems, including simple cycle, combined cycle, 1on1, and 2on1 configurations.</li><li>Work with circuit routing, duct banks, and cable trays.</li><li>Utilize AutoCAD Electrical and Inventor or other 3D software for electrical design.</li></ul><h2>Essential Skills</h2><ul><li>Experience in conventional power generation design, including simple cycle, combined cycle, 1on1, and 2on1.</li><li>Proficiency in circuit routing, duct bank, and cable tray design.</li><li>Proficiency in AutoCAD Electrical and Inventor or other 3D software.</li></ul><p><br></p><p><br></p><h2>REMOTE OR HYBRID - depending on experience level and location-first 90 days are in-office for training</h2>

Remote Power Generation Designer

<h1 style="font-weight: 700;">Job Title: VDC Designer</h1><br><h2>Job Description</h2><p>As a VDC Designer, you will play a crucial role in ensuring the accuracy and efficiency of virtual design and construction processes. Your primary responsibilities will include linking Revit files, creating and modifying schedules for drawings, and setting up view filters and templates. You will be responsible for accurately laying out conduit racks with proper parameters and ensuring that all modeling is done to avoid clashes. Additionally, you will model electrical equipment and light fixtures in accordance with project specifications and submittals, and perform clash detection tests. Your role will also involve reviewing and marking up drawings, placing and coding APL points, and exporting point files from projects.</p><br><h2>Responsibilities</h2><ul><li>Link Revit files and manage schedules for drawings.</li><li>Set up view filters and templates for projects.</li><li>Layout conduit racks with correct parameters, spacing, and sizing.</li><li>Model electrical equipment and light fixtures following project specs.</li><li>Perform clash detection and export NWC files for tests.</li><li>Review, markup, and ensure corrections on drawings by others.</li><li>Place and code APL points and export point files from projects.</li></ul><h2>Essential Skills</h2><ul><li>Proficiency in BIM, Revit MEP, Navisworks, and Bluebeam.</li><li>Experience with BIM 360 and electrical systems.</li><li>BS in Construction Management, Engineering, Architecture, or BIM Technology.</li><li>5-7 years of field and/or technical experience, or 3-4 years of software experience.</li><li>Advanced understanding of NEC and BICSI codes.</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>Experience in electrical and specialty systems field.</li><li>Job-related experience in 2D and 3D modeling.</li><li>Familiarity with Google Suite, Smartsheet, and Excel.</li></ul><h2>Work Environment</h2><p>The work environment involves collaborative use of advanced design software such as Revit, Navisworks, and Bluebeam. You will work in a dynamic setting that requires coordination with various project teams. The role may require occasional site visits to ensure design accuracy and compliance.</p><br>

Remote VDC Designer

<h1 style="font-weight: 700;">Job Title: Requirements Engineer</h1><br><h2>Job Description</h2><p>We are seeking a highly skilled Requirements Engineer who excels at translating user needs into testable software requirements. The ideal candidate will lead and coach users in defining their needs while being an expert in software and systems life cycle controls for both waterfall and Agile methodologies. This role requires expertise in system deliverables, including documenting requirements (User &amp; System), software classification, risk assessment, and V&amp;V Plans/Reports. Candidates must be knowledgeable in Quality Systems used for ISO and FDA compliance and possess excellent technical writing skills.</p><br><h2>Responsibilities</h2><ul><li>Translate user needs into clear, testable software requirements.</li><li>Lead and coach users in defining their requirements.</li><li>Document system deliverables such as User and System requirements, software classification, risk assessment, and V&amp;V Plans/Reports.</li><li>Ensure compliance with ISO and FDA standards in software and systems life cycle controls.</li><li>Provide expertise in both waterfall and Agile methodologies.</li></ul><h2>Essential Skills</h2><ul><li>Expertise in systems engineering, software validation, and software quality.</li><li>Strong requirement documentation skills.</li><li>Excellent understanding and working knowledge of ISO/IEC standards.</li><li>Previous experience as a Requirements Engineer.</li><li>Understanding of V&amp;V to write testable requirements.</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>Experience in environments that have implemented ISO/IEC standards.</li><li>Demonstrated ability to transform customer input into user requirements.</li><li>Familiarity with project/program management as it relates to requirements engineering.</li></ul>

Requirements Engineer

<h1><strong>Job Title: Research and Development Engineer</strong></h1><p><br></p><h2>Job Description</h2><p>This position is focused on the design of new industrial packaging equipment. The role involves designing and developing parts and assemblies using SolidWorks, creating models, assembly drawings, and manufacturing/fabrication drawings.</p><p><br></p><h2>Responsibilities</h2><ul><li>Conduct market research to identify emerging trends, technologies, and materials.</li><li>Collaborate with teams to translate voice of customer and market needs into product concepts.</li><li>Evaluate and experiment with materials to enhance performance, sustainability, and cost-effectiveness.</li><li>Oversee the prototyping and testing phases of new product development.</li><li>Implement testing protocols to validate the performance and durability of new packaging concepts.</li><li>Work closely with internal teams to ensure integration of new products into the sales and production pipeline.</li><li>Communicate with external partners, suppliers, and industry experts.</li><li>Prepare reports and presentations to update stakeholders on the progress of ongoing projects.</li><li>Support existing products including root cause analysis, engineering change requests, and manufacturing support.</li></ul><h2>Essential Skills</h2><ul><li>Bachelor’s degree in engineering.</li><li>3 plus years of experience in the packaging industry with a focus on food and/or beverage.</li><li>Proficiency in SolidWorks or Autodesk Inventor.</li><li>Strong understanding of materials, manufacturing processes, and quality standards.</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>Experience in research and development of new products.</li><li>Experience with Mathcad, FEA, or CFD.</li><li>Knowledge of Product Manufacturing Information (PMI) and machine tools.</li><li>Experience in conveyance and new product development.</li></ul><h2>Work Environment</h2><p>The position is based in a large manufacturing facility with automated equipment, offering a clean and updated office space. The work schedule is hybrid, with four days onsite and one day remote. The team consists of 12 engineers, with 4 dedicated to R&amp;D, and the facility supports a diverse range of exciting new projects.</p>

Research And Development Engineer

<h1><strong>Job Title: Research Assistant - Chemist</strong></h1><p><br></p><h2>Job Description</h2><p>Become a Research Assistant and play a crucial role in performing biological extractions on samples such as urine, blood, and plasma. Initially, you will focus on wet lab extractions, progressing to LC-MS (HPLC-Mass Spec) after training on instrumentation. Your responsibilities will also include running robotics for liquid handling and utilizing lab equipment such as balances, pH meters, and pipettes. You will work under GLP regulations and use software like eWorkbook, with each chemist equipped with a tablet.</p><p><br></p><h2>Responsibilities</h2><ul><li>Perform biological extractions on various samples including urine, blood, and plasma.</li><li>Focus on wet lab extractions, transitioning to LC-MS after training.</li><li>Operate robotics for liquid handling.</li><li>Utilize lab equipment such as balances, pH meters, and pipettes.</li><li>Work under GLP regulations and maintain accurate records using eWorkbook software.</li></ul><h2>Essential Skills</h2><ul><li>B.S. in Chemistry, Biochemistry, Biology, Microbiology, or related Life Science degree.</li><li>1-2 years of experience in a chemistry lab.</li><li>Proficiency in HPLC and experience or willingness to learn other chromatography techniques.</li><li>Strong attention to detail and excellent communication skills.</li><li>Ability to work effectively as a team player.</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>Mass Spec experience is advantageous.</li><li>Experience in food service, bartending, or client-facing roles is beneficial for fast-paced environments.</li><li>Demonstrated ability to multitask and work under pressure.</li><li>High ownership and responsibility for personal work and error recognition.</li></ul><h2><br></h2>

Research Assistant

<p><strong style="font-size: 16px;">Research Assistant – Entry Level</strong></p><p>We are seeking a detail-oriented and motivated Research Assistant to support clinical study operations in a dynamic and collaborative environment. This is an excellent opportunity for individuals interested in gaining hands-on experience in clinical research and healthcare.</p><p><br></p><p><strong>Key Responsibilities:</strong></p><ul><li>Assist study coordinators with daily clinic procedures, including participant check-ins, informed consent processes, administering electronic questionnaires, and supporting instrumentation and photography tasks.</li><li>Perform administrative duties such as preparing test materials, making appointment reminder calls, and quality-checking study documents.</li><li>Support the development and organization of study paperwork and documentation.</li><li>Ensure punctual attendance for all assigned studies and maintain a professional presence in the clinic.</li><li>Follow Good Clinical Practice (GCP) guidelines, standard operating procedures (SOPs), and applicable regulations.</li><li>Collaborate with other departments as needed and contribute to a positive team environment.</li><li>Deliver excellent customer service to both clients and study participants, maintaining respectful and professional interactions at all times.</li><li>Adhere to all safety and operational integrity protocols.</li></ul><p><strong>Qualifications:</strong></p><ul><li>Strong customer service orientation and communication skills.</li><li>Interest or experience in medical or clinical environments is a plus.</li><li>Comfortable using standard office equipment, including computers and phones.</li><li>Ability to work in a fast-paced, professional setting with attention to detail.</li></ul><p><strong>Experience Level:</strong> Entry Level</p><p><strong>Work Environment:</strong> Professional office and clinical setting. Monday - Friday 8am-5pm </p><p>Once sequester studies start end of Sept/October some studies will be 8 hours and some will be 12 hours</p><p>Schedule for sequester days will start at 6 or 7am and run through the end of the study (8 hours or 12 hours) - If working 12 hour study next day will be a short day.</p><p>Cosmetics research office</p>

<h1><strong>Job Title: Research Associate, Process Analytics</strong></h1><p><br></p><h2>Job Description</h2><p>Join a dynamic Process Analytics team as a Research Associate or <span style="color: rgb(8, 7, 7); background-color: none;">Senior</span> Research Associate to support the characterization of Lentiviral Vector (LVV). You will be trained by <span style="color: rgb(8, 7, 7); background-color: none;">senior</span> staff to perform a variety of molecular, cellular, biophysical, and biochemical protocols, working closely with other functions to test LVV samples. This role is pivotal in advancing pipeline and Analytical Development capabilities.</p><p><br></p><h2>Responsibilities</h2><ul><li>Assist with experimental design, execution, and analysis to support the development of gene therapy products.</li><li>Perform routine impurity and characterization testing, such as ELISA, qPCR, ddPCR, and flow cytometry, to support process development.</li><li>Maintain clear records of experimental work using an electronic notebook system in adherence to company guidelines.</li><li>Manage sample submissions for assigned methods and provide timely turnaround of data.</li><li>Exemplify company core values and adhere to company policies to ensure the safety and quality of gene therapy products and facilities.</li><li>Train on initial methods for qualification experiments, and upon proficiency, advance to additional methods.</li><li>Conduct daily experiments involving plate design, sample preparation, data analysis, and electronic notebook submission for review.</li><li>Maintain inventory of reagents and other lab supplies.</li></ul><h2>Essential Skills</h2><ul><li>Quality control and GMP knowledge.</li><li>Proficiency in laboratory techniques including aseptic techniques, chemistry, and QC.</li><li>Experience with ELISA, qPCR, ddPCR, flow cytometry, impurity testing, and characterization testing.</li><li>Familiarity with analytical development, process development support, and LIMS/QMS systems.</li><li>Understanding of gene therapy and viral transduction.</li><li>Experience with cell culture, PBMC, multi-channel flow cytometry, and T cell flow.</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>A BS in Biology, Biochemistry, or related discipline with no previous industry experience or an Associate’s Degree and 2 years of hands-on laboratory experience.</li><li>Hands-on experience with techniques such as ddPCR, qPCR, ELISA, and flow cytometry.</li><li>Excellent communication skills and ability to build collaborative relationships.</li><li>Experience with basic data analysis is a plus.</li><li>Self-motivated, organized, and clear documentation skills.</li><li>Ability to work in a fast-paced environment and manage multiple projects.</li></ul><h2><br></h2>

Research Associate, Process Analytics

<h2><strong>Job Title: Clinical Research Nurse Practitioner/Sub-Investigator</strong></h2><p><br></p><h2>Job Description</h2><p>Looking for a Clinical Research Nurse Practitioner/Sub-Investigator to provide clinical assessment and care, within the scope of licensure and in accordance with trial protocols, FDA Regulations, and ICH/GCP Guidelines, for research volunteers participating in Phase I-IV industry-sponsored and investigator-initiated/behavior focused clinical trials. </p><p><br></p><h2>Responsibilities</h2><ul><li>Utilize knowledge and skill to care for adult and pediatric patients in a clinical setting.</li><li>Document essential history information and physical exam components that support the study protocol.</li><li>Counsel, refer, and order as documented on the record.</li><li>Interpret diagnostic testing and refer abnormal results to physicians when necessary.</li><li>Refer to supervising physician or other healthcare providers as needed.</li><li>Maintain an active presence in local and national professional associations.</li><li>Meet productivity standards set by the department.</li><li>Participate in training programs to stay current on applicable knowledge and skills.</li><li>Complete Employee Assessment Form and plan for career development.</li><li>Assist in protocol development and review of research drafts for publication submission.</li><li>Perform other duties as assigned to ensure smooth department operations.</li></ul><h2>Required Skills &amp; Experience</h2><ul><li>Clinical research experience</li><li>Nurse Practitioner certification/licensure or previous Sub-Investigator experience</li><li>Physical assessment skills</li></ul><h2>Work Environment</h2><p>The work environment is hospital-based, providing a dynamic setting to engage in clinical trials and research. The role involves collaboration with various healthcare professionals and participation in ongoing training to ensure high standards of clinical care and research.</p>

Research Nurse Practitioner/Sub Investigator

<h1 style="font-weight: 700;">Job Title: Research Scientist - Mammalian Cell Lines</h1><br><h2>Job Description</h2><p>We are seeking a highly skilled scientist contractor with significant experience in transient transfection of mammalian cell lines, in vitro mammalian cell assays, cell line construction, and detailed scientific report writing in compliance with ALCOA+ standards. This contractor role is ideal for an industrious, detail-oriented scientist seeking to contribute expertise in mammalian cell engineering and assay development to support drug discovery and biotherapeutic projects at the cutting edge of pharmaceutical research.</p><br><h2>Responsibilities</h2><ul><li>Perform and optimize transient transfection protocols in mammalian cell lines such as HEK293, CHO, and other relevant models.</li><li>Design and execute a variety of in vitro assays to support cell line characterization, functional validation, and process development.</li><li>Construct stable and clonal mammalian cell lines for candidate evaluation, including vector construction, cloning, single cell selection, screening, and cell banking.</li><li>Maintain, troubleshoot, and scale mammalian cell cultures for both small- and midscale applications.</li><li>Precisely document all work in alignment with ALCOA+ principles for regulatory and quality compliance.</li><li>Generate comprehensive study reports, experimental protocols, and presentations for internal and external stakeholders.</li></ul><h2>Essential Skills</h2><ul><li>MS or PhD or equivalent experience in Biology, Molecular Biology, Cell Biology, Biochemistry, or a related field.</li><li>Demonstrated expertise in transient transfection and cell line construction in an industrial environment.</li><li>Hands-on experience with a wide range of in vitro cellular assays (ELISA, cytotoxicity, FACS, etc.) and routine sterile cell culture methods.</li><li>Strong scientific writing and documentation skills, with practical familiarity with ALCOA+ data integrity standards.</li><li>Proficiency in analyzing and presenting complex data, with attention to accuracy and regulatory requirements.</li><li>Excellent organizational skills; ability to manage multiple projects and deliverables in parallel within tight timelines.</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>Experience with all aspects of mammalian cell culture and multiple assay types.</li><li>Familiarity with regulatory requirements for cell bank manufacturing and documentation.</li><li>Strong interpersonal and communication skills for effective collaboration in a dynamic, multidisciplinary environment.</li><li>5+ years of experience.</li></ul><h2>Work Environment</h2><p>The position is based in a brand new biologic lab, offering an innovative and collaborative work environment. The contractor will be involved in designing and executing assays, performing transient transfection within cell lines, and writing all reports in compliance with ALCOA standards. The facility boasts no attrition in three years and is engaged in exciting new collaborations and projects.</p><br>

Research Scientist

<p><strong>Description</strong></p><p>Develop advanced and robust LC-MS analytical methods for the bioanalysis of different molecular formats such as small molecules, oligonucleotides, peptides, and/or proteins.</p><p>Develop and implement innovative high-resolution mass spectrometry-based metabolite profiling and identification platforms</p><p>Perform LC-MS-based small molecule biomarker analysis occasionally</p><p>Review and translate complex LC-MS-based data sets and articulate findings to project teams</p><p>Maintain/document records of all experiments, including QC review data, experimental results, and reports as appropriate into electronic laboratory notebooks</p><p>Contribute to the team’s knowledge through updating scientific literature and discussions</p><p>Maintain and troubleshoot lab instruments such as biological sample extraction systems, HPLC, and LC-MS</p><p><br></p><p><strong>Top Skills Details</strong></p><p>lc-ms,mass spectrometry,gmp,Method development</p><p><br></p><p><strong>Additional Skills &amp; Qualifications</strong></p><p>1. PhD or Master’s degree in pharmaceutical sciences, analytical chemistry, chemistry or related disciplines with relevant bioanalysis experience from industry or academia required. (Fellowship work can be counted as relevant experience, but preference will be given to a scientist with CRO bioanalysis experience)</p><p>2. Hands-on experience in diverse mass spectrometric workflows such as high-resolution and triple quadrupole mass spectrometry to characterize and quantify drug and its metabolites via in vitro and in vivo assays.</p><p>3. Expertise in LC-MS based bioanalysis method development, method validation and sample analysis. Experience with Sciex Analyst™, OS, Xcalibur™ and/or other Mass Spectrometry data-acquisition software packages</p><p>4. Previous knowledge with oligonucleotide and or protein bioanalysis would be a major advantage.</p><p>5. Strong analytical and problem-solving skills; Excellent organizational and time management abilities; Proficiency in data analysis/interpretation and effective communication/teamwork skills.</p><p>6. Please make note of preferred qualifications in JD below.</p><p><br></p><p><strong>Scheudle</strong></p><p>Monday-Friday, 8am-5pm</p><p><br></p>

Research Scientist II

<p style="text-align: center;">Research Technician</p><p>Location: On-site | Hampshire County</p><p>Position Type: Per Diem</p><p>Schedule: Flexible hours between 8:00 AM – 8:00 PM; minimum 2 days/week, up to 4 days/week including potential weekends</p><p>Duration:Through end of October, with potential extension</p><hr><h3>Position Summary</h3><p>We are seeking a detail-oriented and technically skilledResearch Technicianto support the operations of our specialized Core facility. This role is essential in maintaining the high standards of our research environment, ensuring smooth day-to-day operations, and supporting cutting-edge scientific advancements. The ideal candidate will bring a strong <span style="color: rgb(8, 7, 7); background-color: none;">background</span> in laboratory procedures, instrumentation, and medical imaging, along with excellent organizational and communication skills.</p><hr><h3>Key Responsibilities</h3><ul><li>Perform advanced research techniques and procedures in a Core-specific science.</li><li>Supervise daily operations of specialized Core facilities.</li><li>Maintain financial records and databases for invoicing and customer usage tracking.</li><li>Provide timely and effective technical support to user groups.</li><li>Maintain, troubleshoot, and service laboratory instrumentation.</li><li>Assist in implementing new techniques and technologies to maintain a competitive, state-of-the-art Core.</li><li>Collaborate with the Center Director and staff to establish, update, and enforce safety and operational protocols.</li></ul><hr><h3>Essential Skills &amp; Qualifications</h3><ul><li>Minimum 9 months of relevant laboratory or research experience.</li><li>Strong troubleshooting skills in a laboratory setting.</li><li>Knowledge of magnetic resonance and medical laboratory procedures.</li><li>Certification in CRT, ARRT, or ARMRIT.</li><li>Demonstrated understanding of general anatomy, physiology, and medical terminology.</li><li>High-level knowledge of cross-sectional anatomy.</li><li>Excellent interpersonal, oral, and written communication skills.</li><li>Strong organizational and time-management abilities.</li></ul><hr><h3>Work Environment</h3><ul><li>Involves working with pediatric populations (ages 3–5).</li><li>Per diem role with flexible scheduling; coverage needed while primary technician is on leave.</li><li>Opportunity for extension based on workload and lab expansion plans.</li></ul><h1><br></h1>

Research Technician

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