<h1 style="font-weight: 700;">Job Title: QC Compendial Scientist II</h1><br><h2>Job Description</h2><p>In this role, you will utilize a range of analytical tools for large molecule analysis, including Compendial Testing (pH, UV, Osmolality), and other minor equipment. Your work will support GMP manufacturing through commercial product testing and Stability testing, among other client-requested endeavors. This position requires experience in a cGMP environment.</p><br><h2>Responsibilities</h2><ul><li>Perform Compendial Testing (pH, UV, Osmolality) using Spectrometer, Plate Readers, SoloVPE, qPCR, and color metric-based assays like Picogreen and Bradford on In-Process, DS release, and stability samples, ensuring timely project delivery.</li><li>Review laboratory data packets as assigned.</li><li>Perform and author laboratory investigations as assigned.</li><li>Conduct GMP testing in an analytical laboratory environment using HPLC and UPLC test methods such as Reverse Phase, SEC, CEX, etc.</li><li>Compile data for documentation of test procedures and prepare reports while collaborating with team members and other departments like quality assurance and data reviewers.</li><li>Contribute to the development of new concepts, techniques, and standards.</li><li>Recognize and report invalid/lab incident/out-of-specification/out-of-trend results to laboratory management and recommend solutions.</li><li>Perform all duties in compliance with Standard Operating Procedures, Good Manufacturing Practices, and Safety guidelines.</li><li>Participate in laboratory activities, including performing safety inspections and ordering supplies.</li></ul><h2>Essential Skills</h2><ul><li>Proficiency in Compendial Testing (pH, UV, Osmolality)</li><li>Experience with Spectrometer and Plate Readers</li><li>Qualitative pipetting skills</li><li>Knowledge of SoloVPE or A280 techniques</li><li>Bachelor’s degree in chemical pharmaceutical, biology, chemistry, biotechnology or related field</li><li>2+ years of experience in a GMP regulated environment, preferably in pharmaceuticals</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>Experience with qPCR and color metric-based assays like Picogreen and Bradford</li><li>Familiarity with wet chemistry and bioassay techniques</li><li>Flexibility, good organization and planning skills</li><li>Attention to details, positive and collaborative demeanor</li></ul><h2>Work Environment</h2><p>The role operates Monday to Friday from 8am to 4:30pm with a flexible start time. Training on all assays will occur during the first 3-6 months. The team currently consists of 3 members and is expected to grow to 6 members soon.</p><br>

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***QC Compendial Scientist II***

<h1 style="font-weight: 700;">Job Title: Downstream Processing Supervisor</h1><br><h2>Job Description</h2><p>The Downstream Processing Supervisor is accountable for overseeing the success of downstream manufacturing processes in the biopharmaceutical sector. This role involves executing a variety of functions including large-scale chromatography, viral inactivation, filtration techniques, and aseptic filling of bulk drug substances. The supervisor will focus on proactive &#39;right the first time&#39; executions and is responsible for the reconciliation of batch records.</p><br><h2>Responsibilities</h2><ul><li>Execute manufacturing batch records, work instructions, and SOPs with minimal instruction.</li><li>Assist with batch record reconciliation and maintain all department functions such as suite, supplies, equipment, logbooks, and data in accordance with site SOPs and policies.</li><li>Document all activities to meet cGMP requirements and conduct daily record reviews.</li><li>Forecast and resolve supply and raw material deficiencies and identify scheduling conflicts with a one-week outlook.</li><li>Identify deviations, assist in investigations/root cause analysis, and provide input on major/critical deviations.</li><li>Represent the manufacturing team at tier meetings and practice safe work habits adhering to safety procedures.</li><li>Utilize manufacturing process knowledge and investigational skills to resolve manufacturing issues and drive continuous improvement.</li><li>Provide feedback on document revisions and manage batch production records and manufacturing procedures.</li><li>Maintain a safe and clean work environment by educating and directing personnel to ensure compliance with policies and procedures.</li><li>Coordinate training with the team either in class or on the floor as needed.</li><li>Build cross-functional relationships and enhance relationships with team members.</li><li>Provide frequent feedback and coaching to others on improving performance.</li><li>Complete production plans by scheduling and assigning personnel, prioritizing tasks, supervising progress, revising schedules, and reporting results.</li><li>Lead shift exchanges and daily huddles for the team as required, acting as a liaison with other groups within the manufacturing organization.</li></ul><h2>Essential Skills</h2><ul><li>Prior supervisory experience or experience managing direct reports, including HR processes, independent decision-making, and performance management.</li><li>Large-scale pharmaceutical manufacturing experience.</li><li>Bachelor&#39;s degree in STEM with 2+ years in a supervisor role within pharmaceuticals, or 5 years total in manufacturing.</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>5-9 years of experience in lead biopharmaceutical or pharma operating positions with a HS Diploma.</li><li>Experience in cGMP environment preferred.</li><li>Knowledge of cGMP practices.</li><li>Strong math skills, aseptic techniques, and chemical concepts preferred.</li><li>Critical thinking and problem-solving capabilities.</li><li>Detail-oriented and results-driven.</li><li>Efficient in MS Office.</li></ul><h2>Work Environment</h2><p>The role is based in cleanroom/aseptic suites, requiring full gowning attire including bodysuit, gloves, hair and beard nets, face covers, and safety glasses. The night shift operates from 6:15pm to 6:45am on a rotating 12-hour shift schedule. Employees work 7 days out of a 2-week period following a 223 schedule. Candidates must be able to lift a minimum of 25 lbs independently and stand for 80% of the shift.</p><br>

**Downstream Processing Supervisor**

<h1><strong>Calibration/Metrology Technician</strong></h1><h2>Job Description</h2><p>As an Instrument Calibration Technician, you will provide maintenance on various laboratory instrumentation and equipment. Your role includes installing, calibrating, and qualifying routine and remedial maintenance tasks. You will perform and document your work according to standard operating procedures and established maintenance schedules to meet regulatory requirements. Additionally, you will collaborate with lab staff to schedule maintenance and provide training on equipment when necessary.</p><p><br></p><h2>Responsibilities</h2><ul><li>Perform scheduled routine maintenance on active instrumentation and equipment.</li><li>Conduct scheduled calibrations and qualifications on active instrumentation and equipment, including Installation Qualification (IQ), Operational Qualification (OQ), and Performance Qualification (PQ).</li><li>Carry out remedial maintenance on active instrumentation and equipment.</li><li>Oversee the installation of new laboratory instrumentation and equipment.</li><li>Follow vendor documentation related to preventive maintenance, calibration/qualification, and repairs.</li><li>Address audits, both internal and external, concerning laboratory instruments and equipment.</li><li>Evaluate lab support records for compliance with SOPs, ensuring completeness and accuracy, and report findings.</li></ul><h2>Essential Skills</h2><ul><li>Metrology</li><li>Calibration</li><li>Laboratory equipment maintenance</li><li>Troubleshooting</li><li>GMP experience</li><li>Instrument calibrations (e.g., scales, balances, flow meters, temperature and pressure meters, temperature probes, fluke meters)</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>Experience in a GMP-regulated pharmaceutical environment</li><li>Cleanroom experience (ISO 7/8 preferred)</li><li>Technical certification may be required</li><li>Understanding of FDA and GXP regulations and requirements</li><li>Knowledge of laboratory instrumentation and equipment</li><li>Basic troubleshooting, analytical, and problem-solving skills</li><li>Client-focused approach with strong interpersonal skills</li><li>Effective communication with vendors, clients, and staff</li><li>Ability to work collaboratively in a team environment</li></ul><p>#stlsci</p>

**Metrology Technician**

<h1 style="font-weight: 700;">Job Title: QA Associate</h1><br><h2>Job Description</h2><p>The QA Associate is responsible for the rigorous review, verification, and archival of batch records and associated documentation to ensure compliance with internal SOPs, cGMP, and FDA regulations. This role is primarily desk-based and involves close collaboration with production, warehouse, and quality teams to resolve discrepancies and maintain data integrity.</p><br><h2>Responsibilities</h2><ul><li>Perform comprehensive batch record reviews for completeness, accuracy, and compliance with GDP and SOPs.</li><li>Review supporting documentation including logbooks, protocols, packaging records, and inventory records.</li><li>Collaborate with production and management to resolve discrepancies or missing information in batch records.</li><li>Scan and archive completed records into the electronic database and physical storage system.</li><li>Input data into warehouse management systems (e.g., Dynamics 365) and quality systems (e.g., Reliance).</li><li>Ensure inventory values and documentation are accurately recorded and support initiatives within the QA team to build flexibility and coverage.</li><li>Participate in continuous improvement efforts and assist in training production staff on documentation best practices.</li><li>Cross-trained with other QA Associate functions including Document Control and Inventory Control.</li><li>Issue and control batch records, cleaning records, test sheets, and logbooks.</li><li>Maintain and control the company lot number system and ensure proper documentation flow.</li></ul><h2>Essential Skills</h2><ul><li>Strong interpersonal skills; able to work respectfully with cross-functional teams.</li><li>Self-motivated and organized with a high level of accountability.</li><li>Willingness to learn and adapt to evolving processes and systems.</li><li>Proficient in Microsoft Office and comfortable using ERP and quality systems (e.g., Dynamics 365, Reliance).</li><li>Excellent written and verbal communication skills.</li><li>Ability to work independently and collaboratively with minimal supervision.</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>High School Diploma or GED required; Associate’s or Bachelor’s degree in a scientific or technical field preferred.</li><li>1+ year of experience in pharmaceutical QA or FDA-regulated environment preferred.</li><li>Strong attention to detail and ability to work in a fast-paced, documentation-heavy environment.</li></ul><h2>Work Environment</h2><p>This position is a Monday to Friday Day Shift role with a flexible start time between 7:00 - 8:30 AM, working 8-9 hours from there. The role includes 90% desk-based work in a shared office setting, with occasional lifting of up to 50 lbs. The manufacturing building is dusty due to the powdered products produced and is not a sterile environment. The team comprises 3 Inspectors, 1 Supervisor, 3 Batch Record Reviewers, 1 Document Control, and 1 Inventory Control.</p><br>

**QA Associate - Batch Record Reviewer**

<h1 style="font-weight: 700;">Job Title: QA Deviation Investigator</h1><br><h2>Job Description</h2><p>As a QA Deviation Investigator, you will play a crucial role in analyzing and investigating deviations or non-conformances within a regulated environment. Utilizing problem-solving tools like root cause analysis, you will collect and analyze relevant data to identify patterns and potential causes. Your findings will be documented comprehensively, and you will collaborate with various departments to implement corrective and preventive actions (CAPAs). You will also participate in client communications and provide timely written documentation of investigations.</p><br><h2>Responsibilities</h2><ul><li>Analyze and investigate deviations or non-conformances using problem-solving tools such as root cause analysis.</li><li>Collect and analyze relevant data to identify patterns, trends, or potential causes.</li><li>Document findings in a comprehensive and objective manner, ensuring accurate recording of all relevant information.</li><li>Collaborate with various departments to gather information, evaluate causal factors, and implement corrective and preventive actions (CAPAs).</li><li>Provide timely written documentation of investigations and communicate recommendations based on investigation outcomes.</li><li>Participate in client communications and responses, working closely with program team leads, quality, and management.</li></ul><h2>Essential Skills</h2><ul><li>Experience in CAPA, quality assurance, and root cause analysis.</li><li>Knowledge of deviations in pharmaceutical settings and GMP/FDA regulations.</li><li>Strong technical writing and communication skills.</li><li>Proficiency in quality processes and Six Sigma methodologies.</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>BS/BA in biology, biochemistry, chemistry, or other science-related fields.</li><li>1+ years of experience with problem-solving tools like Root Cause Analysis and/or LEAN/Six Sigma.</li><li>1+ years of experience in technical writing and/or deviation writing.</li><li>3+ years of experience in a regulated environment, preferably in biologics/pharmaceuticals.</li><li>Ability to evaluate data and make recommendations based on trends and trend analysis.</li><li>Ability to work effectively in a fast-paced environment and prioritize tasks.</li><li>Ability to facilitate meetings for desired outcomes.</li></ul><h2>Work Environment</h2><p>The role requires working Monday through Friday, with core hours of 9am to 3pm, and flexibility in start and end times. You will collaborate with any department needed for deviations, not necessarily limited to upstream or downstream processes.</p><br>

**QA Deviation Investigator** 38-43/HR

<h1 style="font-weight: 700;">Job Title: QA Inspector</h1><br><h2>Job Description</h2><p>The QA Inspector ensures that all products released for distribution comply with applicable specifications. This role involves managing materials in the warehouse to ensure they are appropriately identified as to status and stored correctly. The QA Inspector is responsible for verifying that only released materials are used in production and that all materials are appropriately sampled, tested, and meet specifications before their use in production.</p><br><h2>Responsibilities</h2><ul><li>Assure compliance with applicable SOPs.</li><li>Ensure manufacturing complies with Batch Record Instructions and requirements.</li><li>Receive and sample all raw materials and components for appropriate testing.</li><li>Quarantine and release finished products for shipping.</li><li>Ensure all items in the plant, including raw materials, components, packaging, labels, finished products, reject materials, and rework materials, are appropriately labeled and stored according to SOPs.</li><li>Administer the label program.</li><li>Inspect production lines.</li><li>Conduct appropriate sampling, storage, and status labeling of pallets of incoming materials until tested for compliance with specifications and released for use.</li><li>Conduct appropriate sampling and storage of finished products until tested and released for production.</li><li>Review batch records to ensure only released ingredients, components, and labeling are used in production.</li><li>Assist the Quality Manager in product investigations where deviations have occurred in manufacturing, or complaints or product failures have been reported.</li><li>Maintain label inventory, issue labels to production, return labels to inventory, and facilitate reconciliation of label inventory.</li><li>Inspect production lines, checking for PPE, labels, codes, weights, and compliance with product specifications.</li></ul><h2>Essential Skills</h2><ul><li>1+ years of quality inspection experience in a GMP environment required, 3+ years preferred.</li><li>HS Diploma required.</li><li>Proficient computer skills to work within the QMS/Database, including basic skills or experience in a similar system like SAP or equivalent ERP.</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>Experience in quality assurance, quality inspection, and quality check processes.</li></ul><h2>Work Environment</h2><p>The QA Inspector will work primarily Monday through Friday from 8:00 AM to 4:30 PM, with moderate overtime of 4-6 hours weekly. There is a possibility of Saturday work, typically one Saturday a month. The team consists of three inspectors and a supervisor, interfacing with production and warehouse personnel. Sampling duties are typically performed one day a week, constituting 80% of the workday compared to 20% in the office. Other days will involve 70% office release work and 30% inspections and auditing in production/warehouse environments. The work environment can be dusty due to the powdered products or animal feed-based products. The role offers 6 paid holidays and 40 hours of PTO, with a plan for conversion at the end of the assignment as there is an open headcount already approved.</p><br>

**QA Inspector**

<h1 style="font-weight: 700;">Job Title: QA Specialist</h1><br><h2>Job Description</h2><p>We are seeking a proactive and detail-oriented Quality Assurance (QA) Associate to support clinical and commercial manufacturing operations. This role will focus on reviewing and managing documentation for registration and clinical batches, ensuring compliance with regulatory requirements, and supporting R&amp;D and feasibility projects. The ideal candidate will be comfortable working independently on smaller projects, collaborating cross-functionally, and maintaining high standards of quality and accountability.</p><br><h2>Responsibilities</h2><ul><li>Review and understand batch records, manufacturing protocols, and registration/clinical batch documentation.</li><li>Ensure documentation aligns with FDA and other regulatory agency requirements.</li><li>Manage deviations, change controls, and CAPAs as they arise.</li><li>Evaluate method validation and equipment qualification protocols and reports.</li><li>Ensure SOPs are followed and documentation is complete and accurate.</li><li>Provide feedback on validation documents and ensure alignment with regulatory expectations.</li></ul><h2>Essential Skills</h2><ul><li>Quality assurance experience with a focus on batch record review and GMP compliance.</li><li>2-4 years of experience in a QA role, specifically in document review of Batch Records, Equipment Records, Validation Records, etc.</li><li>Collaboration and initiative to seek help or additional work.</li><li>Attention to detail and accountability.</li><li>Ability to prioritize tasks and review protocols effectively.</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>AS/BS Degree Preferred, HS Diploma Required.</li><li>2+ years in a Quality/GMP Environment with at least 2 years directly in a QA role.</li><li>Pharmaceutical industry experience strongly preferred.</li><li>Experience reviewing batch records in a commercial setting and understanding supporting documents such as Deviations and Change Controls.</li><li>Well-rounded experience in reviewing documentation for GMP compliance.</li></ul><h2>Work Environment</h2><p>The QA Specialist will work on the R&amp;D side of the building, which offers a quieter environment than the operations side. The role involves walking through scale-up production environments or entering the operations building for final clinical batch compliance. The position provides an individual office space, with primarily onsite work and occasional flexibility for minimal remote work if necessary. The work schedule is Monday to Friday, from 7:30 AM to 4:00 PM, or a similar variation. Collaboration with internal teams is essential, and the position occasionally supports CDMO-related tasks. The role promises exposure to diverse QA experiences and a supportive R&amp;D team, with potential for role extension into 2026.</p><br>

**QA Specialist** 25-30/HR

<h1><strong>QC Scientist</strong></h1><p><br></p><h2>Job Description</h2><p>The QC Scientist  will perform HPLC/UPLC testing on various samples, including In-Process DS release, DP release, DS stability, DP Stability, process validation, analytical method validation/transfer, method establishment/qualification, and non-routine samples. The role involves demonstrating proper laboratory safety and housekeeping practices through regular audits and inspections, ensuring all activities meet EHS requirements. Conduct GMP testing in an analytical laboratory environment using HPLC and UPLC test methods, including Reverse Phase, SEC, Titer concentration, and CEX.</p><p><br></p><h2>Responsibilities</h2><ul><li>Accurately record and report analysis results following lab procedures and quality systems.</li><li>Recognize and report out-of-specification/out-of-trend results to laboratory management and recommend solutions.</li><li>Maintain and troubleshoot analytical instrumentation and workspace as needed.</li><li>Perform method validation and/or qualification testing as required.</li><li>Author and/or review SOPs, test methods, forms, etc., in the document management system eDMS.</li><li>Ensure compliance with Standard Operating Procedures, Good Manufacturing Practices, Good Laboratory Practices, and Safety guidelines.</li><li>Work with internal and external customers to ensure clear and open communication when resolving and raising issues.</li><li>Collaborate with QC leads, PMs, and clients to maintain the health of client programs.</li></ul><h2>Essential Skills</h2><ul><li>Minimum of 1 year of HPLC/UPLC experience in quality/analytical/pharmaceutical industry or similar experience.</li><li>Proficiency in HPLC, GMP, chemistry, and EMPOWER.</li><li>Knowledge of GMP regulations in a cGMP manufacturing environment.</li><li>Working knowledge of scientific principles for a wide range of analytical techniques.</li></ul><h2><strong>Work Environment: </strong></h2><p>Monday-Friday 8am-4:30pm</p><p>Bench work</p>

**QC Scientist II/III** 30-43/HR

*QA Deviation Investigator* -38-43/HR

<h3><strong>Low Voltage Technician</strong></h3><p>Location: Nationwide Travel Required</p><h4>Job Summary</h4><p>We are seeking a skilled and motivated Low Voltage Technician to join our team. In this role, you will travel to job sites across the United States to install, calibrate, test, and troubleshoot a variety of low voltage control systems. Your work will be critical in ensuring the performance, reliability, and safety of systems such as CCTV, access control, perimeter detection, and audio communication.</p><hr><h3><strong>Key Responsibilities</strong></h3><ul><li>Install, calibrate, test, and troubleshoot low voltage control systems.</li><li>Read and interpret electronic schematics, wiring diagrams, and technical drawings.</li><li>Install and configure CCTV, access control, perimeter detection, and audio communication systems.</li><li>Pull, terminate, and testCat5/Cat6cabling.</li><li>Perform system diagnostics and resolve technical issues on-site.</li><li>Maintain accurate documentation of installations, service calls, and system configurations.</li><li>Ensure compliance with safety standards and job site protocols.</li><li>Communicate effectively with project managers, clients, and team members.</li></ul><hr><h3><strong>Essential Skills &amp; Qualifications</strong></h3><ul><li>Proficiency in low voltage systems and structured cabling.</li><li>Experience with Cat5/Cat6 installation and termination.</li><li>Ability to read and interpret electronic schematics and wiring diagrams.</li><li>Strong troubleshooting and problem-solving skills.</li><li>Excellent attention to detail and organizational skills.</li></ul><hr><h3><strong>Additional Qualifications</strong></h3><ul><li>Minimum1 year of experience in low voltage or related technical field preferred.</li><li>Willingness to travel extensively across the United States (up to 75–100% travel).</li><li>Valid driver’s license and clean driving record.</li><li>Ability to work independently and in a team environment.</li><li>Experience with hand tools, power tools, and testing equipment.</li><li>OSHA 10 or 30 certification is a plus.</li></ul><hr><h3><strong>Work Environment</strong></h3><ul><li>This is a field-based role requiring frequent travel to job sites nationwide. Work may involve climbing ladders, lifting equipment, and working in various indoor and outdoor environments.</li></ul>

*TRAVEL*  Low Voltage Technician

<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>Job Description</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>Responsibilities</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>Essential Skills</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>Additional Skills &amp; Qualifications</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>Work Environment</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>

100% Remote Pharmacist

<h1><strong>AI Engineering Manager - Phoenix, AZ</strong></h1><h2>Job Description</h2><p>As the Manager of Agentic AI Engineering, you will lead a highly specialized team driving the development of cutting-edge AI systems. The manager will lead efficiency across three key areas: Data Cleaning, Model Fine-Tuning, and Agentic AI Creation. This individual will oversee a team of <span style="color: rgb(8, 7, 7); background-color: none;"><span style="color: rgb(8, 7, 7); background-color: none;">senior</span></span> engineers and work closely with leadership, product, and research teams to drive the development of innovative AI systems.</p><p>This is an exciting opportunity for someone with relevant experience to join a cutting-edge Semiconductor Manufacturing team that is continuing to grow in the Phoenix, AZ, area. This will be a long-term opportunity. </p><h2>Responsibilities</h2><ul><li>Lead and manage a cross-functional team focusing on data, model behaviors, and autonomous agents.</li><li>Define and implement the strategic vision for the team, balancing short-term goals with long-term AI development.</li><li>Mentor and guide <span style="color: rgb(8, 7, 7); background-color: none;"><span style="color: rgb(8, 7, 7); background-color: none;">senior</span></span> engineers, fostering a collaborative and innovative environment.</li><li>Serve as the liaison between engineering, leadership, and external stakeholders.</li></ul><h2>Essential Skills</h2><ul><li>Bachelor&#39;s degree in Computer Science, Machine Learning, or a related field.</li><li>6+ years of experience in AI, ML, or automation, with at least 3 years in a leadership role.</li><li>Strong expertise across the entire lifecycle: data, model tuning, and agent systems.</li><li>Experience with foundational models, RLHF, and multi-agent systems.</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>5+ years of experience in Data Cleaning, Model Fine-Tuning, and Agentic AI Creation.</li><li>3+ years of experience in Project Management and Team Management.</li><li>Proficiency in machine learning, artificial intelligence software, Python, SQL, C#, and software development.</li></ul><h2>Work Environment</h2><p>The work environment consists of desk work with a casual attire policy. The team is composed of five people, and external technology is not allowed inside the building. The company will provide a work phone, and lockers are available in the lobby to store personal items not permitted inside. Employees must go through security checks each day upon entering and leaving the building.</p>

AI Engineering 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;">Senior</span></span> AI Model Fine-Tuning Engineer</h1><br><h2>Job Description</h2><p>As a <span style="color: rgb(8, 7, 7); background-color: none;"><span style="color: rgb(8, 7, 7); background-color: none;">Senior</span></span> AI Model Fine-Tuning Engineer, you will play a pivotal role in enhancing the adaptability and intelligence of AI models, aligning them with real-world applications. You will employ advanced techniques such as prompt engineering, Reinforcement Learning from Human Feedback (RLHF), and instruction tuning to ensure high-quality, context-aware responses from our models.</p><br><h2>Responsibilities</h2><ul><li>Lead the fine-tuning process for large pre-trained models, ensuring they behave appropriately across various contexts, such as instruction following, question answering, and task performance.</li><li>Design and implement prompt engineering strategies to produce accurate, relevant, and coherent outputs from AI models.</li><li>Apply RLHF and other behavioral fine-tuning methods to improve model alignment with user needs and ethical standards.</li><li>Collaborate with data teams to integrate relevant data for continuous model behavior improvement.</li><li>Conduct model evaluations using performance metrics such as accuracy, bias detection, and user feedback to identify areas for enhancement.</li><li>Iterate and experiment with different fine-tuning methods to achieve optimal performance for specific use cases.</li><li>Monitor model drift to ensure models remain consistent, reliable, and safe over time.</li></ul><h2>Essential Skills</h2><ul><li>Bachelor&#39;s degree in Computer Science, Data Science, or a related field.</li><li>5+ years of experience fine-tuning large-scale models like GPT, T5, or BERT, with a focus on behavior and functionality.</li><li>Expertise in advanced tuning methods such as RLHF, prompt engineering, and zero-shot learning.</li><li>Experience with transformer architectures and frameworks like Hugging Face, TensorFlow, or PyTorch.</li><li>Proficiency in Python and experience with libraries for model fine-tuning, such as Transformers and DeepSpeed.</li><li>Understanding of LLM behaviors, including instruction-following, task completion, and ethical output considerations.</li><li>Experience in evaluating model performance using metrics such as BLEU, ROUGE, and perplexity.</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>Experience with ethical AI and safety considerations, including bias minimization and adversarial input handling.</li><li>Experience with model deployment and real-time experimentation, such as A/B testing.</li></ul><h2>Work Environment</h2><p>The role requires candidates to work on-site at our Phoenix, Arizona facility, which is a state-of-the-art technology environment. The work setting is highly regulated, prohibiting the use of personal cell phones. Employees benefit from an average of 85+ hours of learning programs annually, focusing on technical training, leadership development, and cross-functional mobility. Additional benefits include health coverage, wellness programs, family care support for childcare, eldercare, and pet care, fitness resources, mental health support, travel-related benefits, and funding for professional development and community service activities.</p><br>

AI Model Fine-Tuning Engineer

<h1><strong>AMHS Manager - Phoenix, AZ</strong></h1><p>Join a leading semiconductor manufacturer in Phoenix, AZ, at its advanced 4-nanometer fabrication facility! We are hiring an AMHS (Automated Material Handling System) Manufacturing Manager to lead efforts in new technology transfers and production line setups, focusing on wafer manufacturing across multiple modules and departments. This person will be responsible for driving production improvements and ensuring smooth operations, while also managing people and business-related functions. We believe brilliance can ignite a world of innovation and launch a promising future. Our team is in the pursuit of excellence with the goal to transform ideas into world-changing products that impact millions of lives.</p><h2>Job Responsibilities</h2><ul><li>Lead new Technology Transfers and Production Line Setups.</li><li>Improve Production Operations and manage people-related initiatives.</li><li>Work with DFK or Muratec AMHS systems, or other relevant AMHS equipment.</li><li>Enhance Wafer-Focused Manufacturing across multiple modules and departments.</li><li>Elevate Semiconductor Manufacturing System Excellence by improving Equipment Productivity and Delivery Cycle Time.</li><li>Integrate Machinery and Equipment Applications to maintain effective Scheduling Systems that enhance Fab Production Capacity.</li><li>Provide insight to achieve Production Capacity Targets, improve the Operation Control Capability of the Fab, and reduce Variability.</li><li>Collaborate with Engineering Teams, Process Integration, and Yield Improvement Teams to meet customer requirements.</li></ul><h2>Job Requirements</h2><ul><li>B.S. in Computer Science, Industrial, Manufacturing, Mechanical, or Automation Engineering</li><li>7+ years of experience in the Semiconductor Industry</li><li>2+ years of experience on Automated Material Handling Systems</li><li>2+ years of experience in Managing and Developing Direct Reports</li><li>Demonstrated knowledge of Scheduling Systems or Optimization Algorithms</li><li>Strong understanding of Statistical Process Control (SPC) or Design of Experiments (DOE) principles</li><li>Strong technical understanding of IC Processing Equipment, Integrated Flow, Chemistry, and Physics</li></ul><h2>Work Environment</h2><p>This role is based in a fast-paced fabrication environment. This person may be required to be on-call during weekends and off-hours as needed. This position will include a year-one road map with training and development geared towards long-term success. After the initial first year of training onsite, this person may be asked to travel internationally for additional skill and business development. You will be working in a dynamic setting where brilliance can ignite a world of innovation and launch a promising future. This team values Integrity, Innovation, Accountability, Customer Focus, Enthusiasm, and a strong sense of Reliability and Commitment.</p>

AMHS Manager

<h1 style="font-weight: 700;">Job Title: Accessioner</h1><br><h2>Job Description</h2><p>We are seeking an organized and detail-oriented Accessioner to join our team. This role involves following laboratory procedures and policies while assisting with various administrative functions. You will be responsible for maintaining clinical records, organizing document management systems, and ensuring the availability of laboratory supplies. Additionally, you will assist in quality control and improvement activities and complete all mandatory training.</p><br><h2>Responsibilities</h2><ul><li>Follow all laboratory procedures and policies.</li><li>Assist with maintaining clinical records and logs.</li><li>Maintain an organized document management system for easy access and retrieval of records and forms.</li><li>Ensure the availability of clinical laboratory supplies.</li><li>Identify and consult with a Supervisor regarding administrative problems that may affect test reports.</li><li>Perform and document corrective actions as assigned.</li><li>Assist in quality control and improvement activities.</li><li>Complete and document all mandatory training, including annual safety training.</li><li>Work 60% of the time in the lab environment, handling documentation related to samples.</li></ul><h2>Essential Skills</h2><ul><li>Proficiency in data entry and accessioning.</li><li>Experience with Excel and sample processing.</li><li>Ability to keep up with a high workload and fast-paced environment.</li><li>Attention to detail is critical due to the volume and amount of data.</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>Experience in similar roles is required.</li><li>A degree is not required but would be helpful.</li><li>Candidates must be a <span style="color: rgb(8, 7, 7); background-color: none;"><span style="color: rgb(8, 7, 7); background-color: none;">U.S. Citizen</span></span> or <span style="color: rgb(8, 7, 7); background-color: none;"><span style="color: rgb(8, 7, 7); background-color: none;">Green Card</span></span> Holder.</li><li>Basic skills in Excel and Word are necessary.</li></ul><h2>Work Environment</h2><p>This position requires working in a lab environment 60% of the time, handling documentation related to bodily fluid samples, including nasal swabs. The remaining 40% of the time will be spent at a desk. The office environment is relaxed, with a business casual dress code, including jeans. The company offers a supportive and employee-centric culture, with opportunities for growth and a generous 401K matching program. The work schedule is Tuesday to Saturday, with a 20% differential pay for weekend work. Average tenure at the company is seven years, reflecting a stable and rewarding workplace.</p><br>

Accessioner

<h1><strong>Job Title: Accessioner</strong></h1><p><br></p><h2>Responsibilities</h2><ul><li>Manage inbound calls from patients and doctor&#39;s offices. </li><li>Provide exceptional customer service and support to callers.</li><li>Participate in outbound calling as required by patient or client situations.</li><li>Maintain accurate data entry and processing for samples and calls.</li><li>Assist and train in the medical lab</li></ul><h2>Essential Skills</h2><ul><li>High School Diploma</li><li>Attention to detail</li><li>Experience with phone call handling</li><li>Experience in sample collection and processing</li><li>Customer service skills</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>Spanish speaking skills are desirable</li></ul><h2>Work Environment</h2><p>The work schedule is Monday to Wednesday, 7:00am - 3:30pm, and Thursday to Friday, 8:30am - 5:00pm, with weekends off. The first week of training is Monday to Friday, 9:30am – 5:00pm. Overtime may be required based on business needs. The job requires flexibility for occasional changes to the schedule.</p>

<h1><strong>Job Title: Accessioner</strong></h1><p><br></p><h2>Job Description</h2><p>We are seeking an organized and detail-oriented Accessioner to join our team. This role involves following laboratory procedures and policies while assisting with various administrative functions. You will be responsible for maintaining clinical records, organizing document management systems, and ensuring the availability of laboratory supplies. Additionally, you will assist in quality control and improvement activities and complete all mandatory training.</p><p><br></p><h2>Responsibilities</h2><ul><li>Follow all laboratory procedures and policies.</li><li>Assist with maintaining clinical records and logs.</li><li>Maintain an organized document management system for easy access and retrieval of records and forms.</li><li>Ensure the availability of clinical laboratory supplies.</li><li>Identify and consult with a Supervisor regarding administrative problems that may affect test reports.</li><li>Perform and document corrective actions as assigned.</li><li>Assist in quality control and improvement activities.</li><li>Complete and document all mandatory training, including annual safety training.</li><li>Work 60% of the time in the lab environment, handling documentation related to samples.</li></ul><h2>Essential Skills</h2><ul><li>Proficiency in data entry and accessioning.</li><li>Experience with Excel and sample processing.</li><li>Ability to keep up with a high workload and fast-paced environment.</li><li>Attention to detail is critical due to the volume and amount of data.</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>Experience in similar roles is required.</li><li>A degree is not required but would be helpful.</li><li>Candidates must be a U.S. passport holder or permanent resident.</li><li>Basic skills in Excel and Word are necessary.</li></ul><h2>Work Environment</h2><p>This position requires working in a lab environment 60% of the time, handling documentation related to bodily fluid samples, including nasal swabs. The remaining 40% of the time will be spent at a desk. The office environment is relaxed, with a business casual dress code, including jeans. The company offers a supportive and employee-centric culture, with opportunities for growth and a generous 401K matching program. The work schedule is Tuesday to Saturday, with a 20% differential pay for weekend work. Average tenure at the company is seven years, reflecting a stable and rewarding workplace.</p>

<h1><strong>Job Title: Non-Profit Account Manager</strong></h1><p><br></p><h2>Job Description</h2><p>This role involves driving awareness in the PACE Program sharing information about medical benefits with the elderly, with a focus on community-based long-term care services. The ideal candidate will have a minimum of two years&#39; experience in healthcare field awareness, preferably related to MLTC, MAP, PACE programs, or homecare. Strong interpersonal skills, both written and verbal, are essential, along with proficiency in Microsoft Word and Outlook. Preferred qualifications include experience with CRM platforms such as Care Compass, as well as knowledge of the PACE program benefits.</p><p><br></p><h2>Responsibilities</h2><ul><li>Educate prospective community leaders, providers, participants, caregivers, and other audiences on PACE program benefits, highlighting differentiators from other healthcare options.</li><li>Provide program education through lectures, presentations, events, meetings, or other necessary communications to facilitate PACE referral generation.</li><li>Manage assigned accounts, ensuring continuous and effective communication with contacts and responding to all inquiries, requests, and referrals promptly.</li><li>Collaborate with the Events and Marketing teams to identify appropriate events, community partners, or resources to educate the community about PACE.</li><li>Develop informational trainings and create handouts/packets with approved marketing materials.</li><li>Track all generated referrals and consistently measure and evaluate individual performance to improve outreach efforts and maximize referral opportunities.</li><li>Assist intake and provider relations with introductory calls, general qualification screening, documentation collection, benefit education/applications, site tours, home visits, and follow-up for enrollment or education.</li></ul><h2>Essential Skills</h2><ul><li>Minimum 2 years work experience in healthcare business development.</li><li>Knowledge of community-based long-term care services for dual eligible and frail adult population.</li><li>Strong interpersonal skills (written and verbal).</li><li>Experience with CRM platforms, preferably Care Compass.</li><li>Proficiency in Microsoft Word and Outlook.</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>Bachelor&#39;s degree preferred.</li><li>Knowledge of PACE program benefits is a plus.</li><li>Bilingual Spanish speaker preferred</li><li>Car and valid driver&#39;s license for traveling.</li></ul><h2>Work Environment</h2><p>The position operates in a professional setting with regular business hours from 8:30 AM to 5:30 PM. The role involves traveling to various locations to provide education and support. The candidate should be comfortable working independently and collaboratively with teams.</p>

Account Manager

<p><strong>This is a Part Time Opportunity - 16 to 20 Hours a Week. Fully Remote After 1 Week of Onsite Training in Bothell, WA</strong></p><p><br></p><p><strong>Description</strong></p><p>We are seeking a detail-oriented and organized Accounts Payable Assistant to join our team. The successful candidate will be responsible for invoice processing in SAP &amp; Ariba and monitoring the organizations vendor invoice mailbox. Additionally you will handle contract management tasks and submitting change orders.</p><p><br></p><p><strong>Skills</strong></p><p>Administrative support, Project coordination, Data entry, administrative assistance, database management, database administrator, Compliance, Audit, Document control, inventory system, vendor communication, vendor maintenance</p><p><br></p><p><strong>Additional Skills &amp; Qualifications</strong></p><p>Qualifications:</p><p>High school diploma or equivalent; additional qualifications in office administration are a plus.</p><p>Proven experience in an administrative role, preferably handling sensitive information.</p><p>Strong organizational skills and attention to detail.</p><p>Excellent communication and interpersonal skills.</p><p>Proficiency in Microsoft Excel</p><p>Ability to handle confidential information with discretion.</p>

Accounts Payable Associate (Remote)

<p> Now Hiring: Accountant | Join a Team That Values Precision and People! </p><p> Schedule: Full-Time | On-Site</p><p> Department: Finance &amp; Administration</p><p>Are you a detail-driven accounting professional who thrives in a fast-paced, collaborative environment? Do you love balancing books <em>and</em> being a go-to team player? If so, we want to meet you!</p><p>We’re looking for an Accounting &amp; Operations Specialist to join our growing team. This hybrid role blends core accounting responsibilities with operational support, offering variety, challenge, and the chance to make a real impact every day.</p><h3>What You’ll Do</h3><ul><li>Maintain accurate financial records and ensure compliance with GAAP</li><li>Manage Accounts Receivable and assist with Accounts Payable</li><li>Perform data entry and reconciliation in QuickBooks</li><li>Investigate and resolve discrepancies with a sharp eye for detail</li><li>Support internal financial controls and process improvements</li><li>Assist with invoicing, purchasing, and submitting purchase orders</li><li>Pitch in with administrative tasks like answering phones and greeting guests</li><li>Keep things organized with top-notch filing and documentation</li></ul><h3>What You Bring</h3><ul><li>Proficiency in QuickBooks and Microsoft Office Suite</li><li>Bachelor’s degree in Accounting, Finance, or Business (preferred)</li><li>3+ years of accounting experience (preferred)</li><li>High mathematical aptitude and analytical mindset</li><li>A proactive, team-oriented attitude with strong communication skills</li></ul><h3>Bonus Points If You…</h3><ul><li>Love solving puzzles and streamlining processes</li><li>Enjoy wearing multiple hats and helping where needed</li><li>Thrive in a collaborative, people-first culture</li></ul>

Accounts Receivable Specialist

<h1>Additive Manufacturing Engineer</h1><p><br></p><h2>Job Description</h2><p>We are seeking a highly motivated and skilled Manufacturing Engineer to lead the setup and operation of a state-of-the-art 3D printing lab at the Electrified Powertrain Center. This role involves the installation and commissioning of 20 brand new 3D printing machines, establishing lab protocols, and ensuring seamless integration with plant production processes. The engineer will also be responsible for ongoing lab operations and reporting on the efficiencies and benefits provided to the production line as the lab matures.</p><p><br></p><h2>Responsibilities</h2><ul><li>Lead the setup and commissioning of 20 new 3D printing machines.</li><li>Design and implement lab layout, workflows, and safety protocols.</li><li>Coordinate with vendors and internal teams for equipment installation.</li><li>Develop and document standard operating procedures (SOPs) for lab operations.</li><li>Oversee daily operations of the 3D printing lab, ensuring optimal performance and uptime.</li><li>Collaborate with production teams to identify opportunities for 3D printing applications.</li><li>Monitor and analyze lab output to assess impact on production efficiency.</li><li>Generate regular reports on lab performance, cost savings, and process improvements.</li><li>Train and support lab technicians and other personnel in 3D printing technologies.</li><li>Ensure compliance with all safety and quality standards.</li></ul><h2>Essential Skills</h2><ul><li>Experience with 3D printing technologies and equipment.</li><li>Proven leadership skills.</li><li>Bachelor’s degree in Manufacturing Engineering, Mechanical Engineering, or a related field.</li><li>Experience within an automotive manufacturing facility.</li><li>Strong project management and organizational skills.</li><li>Ability to analyze data and report on operational efficiencies.</li><li>Strong communication and interpersonal skills.</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>Experience with CAD software and digital manufacturing tools is a plus.</li><li>Proven experience in setting up and managing manufacturing or prototyping labs.</li></ul><h2>Work Environment</h2><p>The role is based in a modern 3D printing lab within the Electrified Powertrain Center. The work involves collaboration with various teams and vendors, with an emphasis on safety and quality standards. The environment promotes innovation and continuous improvement in production efficiency through advanced 3D printing technologies.</p>

Additive Manufacturing Engineer

<h1 style="font-weight: 700;">Job Title: Engineering Administrative Assistant</h1><br><h2>Job Description</h2><p>This position provides organizational and administrative support to the Director overseeing the estimating and sales team. The role involves monitoring an inbox for various RFQs and customers to ensure the appropriate manager or team member receives them. Additionally, the assistant will manage the director&#39;s calendar and assist with organizational projects for customers, such as printing proposals and documents, organizing blueprints and drawings, and handling related files. The position requires performing administrative and organizational tasks for the estimating department.</p><br><h2>Responsibilities</h2><ul><li>Monitor inbox for RFQs and customer inquiries.</li><li>Ensure proper assignment of queries to the estimating team.</li><li>Manage the director&#39;s calendar and day-to-day activities.</li><li>Assist with organizational projects for customers.</li><li>Print proposals and documents as needed.</li><li>Organize blueprints, drawings, and related files.</li><li>Perform administrative tasks for the estimating department.</li><li>Maintain constant communication with the estimating team and manager.</li><li>Collaborate with another member of the administrative support team.</li></ul><h2>Essential Skills</h2><ul><li>Administrative support</li><li>Data entry</li><li>Engineering administration</li><li>Calendar management</li><li>Proficiency in Microsoft Office</li><li>Organizational skills</li><li>Proficiency in Outlook</li><li>Executive support</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>2+ years working in an administrative support position</li><li>Exposure to a manufacturing or engineering environment is a plus</li><li>Experience with Microsoft Office and Outlook</li></ul><h2>Work Environment</h2><p>The role is based in an office environment alongside the estimating and sales teams. The assistant will work closely with another <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> administrative team member who will provide training and support. The company fosters a family-oriented culture with low turnover and treats employees well, offering opportunities for growth and merit increases based on performance.</p><br>

Administrative Assistant

<h1><strong>Job Title: Administrative Coordinator</strong></h1><p><strong><em><u>For immediate consideration, please email your resume and interview availability to (sanmalik@actalentservices.com) ASAP today or tomorrow. I am conducting interviews this week and looking to hire immediately.</u></em></strong></p><p><br></p><p><strong><em><u>Please apply if you have experience working on a shopfloor and handling the administrative side of things throughout the day. </u></em></strong></p><h2>Job Description</h2><p>The successful candidate will be responsible for ensuring that parts move through the repair station efficiently and in a timely manner. This role involves anticipating lead times and coordinating the flow of parts through various stages including machining, assembly, welding, paint, NDT, X-ray, and other secondary processes according to the engine manual for overhaul and repair processes.</p><p><br></p><h2>Responsibilities</h2><ul><li>Monitor, anticipate, and manage the movement of parts through the facility to ensure timely progression through machining, assembly, welding, paint, NDT, and X-ray processes.</li><li>Maintain accurate WIP/HOLD for concessions inventory records and ensure parts are correctly logged and tracked.</li><li>Utilize Excel and Teams to manage inventory data, track part movement, and communicate with team members.</li><li>Collaborate with different departments to resolve any issues that may delay the movement of parts.</li><li>Anticipate the adequacy of detail levels and initiate the process to obtain material, schedule the work to produce sleeves, liners, threaded plugs internally.</li><li>Conduct regular inventory audits to ensure accuracy and completeness of records.</li><li>Assist in the development and implementation of part management/tracking inventory management procedures.</li><li>Provide support to engineering and production control teams as needed.</li></ul><h2>Essential Skills</h2><ul><li>Proficiency in Microsoft Excel and Teams.</li><li>Strong attention to detail and organizational skills.</li><li>Excellent communication and interpersonal skills.</li><li>Ability to work independently and as part of a team.</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>Previous experience in inventory management or a related field is preferred.</li><li>Knowledge of manufacturing processes and stages in an aerospace environment (machining, assembly, welding, paint, NDT, X-ray) is a plus.</li></ul><h2>Work Environment</h2><p>This position offers a clean manufacturing floor and updated office spaces with ample windows that look onto the manufacturing floor. The company provides a business casual dress code. Employees benefit from 100% medical coverage, a 401K plan with a 2.5% match, and 2-3 weeks of PTO to start. Spot bonuses are paid out 2-3 times per year based on company and individual performance, ranging from 8-10% of yearly salary for engineering roles. Flexible start and stop times are available. The company specializes in complex machining, NADCAP accredited welding and chemical processing/painting, CMSP, and assembly.</p>

Administrative Coordinator

<h1><strong>Job Description: Design Checker</strong></h1><p>As a Design Checker, you will play a crucial role in verifying engineering drawings for accuracy and completeness. You will ensure that all drawings comply with industry standards and project specifications, identify and correct errors, omissions, or discrepancies in drawings, and collaborate with engineers and designers to resolve drawing issues.</p><p><br></p><h2>Responsibilities</h2><ul><li>Verify engineering drawings for accuracy and completeness.</li><li>Ensure all drawings comply with industry standards and project specifications.</li><li>Identify and correct errors, omissions, or discrepancies in drawings.</li><li>Collaborate with engineers and designers to resolve drawing issues.</li><li>Maintain updated records of drawing revisions and approvals.</li><li>Utilize specialized software to review and edit drawings.</li><li>Participate in the development and implementation of quality control procedures for drawings.</li><li>Provide feedback and recommendations for improving drawing accuracy and clarity.</li></ul><h2>Essential Skills</h2><ul><li>Expertise in blueprint reading.</li><li>Proficiency in GD&amp;T (Geometric Dimensioning and Tolerancing).</li><li>Experience as a checker.</li><li>SolidWorks proficiency.</li><li>Design and drafting skills.</li><li>5+ years of experience in design checking.</li><li>Experience with tolerance stack-ups.</li><li>Aerospace industry experience.</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>Associates or Bachelor&#39;s degree preferred.</li><li>SolidWorks experience preferred.</li></ul>

Aerospace Design Checker

<h1><strong>URGENT: Aftermarket Sales and Steel Fabrication Estimator</strong></h1><p><br></p><h2>Job Description</h2><p>This position offers a unique blend of responsibilities, evenly divided between aftermarket sales and steel estimating. The role requires engaging with existing customers and discovering new prospects, focusing on selling replacement components manufactured within the industry. The individual will prepare quotes based on customer needs, including breakdown situations and preventative maintenance. Additionally, the role involves training to help understand component needs and questions to ask. The other half of the role is dedicated to quoting steel fabrication projects, including conveyor systems and structural steel work.</p><p><br></p><h2>Responsibilities</h2><ul><li>Engage with existing customers and identify new prospects for aftermarket sales.</li><li>Sell replacement components manufactured by other industry companies.</li><li>Prepare quotes based on customer needs, including breakdown situations and preventative maintenance.</li><li>Train and understand various components and necessary questions.</li><li>Quote steel fabrication projects, including conveyor systems and structural steel.</li><li>Operate independently once trained, rebuilding and growing the aftermarket business.</li></ul><h2>Essential Skills</h2><ul><li>Advanced Excel proficiency, essential for the role, with complex function utilization.</li><li>Ability to navigate and utilize an internal system for parts and component selection.</li><li>Self-motivation and initiative to learn independently and explore resources.</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>Experience with structural steel and conveyor systems is a plus.</li><li>Familiarity with structural components is a plus.</li></ul><h2>Work Environment</h2><p>The work environment is a large square-footage assembly shop, offering a comprehensive project management experience from initial sale to full operation. The company provides an all-encompassing service, managing projects from selling to manufacturing and installation. The facility operates as a one-stop shop, ensuring projects are handled effectively from start to finish. With a history of dedicated employees since 1997, the role provides an opportunity to experience the entire process, from quoting to shipping equipment.</p>

Aftermarket Sales And Steel Fabrication Estimator

<h1><strong><span style="color: rgb(8, 7, 7); background-color: none;">Senior</span> Autonomous Agent Developer - Phoenix, AZ</strong></h1><h2>Job Description</h2><p>We are actively hiring a <span style="color: rgb(8, 7, 7); background-color: none;">Senior</span> Autonomous Agent Developer to join our growing team for Semiconductor Manufacturing in Phoenix, AZ! As a <span style="color: rgb(8, 7, 7); background-color: none;">Senior</span> Autonomous Agent Developer, you will design and build autonomous agents capable of reasoning, decision-making, and interacting with external systems. Your work will focus on developing systems that allow agents to autonomously carry out tasks, plan actions, and collaborate with other agents while ensuring their behavior is safe, reliable, and ethical. Utilizing cutting-edge AI technologies, you will extend the capabilities of language models through integration with APIs, tools, and external software environments. This is an excellent opportunity to work with cutting-edge technology in a long-term position with a stable company.</p><h2>Responsibilities</h2><ul><li>Design and implement autonomous agent systems with a focus on behavior modeling, task execution, and collaboration.</li><li>Integrate language models with tools, APIs, and software environments to enhance agents&#39; capabilities.</li><li>Develop agent memory systems, task tracking mechanisms, and goal-directed behaviors for autonomous action in dynamic environments.</li><li>Implement multi-agent systems to facilitate collaboration, knowledge sharing, and problem-solving.</li><li>Ensure agents&#39; actions comply with ethical and safety constraints to minimize risks.</li><li>Test and evaluate agents in real-world scenarios, iterating on designs based on feedback and performance metrics.</li><li>Research and experiment with emerging multi-agent frameworks to improve efficiency and capability.</li></ul><h2>Job Requirements</h2><ul><li>Bachelor’s or Master’s degree in Computer Science, AI, Machine Learning, or a related technical field.</li><li>5+ years of experience in Developing Autonomous Systems or Intelligent Agents.</li><li>Proficiency with Agent Architectures and Techniques, such as Task Planning and Agent Coordination.</li><li>Experience with Multi-Agent Systems, including Agent Communication and Task Distribution.</li><li>Deep understanding of language models and their integration with external APIs.</li><li>Strong Programming skills in Python and experience with AI frameworks.</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>3-8 years in Integrate Language Models; Reinforcement Learning; Artificial Intelligence; and Design Machine learning.</li><li>Familiarity with AI safety and ethics to prevent unwanted behaviors in autonomous systems.</li><li>Familiarity with cognitive architectures or symbolic reasoning for agent systems.</li></ul><h2>Work Environment</h2><p>This fab is state-of-the-art, but still undergoing expansion and construction in some areas, which can create a transitional atmosphere. The environment offers exposure to cutting-edge semiconductor technology and complex systems, which can be beneficial experience for engineers and technicians. AI is a fast-moving field, and this position at this facility allows employees to a great opportunity to stay competitive and updated with their skillsets.</p><p>Candidates must be willing and able to work on-site at our Phoenix, Arizona facility. The role requires dedication with long working hours. The company offers an average of 85+ hours of learning programs per employee annually, with a strong focus on technical training, leadership development, and cross-functional mobility. Benefits include health coverage, wellness programs, support for family care, and professional development funding.</p>

Agent AI Engineer

<h2>Job Description</h2><p>You will be involved in the layout of mixed analog and digital designs, including line voltage traces and multilayer board designs. You will generate and apply design rules and scripts, voltage maps, spacing, and perform DRC checks. Additionally, you will create and manage templates and libraries, develop and migrate file-based libraries to Altium 365, and generate output files for manufacturing. A thorough understanding of DFM and DFT requirements of PCB layout and design is essential. You will also need to execute projects on tight deadlines and quickly adapt between different PCB designs.</p><p><br></p><h2>Responsibilities</h2><ul><li>Design PCB layouts for mixed analog and digital systems.</li><li>Create multilayer board designs with precise line voltage traces.</li><li>Generate and apply design rules, scripts, voltage maps, and spacing.</li><li>Conduct DRC checks and ensure compliance with design standards.</li><li>Develop and manage templates and libraries for efficient design processes.</li><li>Migrate and develop file-based libraries to Altium 365, including symbols, footprints, and standardized parameters.</li><li>Produce output files for manufacturing and ensure their accuracy.</li><li>Understand and implement DFM and DFT requirements in PCB layout and design.</li><li>Execute projects under tight deadlines and adapt quickly to different PCB designs.</li></ul><h2>Essential Skills</h2><ul><li>Proficiency in PCB Layout and PCB Design.</li><li>Experience creating component libraries in Altium.</li><li>Knowledge of Altium 365 for managing mixed signal and voltage designs.</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>5+ years of experience using Altium Designer in a collaborative role.</li><li>Minimum 2 years of experience with component library and template management using Altium 365.</li><li>3 years of experience in 4–6-layer mixed signal PCB boards design with AC line voltage power.</li><li>Bachelor of Science in Electrical Engineering (BSEE) or equivalent experience.</li><li>Basic understanding of electronic components.</li><li>Proficiency in MS-Office applications like Word, Excel, and Teams.</li></ul>

Altium Drafter (Remote)

<h1><strong>Job Title: Analysis Engineer</strong></h1><p><br></p><h2>Job Description</h2><p>We are seeking a skilled Analysis Engineer who excels in finite element modeling and analysis, particularly using FEMAP. The ideal candidate will have a strong <span style="color: rgb(8, 7, 7); background-color: none;">background</span> in composites, with proficiency in Python for automation and data processing. This role requires an individual who thrives in a fast-paced, production-driven environment and can contribute immediately to reducing a significant backlog of non-conformances over a 6-month period.</p><p><br></p><h2>Responsibilities</h2><ul><li>Perform finite element modeling and analysis using FEMAP.</li><li>Utilize Python for automation and data processing tasks.</li><li>Provide production support with a focus on non-conformance resolution.</li><li>Apply materials knowledge in composites to support production processes.</li><li>Adapt to a fast-paced, ever-changing environment and contribute to operational efficiency.</li></ul><h2>Essential Skills</h2><ul><li>Proficiency in FEMAP for finite element modeling and analysis.</li><li>Experience with Python for automation and data processing.</li><li>Strong <span style="color: rgb(8, 7, 7); background-color: none;">background</span> in composites, including materials knowledge and production support.</li><li>Ability to work in a fast-paced, production-driven environment.</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>Experience in manufacturing with hands-on involvement.</li><li>Knowledge of stress analysis, thermal analysis, and GD&amp;T.</li><li>Understanding of aerospace engineering principles.</li><li>Experience in structural analysis and mechanical engineering.</li></ul><h2>Work Environment</h2><p>The position is onsite at a facility in Trinity, Decatur, Alabama. The work environment is fast-paced and requires adaptability to constant changes. Dress code is professional and appropriate for a manufacturing setting.</p>

Analysis Engineer

<h1 style="font-weight: 700;">Job Title: Analytical Chemist</h1><br><h2>Job Description</h2><p>We are seeking a skilled Analytical Chemist to perform routine analytical chemical testing on a variety of samples including raw materials, in-process batches, finished goods, water samples, and more. This role involves conducting specialized analytical testing to support development projects and troubleshoot methods as needed.</p><br><h2>Responsibilities</h2><ul><li>Conduct routine analytical chemical testing on products submitted to the lab, including raw materials, in-process batches, finished goods, water samples, and cleaning samples.</li><li>Perform specialized analytical testing as directed by the Laboratory Manager to support development projects and troubleshoot methods.</li><li>Document all results according to Standard Operating Procedures and Work Instructions.</li><li>Review the work of other laboratory personnel as required.</li><li>Learn and practice all aspects of laboratory instrumentation, including gas chromatography (GC), High-Pressure Liquid Chromatography (HPLC), UV/Visible Spectrophotometry, and FTIR.</li><li>Support cleaning validations and engineering trials through analytical work.</li><li>Compile and summarize data as required.</li><li>Perform general housekeeping and glassware cleaning.</li><li>Communicate verbally and in writing with management, coworkers, suppliers, and customers.</li><li>Maintain and promote strong work ethics and uphold all policies and procedures.</li><li>Perform additional assignments as requested by the Lab Manager.</li></ul><h2>Essential Skills</h2><ul><li>Proficiency in HPLC and GC techniques.</li><li>Strong foundation in analytical chemistry.</li><li>Ability to document and review laboratory results accurately.</li><li>Experience with laboratory instrumentation such as UV/Visible Spectrophotometry and FTIR.</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>Bachelor&#39;s Degree in Chemistry or any Laboratory Sciences Degree.</li><li>1+ years of experience in a GMP lab is preferred.</li></ul><h2>Work Environment</h2><p>The work environment is an OTC Manufacturing Analytical Chemistry Laboratory with hours on the 3rd shift, Monday to Friday, from 11 p.m. to 7 a.m. Candidates must be able to work extra hours, including some limited weekend work, when necessary to handle spikes in workload and meet deadlines.</p><br>

Analytical Chemist

<h1 style="font-weight: 700;">Job Title: Lab Technician</h1><br><h2>Job Description</h2><p>Join our dynamic team providing analytical services for a diverse range of products. As a Lab Technician, you will perform a variety of analytical testing procedures and support laboratory operations while adhering to Good Laboratory Practices.</p><br><h2>Responsibilities</h2><ul><li>Conduct analytical testing using FTIR, Carbon/Sulfur analysis, ICP, DSC, HPLC, and GC.</li><li>Support laboratory operations including glassware cleaning and sample preparation.</li><li>Follow established procedures and document all activities in compliance with Good Laboratory Practices (GLP).</li><li>Communicate effectively with team members to coordinate sample workflows and meet testing schedules.</li><li>Participate in continuous improvement initiatives and cross-functional team activities.</li><li>Assist in identifying and troubleshooting test method failures.</li><li>Support both development and commercial Quality Control (QC) release activities.</li><li>Learn and understand the manufacturing processes supported by the lab.</li></ul><h2>Essential Skills</h2><ul><li>Bachelor’s degree in Chemistry, Biochemistry, or a related scientific field.</li><li>6+ months of experience in a laboratory environment, preferably contract testing lab.</li><li>Proficiency in analytical techniques such as DSC, FTIR, GC, HPLC, ICP.</li><li>Strong attention to detail and commitment to quality.</li><li>Excellent communication and organizational skills.</li><li>Ability to work under pressure and manage multiple priorities effectively.</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>Previous experience in a regulated environment.</li><li>Contract testing lab experience.</li></ul><h2>Work Environment</h2><p>Join a close-knit team of 14 professionals where collaboration and teamwork are highly valued. The role requires 100% onsite presence, with daily meetings at 10 AM. Flexible hours are available around the meeting schedule, allowing for a balanced work-life experience.</p><br>

Analytical Chemistry Lab Technician

<h2>Analytical Chemistry Technician</h2><h2><br></h2><h2>Job Description</h2><p>Join our dynamic team providing analytical services for a diverse range of products. As a Lab Technician, you will perform a variety of analytical testing procedures and support laboratory operations while adhering to Good Laboratory Practices.</p><p><br></p><h2>Responsibilities</h2><ul><li>Conduct analytical testing chromatography instrumentation.</li><li>Support laboratory operations including glassware cleaning and sample preparation.</li><li>Follow established procedures and document all activities in compliance with Good Laboratory Practices (GLP).</li><li>Communicate effectively with team members to coordinate sample workflows and meet testing schedules.</li></ul><p><br></p><h2>Essential Skills</h2><ul><li>Bachelor’s degree in Chemistry, Biochemistry, or a related scientific field.</li><li>6+ months of experience in a laboratory environment, preferably fast paced lab experience.</li></ul><h2><br></h2><h2><br></h2>

Analytical Chemistry Technician

<h1 style="font-weight: 700;">Job Title: Analytical Data Reviewer</h1><br><h2>Job Description</h2><p>As an Analytical Data Reviewer, you will be responsible for developing and maintaining critical documentation related to Quality Control and Analytical Development. This includes writing, editing, and updating Standard Operating Procedures, test methods, specifications, and protocols. You will ensure all documentation is consistent, clear, and compliant with regulatory guidelines, while maintaining accurate version control and document tracking.</p><br><h2>Responsibilities</h2><ul><li>Write, edit, and maintain Standard Operating Procedures (SOPs), test methods, specifications, work instructions, and protocols related to Quality Control and Analytical Development.</li><li>Develop and update analytical test reports, validation protocols (IQ/OQ/PQ), and stability study reports.</li><li>Prepare method validation protocol/reports, method transfer protocol/reports, and technical documents including change controls, deviations, CAPAs, and OOS investigations.</li><li>Ensure consistency, clarity, and compliance in all documentation.</li><li>Maintain up-to-date copies of all cGMP documents in the laboratory and relevant databases.</li><li>Ensure all QC documentation aligns with FDA, ICH, USP, EP, cGMP, and other regulatory guidelines.</li><li>Assist in preparing documentation for regulatory submissions and audits.</li><li>Maintain accurate version control and document tracking within electronic document management systems.</li><li>Collaborate closely with QC analysts, Outside Contract Testing Laboratories, customers, equipment manufacturers, and Quality Assurance to gather technical information.</li><li>Assist in reviewing and updating documents based on feedback from Quality Assurance and Customers.</li><li>Provide guidance to QC personnel on documentation best practices and compliance requirements.</li><li>Develop training materials for QC team members on updated SOPs, specifications, and test methods.</li><li>Support quality improvement initiatives by identifying gaps in documentation and recommending improvements.</li><li>Stay up-to-date with industry best practices, regulatory changes, and advancements in pharmaceutical quality control.</li></ul><h2>Essential Skills</h2><ul><li>4-5 years of bench experience as a chemist with expertise in HPLC, Dissolution, KF Wet Chem Sample preparation.</li><li>Strong understanding of analytical techniques and laboratory procedures such as HPLC, GC, UV-Vis, FT-IR, Malvern PSD, Water by KF, and Dissolution.</li><li>Familiarity with regulatory guidelines such as FDA, ICH, USP, EP, cGMP, and GLP.</li><li>Excellent writing, editing, and organizational skills.</li><li>Highly skilled in Microsoft Office Suite, including Word, Excel, and PowerPoint.</li><li>Strong attention to detail and ability to translate complex scientific information into clear documentation.</li><li>Ability to work independently and collaborate effectively with cross-functional teams.</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>Bachelor&#39;s or Master’s degree in Pharmaceutical Sciences, Chemistry, Microbiology, Biotechnology, or a related field.</li><li>2-5 years of experience in technical writing within the pharmaceutical or biotech industry, preferably in Quality Control/Analytical Development.</li><li>Experience with Empower Software and solid oral dosage forms.</li><li>Ability to identify non-conformances and conduct laboratory investigations.</li></ul><h2>Work Environment</h2><p>You will work in a laboratory setting with approximately 10 colleagues. The environment is supportive of growth and continuous improvement, with opportunities to engage in high-pay projects within a new facility. The role encourages collaboration and communication among team members to ensure compliance and quality.</p><br>

Analytical Data Reviewer

<h1 style="font-weight: 700;">Job Title: Analytical Data Reviewer</h1><br><h2>Job Description</h2><p>As an Analytical Data Reviewer, you will be responsible for developing and maintaining essential documentation related to Quality Control and Analytical Development. Your role will ensure compliance with regulatory guidelines, support collaborative efforts, and contribute to continuous improvement initiatives within the laboratory.</p><br><h2>Responsibilities</h2><ul><li>Write, edit, and maintain Standard Operating Procedures (SOPs), test methods, specifications, work instructions, and protocols related to Quality Control and Analytical Development.</li><li>Develop and update analytical test reports/Certificate of Analysis, validation protocols (IQ/OQ/PQ), and stability study reports.</li><li>Prepare method validation protocol/reports, method transfer protocol/reports, technical documents, including change controls, deviations, CAPAs, and OOS (Out of Specification) and laboratory investigations.</li><li>Ensure consistency, clarity, and compliance in all documentation.</li><li>Maintain up-to-date copies of all cGMP documents in the laboratory and relevant databases.</li><li>Ensure all QC documentation aligns with FDA, ICH, USP, EP, cGMP, and other regulatory guidelines.</li><li>Assist in preparing documentation for regulatory submissions and audits (internal and external).</li><li>Maintain accurate version control and document tracking within electronic document management systems (ACE).</li><li>Work closely with QC analysts, outside contract testing laboratories, customers, equipment manufacturers, and Quality Assurance to gather technical information.</li><li>Assist in reviewing and updating documents based on feedback from Quality Assurance and Customers.</li><li>Provide guidance to QC personnel on documentation best practices and compliance requirements.</li><li>Develop training materials for QC team members on updated SOPs, specifications, and test methods.</li><li>Support quality improvement initiatives by identifying gaps in documentation and recommending improvements.</li><li>Stay up to date with industry best practices, regulatory changes, and advancements in pharmaceutical quality control.</li></ul><h2>Essential Skills</h2><ul><li>4-5 years of bench experience as a chemist.</li><li>Proficiency in HPLC Dissolution, KF Wet Chemistry, Sample preparation.</li><li>Experience with Solid Oral Dosage and Empower Software.</li><li>Ability to identify non-conformance in laboratory settings.</li><li>Strong understanding of analytical techniques (HPLC, GC, UV-Vis, FT-IR, Malvern PSD, Water by KF and Dissolution, etc.) and laboratory procedures.</li><li>Familiarity with regulatory guidelines such as FDA, ICH, USP, EP, cGMP, and GLP.</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>Bachelor&#39;s or Master’s degree in Pharmaceutical Sciences, Chemistry, Microbiology, Biotechnology, or a related field.</li><li>2-5 years of experience in technical writing within the pharmaceutical or biotech industry, preferably in Quality Control/Analytical Development.</li><li>Excellent writing, editing, and organizational skills.</li><li>Proficiency in Microsoft Office Suite, including Word, Excel, and PowerPoint.</li><li>Strong attention to detail and ability to translate complex scientific information into clear documentation.</li><li>Ability to work independently and collaborate effectively with cross-functional teams.</li></ul><h2>Work Environment</h2><p>The role is based in a laboratory setting with a team of 10 people. The facility is new, offering a dynamic and growing environment. High pay and opportunities within a growing Contract Manufacturing Organization (CMO) make this role attractive.</p><br>

<h1 style="text-align: center;"><strong><u>Lab Technician</u></strong></h1><p style="text-align: center;"><br></p><p style="text-align: center;">INTERESTED CANDIDATES MAY SEND UPDATED RESUMES TO: JGASSER @ ACTALENTSERVICES.COM </p><p style="text-align: center;">OR TEXT JENNA TO SETUP A PHONE INTERVIEW: 419. 980. 5823 </p><p><br></p><p><strong><u>Job Description</u></strong></p><p>This role involves performing various laboratory tests and analyzing samples, while maintaining accurate records and adhering to strict lab standards. The lab technician will prepare samples for analysis by weighing, diluting, and mixing according to established procedures. The position requires operating analytical instruments, primarily HPLC, and conducting analytical analyses.</p><p><br></p><p><strong><u>Responsibilities</u></strong></p><ul><li>Perform various lab tests and analyze samples.</li><li>Maintain accurate records and adhere to strict lab standards.</li><li>Prepare samples for analysis by weighing, diluting, and mixing according to established procedures.</li><li>Operate analytical instruments, mainly HPLC.</li><li>Conduct analytical analyses.</li><li>Perform tests including viscosity, titration, and pH measurements.</li><li>Collaborate with scientists to develop analytical methods.</li><li>Perform sample preparation and reference sample preparation.</li><li>Prepare sample solutions for scientists.</li></ul><p><strong><u>Essential Skills</u></strong></p><ul><li>Proficiency in chemistry and laboratory practices.</li><li>Quality control and analytical chemistry skills.</li><li>Experience with wet chemistry techniques.</li><li>Ability to conduct lab testing.</li></ul><p><strong><u>Additional Skills &amp; Qualifications</u></strong></p><ul><li>Bachelor&#39;s degree in Science, with completion of General Chemistry I and II with labs.</li><li>Basic understanding of lab equipment.</li><li>Preferably, some lab experience outside of school.</li></ul><p><strong>Work Environment</strong></p><p>The lab technician will work in a laboratory setting, offering exposure to various tests and R&amp;D projects. The position is part of a long-term contract, providing ample opportunities for learning and development.</p>

Analytical Lab Technician

<h1><strong> Analytical Lab Technician</strong></h1><p><br></p><h2>Job Description</h2><p>Support laboratory operations by independently performing standard testing procedures and preparing samples for analysis.</p><p><br></p><h2>Responsibilities</h2><ul><li>Execute established testing protocols and prepare materials for analysis with minimal oversight.</li><li>Assemble and operate experimental setups under direction from team members.</li><li>Perform routine maintenance and calibration of lab instruments to ensure optimal performance.</li><li>Accurately document test results and maintain comprehensive logs of experimental activities.</li><li>Assist in tracking and replenishing laboratory inventory and consumables.</li><li>Adhere to safety standards and contribute to maintaining a clean and organized lab environment.</li></ul><h2>Essential Skills</h2><ul><li>Experience in a laboratory setting</li><li>Proficiency in chemistry and data entry.</li><li>Strong documentation skills.</li></ul><h2>Qualifications</h2><ul><li>1-3 years of lab experience. Associate&#39;s degree preferred</li><li>Verbal and written communication skills for interaction with internal and external customers.</li><li>Ability and willingness to work in a multinational team environment.</li><li>Proficiency in PC skills, including Windows (Word, Excel, PowerPoint).</li></ul><h2>Work Environment</h2><p>Work in an analytical and materials testing lab. The environment fosters growth and development within a small team that contributes to larger projects. The role is ideal for those looking for a long-term opportunity rather than a short-term stepping stone.</p>

<h1 style="font-weight: 700;">Job Title: Analytical Lab Technician</h1><br><h2>Job Description</h2><p>Support laboratory operations by independently performing standard testing procedures and preparing samples for analysis.</p><br><h2>Responsibilities</h2><ul><li>Execute established testing protocols and prepare materials for analysis with minimal oversight.</li><li>Assemble and operate experimental setups under direction from <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> team members.</li><li>Perform routine maintenance and calibration of lab instruments to ensure optimal performance.</li><li>Accurately document test results and maintain comprehensive logs of experimental activities.</li><li>Assist in tracking and replenishing laboratory inventory and consumables.</li><li>Adhere to safety standards and contribute to maintaining a clean and organized lab environment.</li></ul><h2>Essential Skills</h2><ul><li>Experience in laboratory operations and sample preparation.</li><li>Proficiency in chemistry and data entry.</li><li>Strong documentation skills.</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>Non-degree candidate or associates degree level candidate with 1-3 years of lab experience.</li><li>Verbal and written communication skills for interaction with internal and external customers.</li><li>Ability and willingness to work in a multinational team environment.</li><li>Proficiency in PC skills, including Windows (Word, Excel, PowerPoint).</li></ul><h2>Work Environment</h2><p>Work in an analytical and materials testing lab located at the Maple Grove site. The environment fosters growth and development within a small team that contributes to larger projects. The role is ideal for those looking for a long-term opportunity rather than a short-term stepping stone.</p><br>

<h1><strong> Analytical Lab Technician</strong></h1><p><br></p><h2>Job Description</h2><p>Support laboratory operations by independently performing standard testing procedures and preparing samples for analysis.</p><p><br></p><h2>Responsibilities</h2><ul><li>Execute established testing protocols and prepare materials for analysis with minimal oversight.</li><li>Assemble and operate experimental setups under direction from <span style="color: rgb(8, 7, 7); background-color: none;">senior</span> team members.</li><li>Perform routine maintenance and calibration of lab instruments to ensure optimal performance.</li><li>Accurately document test results and maintain comprehensive logs of experimental activities.</li><li>Assist in tracking and replenishing laboratory inventory and consumables.</li><li>Adhere to safety standards and contribute to maintaining a clean and organized lab environment.</li></ul><h2>Essential Skills</h2><ul><li>Experience in a laboratory setting</li><li>Proficiency in chemistry and data entry.</li><li>Strong documentation skills.</li></ul><h2>Qualifications</h2><ul><li>1-3 years of lab experience. Associate&#39;s degree preferred</li><li>Verbal and written communication skills for interaction with internal and external customers.</li><li>Ability and willingness to work in a multinational team environment.</li><li>Proficiency in PC skills, including Windows (Word, Excel, PowerPoint).</li></ul><h2>Work Environment</h2><p>Work in an analytical and materials testing lab. The environment fosters growth and development within a small team that contributes to larger projects. The role is ideal for those looking for a long-term opportunity rather than a short-term stepping stone.</p>

<h1 style="font-weight: 700;">Job Title: Quality Assurance Technician</h1><br><h2>Job Description</h2><p>As a Quality Assurance Technician, you will be responsible for reviewing compliance documentation related to raw materials, in-process samples, and finished product analyses. You will monitor adherence to current Good Laboratory Practices (cGLP) by laboratory personnel during routine operations to ensure procedural compliance. Additionally, you will verify that laboratory chemicals, reagents, and standards are properly labeled in accordance with standard operating procedures (SOPs).</p><br><h2>Responsibilities</h2><ul><li>Review laboratory audit trails during data assessments to ensure alignment with SOPs.</li><li>Coordinate with Analytical Laboratory Teams to compile and provide necessary documentation to cross-functional teams.</li><li>Manage incoming documentation, including tracking, recording, storing, and archiving in an organized manner.</li><li>Identify system gaps during routine monitoring and notify supervisors of areas requiring improvement.</li><li>Understand laboratory equipment operation, qualification, and calibrations, including their software audit trail reviews.</li><li>Actively participate in the review of data related to laboratory investigations and incidents to ensure regulatory compliance.</li><li>Support departmental and cross-functional initiatives and complete assignments as directed by the manager or supervisor.</li></ul><h2>Essential Skills</h2><ul><li>Strong documentation and technical writing skills, with the ability to apply relevant scientific principles and practices.</li><li>Ability to work under minimal supervision, independently, and in a team environment.</li><li>Proficiency in computer skills and software applications such as Microsoft Office tools and Quality applications and software programs.</li><li>Experience in analytical quality assurance with a focus on inhalation products (MDI) is a plus.</li><li>Effective interpersonal relationship skills and the ability to work in a team environment.</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>Possess a minimum bachelor&#39;s degree in Chemistry, Pharmaceutical Sciences, or related field from an accredited institution. A master&#39;s degree is preferred.</li><li>A minimum of 1-3 years of experience in analytical quality assurance.</li><li>Proficiently speak English as a first or second language and ability to read, write, and communicate effectively.</li><li>Self-starter with the initiative to seek additional training or direction as needed.</li><li>Knowledge and experience with analytical laboratory activities in areas such as active pharmaceutical ingredients (API), drug products, analytical development, Quality Control (QC), Good Laboratory Practices (GLP)/Good Manufacturing Practices (GMP)/Good documentation Practices (GDP).</li><li>Willingness to work any assigned shift ranging from first or second shift; work schedules may be Monday to Friday.</li></ul><h2>Work Environment</h2><p>Work primarily during the first shift from 8:30 AM to 5:00 PM, Monday to Friday. You will be part of a supportive team of 15-20 people, collaborating with the manufacturing team. Reporting directly to the QA Manager, you will be required to stand or walk unassisted for 75% or more of an 8-hour period and may need to lift up to 10 kg unassisted. Appropriate personal protective equipment must be worn when required. You will spend considerable time sitting at a desk and working at a computer or other screens.</p><br>

Analytical Quality Assurance Associate

<h1 style="font-weight: 700;">Job Title: Analytical Research and Development Chemist</h1><br><h2>Job Description</h2><p>The Analytical Chemist will collaborate with a project team of chemists in a laboratory setting to analyze and develop HPLC and GC methods. These methods are used for assays, impurity analysis, dissolution, residual solvents testing, and particle size distribution of active pharmaceutical ingredients, excipients, and finished dosage forms.</p><br><h2>Responsibilities</h2><ul><li>Perform Method Development/Method Validation/Stability Testing for various dosage forms including Tablets, Hard Gelatin Capsules, Oral/Topical Liquids, Oral Suspensions, Powder for Oral Suspensions, and Nasal Products with minimal supervision.</li><li>Support the Product Development team in the creation of new products.</li><li>Identify and characterize unknown impurities in drug products and substances.</li><li>Conduct Elemental Impurity Testing using ICP-MS/ICP-OES.</li><li>Troubleshoot analytical issues to achieve desired results.</li><li>Write reports suitable for regulatory submission with minimal supervision.</li><li>Perform other duties as assigned.</li></ul><h2>Essential Skills</h2><ul><li>Bachelor&#39;s Degree in Chemistry, Biology, or a related field; a Master&#39;s Degree is a plus.</li><li>3-10 years of experience as an R&amp;D Chemist in a pharmaceutical setting.</li><li>Operational and technical expertise in HPLC, GC, Dissolution, and Particle Size Distribution.</li><li>Experience in pharmaceutical Method Development, Method Validation, and Stability Testing.</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>Capable of writing comprehensive reports for regulatory submissions with minimal supervision.</li></ul><h2>Work Environment</h2><p>This role is based in Somerset, New Jersey, within a laboratory environment that involves working with chemicals, reagents, and solvents. The position may require occasional lifting of up to 20 pounds. The location serves as one of the fifteen global commercial manufacturing sites and houses additional Research and Development teams.</p><br>

Analytical Research And Development Chemist

<h1><strong>Job Title: Scientist - Analytical</strong></h1><p><br></p><h2>Job Description</h2><p>The Scientist will support the Quality Control Method Transfer and Validation team by performing method validation activities, including drafting protocols and reports, executing validation assays, and conducting data analysis. Additionally, the Scientist will be responsible for reviewing reports and data in accordance with cGMP and data integrity principles.</p><p><br></p><h2>Responsibilities</h2><ul><li>Independently conceptualize, plan, and execute laboratory experiments.</li><li>Collaborate with colleagues and subject matter experts to determine suitable analytical methodologies for project initiatives, including computational predictive tools, modeling software, and data visualization tools.</li><li>Lead and manage multiple projects, assisting teams in developing effective strategies for analytical needs and controls.</li><li>Engage with the method development team and participate in both in-process and final product sample analyses.</li><li>Author relevant sections of technical reports to support interdepartmental technology and method validation and transfer processes.</li><li>Prepare technical reports, critically review data, and evaluate new instrumentation and analytical techniques/approaches as required.</li><li>Independently analyze experimental data and provide conclusive insights.</li><li>Mentor junior scientists and offer technical guidance when required.</li><li>Support the technical leads and the Scientist II with project activities to meet deadlines.</li></ul><h2>Essential Skills</h2><ul><li>Experience with GMP, HPLC, UPLC, and Empower.</li><li>Capability to independently execute laboratory assays and draft protocol deviations under supervision.</li><li>Proficiency in performing data reviews.</li><li>Applicable relevant experience in pharmaceutical chemistry.</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>Bachelors, Masters, or PhD in a related field.</li><li>Experience in assay development, method validation, method development, and method transfer.</li><li>Knowledge of cGMP, quality control, and LIMS.</li><li>Experience with Waters HPLC, capillary electrophoresis, PA 800, and chemistry plate-based assays.</li></ul><h2>Work Environment</h2><p>This large pharmaceutical manufacturing organization focuses on vaccine and mAb intermediate manufacturing. The position involves working in both office and lab environments. The work schedule is 1st Shift, Monday through Friday, from 8 AM to 5 PM, with occasional weekend work on a rotating basis as needed for specific projects.</p>

Analytical Scientist

<p><strong>Description</strong></p>
					<p>Description:

Breeds, raises and cares for small research animals on behalf of, or for sale to, customers. Follows proper breeding and animal care procedures. Monitors animal behavior and physical attributes to ensure animal health and confirm appropriate phenotype; reports any findings. Ensures biosecurity. Coordinates with Customer Service on scheduling and order status.

Basic Animal Husbandry
Physical job/on feet/climbing stairs to work on second level/repetitive motion
Need Ability to work with tablet computers
Attention to detail required
Strict Animal Welfare compliance – the health and treatment of our animals is paramount
Needs to be focused, punctual and engaged
Education: High School up to College
<span style="color: rgb(8, 7, 7); background-color: none;"><span style="color: rgb(8, 7, 7); background-color: none;">Background</span></span>: previous work with animals preferred but not required</p>
					<p><strong>Skills</strong></p>
					<p>animal care, Husbandry, Sterilization, Animal health, Veterinary, Laboratory, animal science, animal handling, animal husbandry, animal research, customer service</p>
					<p><strong>Top Skills Details</strong></p>
					<p>animal care,Husbandry,Sterilization,Animal health,Veterinary,Laboratory</p>
					<p><strong>Additional Skills &amp; Qualifications</strong></p>
					<p>They will take a HS diploma or GED</p>
					<p><strong>Experience Level</strong></p>
					<p>Entry Level</p>

Animal Care Technician

<h2 style="text-align: center;"><strong style="font-size: 22px;">**Immediate Opening: Animal Research Tech - HIRING NOW**</strong></h2><p style="text-align: center;"><em style="font-size: 14px;"><u>*Interview availability this week*</u></em></p><p><br></p><p style="text-align: center;"><strong>Interested in this role? </strong>Reach out directly to apply <strong>TODAY </strong>to <strong>Grace Williams </strong>at <strong>grawilliams@actalentservices .com</strong></p><h2><br></h2><p><strong>Description</strong></p><p>A globally recognized biotechnology leader, specializing in drug target validation and functional genomics, is expanding its Indianapolis team. We are currently seeking an Animal Lab Research Technician to support our growing operations. In this role, you will play a key part in the daily care and maintenance of the animal facility, contributing to essential research and development efforts. </p><p><br></p><p><strong>Responsibilities:</strong></p><ul><li>Ensure the health of all animals are properly cared for. Fed, watered, and have clean bedding at all times</li><li>Perform all animal care tasks in strict accordance with animal welfare regulations</li><li>Coordinate the receipt, handling, and delivery of vivarium supplies</li><li>Wash, dry, and autoclave equipment and materials as needed</li><li>Accurately maintain relevant records, manually and electronically</li><li>Complete scheduled tasks to ensure cleanliness and sterility of designated areas</li><li>Keep the vivarium, storage, and office spaces organized and hygienic</li><li>Adhere to all Occupational Health and Safety (OHS) policies and procedures to ensure a safe working environment</li><li>Monitor and uphold OHS standards throughout the facility</li><li>Follow quarantine protocols for designated facility zones</li><li>Appropriately dispose of biohazard waste in compliance with safety guidelines</li><li>Assist with GLP (Good Laboratory Practice) studies and accurately document findings</li><li>Conduct clinical observations and record body weights of rodents (rats and mice)</li><li>Perform other duties as assigned to support research and facility operations</li></ul><p><br></p><p> <strong>Organizational Capability Duties:</strong></p><ul><li>Actively participate in team workshops and provide support across departments as needed</li><li>Promote and facilitate learning and understanding of the Organizational Capability Program (OCP)</li><li>Assist other team members in all duties by providing training, guidance and support.</li><li>Communicate effectively to ensure safe and efficient collaboration with colleagues</li><li>Contribute to the continuous improvement of operational processes throughout the organization</li><li>Assist in the management of equipment, materials, and supplies within the work area</li><li>Take accountability for setting work priorities, making informed decisions, assigning tasks, and monitoring work practices</li><li>Engage in research and development projects aimed at advancing organizational capabilities</li></ul><p><br></p><p><strong>Skills</strong></p><p>Animal Handling, Laboratory, Animal Care, Vivarium, Husbandry, Animal husbandry, Animal science, Animal Breeding, PCR, Embryology, Animal Welfare, Animal Tech, Animal Laboratory, Case Studies, Animal Observation, Animal Health</p><p><br></p><p><strong>Additional Skills &amp; Qualifications</strong></p><p>1) Bachelor&#39;s Degree in Life Science </p><p>2) 2+ months of vivarium experience</p><p>3) Proficient computer skills (Microsoft Office Suite, LIMS, etc.)</p><p>4) Experience being responsible for animal husbandry and maintaining vivarium colonies</p><p>5) Ability to work independently and efficiently</p><p>6) Strong communication skills, as this individual will work with partners all across the world</p><p><br></p><p><strong><u>INTERESTED IN THIS ROLE? SEE BELOW TO APPLY NOW FOR IMMEDIATE CONSIDERTATION:</u></strong></p><p><em><u>*Interview availability this week*</u></em></p><ul><li>I am scheduling interviews for this position and conducting phone interviews as early as today. All candidates will be considered immediately within 24 hours of applying directly to <strong>Grace Williams</strong>.</li><li><strong>HOW TO APPLY DIRECTLY: </strong>Email your updated resume, brief intro about your interest, preferred method of communication for you (i.e., call, email, text) to <strong>grawilliams@actalentservices. com </strong>or call me directly at <strong>(317-567 -6610)</strong></li></ul><h2><br></h2><p><br></p>

Animal Lab Technician - IMMEDIATE OPENING

<h1 style="font-weight: 700;">Job Title: Application Engineer</h1><br><h2>Job Description</h2><p>The successful candidate will be responsible for providing technical application support, training, and product overviews to meet the needs of the sales force, internal teams, and external customer inquiries.</p><br><h2>Responsibilities</h2><ul><li>Manage and resolve application-related inquiries from customers, internal teams, and end-users.</li><li>Address technical questions regarding the operation and functionality of products.</li><li>Support pricing inquiries for inside and outside sales teams, distributors, and sales representatives.</li><li>Collaborate with Global Product Management, Centers of Excellence, and Portfolio Managers to translate customer needs into product requirements.</li><li>Assist in research and compliance reviews for products.</li><li>Provide product training for new employees and internal/external sales channels as needed.</li><li>Develop and maintain technical content for datasheets, price lists, catalogs, and installation/operation manuals.</li><li>Create tools to aid inside sales with product information.</li><li>Represent the company at industry trade shows and support technical inquiries.</li><li>Support engineering teams in assigned duties.</li><li>Stay updated on product applications, business operations, and industry standards.</li><li>Perform additional technical support tasks and ancillary duties as required.</li></ul><h2>Essential Skills</h2><ul><li>BS Degree or equivalent in Mechanical Engineering or related field.</li><li>Experience in a manufacturing engineering type of knowledge.</li><li>Strong knowledge of mechanical systems such as load cells, strain gauges, and pressure sensors.</li><li>Proficiency in MS Office Suite (Word, Excel, PowerPoint, Outlook).</li><li>Strong communication and customer interaction skills.</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>Experience with CRM or Engineering Software.</li><li>Experience in a customer-facing role.</li><li>Strong organizational skills with the ability to manage multiple priorities.</li></ul><h2>Work Environment</h2><p>The position is based in an office setting at Lewis Center. The company boasts a very modern and clean facility with a smaller, family-feel environment. Employees have the flexibility to work from home 1-2 days a week, based on performance. The role includes up to 20% travel with the Sales Team for customer site visits.</p><br>

Application Engineer

<h1 style="font-weight: 700;">Job Title: Application Engineer</h1><br><h2>Job Description</h2><p>The Application Engineer provides technical and modification parts support to sales, PPC, shop, and NP teams to facilitate order management and completion, thereby achieving departmental goals. This role involves conducting research projects to assist in enhancing departmental efficiencies and capabilities.</p><br><h2>Responsibilities</h2><ul><li>Review requests from sales to provide quick information for processing motor modification quotes/orders through various communication channels such as emails and phone calls.</li><li>Develop and improve shop procedures to document current practices and methods, ensuring continuous improvement and uniform implementation. This includes conducting time studies to ensure accurate operation routings for capacity calculations.</li><li>Assist PPC, shop, and NP teams with technical support as needed.</li><li>Consistently mentor and train sales teams on technical information related to motor modifications.</li><li>Collaborate with product engineers and QA personnel to evaluate potential factory issues.</li><li>Maintain and update all motor modification technical tools to ensure accuracy and reliability for users.</li><li>Conduct training sessions for sales groups and field sales teams on motor modification processes and procedures.</li><li>Support stock inventory conversions through the modifications process.</li><li>Source and develop new parts for inventory addition or special projects.</li></ul><h2>Essential Skills</h2><ul><li>Bachelor&#39;s degree in a relevant field or 2 to 4 years of related experience and/or training.</li><li>Understanding of electric motor mechanical assembly at the component level.</li><li>Ability to read and interpret electrical drawings and nomenclature.</li><li>Proficiency in Microsoft Excel, PowerPoint, Word, and Outlook.</li><li>Technical writing skills.</li><li>Familiarity with basic industry standards such as NEMA, IEC, IEEE, UL.</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>Experience with design, mechanical engineering, motors, SAP, BOM, drawings, and PLM.</li><li>Ability to handle multiple projects simultaneously.</li><li>Demonstrated skills in attention to detail, organization, time management, teamwork, initiative, problem-solving, analytical thinking, negotiation, leadership, customer focus, and communication.</li></ul><h2>Work Environment</h2><p>This role is 100% onsite in Duluth, providing a dedicated desk and computer in a professional office setting with visits to the mod shop as needed. The mod shop is equipped with 7 cranes and staffed by 10 people. The team is composed of 6 engineers, 2 operations personnel, 1 manufacturing professional, 1 process engineer, and 1 training specialist. There is no regular travel required, though occasional travel to other mod shops may occur with ample advance notice.</p><br>

<h2>Job Overview</h2><p>We are looking for an Application Engineer with 2-5 years of experience to serve as a key customer-facing technical expert. The ideal candidate will have a passion for solving complex technical challenges, excellent communication skills, and a strong <span style="color: rgb(8, 7, 7); background-color: none;"><span style="color: rgb(8, 7, 7); background-color: none;">background</span></span> in engineering. This role involves working closely with customers to understand their needs, providing technical support, and ensuring successful implementation of our products.</p><h2>Key Responsibilities</h2><ul><li><strong>Customer Engagement</strong>: Act as the primary technical point of contact for customers, addressing their needs and providing tailored solutions.</li><li><strong>Technical Support</strong>: Assist customers with product integration, troubleshooting, and optimization to ensure optimal performance.</li><li><strong>Solution Development</strong>: Collaborate with sales and product development teams to design and propose technical solutions that meet customer requirements.</li><li><strong>Product Demonstrations</strong>: Conduct product demos and presentations to showcase capabilities and benefits to prospective and existing customers.</li><li><strong>Training and Documentation</strong>: Develop and deliver technical training sessions for customers and create user-friendly documentation, including guides and FAQs.</li><li><strong>Feedback Loop</strong>: Gather customer feedback to inform product improvements and relay insights to engineering and product teams.</li><li><strong>Project Management</strong>: Manage customer projects, ensuring timely delivery and alignment with technical specifications.</li></ul><h2>Qualifications</h2><ul><li><strong>Experience</strong>:<ul><li>2-5 years of experience in an application engineering or customer-facing technical role, preferably in a high-tech industry.</li><li>Experience working directly with customers to address technical challenges and deliver solutions.</li></ul></li><li><strong>Education</strong>: Bachelor’s degree in Mechanical Engineering (ME) preferred, or a related engineering field, or equivalent professional experience.</li><li><strong>Skills</strong>:<ul><li>Strong problem-solving and analytical skills.</li><li>Excellent verbal and written communication skills for effective customer interactions.</li><li>Proficiency in technical tools such as CAD software, simulation tools, or other engineering applications.</li><li>Ability to work independently and in a team-oriented environment.</li><li>Strong organizational and project management skills.</li></ul></li><li><strong>Availability</strong>: Willingness to travel occasionally to customer sites as needed.</li></ul><h2>Preferred Qualifications</h2><ul><li>Experience in industries such as manufacturing, aerospace, or electronics.</li><li>Familiarity with CRM systems (e.g., Salesforce) and technical support platforms.</li><li>Knowledge of programming or scripting languages (e.g., Python, MATLAB) for automation or data analysis.</li></ul><h2>Why Join Us?</h2><ul><li><strong>Competitive Compensation</strong>: Attractive salary and comprehensive benefits package, including health, dental, and retirement plans.</li><li><strong>Career Growth</strong>: Opportunities for professional development and advancement in a rapidly growing company.</li><li><strong>Innovative Environment</strong>: Work with cutting-edge technology and collaborate with a talented, forward-thinking team.</li><li><strong>Impactful Role</strong>: Make a direct impact on customer success and product innovation.</li></ul><h2><br></h2>

<h1><strong>Job Title: Applications Engineer</strong></h1><p><br></p><h2>Job Description</h2><p>This position is responsible for accurately targeting and defining product design requirements and specifications and developing designs to meet customer and internal production needs. The Applications Engineer will prepare costing, proposals, and bid packages for all projects within defined market segments, while providing technical support to the Regional Sales Manager. This role focuses on serving as a liaison between engineering and sales, supporting the sales team with quotes, specifications, pricing, strategy, and bid documentation, as well as aiding in lead generation and customer interaction.</p><p><br></p><h2>Responsibilities</h2><ul><li>Size and develop cost-effective process solutions to meet customer needs.</li><li>Prepare technical bids and proposals associated with products in the portfolio.</li><li>Participate in design and process risk reviews for proposed solutions.</li><li>Communicate with Regional Sales Manager, external sales representatives, internal engineering departments, engineering consultants, and customers.</li><li>Ensure all designs conform to contract specifications and drawings.</li><li>Write up orders, clearly identifying what was sold and resolving conflicts regarding price, scope, and delivery schedule.</li></ul><h2>Essential Skills</h2><ul><li>Experience working in a manufacturing environment.</li><li>Proficiency in AutoCAD and ability to review PID/PFD drawings.</li><li>Excellent communication skills, particularly with customers.</li><li>Experience in lead generation and sales.</li><li>Strong technical and writing skills.</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>Bachelor&#39;s degree in chemical, environmental, or civil engineering or related is required.</li><li>2-5 years&#39; experience as an Applications Engineer or in a related field.</li><li>Strong process engineering experience and knowledge of wastewater treatment.</li><li>Proficiency in MS Office.</li></ul><h2>Work Environment</h2><p>The role operates in a new innovation center alongside engineers, offering a collaborative environment with freedom to explore ideas. The position reports to the Applications Engineering Manager and works a standard 40-hour week from 8am to 5pm. Employees have their own cubicle and benefit from working in a dynamic industry with interesting equipment, experiencing growth opportunities and becoming experts in their field. </p>

Applications Engineer

<p><strong>HIRING ASAP!</strong>If interested in more information/direct feedback, please reach out to me at<strong><u>gcollier@actalentservices. com</u>and attach your resume and contact information.</strong></p><p><br></p><p><strong><u>﻿</u></strong><u>Below are some details about the position:</u></p><ul><li><strong><u>BENEFITS:</u></strong>YES</li><li><strong><u>PAY: </u></strong>$43-53 an hour depending on experience</li><li><strong><u>SCHEDULE/ENVIRONMENT: </u></strong>Hybrid with <strong><u>Travel (up to 80% during projects, BUT typically 1 week out of every month)</u></strong></li></ul><h2><strong>Job Description</strong></h2><p>This role demands mastery in AutoCAD and complete ownership of facility layouts for multiple high-volume automated pharmacies and office facilities. Collaborate with the broader operations team and capacity planning to draft facility concepts that align with state-of-the-art processes and equipment. Prepare Requests for Proposal with pharmacy automation vendors for expansion and efficiency needs. Manage vendor selection and collaborate closely with partners, operations, facilities, and IT on detailed project planning. Oversee facility modification installations. This position requires significant travel, up to 80% during projects going-live, followed by periods of reduced travel. Collaborate directly with the Sr Vice President of Operations on cost estimation and building of pharmacy capital budgets. Design office spaces, automation, and detailed engineering. This is a hybrid role when not traveling.</p><p><br></p><h2><strong>Responsibilities</strong></h2><ul><li>Draft facility layouts for high-volume automated pharmacies and office facilities using AutoCAD.</li><li>Collaborate with operations team and capacity planning to develop facility concepts.</li><li>Prepare Requests for Proposal with pharmacy automation vendors.</li><li>Manage vendor selection and work closely with partners, operations, facilities, and IT on project planning.</li><li>Oversee facility modification installations.</li><li>Travel up to 80% during project launches, with reduced travel afterward.</li><li>Work directly with Sr Vice President of Operations on cost estimation and capital budgets.</li><li>Design office spaces and automation systems.</li></ul><p><strong><u>MUST HAVES:</u></strong></p><ul><li>Proficiency in AutoCAD (2D or 3D) with over 5 years of experience.</li><li>Facility layout and new equipment location drafting experience.</li><li>Coordination of equipment relocation and installation.</li><li>Project planning and coordinating skills.</li><li>Utilities delivery engineering knowledge.</li><li>Project management experience.</li><li>Capital planning and budgeting expertise.</li></ul><p><strong><u>NICE TO HAVES:</u></strong></p><ul><li>Bachelor&#39;s degree preferred.</li><li>Network drops and IT installation coordination.</li><li>Vendor selection and requests for quotation.</li><li>Software/hardware familiarity.</li><li>Process engineering skills.</li></ul>

Applications Engineer (Designer) - Hybrid

Applications/sales Engineer

<p><strong>Description</strong></p>
					<p>Lead design development and documentation for commercial projects from concept through construction.
Collaborate with clients, consultants, and internal teams to ensure design excellence and technical accuracy.
Prepare and review construction documents, specifications, and permit submissions.
Coordinate with contractors during construction administration to ensure design intent is maintained.
Design and create renderings in Revit</p>
					<p><strong>Skills</strong></p>
					<p>Revit, Construction administration, Construction document, Autocad, Design, architecture, enscape</p>
					<p><strong>Top Skills Details</strong></p>
					<p>Revit</p>
					<p><strong>Additional Skills &amp; Qualifications</strong></p>
					<p>Professional degree in Architecture and 5–8 years of relevant experience.
Proficiency in Revit, AutoCAD, and Adobe Creative Suite.
Strong understanding of building codes, zoning regulations, and commercial construction methods.
Excellent communication and project coordination skills.
Licensure or progress toward licensure preferred.</p>
					<p><strong>Experience Level</strong></p>
					<p>Entry Level</p>

Architect

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