<h1 style="font-weight: 700;">Job Title: Quality Control Electrical Distribution Designer</h1><br><h2>Job Description</h2><p>The individual will be responsible for performing quality control inspections on electrical overhead and underground distribution design systems for electric utility customers. The individual will either correct the issues they identified in the design during their quality control check OR set and manage expectations for the Designer that submitted the design to make the needed corrections by a set date. This will be a hybrid position with offices located across Michigan and flexibility in the number of days worked at home and in the office.</p><br><h2>Responsibilities</h2><ul><li>Perform quality control checks of distribution designs before submission to the power utility client.</li><li>Correct identified issues in designs during quality control checks or manage expectations for the Designer to make necessary corrections.</li><li>Potentially lead the Quality Control team based on the volume of checks performed.</li><li>Collaborate with the Utility Energy Division to support distribution and reliability work.</li></ul><h2>Essential Skills</h2><ul><li>Power Distribution Design</li><li>Quality control</li><li>Electrical engineering</li><li>Experience with the National Electric Safety Code (NESC)</li><li>Distribution construction &amp; design standards</li><li>QA/Quality Assurance or QC/Quality Control</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>Experience with electric utilities such as Consumers Energy, DTE, AEP, Direct Energy, Atlantic Energy, Great American Power, Horizon Power and Light, Duke Energy, NIPSCO</li><li>Experience with electric utility consulting firms like Sigma Technologies, Pike, Orbital, Metro Engineering Solutions, Burns and Mac</li><li>Experience in writing process standards</li><li>Engineering Intern (EIT) certification</li></ul><h2>Work Environment</h2><p>Offices are available in Traverse City, Gaylord, Bay City, Grand Rapids, Flint, and other locations. This hybrid position offers flexibility with the number of days working from home. Work is directly connected to the Utility industry, Construction Services, Site Development, Survey, Storm Water, Transportation, and Waste Water. Employees receive one week vacation and six holidays during their initial nine months, transitioning to two weeks vacation, six sick days, and nine holidays once direct.</p><br>

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Quality Control Electrical Distribution Designer

<h3>Position Overview</h3><p>We are seeking a detail-oriented and safety-consciousQuality Control Lab Technicianto join our team in a fast-pacedchemical manufacturing environment. In this role, you will be responsible for performing analytical testing on raw materials, in-process samples, and finished chemical products to ensure compliance with internal specifications and regulatory standards. You will work in a modern laboratory equipped with advanced instrumentation, supporting our mission to deliver high-quality, consistent, and compliant chemical products.</p><hr><h3>Key Responsibilities</h3><h4>Analytical Testing &amp; Instrumentation</h4><ul><li>Conduct qualitative and quantitative analysis using:<ul><li>Gas Chromatography (GC)</li><li>High-Performance Liquid Chromatography (HPLC)</li><li>UV-Visible and Infrared (IR) Spectrophotometers</li><li>pH meters, viscometers, and other wet chemistry tools</li></ul></li><li>Perform specialized tests including:<ul><li>FTIR analysis for material identification</li><li>Karl Fischer titration for moisture content</li><li>Residue after evaporation and fluorescence testing</li></ul></li></ul><h4>Sample Management &amp; Prioritization</h4><ul><li>Receive, log, and prioritize samples from production batches, raw material shipments, and final product lots</li><li>Ensure timely and accurate testing to support production schedules and shipping deadlines</li></ul><h4>Documentation &amp; Compliance</h4><ul><li>Record and interpret test results in accordance withGood Documentation Practices (GDP)andISO/GMP standards</li><li>Maintain accurate lab records, test logs, and Certificates of Analysis (CoAs)</li><li>Support internal and external audits by ensuring traceability and data integrity</li></ul><h4>Equipment Calibration &amp; Maintenance</h4><ul><li>Set up, calibrate, and maintain laboratory instruments per SOPs</li><li>Perform routine maintenance and troubleshoot equipment issues to minimize downtime</li></ul><h4>Cross-Functional Collaboration</h4><ul><li>Work closely with Production, R&amp;D, and Quality Assurance teams to resolve quality issues and support process improvements</li><li>Participate in root cause investigations and corrective/preventive action (CAPA) initiatives</li></ul><h4>Safety &amp; Continuous Improvement</h4><ul><li>Follow allchemical safety protocols, including proper handling, labeling, and disposal of hazardous materials</li><li>Contribute to continuous improvement efforts within theQuality Management System (QMS)</li></ul><h3>Qualifications</h3><h4>Required:</h4><ul><li>Solid understanding of chemistry and laboratory techniques</li><li>Experience with wet chemistry, titration, and viscosity testing</li><li>Strong attention to detail and analytical problem-solving skills</li><li>Ability to work independently and follow SOPs in a regulated environment</li></ul><h4>Preferred:</h4><ul><li>Bachelor’s degree in Chemistry, Biochemistry, or a related field</li><li><em>(Entry-level candidates with academic lab experience are encouraged to apply!)</em></li></ul><h3><br></h3>

Quality Control Lab Technician

<p><strong>Overview:</strong></p><p>Join our dynamic team as a Quality Control Lab Technician, where you&#39;ll play a key role in ensuring our products meet the highest quality standards. You&#39;ll work hands-on in a modern laboratory environment, using advanced analytical instruments and techniques to test raw materials, in-process samples, and finished goods.</p><hr><h3><strong>Key Responsibilities:</strong></h3><ul><li>Conduct analytical testing using instruments such as:<ul><li>Gas Chromatography (GC)</li><li>High-Performance Liquid Chromatography (HPLC)</li><li>UV-Visible and Infrared Spectrophotometers</li><li>pH meters and other wet chemistry tools</li></ul></li><li>Perform specialized tests including:<ul><li>FTIR analysis</li><li>Residue after evaporation</li><li>Fluorescence and optical absorption testing</li></ul></li><li>Interpret and document test results in accordance with Good Documentation Practices (GDP)</li><li>Set up and calibrate lab equipment, including daily standards and Karl Fischer titrations</li><li>Plan and prioritize testing for incoming samples</li><li>Collaborate with cross-functional teams to support quality initiatives</li><li>Contribute to continuous improvement efforts within the Quality Management System</li><li>Perform additional duties as assigned</li></ul><h3>What You Bring:</h3><ul><li>Solid foundation in chemistry and laboratory techniques</li><li>Hands-on experience with wet chemistry, titration, and viscosity testing</li><li>Strong analytical thinking and attention to detail</li><li>Ability to work independently and follow established procedures</li></ul><hr><h3>Preferred Qualifications:</h3><ul><li>Bachelor’s degree in Chemistry, Biochemistry, or a related field</li><li><em>(Entry-level candidates with strong academic lab experience are welcome!)</em></li><li>Associate’s degree in Science with 1+ year of industry experience</li><li>High school diploma with 2–3 years of recent lab experience in a chemical setting</li></ul><h1><br></h1>

<h1 style="font-weight: 700;">Job Title: QC Lab Technician</h1><br><h2>Job Description</h2><p>The QC Lab Technician plays a crucial role in supporting QC Lab Chemists by performing physical and chemical analysis to ensure all materials meet quality specifications. This position offers exposure to both chemistry and microbiology within a growing company, providing ample room for professional growth and development.</p><br><h2>Responsibilities</h2><ul><li>Assist QC Lab Chemists in testing raw and finished products using various test methods and instrumentation such as pH meters, Water Activity, FTIR, and HPLC.</li><li>Enter data and manage records on computers, ensuring accurate file management.</li><li>Perform lab maintenance and general cleaning duties.</li><li>Discard old, retained samples according to standard operating procedures (SOP).</li><li>Conduct QC testing and data review.</li><li>Coordinate and perform sensory analysis of incoming samples with a trained team according to established procedures.</li><li>Organize and catalogue retained library samples, folders, and paperwork, and order retains to support QC evaluation.</li><li>Maintain cleanliness of the lab in accordance with Good Laboratory Practices.</li><li>Perform other related duties as assigned.</li></ul><h2>Essential Skills</h2><ul><li>Proficiency in Chemistry, Quality Control, and GMP.</li><li>Experience with analytical techniques such as FTIR and HPLC.</li><li>Ability to read and interpret safety rules, operating and maintenance instructions, and SDS sheets.</li><li>Strong oral and written communication skills.</li><li>Proficient in using computer software including Microsoft Word, Excel, and Access.</li><li>Sound judgment and decision-making skills.</li><li>Attention to detail and thoroughness in documentation.</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>High School Education required; additional 2 years of college preferred.</li><li>Two years of relevant industry experience within a cGMP environment.</li><li>Ability to solve moderately complex problems with multiple variables.</li><li>Competence in basic arithmetic operations using whole numbers, fractions, and decimals.</li><li>Capability to apply common sense understanding to instructions in written, oral, or diagram form.</li></ul><h2>Work Environment</h2><p>The role operates within a GMP Lab with minimal gowning requirements and follows a first shift schedule from 7:30 am to 3:30 pm, Monday through Friday. The environment fosters a great team culture with no mandatory weekend work, though additional hours can be taken if desired. The position includes benefits such as PTO and holidays.</p><br>

<h1><strong>Quality Control Lab Technician</strong></h1><p>We are seeking a diligent and detail-oriented Quality Control Lab Technician to join our team. This role involves conducting hands-on quality testing in a chemistry lab, focusing on finished material testing and ensuring the highest standards of quality control. You will play a crucial part in testing and verifying finished goods, identifying process failures, and participating in continual improvement activities.</p><p><br></p><p><em>INTERESTED CANDIDATES CAN SEND UPDATED RESUMES TO MAMCDONOUGH @ACTALENTSERVICES .COM OR TEXT MARISA AT 330 .397. 1302 TO SET UP A PHONE INTERVIEW!</em></p><p><br></p><h2>Responsibilities</h2><ul><li>Test and verify all finished materials according to Test Procedure/SOP.</li><li>Determine if materials can be adjusted based on control plans and FMEAs.</li><li>Write clear and concise directions for batch adjustments.</li><li>Assist in flagging, tagging, and documenting materials as scrap per Non-Conformance procedures.</li><li>Maintain manual product quality files for raw materials and finished goods.</li><li>Perform statistical analysis on finished goods to ensure process control.</li><li>Observe production processes and verify adherence to written instructions.</li><li>Participate in SPC and testing method evaluations.</li><li>Assist Quality Manager/<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> QC Technician with minor material quality issues.</li><li>Recommend process improvements to eliminate rework and enhance product quality.</li><li>Perform housekeeping duties including cleaning freezers and ovens, maintaining test equipment, and verifying equipment calibration.</li><li>Dispose of retains monthly and maintain organized workspaces.</li><li>Conduct line audits, dock audits, and work order staging as required.</li><li>Test all incoming raw materials per customer/NCU requirements and prepare reports.</li><li>Handle chemicals safely and wear required PPE.</li><li>Label QC-approved incoming materials and participate in inventory control.</li><li>File work orders, packaging tickets, and certificates of analysis into ERP.</li><li>Engage in improvement processes and training activities.</li></ul><h2>Essential Skills</h2><ul><li>Great communication skills.</li><li>Bachelor&#39;s degree in Science (Chemistry).</li><li>Attention to detail and focus.</li><li>0-2 years of industry experience performing chemistry lab testing.</li><li>Knowledge of quality control, assurance, chemical manufacturing, GMP, SOP, and laboratory practices.</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>Fundamental understanding of QC requirements is preferred.</li><li>Experience with viscosity, FTIR, UV-vis, DSC, and ISO 9001 is advantageous.</li></ul><h2><br></h2>

<h1><strong>Job Title: Quality Control Analyst </strong></h1><h1><strong>Shift: M-F 3:00pm-11:30pm </strong></h1><h1><strong>Pay: $22/hr</strong></h1><p><br></p><h2>Job Description</h2><p>As a Quality Control Analyst, you will be responsible for testing raw materials and finished products in our Quality Control laboratory. This role requires precision and attention to detail to ensure compliance with established specifications and standards.</p><p><br></p><h2>Responsibilities</h2><ul><li>Conduct routine and non-routine chemistry and microbiological analysis of raw materials, in-process formulations, and final products.</li><li>Utilize and operate laboratory equipment and instruments according to laboratory procedures, including pH, conductivity, UV, KF, FTIR, and titrations.</li><li>Understand and follow Quality Control test methods or compendia methods (USP, EP, BP, JP, or ACS) and EXCIPACT standards.</li><li>Calculate and generate data for compliance to specifications and report results.</li><li>Perform technical review of lab data forms, such as water, environmental monitoring, and direct measure analysis.</li><li>Calibrate and maintain lab equipment.</li><li>Enter final results and raw data for tested materials or products in the Laboratory Information Management System (LIMS) as needed.</li><li>Perform investigative analysis to support investigations, complaints, or instrument troubleshooting.</li><li>Conduct Environmental Monitoring duties, which require gowning into cleanroom and collecting air and surface samples.</li><li>Review for discrepancies in data, manufacture COA, COC, and perform data verification in accordance with company procedures.</li><li>Apply appropriate disposition labels to materials (accepted, rejected, etc.).</li><li>Handle hazardous materials using all appropriate or mandatory safety PPE and safety equipment.</li><li>Complete documentation in a legible manner and review for accuracy.</li><li>Perform sampling and testing for USP Purified water and Water for Injection.</li><li>Author, review, or update lab procedures and Lab instruments Work Instructions.</li><li>Perform microbiological tests such as bioburden, endotoxin, Dnase, Rnase, Protease, and Phosphatase using proper aseptic techniques.</li><li>Prepare and properly dispose of microbial media.</li></ul><h2>Essential Skills</h2><ul><li>Quality control</li><li>GMP</li><li>Laboratory</li><li>Chemistry</li><li>Microbiology</li><li>Quality assurance</li><li>Biology</li><li>Environmental monitoring</li><li>Biochemistry</li><li>Wet chemistry</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>Bachelor&#39;s degree in a science discipline with knowledge and experience in Chemistry, Biology, or Biochemistry.</li><li>3 years of laboratory experience in a related field.</li><li>Wet chemistry and microbial testing experience preferred (e.g., Acid/Base Titrations, water content, Bioburden, Endotoxin).</li></ul><h2>Work Environment</h2><p>Typically works in a lab and office environment with adequate lighting and ventilation and a normal range of temperature and noise level. At times, may be exposed to various chemicals, including flammables, corrosives, and oxidizers. Work assignments are diversified, with examples of past precedent used to resolve work problems, and new alternatives may be developed to resolve issues. A frequent volume of work and deadlines impose strain on a routine basis. Minimal physical effort is required, as work is mostly sedentary but does require walking, standing, bending, reaching, lifting, or carrying objects that typically weigh less than 10 lbs.</p>

Quality Control Laboratory Technician

<h1 style="font-weight: 700;">Job Title: Quality Control Laboratory Technician</h1><br><h2>Job Description</h2><p>The Quality Control Laboratory Technician will work in a satellite lab located above the manufacturing floor to conduct quality checks and testing on raw materials, in-process, and finished goods. This role involves a blend of laboratory and quality assurance duties, with the technician spending 60% of their time on the plant floor and 40% in the laboratory. Candidates should be comfortable working in a manufacturing setting and being on their feet.</p><br><h2>Responsibilities</h2><ul><li>Perform multiple daily sample collections from the plant floor for laboratory testing.</li><li>Retrieve quality assurance and regulatory documentation from the plant floor.</li><li>Ensure plant personnel adhere to procedures such as GMP and PPE usage.</li><li>Communicate effectively with production personnel to address issues or potential issues.</li><li>Conduct formulation checks including salt, acid, and pH levels.</li><li>Perform titrations and mass-volume calculations.</li><li>Conduct sensory testing twice per shift.</li><li>Calibrate laboratory instruments.</li><li>Perform basic microbiological testing and solution preparation.</li><li>Utilize the SAP system and Microsoft applications for data entry.</li></ul><h2>Essential Skills</h2><ul><li>Bachelor&#39;s degree in sciences such as biology or food science.</li><li>Experience in food manufacturing, preferably in quality roles.</li><li>Basic proficiency in Microsoft Excel for data entry.</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>Experience with microbiological plating and analytical chemistry testing is preferred.</li><li>Strong communication skills for frequent interaction with production personnel.</li><li>Ability to think quickly and make fast decisions in a fast-paced environment.</li><li>Proactive in completing tasks and taking on additional projects.</li><li>Flexibility to work various shifts, including potential overtime as needed.</li></ul><h2>Work Environment</h2><p>The position requires flexibility to work 2nd shift (2 PM - 10:30 PM, M-F) and 3rd shift (10 PM - 6:30 AM, M-F), with training starting on the 2nd shift. The work environment is a mix of laboratory and plant operations, involving quality assurance in a fast-paced manufacturing setting with GMP/GLP standards. The manufacturing area has a strong odor due to the production of mayonnaise, while the laboratory is odor-free. The dress code includes long pants, steel-toed safety shoes, hair/beard nets, smocks, and no jewelry or painted nails. The organization provides a supportive culture with monthly engagement activities, offering growth opportunities within various areas such as lab operations, plant operations, and quality assurance/control.</p><br>

<h1 style="font-weight: 700;">Job Title: Quality Control Laboratory Technician</h1><br><h2>Job Description</h2><p>Perform essential quality control testing of in-process products using prescribed procedures and techniques. Make necessary formula adjustments based on test results to ensure products meet specifications. Document adjustments on the batch ticket and QC card, and approve finished goods that meet specifications.</p><br><h2>Responsibilities</h2><ul><li>Conduct quality control testing of in-process products using prescribed procedures.</li><li>Make necessary formula adjustments based on quality control results to bring products into specification.</li><li>Document any adjustments made on the batch ticket and QC card.</li><li>Approve finished goods that meet specifications and sign off on the batch ticket and QC card.</li><li>Test and sample every in-process product.</li></ul><h2>Essential Skills</h2><ul><li>Proficiency in Chemistry, FTIR, and Microscopy.</li><li>Experience with Microsoft Word and Excel.</li><li>Associates or Bachelors degree in Chemistry.</li><li>Exposure to FTIR and Microscopy in an academic setting.</li><li>Proficient in laboratory techniques and color matching.</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>Good communication skills.</li><li>Team player.</li><li>Motivated and shows initiative.</li></ul><h2>Work Environment</h2><p>Join a leading color manufacturer in the plastics industry, known for its collaboration with large companies. The position requires computer proficiency, particularly in Word and Excel. The work environment values teamwork and motivation.</p><br>

<h1><strong>Quality Control Laboratory Technician</strong></h1><p><br></p><h2>Job Description</h2><p>This role involves performing analytical testing and reporting to support production, raw material, and product release. The individual will be responsible for laboratory equipment and instrument maintenance, as well as day-to-day operations.</p><p><br></p><h2>Responsibilities</h2><ul><li>Perform tests and generate reports to support production, raw material, product release, product development, and stability, ensuring compliance with procedural and cGMP requirements.</li><li>Operate lab instruments, conduct system suitability checks, perform calibrations, and carry out maintenance tasks.</li><li>Manage lab supplies, reagents, and standards, and maintain a clean and organized work area.</li><li>Create and issue batch records, write Out-of-Specification (OOS) investigations, and generate Certificates of Analysis (CoA).</li><li>Assist in Corrective and Preventive Actions (CAPAs) and Deviations, review and control QC data, and execute stability studies.</li><li>Perform additional support tasks as assigned and work independently with minimal supervision from <span style="color: rgb(8, 7, 7); background-color: none;"><span style="color: rgb(8, 7, 7); background-color: none;">senior</span></span> Quality personnel.</li></ul><h2>Essential Skills</h2><ul><li>Proficiency in quality control and chemistry.</li><li>Experience with gas chromatography, pH testing, viscosity testing, NIR, and FTIR.</li><li>Ability to track plant-wide calibrations and participate in quality investigations.</li><li>Technical writing skills and ability to update procedures.</li><li>Knowledge of analytical chemistry, titration, diagnosis, and wet chemistry.</li><li>Attention to detail and documentation practices.</li><li>Ability to read and follow written procedures.</li><li>Strong communication skills, both oral and written.</li><li>Proficiency in Microsoft Outlook or similar, and comfortable working in Microsoft Word and Microsoft Excel.</li></ul><h2>Skills &amp; Qualifications</h2><ul><li>Associate’s degree in scientific discipline or equivalent work experience in a scientific or pharmaceutical field.</li><li>Bachelor’s degree preferred.</li><li>Experience in a QC laboratory setting preferred.</li><li>Previous Quality experience in a regulated environment preferred.</li><li>Computer skills and use of databases for specifications.</li></ul><h2>Work Environment</h2><p>The position is based in the Omaha facility, where flea &amp; tick medication, shampoos, and toothpaste are made. The role involves working alone most of the time in the lab, with a 4-10 shift from 9am-7pm, Monday - Thursday.</p>

<h1><strong>Job Title: Quality Control Laboratory Technician </strong></h1><h1><strong>Pay: $40k-45k</strong></h1><p><strong>Shift: </strong>2nd shift (4-10s) </p><p>Sunday-Wednesday (3:00pm-1:30am) </p><p>Wednesday-Saturday (3:00pm-1:30am) </p><p><br></p><h2>Job Description</h2><p>The Quality Control Laboratory Technician will perform critical quality checks on the production floor and in the laboratory to ensure product standards are met. This role involves conducting thorough testing and analysis of raw, in-process, and finished samples, while maintaining accurate records and proper labeling. The technician will play a key role in supporting production quality and compliance.</p><p><br></p><h2>Responsibilities</h2><ul><li>Conduct product pulls of raw, in-process, and finished samples for testing as needed.</li><li>Keep records and administer proper labels of products and conduct various shelf life evaluations.</li><li>Verify product labeling and code dates.</li><li>Perform all chemical and microbiological testing on all raw, process control, and finished product samples.</li><li>Perform sensory analysis on finished product, including tasting and smelling.</li><li>Conduct plant audits and checklists.</li><li>Perform benchtop testing in the lab.</li><li>Operate lab equipment such as titrators and perform calibrations as required by SOP, troubleshooting as necessary.</li><li>Maintain organization and cleanliness within the laboratory.</li><li>Communicate crucial process control testing and product evaluation results to management as specified by SOPs.</li><li>Maintain company LIMS by performing daily data entry of sample identification and results.</li><li>Verify supply inventories, restock, and prepare supplies as needed.</li><li>Perform any other duties as assigned by the supervisor and work within a team.</li></ul><h2>Essential Skills</h2><ul><li>Quality control and assurance</li><li>Chemistry and microbiology expertise</li><li>Experience with GMP and wet chemistry</li><li>Visual inspection and titration skills</li><li>Ability to prioritize duties and efficiently manage time</li><li>Ability to read SOPs</li><li>Strong teamwork capabilities</li><li>Adaptability to changing tasks and schedules</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>Bachelor&#39;s degree in a Science (Food Science, Food Technology, Chemistry, etc.)</li></ul><h2>Work Environment</h2><p>The technician will work in a laboratory and on the production floor, which will be kept cool due to dairy product requirements. Responsibilities include performing quality checks, such as swabbing and temperature checks, on the plant floor as well as conducting tests in the lab. The company offers room for growth and excellent benefits, with expanding opportunities in R&amp;D, Quality, Leadership, and Microbiology.</p>

<h1><strong><em>Job Title: Quality Control Line Tech</em></strong></h1><p><strong><em>***Working 10hr shifts 4 days a week!!!</em></strong></p><h2><strong>MUST HAVE</strong></h2><ul><li><strong><em>1 year of Inspection, Quality assurance/Inspection experience </em></strong></li><li><strong><em>Documentation</em></strong></li><li><strong><em>GMP experience </em></strong></li><li><strong><em>Quality check</em></strong></li><li><strong><em>HS Diploma</em></strong></li></ul><h2>Job Description</h2><p>Assist the Quality Systems Supervisor in directing all activities of Quality personnel. Train QC Techs, assist in the disposition of all raw materials, components, and finished products as directed by the Supervisor. Assist in developing and maintaining Master Product Records for all products manufactured at the facility. Perform quality checks using weight, measurement, and visual inspections. Document results and tests accurately and timely. Communicate quality variances to management and monitor processes to ensure compliance with the quality system. Operate testing equipment such as pH meter, balance, vacuum test equipment, etc. Ensure identification and traceability of material on the production line. Create visual tools and aides to assist the production line.</p><p><br></p><h2>Responsibilities</h2><ul><li>Assist the Quality Systems Supervisor in directing all activities of Quality personnel.</li><li>Train QC Techs.</li><li>Assist in the disposition of all raw materials, components, and finished products as directed by the Supervisor.</li><li>Assist in developing and maintaining Master Product Records for all products manufactured at the facility.</li><li>Perform quality checks using weight, measurement, and visual inspections.</li><li>Document results and tests accurately and timely.</li><li>Communicate quality variances to management.</li><li>Monitor processes to ensure compliance with the quality system.</li><li>Operate testing equipment such as pH meter, balance, vacuum test equipment, etc.</li><li>Ensure identification and traceability of material on the production line.</li><li>Create visual tools and aides to assist the production line.</li></ul><h2>Work Environment</h2><p>The work environment includes working with various testing equipment such as pH meter, balance, vacuum test equipment, etc. Company promotes 20% of its workforce every year and has never had a formal lay-off.</p>

Quality Control Line Tech

<h1><strong>Job Title: Travelling Construction Quality Control Manager</strong></h1><p><br></p><h2>Job Description</h2><p>We are seeking a Quality Control Manager to oversee and manage a full substation installation project, including all electrical work, at the Allegany Ballistic Laboratory. The ideal candidate will have over 5 years of experience in federal construction quality control management and hold relevant certifications. THIS IS A TRAVELING ROLE AND PER DIEM IS AVAILABLE.</p><p><br></p><h2>Responsibilities</h2><ul><li>Provide full oversight of the subcontractor for the construction project.</li><li>Ensure all electrical work is completed to the highest standards.</li><li>Manage and implement quality control processes and procedures.</li><li>Work closely with the safety officer, lead superintendent, and subcontractor to ensure project success.</li><li>Conduct regular site inspections and audits to ensure compliance with federal construction standards.</li></ul><h2>Essential Skills</h2><ul><li>5+ years of federal construction quality control management experience.</li><li>USACE Quality Control Manager (QCM) certification.</li><li>OSHA 30 certification.</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>EM385-1-1 certification (preferred).</li><li>Must be Clearable</li></ul><h2>Work Environment</h2><p>Work will be performed on-site at Allegany Ballistic Laboratory in &#39;Rocket City&#39;, WV. The role involves collaboration with a safety officer, a lead superintendent, and Freestate Electrical as the sole subcontractor. The company offers a great culture with profit sharing, balancing the workload of large general contractors with the work-life balance of a small family-run firm.</p>

Quality Control Manager

<h1><strong>Job Title: Quality Control Manager</strong></h1><p><br></p><h2>Job Description</h2><p>We are seeking a Quality Control Manager to oversee a $2M interior renovation project at the Naval Academy in Annapolis, MD. This project involves mechanical, electrical, and general construction aspects. The ideal candidate will manage and oversee the day-to-day operations, review the scope of work, uphold quality standards, and communicate project progress in meetings. You will be responsible for supervising multiple subcontractors on site.</p><p><br></p><h2>Responsibilities</h2><ul><li>Oversee the day-to-day operational aspects of the renovation project.</li><li>Review and uphold quality standards and the scope of work.</li><li>Communicate project progress in meetings.</li><li>Supervise multiple subcontractors on site.</li></ul><h2>Essential Skills</h2><ul><li>Experience in quality control management.</li><li>QCM certification.</li><li>OSHA 30 certification.</li><li>Experience in construction management.</li><li>High communication skills.</li><li>Ability to oversee and manage multiple subcontractors.</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>Experience in large commercial construction.</li><li>3-4 years of experience in federal construction projects preferred.</li><li>Clean record is a must.</li><li>US citizenship required.</li></ul><h2>Work Environment</h2><p>The work will be performed on-site at the Naval Academy in Annapolis, MD. You will work alongside a project manager, superintendent, and site safety officer. The company is well-established, focusing strictly on federal contracts, with projects across local bases in the DMV area</p>

<h1><strong>Job Title: Quality Control Manager</strong></h1><p><br></p><h2>Job Description</h2><p>A Quality Control Manager is needed to oversee the renovation of a rifle firing range at the Naval Academy in Annapolis. This is a $10 million design-bid-build project, and the successful candidate will begin a week prior to the mobilization date to become acquainted with the project, team, and Navy officials.</p><p><br></p><h2>Responsibilities</h2><ul><li>Manage and oversee the day-to-day operational aspects of the project.</li><li>Review the scope of work and ensure quality standards are upheld.</li><li>Discuss project progress in meetings.</li><li>Prepare and submit daily progress reports to NAVFAC.</li></ul><h2>Essential Skills</h2><ul><li>Quality assurance expertise.</li><li>Safety management skills.</li><li>Experience with RFIs and federal construction inspection.</li><li>CQM certification and OSHA30 certification are required.</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>5-8 years of previous federal construction experience.</li><li>NAVFAC experience is highly desired.</li><li>EM385-1-1 certification is an added bonus.</li><li>Must be a US Passport holder.</li></ul><h2>Work Environment</h2><p>Work will be performed fully on-site at the Naval Academy in Annapolis, MD. The position offers growth potential and full-time opportunities post-contract. The company values work/life balance and is actively bidding and winning projects, especially in collaboration with Belt Built Contracting.</p>

<p>My client is a established and growing commercial contractor that is looking to add a <strong>Construction Quality Control Manager </strong>to their team. They are working on some of the Tri-States largest infrastructure projects and have close to $70 million+ in backlogged worked. This opportunity offers stability, benefits, and competitive pay!</p><p><br></p><p><strong>Job Description</strong></p><ul><li>Develop and execute QC Plan following three phases of control.</li><li>Ensure all personnel on project, including subcontractors are complying with QC requirements</li><li>Maintain compliance with contract documents and specifications</li><li>Work close with the Project Manager to have a complete knowledge and understanding of the contract, each subcontract, to develop onsite procedures.</li><li>Conduct preparatory, initial and follow-up meetings/inspections to establish an understanding of the standards of care desired for each feature of work.</li><li>Complete inspection reports</li><li>inspect and evaluate adequacy of work performed and identify non-conformities</li><li>Maintain daily paperwork such as reports and log updates</li><li>Conduct pre-final/final inspections; establish punch list; and ensure all deficiencies are corrected.</li></ul><p><strong>Additional Skills &amp; Qualifications</strong></p><ul><li>Bachelor&#39;s degree in construction management, engineering, or project management is desirable. (10+ yrs of construction management experience will be accepted in place of education.</li><li>Minimum of 3-5 years experience as a CQC Manager overseeing construction projects.</li><li>Proficient skill level in MS Word, Excel, Outlook, and MS Projects.</li><li>Primavera P6 software knowledge is highly desirable.</li><li>Procore software knowledge is highly desirable.</li><li>Valid state driver&#39;s license with an acceptable driving record.</li></ul>

<h1><strong>Job Title: Quality Control Manager</strong></h1><p><br></p><h2>Job Description</h2><p>We are seeking a dedicated Quality Control Manager to oversee a 12-month project involving the renovation of a hanger at Norfolk Naval. This role offers a manageable workload and the opportunity for involvement in various projects across the portfolio. The position requires an active Quality Control Management (QCM) certification and a minimum of two years of experience as a Quality Control Manager.</p><p><br></p><h2>Responsibilities</h2><ul><li>Develop and implement project-specific quality control procedures.</li><li>Inspect and evaluate work areas according to plans, specifications, and contract documents, reporting deficiencies and elevating issues as necessary to ensure safety and quality.</li><li>Develop, gather, maintain, and submit work plans, submittals, reports, etc.</li><li>Ensure subcontractors are informed of all project quality control expectations.</li><li>Plan and conduct a three-phase inspection program, including preparatory meetings and reports, initial phase inspections, follow-up inspections, and final phase inspections.</li><li>Lead and document quality control meetings with the project team and customers, providing written minutes.</li><li>Provide daily quality control reports to achieve quality outcomes in a timely manner, reinforcing activities constructed in conformance with project standards, and addressing non-conformance constructively.</li><li>Verify and document that all materials/equipment received conform to approved submittals, are handled and stored correctly, and are suitable for use in the project; check for damaged and defective materials and coordinate and document all required code and independent inspections.</li><li>Clearly document, correct, and re-inspect all non-conformances before covering up work.</li><li>Review as-built drawings to ensure they are current and reflect deviations from contract drawings.</li><li>Review the Job Site Safety Plan, verify hazard analysis approval prior to specific work features during the preparatory phase of control, ensure safety measures during the initial phase, and conduct safety inspections during follow-up.</li><li>Stop work, reject materials/equipment, and direct the removal and replacement of work not compliant with contract documents, codes, building standards, or construction engineering principles.</li><li>Communicate and interact professionally as a team member with trades, manufacturers, suppliers, construction staff, and customer representatives.</li></ul><h2>Essential Skills</h2><ul><li>Active QCM certification and two years of tenure as a Quality Control Manager.</li><li>Experience working on Federal Construction projects.</li><li>Ability to obtain security clearance for federal projects.</li><li>Minimum of five years of experience in programs of similar size and scope.</li><li>Current OSHA 30, First Aid/CPR, and USACE Construction Quality Control Management certifications or ability to obtain within 30 days of hire.</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>Bachelor&#39;s degree in construction management, construction science, engineering, or a related field preferred.</li><li>Safety experience is a strong plus.</li><li>CHST, OSHA 30, CPR, and EM385 certifications are required.</li><li>Strong verbal communication skills and ability to resolve conflict.</li><li>Excellent listening skills and detailed documentation ability.</li><li>Proficient computer skills in Microsoft Office Suite, BlueBeam, and various software.</li><li>Valid driver&#39;s license.</li><li>CQC experience preferred.</li></ul><h2>Work Environment</h2><p>The role involves on-site QC management of a hanger renovation project at Oceana. Construction work attire is required, and typical work hours are 7:30 AM to 4:00 PM. The company offers great pay, benefits, including two weeks of PTO and 10 holidays. The organization provides a supportive work culture, with diversified construction projects across military installations and large private construction initiatives.</p>

<h1 style="font-weight: 700;">Job Title: Quality Control Specialist - Raw Materials</h1><br><h2>Job Description</h2><p>We are seeking a dedicated Quality Control Specialist to develop and manage a QC raw materials testing program that supports commercial manufacturing. The successful candidate will oversee inspection, sampling, and testing of incoming raw materials while ensuring compliance with US and EU GMP requirements.</p><br><h2>Responsibilities</h2><ul><li>Oversee the inspection, sampling, and testing of incoming raw materials prior to use in manufacturing, ensuring compliance with US and EU GMP requirements.</li><li>Ensure materials are sampled according to SOPs, entered into data management systems, and available for use on time.</li><li>Participate in the qualification of raw materials via external and in-house testing.</li><li>Serve as subject matter expert in reviewing raw material specifications.</li><li>Participate in vendor audits as a technical advisor.</li><li>Oversee daily routine activities of the raw materials group, provide data review, and ensure compliance at all times.</li><li>Collaborate with Quality Assurance, Manufacturing, Materials Management, external vendors, and other functions to meet internal timelines, testing TAT, and team milestones.</li><li>Author and maintain required cGMP documentation such as SOPs and guidance documents.</li><li>Oversee verification of assays at external testing labs.</li><li>Identify gaps, design collaborative solutions, and implement improvements.</li><li>Participate in QC laboratory investigations, deviations, and onboarding and qualification of analytical equipment at external testing labs.</li></ul><h2>Essential Skills</h2><ul><li>Extensive experience with raw material sampling, including handling of powders and liquids, using aseptic techniques.</li><li>Knowledge of cGMP raw materials tests including pH, conductivity, osmolality, moisture, appearance, FTIR, HPLC, etc.</li><li>Minimum of 3+ years of hands-on, industry experience managing a cGMP QC laboratory.</li><li>Knowledge of verification and validation of assays required for raw material testing.</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>BS in Chemistry, or related field with a minimum of 5+ years of relevant experience within the pharmaceutical industry.</li><li>Extensive knowledge of regulatory requirements and guidelines (ICH, CFR, FDA).</li><li>Extensive knowledge of GDPs, GMPs multi-compendial assays (USP, EP, JP).</li><li>Excellent communication and collaboration skills.</li><li>Attention to detail, highly organized, able to meet schedules and timelines and handle multiple priorities.</li></ul><h2>Work Environment</h2><p>The work environment involves collaboration with various departments including Quality Assurance, Manufacturing, Materials Management, and external vendors. The role requires a highly organized individual capable of handling multiple priorities and meeting strict schedules and timelines.</p><br>

Quality Control Manager - Raw Materials

<p>Seeking a <strong>Quality Control Manager/Certified</strong> Welding Inspector that oversees all welding-related quality control operations, ensuring compliance with industry standards and internal specifications. This role is responsible for maintaining welding documentation, procedures, and quality systems in accordance with ASME standards, while managing inspections throughout the production process.</p><p><br></p><p>Key Responsibilities:</p><ul><li>Develop, implement, and maintain quality control systems to ensure product reliability and compliance with established standards.</li><li>Inspection &amp; Testing:</li><li>Conduct inspections and tests on materials, equipment, and welds. Perform visual weld inspections and verify adherence to welding procedures.</li><li>Documentation &amp; Reporting:</li><li>Maintain accurate quality records and documentation. Generate detailed inspection reports and recommend corrective actions as needed.</li><li>Team Leadership:</li><li>Lead and support the quality control team. Oversee recruitment, training, and performance to ensure a high-functioning department.</li><li>Customer Engagement:</li><li>Collaborate with customers to define quality criteria, resolve concerns, and maintain clear, timely communication.</li><li>Regulatory Compliance:</li><li>Ensure all activities comply with safety regulations and applicable codes, standards, and procedures.</li><li>Training &amp; Development:</li><li>Identify training needs and provide guidance to welders and junior inspectors to uphold quality standards.</li><li>Issue Resolution:</li><li>Troubleshoot production issues in collaboration with engineering and project teams to minimize delays and costs.</li></ul><p>Qualifications:</p><ul><li>Minimum 5 years in quality control, with strong knowledge of AWS and ASME quality systems.</li><li>Certifications:<ul><li>Certified Welding Inspector (CWI), valid driver’s license, and a clean driving record.</li></ul></li></ul><h2><br></h2>

Quality Control Manager/Certified Welding Inspector

<h2>Job Description</h2><p>This is an excellent opportunity for entry-level engineers to gain experience working on healthcare, education, data centers, and large commercial projects.</p><p><br></p><h2>Responsibilities</h2><ul><li>Review shop drawings in the fabrication shop to ensure mechanical systems, including plumbing and HVAC, are fabricated, built, and assembled correctly.</li><li>Inspect mechanical and plumbing systems in the fabrication shops before they are shipped to client job sites.</li><li>Conduct audits to ensure compliance with design specifications.</li><li>Collaborate with the fabrication team to provide guidance on correctly building HVAC or mechanical systems.</li></ul><h2>Required Skills &amp; Qualifications</h2><ul><li>Associate or Bachelor, Mechanical Engineering degree.</li><li>Understanding of fabrication drawings preferred</li><li>Interest in working for a mechanical contractor and in a fabrication shop.</li></ul>

Quality Control Mechanical Engineer

<h1><strong>Job Title: Quality Control Specialist</strong></h1><p><br></p><h2>Job Description</h2><p>The Quality Control Specialist is responsible for reviewing documentation, including records, procedures, and forms, to ensure quality endpoints and compliance requirements are achieved. This role involves actively leading or contributing to data relevant to Quality Systems Compliance during periodic Management Review meetings, as well as assisting Quality Management in coordinating and actively participating in Quality or Compliance related projects.</p><p><br></p><h2>Responsibilities</h2><ul><li>Conduct product tests and assessments in an industrial or warehouse setting to ensure that specifications are met and that the product, material, or supply will function as intended.</li><li>Perform in-process and final product/result inspections and clearances on the production floor to ensure consistency.</li><li>Identify product defects or potential issues and determine resolutions.</li><li>Analyze lab or usability test results to identify defects and ensure they do not persist.</li><li>Maintain detailed records of product defects or manufacturing issues to help identify and eliminate recurring problems and provide accountability and error reporting.</li><li>Report issues or defect findings to supervisors or plant managers to aid in manufacturing decisions.</li><li>Support process improvements throughout testing and quality assurance processes.</li><li>Suggest improvements to address systemic problems found during quality control, ensuring consistent product production and error elimination.</li></ul><h2>Essential Skills</h2><ul><li>Quality control expertise</li><li>Laboratory experience</li><li>Data entry proficiency</li><li>Knowledge of Standard Operating Procedures (SOP)</li><li>Bachelor&#39;s or Associate&#39;s degree within a Scientific discipline</li><li>Minimum of 1 year experience in quality control, quality assurance, or laboratory settings</li><li>Document control skills</li><li>Quality assurance knowledge</li><li>Accessioning experience</li><li>Quality inspection capabilities</li><li>Batch record review</li><li>Understanding of FDA regulations</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>Requires an Associate&#39;s Degree</li><li>Preferred one or more years of Quality Assurance or Quality Control experience in a regulated environment or other job-related experience</li></ul><h2>Work Environment</h2><p>The work environment is a clean and regulated laboratory setting with a friendly company culture. The shift is Sunday through Thursday, from 11 pm to 7:30 am, with a training schedule from Sunday to Wednesday, 8 am to 6:30 pm. Training will last approximately 3-4 weeks, during which employees will review testing benches and shadow Technologists. </p>

Quality Control Specialist

<h1><strong>Quality Control Specialist</strong></h1><h2>Job Description</h2><p>The Quality Control Specialist is responsible for reviewing documentation, including records, procedures, and forms, to ensure quality endpoints and compliance requirements are achieved. This role involves actively leading or contributing to data relevant to Quality Systems Compliance during periodic Management Review meetings, as well as assisting Quality Management in coordinating and actively participating in Quality or Compliance related projects.</p><p><br></p><h2>Responsibilities</h2><ul><li>Conduct product tests and assessments in an industrial or warehouse setting to ensure that specifications are met and that the product, material, or supply will function as intended.</li><li>Perform in-process and final product/result inspections and clearances on the production floor to ensure consistency.</li><li>Identify product defects or potential issues and determine resolutions.</li><li>Analyze lab or usability test results to identify defects and ensure they do not persist.</li><li>Maintain detailed records of product defects or manufacturing issues to help identify and eliminate recurring problems and provide accountability and error reporting.</li><li>Report issues or defect findings to supervisors or plant managers to aid in manufacturing decisions.</li><li>Support process improvements throughout testing and quality assurance processes.</li><li>Suggest improvements to address systemic problems found during quality control, ensuring consistent product production and error elimination.</li></ul><h2>Essential Skills</h2><ul><li>Quality Control Expertise</li><li>Laboratory Experience</li><li>Data Entry Proficiency</li><li>Knowledge of Standard Operating Procedures (SOP)</li><li>Bachelor&#39;s or Associate&#39;s Degree</li><li>Minimum of 1 year experience in quality or lab setting</li><li>Document Control Skills</li><li>Quality Assurance Knowledge</li><li>Accessioning Experience</li><li>Quality Inspection Capabilities</li><li>Batch Record Review</li><li>Understanding of FDA Regulations</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>Requires an Associate&#39;s Degree at minimum</li><li>Preferred one or more years of Quality Assurance or Quality Control experience in a regulated environment or other job-related experience</li></ul><h2>Work Environment</h2><p>The work environment is a clean and regulated laboratory setting with a friendly company culture. Training will last approximately 3-4 weeks, during which employees will review testing benches and shadow Technologists. </p>

<h1 style="font-weight: 700;">Job Title: Quality Control Specialist</h1><br><h2>Job Description</h2><p>The Quality Control Specialist is responsible for auditing finished goods and the manufacturing facility, maintaining databases, troubleshooting, and overseeing product disposition. This role includes product hold/release authority, quality inspections, investigations, and reporting issues related to Food Safety and Quality. Employees will receive cross-training in various QC functions to provide backup support as needed. The position involves inspecting finished goods, including Medical Foods, Dietary supplements, and other high-profile contract customer products.</p><br><h2>Responsibilities</h2><ul><li>Enter data into company databases.</li><li>Perform inspections of equipment, products, and production lines.</li><li>Ensure conformance to GMP guidelines and company policies/procedures.</li><li>Inspect and audit facilities, manufacturing equipment, and products as required.</li><li>Identify non-conforming conditions and products related to food safety and quality.</li><li>Place products or materials on hold that do not conform to specifications.</li><li>Initiate investigations into causes of material or product non-conformance.</li><li>Investigate customer complaints with guidance from a Supervisor.</li><li>Perform internal audits based on SQF guidelines.</li><li>Make suggestions to improve safety, food safety, and quality.</li><li>Suggest ways to increase efficiency and cost savings within the department.</li><li>Gather sample products as required.</li><li>Provide training to other employees as directed.</li></ul><h2>Essential Skills</h2><ul><li>1+ years of quality control experience in the food/beverage industry.</li><li>Knowledge of GMPs, HACCP, SQF, FDA regulations for foods and beverages, and internal auditing.</li><li>Proficiency in CAPA investigations and training personnel.</li><li>Ability to complete a skills assessment test including basic math, decimal math, English, color, and comprehension.</li><li>Good computer skills including MS Excel, MS Word, and MS PowerPoint.</li><li>Strong written and oral communication skills in English; Spanish bilingual is a huge plus.</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>Ability to work in a team-based environment.</li><li>Capacity to work independently with proactive behavior.</li><li>Strong analytical skills including observation, attention to detail, and problem-solving.</li><li>Desire to learn, take on challenges and responsibilities, and adapt to change.</li><li>Basic math skills: arithmetic, percentages, ratios, measurements.</li><li>Ability to multitask, organize, and prioritize tasks.</li><li>Good conflict resolution and interpersonal skills.</li><li>Ability to identify and communicate unsafe work conditions to a Supervisor.</li></ul><h2>Work Environment</h2><p>The role is based in a temperature-controlled manufacturing plant, requiring walking throughout the plant all day. Available shifts include 1st, 2nd, and 3rd shifts with mandatory overtime, including Saturdays. The position operates on a rotating Saturday schedule, working every other Saturday, especially during the busy season when production runs on Saturdays.</p><br>

<h1><strong>Job Title: Quality Control Technician</strong></h1><p><br></p><h2>Job Description</h2><p>Responsible for ensuring that production staff are following GMP requirements. Calibrate instruments such as viscosity meters, pH meters, and brix meters. Conduct pH titrations, viscosity, and physical testing on products. Assist with wet chemistry testing and call production holds when products are out of specification. Follow HACCP programs.</p><p><br></p><h2>Responsibilities</h2><ul><li>Ensure production staff adhere to GMP requirements.</li><li>Calibrate instruments including viscosity meters, pH meters, and brix meters.</li><li>Conduct pH titrations, viscosity, and physical testing on products.</li><li>Assist with wet chemistry testing.</li><li>Call production holds when products are out of specification.</li><li>Follow HACCP programs.</li></ul><h2>Essential Skills</h2><ul><li>At least 2 years of experience in a GMP manufacturing setting with compounding, filling, and labeling.</li><li>Experience in the OTC drug, pharmaceutical, and/or dietary supplements industry. Candidates from the food and cosmetic industry will also be considered.</li><li>Strong understanding of documentation.</li><li>Ability to understand and operate fill lines, packaging, and labeling processes.</li><li>Experience with quality control testing, including ATP, environmental testing, pH, and viscosity.</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>High school diploma.</li><li>Bilingual in Spanish is a plus.</li><li>Experience in a fast-paced environment.</li><li>Ability to bring a new perspective and be a go-getter.</li><li>Understanding of the production process from start to finish.</li></ul><h2>Work Environment</h2><p>This site produces essential oils, mouthwashes (with a minty smell), and other OTC products that are dietary supplements. Some cosmetic manufacturing will also be brought in-house. The Quality Control Technician will report directly to the manager and work within a team of 6 people, including 2 QC Technicians in Compounding and 2 QC Technicians performing testing on the production floor. This role is responsible for overseeing 3 production lines. The work environment includes long overlapping shifts covering 4am - 7pm. Initially, the schedule will be 9am - 5:30pm for 2-3 weeks of training, followed by a shift from 4am - 12:30pm.</p>

Quality Control Technician

<h1 style="text-align: center;"><strong><u>﻿Quality Control Technician </u></strong></h1><p><br></p><p><strong><u>Job Description</u></strong></p><p>The Quality Control Chemist performs qualitative and quantitative testing of raw materials, intermediates, finished products, and other samples for the purposes of quality control, product development, and regulatory conformance.</p><p><br></p><p><strong><u>Responsibilities</u></strong></p><ul><li>Analyze raw materials, intermediates, and finished products using Symrise, FCC, USP, and AOAC wet chemical and instrumental testing methods.</li><li>Perform microbiological testing as trained and required.</li><li>Provide first-line operation and day-to-day instrument and data system maintenance and calibration.</li><li>Validate test instruments and methods as required.</li><li>Perform project analysis in support of QA, QC, Divisional and Regulatory requirements.</li><li>Assist other departments and members of the lab with requests for analytical testing and results.</li><li>Conform to documented Roles and Responsibilities for this position.</li><li>Maintain timely and complete test method certification for this position.</li><li>Carry out all related quality testing and quality process responsibilities as assigned by the Supervisor.</li></ul><p><strong><u>Essential Skills</u></strong></p><ul><li>Proficiency in chemistry, quality control, and laboratory techniques.</li><li>Experience with wet chemistry, GMP, SQF, HACCP, microbiology, and quality assurance.</li><li>BS or BA in Chemistry, Food Science, Biology, or a related field with Chemistry coursework.</li></ul><p><strong><u>Additional Skills &amp; Qualifications</u></strong></p><ul><li>Functional understanding of Quality Systems: GLP, SQF, ISO-9001, HACCP.</li><li>Experience with SAP is preferred.</li><li>For candidates without a degree, 3-5 years of experience in food quality is required.</li></ul><p><strong><u>Work Environment</u></strong></p><p>This position operates in a laboratory environment. The role is for a third shift position with flexible start times between 9 PM and 7:30 AM (e.g., 9 PM-5:30 AM or 11 PM-7:30 AM). Training will be provided for 1 week on the first shift (8 AM-4:30 PM) and then for 1 month on the second shift (2 PM-10:30 PM).</p>

<p style="text-align: center;"><strong>Join Our Team as a Quality Control Technician in Great Barrington!</strong></p><p style="text-align: center;"><br></p><p>Are you detail-oriented with a passion for ensuring product excellence? Do you thrive in a fast-paced environment where safety and quality are your top priorities? If so, we want to hear from you! We’re seeking a dedicated <strong>Quality Control Technician</strong> to join our dynamic team in Great Barrington. This is your chance to make a real impact in a company that values quality, safety, and teamwork.</p><hr><p><strong>Why Work With Us?</strong></p><ul><li style="text-align: left;"><strong>Competitive Pay &amp; Benefits</strong></li><li style="text-align: left;"><strong>Training &amp; Development Opportunities</strong></li><li style="text-align: left;"><strong>Supportive Team Environment</strong></li><li style="text-align: left;"><strong>Stable, Full-Time Work with Overtime Potential</strong></li><li style="text-align: left;"><strong>Work in a Beautiful, Friendly Community</strong></li></ul><hr><p><strong>Your Role: Be a Key Player in Quality Assurance</strong></p><p>As a Quality Control Technician, you’ll be the guardian of product quality and safety. Your keen eye and attention to detail will help ensure our products meet the highest standards. You’ll work closely with team members, assist in sampling and testing, and maintain meticulous records—all in a safety-focused environment.</p><hr><p><strong>What You’ll Do:</strong></p><ul><li style="text-align: left;">Collaborate with Sheeter Operators and other team members to uphold quality standards</li><li style="text-align: left;">Verify and maintain precise records for incoming raw materials and finished products</li><li style="text-align: left;">Collect, test, and analyze samples to ensure they meet specifications</li><li style="text-align: left;">Perform visual inspections to detect defects and inconsistencies</li><li style="text-align: left;">Conduct in-process testing including caliper, gloss, and smoothness evaluations</li><li style="text-align: left;">Monitor trends and report any irregularities or concerns to supervisors promptly</li><li style="text-align: left;">Calibrate and maintain testing equipment to ensure accuracy</li><li style="text-align: left;">Follow strict safety protocols, wear protective gear, and keep your workspace organized and hazard-free</li><li style="text-align: left;">Assist with equipment troubleshooting and maintenance when needed</li><li style="text-align: left;">Support the team during start-ups and roll changes to maintain high-quality output</li></ul><hr><p><strong>What We’re Looking For:</strong></p><ul><li style="text-align: left;">A high school diploma or equivalent; related experience or training a plus</li><li style="text-align: left;">Strong attention to detail and commitment to safety</li><li style="text-align: left;">Ability to work independently and as part of a team</li><li style="text-align: left;">Basic math skills and familiarity with computers</li><li style="text-align: left;">Excellent communication skills—both written and verbal</li><li style="text-align: left;">Willingness to work various shifts, including overtime when needed</li><li style="text-align: left;">Knowledge of GMP standards and quality assurance practices is a plus</li></ul><hr><p><strong>Work Environment &amp; Schedule:</strong></p><ul><li style="text-align: left;"><strong>Shift: </strong>Second shift, 4pm – 12am</li><li style="text-align: left;"><strong>Training: </strong>Two weeks on first shift (7 am – 3 pm) to get you up to speed</li><li style="text-align: left;"><strong>Environment: </strong>Be prepared for a lively workspace with moving machinery, loud noise, and exposure to chemicals. We prioritize safety and provide all necessary training, including hazardous waste handling.</li></ul>

<h1 style="font-weight: 700;">Job Title: Quality Control Technician</h1><br><h2>Job Description</h2><p>The Quality Control Technician will conduct analytical testing on incoming raw materials and finished products. Responsibilities include performing basic titrations, utilizing GC and GC headspace techniques, and working with NIR instrumentation. The role also involves creating shipping materials for the warehouse, fulfilling sample requests, method development, equipment calibration, and updating general lab equipment.</p><br><h2>Responsibilities</h2><ul><li>Run analytical testing on raw materials and finished products.</li><li>Perform basic titrations, GC, GC headspace, and NIR instrumentation.</li><li>Create shipping materials for the warehouse.</li><li>Fulfill sample requests throughout the day.</li><li>Participate in method development and equipment calibration.</li><li>Update general laboratory equipment.</li></ul><h2>Essential Skills</h2><ul><li>Bachelor&#39;s degree in Chemistry or related field.</li><li>Extensive coursework in analytical chemistry.</li><li>Proficiency in quality control, chemistry, GC, and NIR.</li><li>3-5 years of quality control or laboratory experience.</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>Experience with auto-titrators, FTIR, refractometer, spectrophotometer, HPLC.</li><li>Skills in validation and method development.</li><li>Organizational and prioritizing abilities.</li><li>Good laboratory practices.</li><li>Proficient computer data entry skills.</li><li>Safe handling of laboratory reagents.</li><li>Strong attention to detail.</li></ul><h2>Work Environment</h2><p>The position operates on a second shift schedule, Monday to Friday from 2:00 pm to 10:30 pm, with an initial training period on the first shift from 6:00 am to 2:30 pm for at least six months. The second shift includes a 5% shift differential. The work is conducted in a well-equipped lab with a variety of instruments including GCs and NIR equipment. The team consists of 40 employees at the Janesville location, part of a national team of 75-80 employees.</p><br>

<h1><strong>Job Title: Quality Control Technician</strong></h1><p><br></p><h2><u>Responsibilities</u></h2><ul><li>Manage samples to support the QC group.</li><li>Ensure all filler operators on the production floor follow Standard Operating Procedures (SOPs) correctly.</li><li>Inspect incoming raw materials for quality and compliance.</li><li>Verify that lot and product numbers match bottle numbers.</li><li>Document production goals for all 9 lines.</li><li>Audit documentation and manufacturing processes.</li><li>Audit incoming raw materials.</li><li>Collect samples from production lines and deliver them to chemists in the lab.</li></ul><h2><u>Additional Skills &amp; Qualifications</u></h2><ul><li>Associate&#39;s degree in Science preferred;</li><li>1+ Years of QC Experience </li></ul>

<h1 style="text-align: center;"><strong>Hiring for a Quality Control Technician in Great Barrington!</strong></h1><p><br></p><h2>Job Description</h2><p>As a Quality Control Technician, you will play a crucial role in ensuring the quality and safety of our products. You will assist the Sheeter Operator and other team members as needed, verify and maintain records for incoming and outgoing products, and conduct tasks in accordance with safety protocols. Your responsibilities will include collecting and testing samples, recording and comparing results, and maintaining organized and accurate records.</p><p><br></p><h2>Responsibilities</h2><ul><li>Assist Sheeter Operator and other team members as necessary.</li><li>Verify and maintain records for incoming and outgoing products.</li><li>Conduct tasks safely, following proper work procedures.</li><li>Maintain a clean, neat, and organized work area free of safety hazards.</li><li>Follow all safety rules and wear required safety equipment.</li><li>Collect representative samples from all lots of incoming materials.</li><li>Test samples using prescribed techniques and checklists.</li><li>Record and compare test results with specifications for each grade.</li><li>Maintain test samples and accurate records, ensuring data and samples can be located as necessary.</li><li>Collect representative samples from start-ups and end-of-rolls from laminators and printers.</li><li>Perform visual analysis of samples to detect defects.</li><li>Conduct and record in-process test results, including caliper, smoothness, and gloss tests.</li><li>Monitor trends and shifts in work-in-process test results, run-to-run, and within-run variability.</li><li>Inform supervisor of questionable materials and test results.</li><li>Notify supervisor immediately of suspected test equipment issues.</li><li>Empty baler as needed.</li><li>Calibrate quality control equipment.</li></ul><h2>Essential Skills</h2><ul><li>Ability to work safely in a fast-paced environment and remain focused during slower periods.</li><li>Capacity to work independently and as part of a team, supporting co-workers.</li><li>Understanding of product quality requirements and the role in ensuring quality.</li><li>Basic mathematical skills, including addition, subtraction, multiplication, and division using units of weight measurement and volume.</li><li>Basic computer skills and familiarity with computer concepts.</li><li>Strong oral and written communication skills.</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>High school diploma or equivalent, or up to one year of related experience or training.</li><li>Ability to understand and follow operating and job procedures.</li><li>Willingness to work various shifts and overtime.</li><li>Troubleshooting skills in a laboratory setting.</li><li>Knowledge of GMP (Good Manufacturing Practice) standards.</li><li>Chemistry and quality assurance skills.</li></ul><h2>Work Environment</h2><p>This position operates on the second shift, from 4 pm to 12 am, with two weeks of training on the first shift from 7 am to 3 pm. The work environment involves proximity to moving mechanical parts and exposure to electrical shock risks, fumes or airborne particles, and toxic or caustic chemicals. The noise level is typically loud. This role may involve handling hazardous waste, requiring annual mandatory training in hazardous waste management procedures relevant to the position.</p>

<h1><strong>Quality Control Technician</strong></h1><p><br></p><h2>Job Description</h2><p>As a Quality Control Technician, you will play a critical role in ensuring the integrity and quality of production records and labels. You will be responsible for creating labels for oil products, monitoring the flow of products, and conducting various tests in the lab to verify product quality. This role requires active participation on the production floor, performing frequent quality checks and ensuring compliance with safety standards.</p><p><br></p><h2>Responsibilities</h2><ul><li>Check and verify production records and spot check labels.</li><li>Create labels for oil products and ensure accuracy.</li><li>Monitor the flow of products and take samples for quality testing.</li><li>Perform PV and OSI testing in the lab, as well as pH and density testing.</li><li>Oversee the production floor and conduct thorough quality checks.</li><li>Engage in frequent physical activities such as moving, standing, and lifting.</li></ul><h2>Skills &amp; Qualifications</h2><ul><li>Experience in food and beverage or quality lab preferred.</li><li>An associate degree in biotech or biology is preferred but not required.</li></ul><h2>Work Environment</h2><p>This position offers a 4-day work week, with a 2nd Shift schedule from 2:30 pm to 1 am, Monday through Thursday. You will spend 60% of your time working in the office with labels, 30% overseeing products on the production floor, and 10% in the lab. The work environment is a food-grade setting, climate-controlled, and requires attention to detail to prevent product recalls. PPE such as safety glasses, lab coats, respirators, and gloves are provided. </p>

<p>If you have 2-3 year&#39;s of Quality Control within an electronics manufacturing setting and open to working an interesting contract please apply</p><p><br></p><p>Other skills:</p><p>CAPA</p><p>Continuous Improvement &amp; Process Improvement</p><p>Troubleshooting technical issues from cradle to grave of product completion</p><p>ISO 9001 experience</p><p>prefer someone with an electronics technology degree</p><p><br></p>

<p><strong>Description</strong></p>
					<p>•       Performance of environmental monitoring. Level 3 gowning qualification is required. There will be events where many hours within the cleanroom at level 3 gowning is required. Work hours may vary dependent on the demands of monitoring.
•       Assist with the maintenance of laboratory/ media supplies and equipment.
•       Supports investigations for environmental excursions; assist and revise standard operational procedures, trend reports, deviations, and corrective actions.
•       Performs other duties as assigned.
•       Performs water sampling and gas testing.
•       Execute aseptic process validations, EM performance qualifications, and gowning qualifications.
•       Inspect aseptic process qualification units.


• Performs Quality Control (QC) biological/cell based testing of Cell Therapy release and stability samples during 3rd shift. Typical test methods performed include flow cytometry based assays, but analyst may also perform proliferation, ELISA, cell counts (manual and automated), and immunofluorescence microscopy/spectroscopy assays.
• Actively participates in support of Cell Therapy technology transfer activities and validation of analytical methods including training on new methodology, setup of new equipment, generation of method standard operating procedures (SOPs), and execution of validation protocols.
• Performs general lab and equipment maintenance duties.
• Performs other duties as assigned</p>
					<p><strong>Skills</strong></p>
					<p>Quality control, Laboratory, Chemistry, Gmp, Biology, microbiology</p>
					<p><strong>Top Skills Details</strong></p>
					<p>Quality control,Laboratory</p>
					<p><strong>Additional Skills &amp; Qualifications</strong></p>
					<p>Bachelor&#39;s Degree in Scientific Discipline required</p>
					<p><strong>Experience Level</strong></p>
					<p>Intermediate Level</p>

<h1><strong>Quality Coordinator </strong></h1><h2>Job Description</h2><p>We are seeking a dedicated Quality Coordinator to support the inventory, setup, and documentation of new equipment acquired. The role involves supporting O2 and CO2 cylinder change outs in both GMP and Non-GMP labs, conducting walkdowns, and performing gauge and equipment checks with required documentation. The Quality Coordinator will also handle manual documentation, technical documentation, and quality checks, as well as oversee on-site contractors and help track timelines.</p><p><br></p><h2>Responsibilities</h2><ul><li>Support inventory, setup, and documentation of new equipment</li><li>Assist with O2 and CO2 cylinder change outs in GMP &amp; Non-GMP labs, ensuring proper documentation in GMP logbooks</li><li>Conduct walkdowns and gauge and equipment checks with necessary documentation</li><li>Perform manual documentation, technical documentation, and quality checks</li><li>Oversee and check on-site contractors and help track timelines</li><li>Support cleaning and upkeep functions in main areas</li></ul><h2>Essential Skills</h2><ul><li>Quality check</li><li>Visual inspection</li><li>Documentation review</li><li>Quality assurance</li><li>Inspection</li><li>Facility management</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>HS Diploma (Associates or Bachelors preferred)</li><li>Prior experience in quality coordination</li><li>Experience with documentation, SOP review, and GMP protocols</li><li>Mechanically inclined</li></ul><p><br></p>

Quality Coordinator

<h1 style="font-weight: 700;">Job Title: Quality Coordinator</h1><br><h2>Job Description</h2><p>We are seeking a dedicated Quality Coordinator with experience in an ISO certified environment. You will play a crucial role in maintaining our ISO certification and ensuring the company remains in compliance with relevant standards.</p><br><h2>Responsibilities</h2><ul><li>Maintain and update ISO certification standards and documentation.</li><li>Ensure compliance with quality assurance and control processes.</li><li>Monitor and improve quality standards across the organization.</li><li>Collaborate with various departments to ensure consistent adherence to ISO standards.</li></ul><h2>Essential Skills</h2><ul><li>Experience with ISO standards and certifications.</li><li>Proficiency in quality assurance and quality control processes.</li><li>Strong administrative skills and computer proficiency.</li><li>Ability to implement and monitor continuous improvement initiatives.</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>Highly organized with a keen attention to detail.</li><li>Computer savvy, with proficiency in relevant software.</li><li>Experience in quality standards administration.</li></ul><h2>Work Environment</h2><p>You will work in a dynamic office and manufacturing setting, where collaboration and attention to detail are key. The position offers a contract-to-hire opportunity, with negotiable paid time off and holiday benefits. The role provides upward mobility for those looking to advance their careers.</p><br>

<h1><strong>Job Title: Quality Engineer</strong></h1><p><strong><em>For immediate consideration, please apply directly to this job posting AND email me at habels @actalentservices.com with the following:</em></strong></p><p><strong>1) Word copy of resume</strong></p><p><strong>2) 2-3 professional references</strong></p><p><strong>3) 4-5 brief bullet points highlighting technical qualifications</strong></p><p><br></p><h2>Job Description</h2><p>Control production processes through the implementation of inspection plans, failure analysis investigations, and continuous improvement activities.</p><p><br></p><h2>Responsibilities</h2><ul><li>Plan and conduct analysis, inspection, design, testing, and integration.</li><li>Perform quality reviews of design documentation for compliance, including vendor quality manuals and company quality records.</li><li>Conduct failure analysis investigations to determine improvement opportunities.</li><li>Direct technical and administrative workers engaged in quality assurance activities.</li><li>Maintain a working knowledge of government and industry quality assurance codes and standards.</li><li>Manage both customer and supplier-facing quality functions for the applicable business unit.</li></ul><h2>Essential Skills</h2><ul><li>Bachelor&#39;s Degree in Engineering.</li><li>3+ years of related experience in Quality Engineering.</li><li>Knowledge of ISO 9000 and AS9100 policies and procedures.</li><li>Familiarity with FAA Part 21 and Part 145 requirements.</li><li>Proficiency in failure analysis and corrective action plans.</li><li>Experience with quality control, manufacturing engineering, validation, and test procedures.</li><li>Understanding of PPAP, first article inspection, PFMEA, GD&amp;T, and audit processes.</li><li>Experience with quality management systems in the aerospace industry.</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>Excellent computer skills in a Microsoft Windows environment.</li><li>Exceptional communication skills with team members and stakeholders.</li></ul><h2>Work Environment</h2><p>Work on-site Monday to Friday, with a commitment to work one Saturday per month. Enjoy a supportive environment that promotes from within, offers great benefits, and feels like a family-run business despite being part of a larger organization. Opportunities for leadership development and the possibility to transfer and work at other locations.</p>

Quality Engineer

<h1><strong>Quality Engineer</strong></h1><p><br></p><h2>Job Description</h2><p>This role requires effective communication skills to engage with people at a cross-functional level. The successful candidate will be responsible for presenting information and responding to inquiries from managers, suppliers, customers, and the public both orally and in writing.</p><p><br></p><h2>Responsibilities</h2><ul><li>Develop and maintain a supplier quality system that ensures a reliable supply base.</li><li>Ensure compliance with procedures outlined in the Supplier Quality Manual, including ISO9001 and IATF16949.</li><li>Lead supplier development activities and implement necessary changes.</li><li>Participate in supplier reviews and provide input to the Purchasing Department regarding supplier quality.</li><li>Perform supplier quality audits according to ISO9001, IATF16949, and VDA6 standards.</li><li>Ensure reliability and accuracy of products from the supply base and timely disposition of nonconforming material.</li><li>Coordinate with suppliers on initiatives related to supplier quality performance, track performance trends, and facilitate corrective actions.</li><li>Utilize lean manufacturing, error proofing, and continuous improvement initiatives to develop robust processes ensuring zero defects.</li><li>Provide support to customers regarding supply-based issues.</li></ul><h2>Essential Skills</h2><ul><li>Thorough knowledge of quality tools and APQP methods such as FMEA, Control Plan, Measurement Equipment including MSA, and PPAP.</li><li>Ability to read technical specifications and drawings.</li><li>Effective problem-solving skills and the ability to implement continuous improvement techniques.</li><li>Ability to facilitate and improve cross-functional communication.</li><li>Proficiency in using business applications software and data analysis tools.</li><li>Six Sigma Green/Black Belt Certification and ISO/IATF auditor certification.</li><li>2-5 years of related audit experience.</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>Experience in Plastic Molding and Assembly processes.</li><li>Must have an Engineering degree.</li><li>Experience in the automotive industry</li></ul>

<h1 style="font-weight: 700;">Job Title: Quality Engineer</h1><br><h2>Job Description</h2><p>The primary objective of this role is to ensure quality in manufacturing and supply chain in support of the development and production of the Aurora Driver, delivering the benefits of self-driving technology safely, quickly, and broadly. A successful candidate is data-driven, excels at complex problem-solving, has a strong quality and product-focused mindset, and can lead cross-functional teams to identify and eliminate quality problems, issues, and risks.</p><br><h2>Responsibilities</h2><ul><li>Create test and inspection plans based on program plans, product requirements, and specifications.</li><li>Coordinate calibration of data acquisition, inspection, and testing equipment, maintaining records and certificates.</li><li>Design or coordinate the design of custom inspection and test fixtures and sensors for quality control.</li><li>Direct and manage all non-conforming product(s) and return material authorization activities.</li><li>Support inspection and testing activities to ensure continuous compliance of products to specifications.</li><li>Collaborate closely with engineering and manufacturing teams to develop manufacturing test requirements, quality standards, and product quality plans.</li><li>Identify critical risks in design and manufacturing and drive actions to mitigate risks with cross-functional teams.</li><li>Develop, validate, and roll out critical quality controls across production lines, in coordination with engineering and manufacturing teams.</li><li>Lead and support the qualification of new production lines and processes by utilizing quality tools and techniques.</li><li>Work with internal and external suppliers to establish requirements and ensure product quality.</li><li>Investigate and resolve product complaints and quality problems in the field and in the process.</li><li>Use lean tools, statistical techniques, and analytical methods for effective problem-solving.</li><li>Track quality performance metrics, prioritize top issues, and drive continuous improvement activities.</li><li>Provide technical support and mentorship to junior-level engineers and technicians.</li><li>Lead and participate in initiatives to support business and quality objectives.</li></ul><h2>Essential Skills</h2><ul><li>Quality Control, QMS, IPC expertise.</li><li>Bachelor of Science in Electrical, Mechanical, Industrial Engineering, or related fields; or equivalent combination of education and experience.</li><li>5+ years in automotive manufacturing, electro-mechanical assembly operations, robotics, or equivalent field experience.</li><li>Excellent data analysis skills, using simulation/modeling tools.</li><li>Ability to interpret regulations and test procedures.</li><li>Ability to operate and use diagnostic scan tools, scopes, meters, and other test equipment.</li><li>Ability to read design/wiring schematics and operate data acquisition systems.</li><li>Understanding of test equipment maintenance, calibration, upgrades, and improvements.</li><li>Investigate, debug, and resolve quality inspection or test problems in the manufacturing process.</li><li>Comprehensive understanding of the quality toolbox (SPC, 8D root cause analysis, tolerancing, control and inspection standards).</li><li>Knowledge of Continuous Improvement, Kaizen, 5S, Six Sigma Process, APQP, PPAP, DFMEA, PFMEA.</li><li>Experience with Google Sheets, Docs, Slides, and Gmail.</li><li>Experienced in ISO-9001.</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>Experience in IATF, ISO standards.</li><li>Experience with Linux operating systems.</li><li>Minitab or other statistical software capabilities.</li><li>Experience programming and scripting (C++, Python or equivalent).</li><li>Experience with Jira.</li><li>Ability to communicate effectively with internal stakeholders and third parties.</li></ul><h2>Work Environment</h2><p>This is an on-site position where you will be working directly on autonomous vehicles.</p><br>

<p><strong>Description</strong></p><p>The Quality Engineer is responsible for verifying the quality of in-process and finished products for custom products before shipment. </p><p><br></p><p><strong>Responsibilities</strong></p><ul><li>Conduct thorough inspections, verify compliance with required standards, and approve necessary documentation</li><li>Perform receiving inspections of vendor- or customer-supplied components to ensure they meet requirements</li></ul><p><strong>Additional Skills &amp; Qualifications</strong></p><ul><li>Experience completing first article inspections</li><li>Familiarity with DOD standards and qualifications</li><li>Experience in a customer facing role </li></ul><p><strong>Soft Skill Requirements:</strong> </p><ul><li>Strong initiative </li><li>Good verbal and written communication skills </li><li>Practical experience with sound technical skills, analytical ability, decisive, good judgment, and strong operational focus. </li><li>Ability to work in team environment </li><li>Results and solution-oriented individual</li></ul><p><strong>Experience Level</strong></p><p>Intermediate Level</p><p><br></p>

<h1 style="font-weight: 700;">Job Title: Quality Engineer</h1><br><h2>Job Description</h2><p>The Quality Engineer plays a crucial role in directing quality assurance efforts to ensure that the company&#39;s products adhere to quality and regulatory standards. This position involves establishing and maintaining quality assurance procedures and controls, managing microbiological procedures such as sterilization, bioburden, residuals, and environmental monitoring. The Quality Engineer supports various systems including the Corrective and Preventive Action System (CAPA), Complaint System, Material Review Board (MRB) System, Internal Audit System, and Management Review System. This role is vital in ensuring organizational compliance with defined quality systems, FDA QSR/GMP regulations, ISO quality system standards, and the Medical Device Directive (MDD) concerning product development and manufacturing.</p><br><h2>Responsibilities</h2><ul><li>Serve as a technical resource for initiating and implementing cost improvement plans for new and existing programs.</li><li>Perform validations (IQ, OQ, PQ, MSA, CQ) in accordance with company SOPs.</li><li>Coordinate new process techniques that enhance overall job efficiencies.</li><li>Implement quality systems and procedures to ensure compliance with Quality Standards.</li><li>Participate in Design Development Process meetings representing quality, where appropriate.</li><li>Facilitate communication between engineering functions, manufacturing, and quality both internally and externally.</li><li>Contribute to the design and development of components, assemblies, and devices for various industries.</li><li>Manage equipment and process validation activities for development programs.</li><li>Manage acceptance of product &amp; deliverables.</li><li>Participate in development teams, as appropriate.</li><li>Provide direct feedback into product/process quality-related decisions.</li><li>Travel to other facilities may be required to support business needs.</li><li>Actively participate in continual improvement/innovation, corrective action, and internal/external customer satisfaction.</li><li>Support regulatory and agency inspections, audits, investigations, and inquiries regarding product design and manufacturing quality.</li><li>Monitor manufacturing of assigned products, ensuring compliance with DMR while providing deviation/waiver guidance and maintaining complete and correct Device History Records.</li><li>Review the adequacy and correctness of changes to Bill of Materials (BOMs), Assembly Procedures, Drawings, Component Specifications, FMEAs, Control Plans, etc.</li><li>Lead generation and completion of protocols and reports for test method validations.</li><li>Interface with Manufacturing to review processes for new and existing products and coordinate process validations and capability studies. Recommend process monitoring devices where applicable.</li><li>Develop various inspection techniques and procedures to ensure product integrity to design specifications. Responsible for writing, approval, and implementation of Incoming, In-Process, and Final Inspection procedures.</li><li>Ensure the disposition of non-conforming materials meets all necessary regulatory requirements and ensure adequacy of corrective actions to prevent re-occurrence.</li><li>Lead and manage complaint investigations.</li><li>Participate in plant CAPA activities, including analysis of data and trends in complaints, supplier quality, nonconforming material, training effectiveness, and root cause analysis.</li><li>Participate in continuous improvement projects.</li><li>Assist with product transfers.</li><li>Work with suppliers, management, engineers, and manufacturing associates to resolve quality problems.</li><li>Mentor and support quality inspectors and technicians.</li><li>Perform other functions as required.</li></ul><h2>Essential Skills</h2><ul><li>Proficiency in quality engineering and quality assurance.</li><li>Experience in CAPA and ISO standards.</li><li>Familiarity with device documentation.</li><li>Ability to perform IQ/PQ validations.</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>Bachelor’s degree in engineering (mechanical, electrical, biomedical, or related field) with 1-3 years of experience in Quality Engineering in a regulated medical device or pharmaceutical industry.</li><li>Master’s degree in engineering (mechanical, electrical, biomedical, or related field) with 1-3 years of experience in Quality Engineering in a regulated medical device or pharmaceutical industry.</li></ul><h2>Work Environment</h2><p>The work environment involves collaboration with engineering, manufacturing, and quality teams. It requires travel to other facilities as needed to support business needs and involves participation in regulatory inspections and audits. The role also involves mentoring and supporting quality inspectors and technicians.</p><br>

<h1 style="font-weight: 700;">Job Title: Quality Engineer</h1><br><h2>Job Description</h2><p>Collaborate with Engineering and Manufacturing departments to develop effective test methods, sampling plans, and acceptance criteria for both new and existing products. Assist in implementing and maintaining a quality system that complies with European, US, Canadian, and other regulatory and Quality System requirements.</p><br><h2>Responsibilities</h2><ul><li>Review and approve change orders for compliance with regulations, standards, customer quality agreements, and internal procedures.</li><li>Work with manufacturing to implement Quality Improvements through complaint investigations, defect analysis, control charts, data analysis, leading Quality and Continuous Improvement (CIP) teams, and Corrective and Preventive Action (CAPA).</li><li>Provide guidance to the team on risk management, regulatory and quality engineering policies, and design control principles and best practices.</li><li>Offer technical expertise regarding validations, verification, and qualifications.</li><li>Investigate and resolve product and process issues within CAPA and Non-Conforming Material Report (NCMR) systems.</li><li>Develop quality plans and project plans, providing technical expertise to project teams.</li><li>Support customer and third-party audits.</li></ul><h2>Essential Skills</h2><ul><li>Proficiency in quality engineering and root cause analysis.</li><li>Knowledge of ISO 13485 and New Product Introduction (NPI).</li><li>Experience with IQ/OQ/PQ protocols and design control.</li><li>Bachelor&#39;s degree in Engineering or a related discipline.</li><li>At least one to three years of work experience in a regulated industry, preferably medical devices.</li><li>Understanding of FDA regulations, Quality System Regulations 21 CFR Part 820, and EU MDR.</li><li>Experience in new product launch teams.</li><li>Excellent verbal and written communication skills for effective interaction with internal and external customers.</li><li>Proficiency in MS Office (Word, Excel, Outlook) and ERP systems.</li><li>Knowledge of statistical methods and principles such as Statistical Process Control (SPC) and Design of Experiments (DOE).</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>American Society of Quality Certified Quality Engineer (ASQ CQE) is a plus.</li><li>Ability to work under pressure and meet deadlines while maintaining a positive attitude and exemplary customer service.</li><li>Independence in carrying out assignments to completion using Good Manufacturing Practice (GMP).</li></ul><h2>Work Environment</h2><p>The role involves working within a dynamic environment where collaboration with cross-functional teams is essential. The use of various technologies and equipment is expected, with a focus on maintaining quality standards. The work requires adherence to regulatory requirements and may include participation in audits and reviews.</p><br>

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