Quality control technician jobs in Manchester, NH - 551 jobs

Quality Inspector III - Weekdays About Us Founded in 2015 to develop the world's first industrially scalable laser metal additive manufacturing solution, our client is reshaping how the world manufactures critical products. They build and operate advanced digital infrastructure that enables innovation, accelerates growth, and supports sustainability across aerospace, defense, medical, and other essential industries. Through vertically integrated capabilities, including scalable additive manufacturing and precision machining, they deliver true end-to-end production at scale by combining cutting-edge technology with a foundation of proven industrial craftsmanship. Their team brings deep expertise in manufacturing, materials science, software, automation, and operations, united by a shared commitment to quality, curiosity, and accountability. They foster an inclusive culture where people take ownership, solve meaningful problems, and continuously learn, because diverse perspectives lead to better outcomes. Job Purpose As a Quality Inspector III at our client, you will work in a diversified role within the Quality Inspection team dedicated to ensuring every product delivered meets the highest standards of precision, safety, and reliability. By applying expertise in inspection methods, quality systems, and problem-solving, this role safeguards customer trust, drives continuous improvement, and supports innovation in metal additive manufacturing. This position operates on the weekday shift: Monday-Friday, 6:00 AM to 2:30 PM. Key Responsibilities Perform First Article Inspections (FAI) and routine part inspections using calipers, micrometers, and other gauges. Verify that materials, equipment, processes, and products comply with quality specifications. Develop and validate inspection and test methods; assist in creating SOPs and inspection protocols. Monitor, analyze, and report on product quality metrics. Support compliance with customer, internal, and industry requirements (AS9100, ISO 9001, ISO 13485) through audits and gap analysis. Assist in developing and implementing process controls, corrective actions, and continuous improvement initiatives. Ensure workflows, processes, and products comply with safety regulations. Investigate and troubleshoot product or production issues. Inspect manufactured parts, issue non-conformance reports, and facilitate MRB hardware disposition and corrective action tasks. Work independently and manage daily priorities with minimal supervision. Communicate and collaborate with operations personnel to ensure production needs are met. Initiate and communicate identified nonconformances. Qualifications 5+ years of experience performing part inspections with strong drawing interpretation skills. Extensive knowledge of GD&T principles. Experience with First Article Inspections (FAI), Test Method Validation (TMV), and developing inspection methods. Proficiency in AQL sampling techniques. Skilled in performing dimensional and visual inspections. Experience with root cause analysis, data analysis, and troubleshooting. Experience in medical device, aerospace, or defense manufacturing required. Hands-on experience with advanced inspection equipment and software, including CMMs, PCMMs, vision systems, profilometers, and blue-light scanners (e.g., Zeiss, Faro, Keyence). Ability to troubleshoot issues encountered with inspection equipment. Self-motivated, hands-on team player with excellent communication skills; adaptable to fast-paced environments and excited by new challenges in metal additive manufacturing.

Adecco Staffing is working with Prototek in Hopkinton, NH to bring on Quality Control Inspectors! This is a full-time, long-term opportunity with room for growth. Job Title: Quality Control Inspector Pay: Based on experience Shifts: All shifts available (varies by department) Job Duties: • Perform detailed inspection of machined and fabricated components using precision measuring tools • Use calipers, micrometers, height gauges, pin gauges, and other QC equipment • Read and interpret blueprints, drawings, and customer specifications • Document inspection findings and maintain accurate quality records • Perform in-process, first-piece, and final inspections as required • Work closely with machinists, welders, and engineering teams to resolve quality concerns • Follow all company quality, safety, and workflow procedures • Support continuous improvement efforts within the quality department • Maintain a clean, organized, and professional work area Requirements: • Previous quality control inspection experience in manufacturing preferred • Strong ability to read and understand engineering drawings • Proficient with precision measuring tools (calipers, micrometers, gauges, etc.) • Comfortable working in a fast-paced environment with tight tolerances • Excellent attention to detail and documentation accuracy • Reliable attendance and willingness to work overtime when needed If you are interested in this position, please apply with an updated resume! Pay Details: $25.00 to $30.00 per hour Benefit offerings available for our associates include medical, dental, vision, life insurance, short-term disability, additional voluntary benefits, EAP program, commuter benefits and a 401K plan. Our benefit offerings provide employees the flexibility to choose the type of coverage that meets their individual needs. In addition, our associates may be eligible for paid leave including Paid Sick Leave or any other paid leave required by Federal, State, or local law, as well as Holiday pay where applicable. Equal Opportunity Employer/Veterans/Disabled Military connected talent encouraged to apply To read our Candidate Privacy Information Statement, which explains how we will use your information, please navigate to The Company will consider qualified applicants with arrest and conviction records in accordance with federal, state, and local laws and/or security clearance requirements, including, as applicable: The California Fair Chance Act Los Angeles City Fair Chance Ordinance Los Angeles County Fair Chance Ordinance for Employers San Francisco Fair Chance Ordinance Massachusetts Candidates Only: It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.

We are seeking a dedicated Lab Technician to operate production equipment following standard operating procedures (SOPs), Batch Records, Manufacturing, Documentation (MD), and Operational Procedures Manual (OPM). The role involves executing procedures for the production of cross-linked hyaluronic acid products, reviewing manufacturing documentation for compliance, coordinating sample preparation and testing, and accurately recording data into Batch Records, log books, and OPMs. The ideal candidate will document all work activities following Good Documentation Practices, recommend document revisions, and report procedural deviations and non-conformance to management. - Operate production equipment as per SOPs, Batch Records, MD, and OPM. - Execute procedures for cross-linked hyaluronic acid product production. - Review manufacturing documentation for compliance. - Coordinate sample preparation and testing. - Record data into Batch Records, log books, and OPMs. - Document work activities following Good Documentation Practices. - Recommend document revisions. - Proficiency in SOP and GMP. - Experience in biotechnology or pharmaceutical manufacturing. - Knowledge of cell culture. - Understanding of chemicals, including acids and bases. - Aseptic technique skills. Skills batch record, SOP, pharmaceutical manufacturing, cell culture, aseptic technique, sample prep, media prep, acids, chemicals, bases, GMP, Biotechnology manufacturing, Cleanroom Top Skills Details batch record,SOP,pharmaceutical manufacturing,cell culture,aseptic technique,sample prep,media prep Additional Skills & Qualifications Associate or BS with biomanufacturing/pharmaceutical experience 4-6 years experience in a biotech manufacturing environment Ability to gown and gain entry to biotechnology/pharmaceutical manufacturing Aseptic technique needed Work with chemicals (Acids & bases) Comfortability working in a cleanroom environment Experience Level Intermediate Level Job Type & Location This is a Contract position based out of Bedford, MA. Pay and Benefits The pay range for this position is $23.00 - $26.50/hr. Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following: - Medical, dental & vision - Critical Illness, Accident, and Hospital - 401(k) Retirement Plan - Pre-tax and Roth post-tax contributions available - Life Insurance (Voluntary Life & AD&D for the employee and dependents) - Short and long-term disability - Health Spending Account (HSA) - Transportation benefits - Employee Assistance Program - Time Off/Leave (PTO, Vacation or Sick Leave) Workplace Type This is a fully onsite position in Bedford,MA. Application Deadline This position is anticipated to close on Jan 29, 2026. About Actalent Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law. If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email actalentaccommodation@actalentservices.com (%20actalentaccommodation@actalentservices.com) for other accommodation options.

Engineering Technician - Medical Device R&D temp to perm Marlboro, MA Support engineers in the development and testing of single-use medical devices. This hands-on role involves working with Engineers testing prototypes, performing validation and system testing, and accurately documenting results in a regulated environment. Responsibilities Perform validation, strength, and system testing on medical devices Work with tubing and small mechanical components Set up and maintain test equipment; perform basic troubleshooting Document test results and communicate findings to engineers Support calibration and quality documentation requirements Qualifications Associate degree or equivalent hands-on experience 1+ year experience in technical, lab, R&D, or manufacturing role Strong mechanical aptitude and troubleshooting skills Ability to follow procedures and document work accurately Medical device or regulated environment experience preferred.

Job Title: Manufacturing Associate I - Cell Therapy Job Duration: 6 Months with potential to extend Shift Schedule: (There will be 6-8 weeks of training 7 AM - 4 PM, Monday to Friday) Rotational shift schedule (Day/Night) PURPOSE AND SCOPE OF POSITION The client seeks Associates within manufacturing who bring enthusiasm, intellectual curiosity, scientific rigor, and a desire to help drive novel programs. The candidate must be goal-oriented, flexible, and able to work efficiently with safety and quality in mind. We are searching for enthusiastic and innovative individuals with a good understanding of good manufacturing practices to support routine manufacturing operations for Cell Therapy. DUTIES AND RESPONSIBILITIES Performing patient process unit operations and support operations described in standard operating procedures and batch records. Work in a cleanroom environment and perform aseptic processing; maintain manufacturing environmental conditions (Non-Viable Particulate(s) and Viable microbial levels per controlled area classification specifications) by performing area disinfection regimen as required to meet global Health Authority requirements. Completing documentation required by process transfer protocols, validation protocols, standard operating procedures, and batch records. Performing tasks in a manner consistent with the safety policies, quality systems, and GMP requirements. Completing training assignments to ensure the necessary technical skills and knowledge. Assisting in setting up manufacturing areas and equipment/fixtures. Perform facility and equipment commissioning activities. Training others on SOPs, Work Instructions to successfully complete manufacturing operations. Executing daily unit operations schedule that includes people, product, and material flow across multiple shifts. REQUIRED COMPETENCIES Education: Bachelor's in a relevant science or engineering discipline is preferred. High school diploma and 2 years of experience in cGMP bioprocessing manufacturing, cell therapy manufacturing, or relevant experience. Preferred Qualifications: Knowledge of cGMP regulations and FDA guidance applicable to biologics and cell therapy manufacturing is preferred.

Responsible for the dispensing of raw materials liquids and powders (hazardous and non-hazardous), acids/bases, under cGMP conditions to support the manufacture of therapeutic proteins (API) Individual will be required to perform and monitor all dispensing processes and weighs, including liquid, powder (hazardous and non-hazardous), acids and bases. All processes will be completed per cGMP guidelines to support the manufacture of therapeutic proteins (API). Required to attain a basic understanding of cGMP compliance while training under close supervision, demonstrating aseptic technique and cross contamination awareness in handling of products and materials. Expected to follow and adhere to all written procedures (SOPs), monitor equipment and processes, perform basic laboratory tasks, including pH, conductivity, and sampling as required. All tasks will be completed while gowned and wearing required PPE while working in a Class C environment. Expected to execute process recipes. Ability to qualify for all assigned tasks and maintain individual training plan. Ability to qualify and perform required functions and scheduled cleans on all Dispensing equipment through routine cleaning and sanitization. Perform peer, First Level Reviews of completed eDispense orders/kits, upon completion of WBT and LQM/PM signoff by area trainer. Ability to report to production via written and electronic documents in accordance with current good manufacturing practice (cGMP) and good documentation practice (GDPs). Complete documentation reviews as appropriate. Prepare materials for transport and delivery to manufacturing suites. Perform material movements both physically and in software systems. Participate in Safety Inspections and submit safety observations to provide safer working conditions for self and others. Administrative tasks to include attendance at shift exchange and required meetings, sending/receiving of emails, and participation in assigned projects. Performs other duties as they are assigned to support Logistics Team. Associates Degree and/or equivalent experience

Supports Quality Assurance and Control activities to ensure products and procedures meet all applicable internal and external requirements. Supports the administration and maintenance of quality systems. Provides support for quality projects dictated by the Quality Leadership. ESSENTIAL FUNCTIONS AND RESPONSIBILITIES * Supports the administration and maintenance of in-process inspection reports, final inspection reports, and First Article inspection Reports compliant with AS9102 using Discus inspection report software. * Maintain calibrated test equipment, ensures equipment is calibrated, validated and maintained properly, maintains the calibration system, prepare test data, and identify areas for improvement. * Reads and interprets work instructions and to determine dimensions and tolerances. * Reads blueprints or specifications to determine dimensions and tolerances. * Collates test data and drafts quality reports. * May interpret test results and compare them to the specifications and control limits in place while providing recommendations on the appropriateness of data. * Supports QMS activities including but not limited to CAPA, Internal Audits, Document Control, Records Management, etc. * Maintain QMS documentation; revise and update documentation, assign training based on documentation changes. * May interpret Geometric Dimensioning & Tolerance * Strong attention to detail, organization, and documentation skills. * May verify specified dimensions of product or raw material using verniers, micrometers, CMM, height gages, comparator, scales or other tools. * Assists in other areas in support of product conformity. * Demonstrates responsibility and accountability for creating a professional, safe, and clean environment evidenced by: being at work on time to perform assigned duties, following the policies of Granite State Manufacturing, always wearing safety glasses in designated areas, maintaining a neat and orderly work area, and following safety practices to prevent errors. * Demonstrates commitment to teamwork by establishing effective relationships and networks with both managers/directors and workers and collaborating with them to accomplish shared purposes and goals. * Complies with federal and state laws, regulations, specifications and company standards. * Abides by GSM Code of Ethics and Business Conduct standards and strictly observes all U.S. and foreign laws and regulations.

Life changing therapies. Global impact. Bridge to thousands of biopharma companies and their patients. We are PCI. Our investment is in People who make an impact, drive progress and create a better tomorrow. Our strategy includes building teams across our global network to pioneer and shape the future of PCI. This position will have the primary responsibility for daily formulation activities to ensure schedule activities are completed, formulation materials and equipment are maintained, as well as the responsibility for performing corrective and preventative actions. As a secondary function, provide troubleshooting expertise for manufacturing of products both internally and externally of the company. Schedule: Sunday - Wednesday 6:00AM - 4:30PM Essential Duties and Responsibilities: To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The basic duties and responsibilities include the following, but other duties may be assigned. Has ownership for the daily formulation activities to ensure scheduled all scheduled tasks/events are completed Is responsible for critical steps in the formulation process including but not limited to, lab setup and process flows, in-process testing, API dissolution and final QS while ensuring safety, batch integrity and prevention or errors that could lead to product and or finical loss Initiate the production of batch documentation used for engineering and cGMP production. Prepare and update Master Production Batch records and SOPs accurately for communicating and initiate the documentation change process for needed documentation changes Complete executed Batch Records accurately and completely prior to submission to supervision for review Comply with all area SOPs and ensure logbooks are completed, and adhere to cGMP requirements Author process deviations when these occur within the department, participate in investigations, and contribute to identifying corrective and preventative actions Cross train to increase technical skills across the department Accountable for timely communication to management and clients of issues, challenges as well as opportunities for process improvements. As a member of the manufacturing team, you will perform other manufacturing tasks for example filling, capping etc., as needed. Work with enabling groups to improve/implement processes. Other duties as assigned. Strong interpersonal skills Strong working knowledge of MS Office suite is preferable Attention to detail and positive attitude are key attributes Able to follow rules and regulations perfectly Works directly with aseptic and non-aseptic personnel. Works closely with Quality Assurance, MTS, Validation etc. Qualifications: The requirements listed below are representative of the knowledge, skill, and/or ability required for the stated position. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. Required: High School education or AS degree or BS degree in Chemical Engineering/ Bio Chemistry or other industry related discipline is preferred Experience and knowledge of formulation/compounding tools and equipment Minimum 1-2 year's work experience in a GMP environment preferably in fill finish pharmaceutical operations Demonstrated ability to prioritize multiple projects and activities Full Professional Proficiency: Ability to speak, read, and write fluently and accurately on all levels pertinent to professional needs. #LI-KC1 Join us and be part of building the bridge between life changing therapies and patients. Let's talk future Equal Employment Opportunity (EEO) Statement: PCI Pharma Services is an Equal Opportunity/Affirmative Action Employer. We do not unlawfully discriminate on the basis of race, color, religion, age, sex, creed, national origin, ancestry, citizenship status, marital or domestic or civil union status, familial status, affectional or sexual orientation, gender identity or expression, genetics, disability, military eligibility or veteran status, or any other protected status. At PCI, Equity and Inclusion are at the core of our company's purpose: Together, delivering life-changing therapies. We are committed to cultivating an inclusive workplace by holding ourselves accountable to the highest standards of understanding, fairness, respect, and equal opportunity - at every level. We envision a PCI community where everyone can belong and grow, and we strive to bring this vision to reality by continuously and intentionally assessing our people practices, policies and programs, marketing approach, and workplace culture.

At QIAGEN, we are driven by a simple but powerful vision: making improvements in life possible. We're dedicated to revolutionizing science and healthcare for the better. From our entrepreneurial roots to our current global presence, we've grown into a force for positive change. With thousands of employees across six continents, collaboration is our greatest strength. We're always striving to identify talented individuals to join our exceptional teams. We have played a pivotal role in shaping modern science and healthcare, and we're just getting started. If you're someone who thrives on new challenges, values diversity and wants to make a tangible difference in people's lives, then QIAGEN is the place for you. At QIAGEN, every day is an opportunity to make a real-life impact. Join us, grow with us, and together, let's shape the future of biological discovery. The Finished Goods Formulation Technician II formulates buffers, diluents, and PCR master mixes for the Finished Goods team. This position is charged with adhering to the Quality System to execute consistent processes that result in repeatable product for on time delivery. Responsibilities include: Job performance will involve a variety of activities including but not limited to: * Perform applicable processes as detailed in work instructions, including but not limited to: o Chemical material handling o Care and use of formulation equipment (i.e., balances, overhead mixes, stir plates, etc.) o Measurement of materials by mass and volume o Annealing oligos o Thawing and handling of enzymes, oligos, and light sensitive products o Line clearance and PPE usage * Perform SAP transactions for order confirmations. * Record production activities on all applicable forms in accordance with Good Documentation Practices. * Assist in maintaining inventory system to keep materials related to Formulation orders organized, stocked, and ensure inventory levels are accurate within SAP. * Contribute to and support department/corporate goals * Work with Supervisor to ensure personal growth through individual goal setting and participate in a dialog around performance reviews. * Complete all required quality documentation training as issued through Master Control. * Contribute to quality documentation development/improvements within and across departments, as needed. * Ensure compliance to applicable ISO Quality and EHS regulations and standards. * Contribute to a strong team mindset with a focus on creative problem solving. * Assist in training additional team members, if applicable. * Assist the Finished Goods Dilutions and/or Fill/Pack teams, as needed. Your profile: * Bachelor's of Science degree and 1 or more years related industry experience or the equivalent combination of education and experience * Understanding of ISO Quality and Lean Manufacturing concepts Personal Requirements * Attention to detail * Strong communication skills What we offer * Bonus/Commission * Local benefits * Referral Program * Volunteer Day * Internal Academy (QIALearn) * Employee Assistance Program * Hybrid work (conditional to your role) Our people are the heartbeat of everything we do. Passion drives us as we push boundaries to innovate and evolve. We inspire with our leadership and make an impact with our actions. We cultivate a collaborative, supportive environment where each individual and team can flourish. We champion accountability and encourage entrepreneurial thinking. QIAGEN is committed to creating a diverse environment and is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, sex, age, national origin, religion, sexual orientation, gender identity, status as a veteran, or disability.

At QIAGEN, we are driven by a simple but powerful vision: making improvements in life possible. We're dedicated to revolutionizing science and healthcare for the better. From our entrepreneurial roots to our current global presence, we've grown into a force for positive change. With thousands of employees across six continents, collaboration is our greatest strength. We're always striving to identify talented individuals to join our exceptional teams. We have played a pivotal role in shaping modern science and healthcare, and we're just getting started. If you're someone who thrives on new challenges, values diversity and wants to make a tangible difference in people's lives, then QIAGEN is the place for you. At QIAGEN, every day is an opportunity to make a real-life impact. Join us, grow with us, and together, let's shape the future of biological discovery. The Finished Goods Formulation Technician II formulates buffers, diluents, and PCR master mixes for the Finished Goods team. This position is charged with adhering to the Quality System to execute consistent processes that result in repeatable product for on time delivery. Responsibilities include: Job performance will involve a variety of activities including but not limited to: · Perform applicable processes as detailed in work instructions, including but not limited to: o Chemical material handling o Care and use of formulation equipment (i.e., balances, overhead mixes, stir plates, etc.) o Measurement of materials by mass and volume o Annealing oligos o Thawing and handling of enzymes, oligos, and light sensitive products o Line clearance and PPE usage · Perform SAP transactions for order confirmations. · Record production activities on all applicable forms in accordance with Good Documentation Practices. · Assist in maintaining inventory system to keep materials related to Formulation orders organized, stocked, and ensure inventory levels are accurate within SAP. · Contribute to and support department/corporate goals · Work with Supervisor to ensure personal growth through individual goal setting and participate in a dialog around performance reviews. · Complete all required quality documentation training as issued through Master Control. · Contribute to quality documentation development/improvements within and across departments, as needed. · Ensure compliance to applicable ISO Quality and EHS regulations and standards. · Contribute to a strong team mindset with a focus on creative problem solving. · Assist in training additional team members, if applicable. · Assist the Finished Goods Dilutions and/or Fill/Pack teams, as needed. Your profile: · Bachelor's of Science degree and 1 or more years related industry experience or the equivalent combination of education and experience · Understanding of ISO Quality and Lean Manufacturing concepts Personal Requirements · Attention to detail · Strong communication skills What we offer Bonus/Commission Local benefits Referral Program Volunteer Day Internal Academy (QIALearn) Employee Assistance Program Hybrid work (conditional to your role) Our people are the heartbeat of everything we do. Passion drives us as we push boundaries to innovate and evolve. We inspire with our leadership and make an impact with our actions. We cultivate a collaborative, supportive environment where each individual and team can flourish. We champion accountability and encourage entrepreneurial thinking. QIAGEN is committed to creating a diverse environment and is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, sex, age, national origin, religion, sexual orientation, gender identity, status as a veteran, or disability.

Job Title: Electrical Quality Technician Company: Munters Schedule: Monday-Thursday, 6:00 AM - 4:30 PM Salary: $26.17/hr. - $33.10/hr. About Us: Munters is a global leader in climate solutions for mission-critical processes. We offer innovative, efficient and sustainable solutions for customers in industries where controlling indoor humidity, temperature and energy efficiency is mission-critical. Climate control systems often account for a large percentage of the energy consumption in many of our customers' operations. With an optimal climate system, we can help them to more efficiently use energy or water resources, and thereby reduce their climate and environmental impact. Sustainability is an important part of Munters' business strategy and value creation. We pride ourselves on fostering a dynamic and inclusive work environment where interns are valued members of the team and are given meaningful projects to work on. Job Description: Work as part of final test team, analyzing and correcting electrical problems. Keeps the Team Leader and Quality Manager informed of all issues affecting the performance of the department or product quality or delivery. Responsibilities: Assumes delegated responsibilities from the Team Leader of the Quality department. When working with lower graded electrical personnel, assumes some responsibility to coordinate the mutual effort and provide guidance and direction to perform the work in a safe and workmanlike manner and the installation be in compliance with specifications, established standards and the National Electric Code Understands electrical theory and practice as applied to the operation of such components as electric motors, motor starters, contractors, control relays, time delay relays, circuit breakers, and other related electrical, pneumatic and mechanical components Applies trade knowledge and experience to recognize errors or potential problems with schematics, assembly drawings, parts lists or instructions. Advise supervisor of problems or questions and, if possible, recommends solutions Prepares, without supervision, electrical components and subassemblies at the bench or on the product following specified methods and techniques. Cuts or extends lead wires, attaches terminals or connections. Interconnects wires according to diagrams or schematics Inspects repair jobs, prepare list of parts to be replaced or repaired. Tests repaired or reconditioned unit for compliance with specifications or established standards Installs, without supervision, a complete electrical and/or pneumatic system utilizing electrical conduits, fittings, boxes and wire, following electrical diagrams and schematics. Insures that the components are secure and free from any interference and functioning properly Performs trouble-shooting as necessary on parts or subassemblies to identify and resolve the problem Tests unit using required test equipment and complete test reports Performs work and/or delegated responsibilities without supervision and with either verbal or written instructions. Ensures work area is clean and orderly Work in other areas when needed. Maintain ISO standards Observe all safety rules Requirements: Understands electrical theory and practice Capability of reading electrical diagrams and schematics Requires at least 1 year of experience in manufacturing or relevant experience High school diploma or equivalent Medium Work: Exerting up to 50 pounds of force occasionally and/or up to 20 pounds of force frequently, and/or up to 20 pounds of force constantly to move objects Climbing, stooping, kneeling, crouching, reaching, standing, walking, pushing, pulling, lifting The worker is required to have close visual acuity to perform an activity such as: preparing and analyzing data, viewing computer terminal, expansive reading, etc. The worker is not substantially exposed to adverse environmental conditions Benefits: Competitive salary Comprehensive health, dental, and vision insurance plans. Flexible work schedule Generous vacation and paid time off. 401(k) retirement savings plan with employer matching. Professional development opportunities, including tuition reimbursement and conference attendance. Company-sponsored social events and team-building activities. State-of-the-art equipment and tools to support your work. Equal Opportunity Employer: We are an equal opportunity employer and value diversity at our company. We do not discriminate on the basis of race, religion, color, national origin, gender, sexual orientation, age, marital status, veteran status, or disability status. All offers are contingent on a pre-employment drug test and background check, as applicable for the position. #HPMUNTERS

Job Description 1st shift (9/80 schedule - every other Friday off) 1st shift hours are: 6a-3:30p, working Friday is 6a-2:30p ABOUT THE JOB! Inspect, measure and test purchased products in accordance with drawings, specification, customer flow down and incoming inspection/test plans. Process customer return materials through the internal RMA process and drive expedites from receipt to final disposition while trying to maintain a cycle time metric to close. RESPONSIBILITIES: Perform visual and mechanical inspection of components in accordance with the inspection plan to detect missing hardware, soldering defects, assembly errors/defects, alignment defects and/or cosmetic defects and to ensure conformance to specified dimensions, specifications and quality standards and maintain appropriate records. Ability to create and process First Article Inspection reports. Process non-conforming product to Material Review Board for disposition. Assure all products meet the requirements of the product drawing, specification, purchase order and the inspection plan. Perform necessary transactions to move product as needed. Trouble shoot product returns to confirm the customer reported issues. Participate in failure analysis investigation process for the product return and update the results in the RMA access database. Troubleshooting test rejects and/or test equipment issues as needed. Build test fixtures as needed to support the troubleshooting/testing function.

Job DescriptionBenefits: 401(k) 401(k) matching Competitive salary Dental insurance Free uniforms Health insurance Paid time off Training & development Vision insurance About Us We are a leading aerospace manufacturer specializing in precision-machined engine components for OEMs and the U.S. Department of Defense. Our team is committed to the highest standards of quality, compliance, and innovation in machining and inspection. Position Overview We are seeking an experienced Quality Technician with strong background in aerospace manufacturing and precision inspection. The ideal candidate will have hands-on inspection expertise, ability to write and run Coordinate Measuring Machine (CMM) programs, and at least 5 years of quality assurance experience in an aerospace environment. Key Responsibilities Develop, edit, and execute CMM inspection programs to support production and first article inspections. Perform dimensional inspection of complex aerospace components to verify compliance with AS9100, OEM, and DoD standards. Interpret engineering drawings, GD&T, and customer specifications. Support root cause analysis, corrective action, and continuous improvement initiatives. Collaborate with machinists, engineers, and quality leadership to maintain high product conformance standards. Qualifications Minimum 5 years of quality/inspection experience in aerospace manufacturing. Proven experience programming and operating CMMs (PC-DMIS, Zeiss Calypso, or equivalent). Strong knowledge of GD&T and precision measurement methods. Familiarity with AS9100, ISO, and NADCAP requirements. Proficiency in using standard metrology equipment (micrometers, bore gages, height gages, surface plates). Ability to work independently and as part of a cross-functional team.

Daily follow-up of supplier-related quality issues on the shop floor - Identification and documentation of defects and non-conformances - Taking photos and videos to support quality records and reporting - Supporting and monitoring supplier rework activities on site - Liaising with Quality and Manufacturing teams to close quality issues - Supporting basic root-cause and problem-solving activities - Ensuring quality and safety compliance within the factory environment We are a company committed to creating diverse and inclusive environments where people can bring their full, authentic selves to work every day. We are an equal opportunity/affirmative action employer that believes everyone matters. Qualified candidates will receive consideration for employment regardless of their race, color, ethnicity, religion, sex (including pregnancy), sexual orientation, gender identity and expression, marital status, national origin, ancestry, genetic factors, age, disability, protected veteran status, military or uniformed service member status, or any other status or characteristic protected by applicable laws, regulations, and ordinances. If you need assistance and/or a reasonable accommodation due to a disability during the application or recruiting process, please send a request to ********************.To learn more about how we collect, keep, and process your private information, please review Insight Global's Workforce Privacy Policy: **************************************************** Skills and Requirements Previous experience in a manufacturing or shop-floor quality role - Experience in HVDC, power transformers, or heavy electrical equipment is desirable - Strong attention to detail and a hands-on working approach - Confident working directly on the shop floor - Basic computer skills (Word, Excel, PowerPoint) - Able to work independently and communicate clearly with multiple stakeholders

Job Description Job Title: Quality Assurance Technician FLSA Status: Non Exempt Developing and maintaining company inspection reports. Inspecting goods or products according to quality and safety standards. Ensuring goods and products comply with company standards as well as Federal and State law. Ensuring test equipment is calibrated and working correctly. This is a 3rd shift position 11:00pm-7:00ajm Key Responsibilities Responsible for maintaining high customer product acceptance through ensuring that products shipped adhere to product specifications at all phases of the operation. This includes inspecting incoming raw materials, purchased parts and outside service (OV) parts. In-process and final product acceptance, first article inspections and dock audits are also required. Responsible for maintaining process acceptance through auditing production process at all phases of production. This auditing will include, but not limited to: 1st pc process, Frequency process, Setup process, Routing Audits, 5S Audits and Safety Audits, all as applicable. Responsible as required, for training machine operators in inspection of product as determined by prints or support documentation. Must have a complete understanding of inspection tools and how to use them. (As applicable to building). Inspection and processing of Returned Goods (RAs), including required data entry, internal and external communications and required reporting. This includes sorting product as applicable. Responsible as required, participate in Root Cause Analysis (RCA) and Corrective & Preventive Actions (CAPA). Must be knowledgeable in the effective use of Lean Six Sigma (LSS) tools and concepts to assist in process improvements as required. Serve as an active participant in LSS programs that promote continuous improvement. Must be knowledgeable in ISO Standards and objectives to maintain and reinforce as needed. Responsible for maintaining and recording accurate quality documentation in various company data collection systems, including first piece sheets, certified operator documentation and in-process records. Must be able to work extended hours when required. Maintains a safe and clean working environment by complying with procedures, rules, and regulations. Contributes to team effort by accomplishing related results as needed. Performs all other duties as assigned. Required Qualifications Must be honest, reliable and conscientious. Task requires comprehension of high school math, reading, and writing skills. Must be able to perform computer work. Must be knowledgeable in Microsoft Excel, Word, e-mail and E2 database. Must be knowledgeable in Standard Operating Procedures as it relates to the Quality Department. Must be able to work well with others. Must be able to read and understand Fabrication blue prints and Machining blue prints including Basic GD&T.(As applicable). Tasks require walking, bending, climbing, lifting and standing. Tasks require the use of small hand tools, instruments and materials 60% of the time. Tasks require visual inspection and reading measurement tools and instruments. Tasks require flexibility and adaptability at a rapid pace Physical and Environmental Conditions Exposure to load noises Regularly required to sit, stand, bend, reach, climb and move about the facility Regularly operates a computer, computer accessories and phone equipment Required to occasionally lift up to 50 lbs. Occasionally stoops, kneels, reaches and carries this is a 3rd shift 11pm-7am Sunday through Thursday

We are seeking a dedicated Lab Technician to operate production equipment following standard operating procedures (SOPs), Batch Records, Manufacturing, Documentation (MD), and Operational Procedures Manual (OPM). The role involves executing procedures for the production of cross-linked hyaluronic acid products, reviewing manufacturing documentation for compliance, coordinating sample preparation and testing, and accurately recording data into Batch Records, log books, and OPMs. The ideal candidate will document all work activities following Good Documentation Practices, recommend document revisions, and report procedural deviations and non-conformance to management. - Operate production equipment as per SOPs, Batch Records, MD, and OPM. - Execute procedures for cross-linked hyaluronic acid product production. - Review manufacturing documentation for compliance. - Coordinate sample preparation and testing. - Record data into Batch Records, log books, and OPMs. - Document work activities following Good Documentation Practices. - Recommend document revisions. - Proficiency in SOP and GMP. - Experience in biotechnology or pharmaceutical manufacturing. - Knowledge of cell culture. - Understanding of chemicals, including acids and bases. - Aseptic technique skills. Skills batch record, SOP, pharmaceutical manufacturing, cell culture, aseptic technique, sample prep, media prep, acids, chemicals, bases, GMP, Biotechnology manufacturing, Cleanroom Top Skills Details batch record,SOP,pharmaceutical manufacturing,cell culture,aseptic technique,sample prep,media prep Additional Skills & Qualifications Associate or BS with biomanufacturing/pharmaceutical experience 4-6 years experience in a biotech manufacturing environment Ability to gown and gain entry to biotechnology/pharmaceutical manufacturing Aseptic technique needed Work with chemicals (Acids & bases) Comfortability working in a cleanroom environment Experience Level Intermediate Level Job Type & Location This is a Contract position based out of Bedford, MA. Pay and Benefits The pay range for this position is $23.00 - $26.50/hr. Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following: • Medical, dental & vision • Critical Illness, Accident, and Hospital • 401(k) Retirement Plan - Pre-tax and Roth post-tax contributions available • Life Insurance (Voluntary Life & AD&D for the employee and dependents) • Short and long-term disability • Health Spending Account (HSA) • Transportation benefits • Employee Assistance Program • Time Off/Leave (PTO, Vacation or Sick Leave) Workplace Type This is a fully onsite position in Bedford,MA. Application Deadline This position is anticipated to close on Feb 2, 2026. About Actalent Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law. If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.

Adecco Staffing is partnering with a reputable manufacturing facility in Peterborough, NH to hire Quality Control Inspectors for all shifts! This is a temp-to-hire or direct-hire opportunity, depending on your level of Inspection experience. The position offers competitive pay rates and the opportunity to join a growing company. Pay Rate: $17-$26 per hour, depending on experience and shift Schedules Available: 1st Shift Monday through Friday 7:00am-3:30pm, OT available 2nd Shift Monday through Friday 3:15pm-11:45pm, OT available 3rd Shift Sunday through Thursday 11:30pm-7:00am (paid for 8), OT available Job Summary: Responsible for ensuring the quality of processes and product within an assigned functional area. Essential Duties and Responsibilities: The following represent general inspection functions which may or may not be required depending upon the functional area in which you are assigned. Inspectors may be reassigned to a different sub function at any time based on the business need, and training will be provided. Perform dimensional inspection using mechanical and visual inspection equipment, such as an optical comparator, contour reader, dial indicators, inspection hand tools, surface plates, height gauges, air gauges, specialized bearing measurement equipment, and gauge blocks. Measure bearing assemblies and/or component features such as roundness, concentricity, perpendicularity, flatness, sphericity, surface finish, surface noise and vibration levels using specialized equipment. Complete basic control charts, run charts, prepare charts, and histograms. Read and understand drawings, specifications, procedures, standards and instructions. Write inspection rejection reports in accordance with company procedures, and maintain detailed inspection records using appropriate forms. Make recommendations regarding quality and manufacturing improvements as needed. Perform visual inspection of bearing assemblies, and/or bearing components, using microscope and the unaided eye. Communicate with Manufacturing & Quality personnel and other disciplines as required in a timely and professional manner. Why Apply? Competitive pay rates with the potential for overtime. Temp-to-hire or direct-hire opportunity based on your level of experience. Work in a high-level manufacturing facility with advanced equipment and processes. Training and growth opportunities available. If you are interested in this exciting opportunity and feel you have the skills to succeed, please apply today with an updated resume or call 603-###-####! We look forward to hearing from you. Pay Details: $17.00 to $26.00 per hour Benefit offerings available for our associates include medical, dental, vision, life insurance, short-term disability, additional voluntary benefits, EAP program, commuter benefits and a 401K plan. Our benefit offerings provide employees the flexibility to choose the type of coverage that meets their individual needs. In addition, our associates may be eligible for paid leave including Paid Sick Leave or any other paid leave required by Federal, State, or local law, as well as Holiday pay where applicable. Equal Opportunity Employer/Veterans/Disabled Military connected talent encouraged to apply To read our Candidate Privacy Information Statement, which explains how we will use your information, please navigate to The Company will consider qualified applicants with arrest and conviction records in accordance with federal, state, and local laws and/or security clearance requirements, including, as applicable: The California Fair Chance Act Los Angeles City Fair Chance Ordinance Los Angeles County Fair Chance Ordinance for Employers San Francisco Fair Chance Ordinance Massachusetts Candidates Only: It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.

Supports Quality Assurance and Control activities to ensure products and procedures meet all applicable internal and external requirements. Supports the administration and maintenance of quality systems. Provides support for quality projects dictated by the Quality Leadership. ESSENTIAL FUNCTIONS AND RESPONSIBILITIES Supports the administration and maintenance of in-process inspection reports, final inspection reports, and First Article inspection Reports compliant with AS9102 using Discus inspection report software. Maintain calibrated test equipment, ensures equipment is calibrated, validated and maintained properly, maintains the calibration system, prepare test data, and identify areas for improvement. Reads and interprets work instructions and to determine dimensions and tolerances. Reads blueprints or specifications to determine dimensions and tolerances. Collates test data and drafts quality reports. May interpret test results and compare them to the specifications and control limits in place while providing recommendations on the appropriateness of data. Supports QMS activities including but not limited to CAPA, Internal Audits, Document Control, Records Management, etc. Maintain QMS documentation; revise and update documentation, assign training based on documentation changes. May interpret Geometric Dimensioning & Tolerance Strong attention to detail, organization, and documentation skills. May verify specified dimensions of product or raw material using verniers, micrometers, CMM, height gages, comparator, scales or other tools. Assists in other areas in support of product conformity. Demonstrates responsibility and accountability for creating a professional, safe, and clean environment evidenced by: being at work on time to perform assigned duties, following the policies of Granite State Manufacturing, always wearing safety glasses in designated areas, maintaining a neat and orderly work area, and following safety practices to prevent errors. Demonstrates commitment to teamwork by establishing effective relationships and networks with both managers/directors and workers and collaborating with them to accomplish shared purposes and goals. Complies with federal and state laws, regulations, specifications and company standards. Abides by GSM Code of Ethics and Business Conduct standards and strictly observes all U.S. and foreign laws and regulations. Requirements QUALIFICATIONS, SKILLS, AND ABILITIES Two-year certification from college or technical school; or ASQ Certified Quality Technician; or 4 years related experience and/or training; or equivalent combination of education and experience. Experience as an inspector or quality technician. Experience working with quality management systems, should know how to interpret Geometric Dimensioning & Tolerance. Must have the ability to work as a team player in a group or team environment and must be able to work independently without supervision. Comfortable using Microsoft Office (Excel, Word, Outlook, PowerPoint) or similar software. Preference for experience in aerospace, defense, other regulated manufacturing environments; experience working with NAVSEA is highly desirable. BENEFICIAL SKILL OR EXPERIENCE Advanced skills in Word and Excel. Strong technical writing skills: ability to create or update procedures and work instructions. Experience operating and setting up CMM's and Faro arms beneficial but not required. Advanced knowledge of inspection, plating and coating processes, and raw materials a plus. A personal and professional background sufficient to secure Government Security Clearance. AAP/EEO STATEMENT Granite State Manufacturing (GSM) is an affirmative action and equal opportunity employer. GSM does not discriminate on the basis of race, color, religion, sex, gender, gender identity or expression, national origin, citizenship, veteran status, age, physical or mental disability, genetic information, marital status, sexual orientation, or any other consideration made unlawful by applicable federal, state, or local laws in its programs, activities, or employment. Benefits Paid time off Floating holidays Paid holidays 401(k) 401(k) company matching Dental & Vision insurance (Company paid) Employee assistance program Flexible spending account Competitive health insurance Health savings account Life insurance Referral program

Manufacturing of therapeutic proteins (API) under cGMP conditions. Associates are expected to execute process recipes, follow written procedures (SOPs), monitor equipment and processes, perform basic laboratory tasks, including pH, conductivity, sampling, and conduct routine sanitization tasks to maintain facility and equipment. They are expected to attain a basic understanding of cGMP compliance while training under close supervision, demonstrating aseptic technique in handling of products and materials. - Set up, operate equipment, and monitor production processes, including clean-in-place (CIP) and steam-in-place (SIP) operations and report production in written and electronic documents in accordance with good manufacturing practice (GMPs) and good documentation procedures (GDPs), review documentation as appropriate. - Perform material movements, transfer raw materials, chemicals into, out of, across the production areas. Skills manufacturing technician, quality control, biology, cell culture, mammalian cell culture, Gmp, Microbiology Top Skills Details manufacturing technician,quality control,biology,cell culture,mammalian cell culture,Gmp,Microbiology Additional Skills & Qualifications Associate's Degree or BS in Life sciences 0+ years experience Detail orientated individuals Experience Level Entry Level Job Type & Location This is a Contract position based out of PORTSMOUTH, NH. Pay and Benefits The pay range for this position is $23.25 - $23.25/hr. Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following: - Medical, dental & vision - Critical Illness, Accident, and Hospital - 401(k) Retirement Plan - Pre-tax and Roth post-tax contributions available - Life Insurance (Voluntary Life & AD&D for the employee and dependents) - Short and long-term disability - Health Spending Account (HSA) - Transportation benefits - Employee Assistance Program - Time Off/Leave (PTO, Vacation or Sick Leave) Workplace Type This is a fully onsite position in PORTSMOUTH,NH. Application Deadline This position is anticipated to close on Feb 2, 2026. About Actalent Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law. If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email actalentaccommodation@actalentservices.com (%20actalentaccommodation@actalentservices.com) for other accommodation options.