NewFM Approvals Engineering Quality Auditor II FMFM Approvals Engineering Quality Auditor IINorwood, MA$74,080–$106,500The role of the Quality Auditor is expected to independently schedule and conduct conformity assessment audits at customer locations. This role will support a team of dedicated auditors who focus on conducting customer at location on-site compliance audits.
NewQuality Assurance Tech ManpowerQuality Assurance TechFall River, MAOur specialized recruiting teams assess and guide talent into meaningful, sustainable employment, while our PowerSuite technology enables deeper insight and smarter matching, helping candidates find opportunities that align with their strengths, experience, and career goals. Manpower® is a global leader in contingent staffing and permanent resourcing, providing companies with strategic and operational flexibility and creating talent at scale.
Senior Engineer, Central Quality & Quality Control | Titleist Acushnet Holdings CorpSenior Engineer, Central Quality & Quality Control | TitleistNew Bedford, MA$107,896–$134,765 / yearPartnering cross-functionally with Manufacturing, R&D, Supply Chain, and external suppliers, the Senior Engineer provides technical expertise in root cause analysis, corrective and preventive actions, and new product introductions. The Senior Engineer, Central Quality & Quality Control plays a critical role in driving excellence across manufacturing operations and supplier networks by ensuring consistent product performance and compliance with Acushnet Company Quality System requirements.
NewSenior Engineer, Central Quality & Quality Control | Titleist TwiceSenior Engineer, Central Quality & Quality Control | TitleistNew Bedford, MA$107,896–$134,765 / yearWhat You BringBachelor's degree in engineering, Chemistry, or closely related field requiredASQ Certified Quality Engineer (CQE) certification preferredMinimum of 5 years in manufacturing and/or Quality EngineeringDemonstrated ability to manage projects independentlyKnowledge of ISO 9001 Quality Systems preferredSupervisory experience preferredAbility to work in industrial and golf course environmentsCapable of lifting up to 40 pounds and standing for extended periodsGood or corrected vision, including accurate color perceptionValid driver's license requiredAbility to travel, occasionally on short noticeFamiliarity with Acushnet Company Safety Policies and PracticesKnowledge of Hazardous Waste Compliance policies and practicesOur Commitment to YouAt Acushnet Company, we are committed to helping our associates thrive both personally and professionally. Partnering cross‑functionally with Manufacturing, R&D, Supply Chain, and external suppliers, the Senior Engineer provides technical expertise in root cause analysis, corrective and preventive actions, and new product introductions.
Senior Engineer, Central Quality & Quality Control | Titleist Acushnet CompanySenior Engineer, Central Quality & Quality Control | TitleistNew Bedford, MassachusettsPartnering cross-functionally with Manufacturing, R&D, Supply Chain, and external suppliers, the Senior Engineer provides technical expertise in root cause analysis, corrective and preventive actions, and new product introductions. The Senior Engineer, Central Quality & Quality Control plays a critical role in driving excellence across manufacturing operations and supplier networks by ensuring consistent product performance and compliance with Acushnet Company Quality System requirements.
Director, Quality Control Oruka TherapeuticsDirector, Quality ControlWaltham, CaliforniaThe Director, Quality Control – Combination Products will provide strategic and operational leadership for the Quality Control function supporting late-stage clinical development, analytical testing oversight for clinical drug substance and drug product, process performance qualification (PPQ), regulatory submissions, and commercial launch readiness for monoclonal antibody drug products and combination products, including pre-filled syringes and autoinjectors. Strong knowledge of cGMP regulations and global regulatory expectations, including 21 CFR Parts 210, 211, and 4. Hands-on experience supporting combination products such as pre-filled syringes, autoinjectors, or related delivery systems.
Associate Director, Quality Control Technical Services Beam TherapeuticsAssociate Director, Quality Control Technical ServicesCambridge, MA$185,000–$225,000 / yearThe successful candidate will work cross‑functionally with Analytical Research & Development, Bioprocess Development, Manufacturing Technical Services, Manufacturing Operations, Regulatory Affairs, and Quality Assurance to drive the transfer, qualification, validation, and lifecycle management of analytical methods for gene‑edited cell therapy products and associated critical materials (e.g., mRNA). In addition, this position will contribute directly to regulatory filings, including specifications, analytical method validation reports, and CMC documentation, and will serve as a QC technical subject matter expert across program teams to ensure compliant, robust, and phase‑appropriate analytical strategies.
Senior Scientist I, Quality Control Candel Therapeutics IncSenior Scientist I, Quality ControlNeedham, MAThis position collaborates with external manufacturing and tech transfer and is focused on Adenovirus and Herpesvirus vectors, associated cell-based potency assays, as well as performing training of new technical staff and troubleshooting and validation of new and established assays. A strong background in one or more analytical techniques such as various HPLC based methods, microplate UV/Vis/Luminescent assays, cell-based assays including virus quantification and potency, qPCR, electrophoresis, sizing techniques such as DLS, etc.
Scientist I, Analytical Development and Quality Control Kailera TherapeuticsScientist I, Analytical Development and Quality ControlWaltham, MassachusettsThe Scientist I, Analytical Development and Quality Control is an experienced scientist within the Analytical Development and Quality Control (AD/QC) organization, with a primary focus on analytical quality control, method validations, stability programs, and data integrity. Evaluate temperature excursions for stability and release samples, assessing potential impact on product quality using scientific judgment, stability data, and relevant regulatory/technical guidance.
Associate Director, Quality Control Technical Services Beam Therapeutics IncAssociate Director, Quality Control Technical ServicesCambridge, MA$185,000–$225,000 / yearThe successful candidate will work cross‑functionally with Analytical Research & Development, Bioprocess Development, Manufacturing Technical Services, Manufacturing Operations, Regulatory Affairs, and Quality Assurance to drive the transfer, qualification, validation, and lifecycle management of analytical methods for gene‑edited cell therapy products and associated critical materials (e.g., mRNA). Primary Responsibilities: Lead and influence QC CMC strategy in partnership with cross‑functional CMC teams for master cell banks (MCBs), plasmids, and mRNA drug substance and critical materials, supporting both ex vivo and in vivo therapy programs across development and commercialization.
Quality Control Analyst- GAS Operations Eversource EnergyQuality Control Analyst- GAS OperationsMA$95,600–$106,220 / yearn* This role works in an environment that often requires the performance of multiple simultaneous activities, where deadlines need to be met and work is performed under pressure while involving significant business commitments and results.\n \nPlease submit a resume with your application.\n \n#gasajd\n \n#LI-ES3\n \nCompetencies:\n \nBuild trusting relationships\n \nManage and develop people\n \nFoster teamwork and cross-functional collaboration\n \nLead change\n \nCommunicate strategic vision\n \nCreate an engaged workforce\n \nFocus on the customer\n \nTake ownership & accountability\n \nCompensation and Benefits: \n \nEversource offers a competitive total rewards program. This includes, but is not limited to, direct company sponsorship, listing Eversource as the employer of record on immigration documents, or any work authorization that requires company involvement or documentation (e.g., H-1B, OPT, STEM OPT, CPT, TN, J-1, O-1, etc.).\n \nRole and Scope of Position:\n \nSupports the implementation, of the Eversource Quality Control (QC) program as it relates to any of the following construction, maintenance, meter service, leak survey, corrosion, damage prevention, LNG and I&R activities at Eversource Gas.
Quality Control Engineer III Hybrid - Boston, MA Cohen Ventures IncQuality Control Engineer III Hybrid - Boston, MABoston, MA$108,000–$118,000 / yearYou will partner dynamically with engineering teams to supercharge test coverage and ensure flawless delivery, while serving as an inspiring technical mentor and peer trainer who elevates junior engineers through hands-on coaching. If you are a seasoned pro with sharp automation skills who can develop automated UI tests with minimal ramp-up and a passion for driving long-term process evolution, we want you to lead the charge in our quality revolution.
Director, Quality Control Emergent BioSolutions IncDirector, Quality ControlCanton, MA$196,000–$237,100 / yearUnsolicited resumes or candidate information submitted to Emergent BioSolutions by search/recruiting agencies not already on Emergent BioSolutions' approved agency list shall become the property of Emergent BioSolutions and if the candidate is subsequently hired by Emergent BioSolutions, Emergent BioSolutions shall not owe any fee to the submitting agency. This role provides strategic and operational leadership for QC laboratories supporting raw materials, in‑process, release, stability, microbiology, environmental monitoring, and sterility assurance activities, ensuring continuous compliance with FDA, EMA, WHO, and global regulatory expectations.
Quality Control Inspector Tech EtchQuality Control InspectorPlymouth, MA$17.50–$25 / hourABOUT THE JOB The Quality Control Inspector conducts in-process inspection sampling of manufactured parts, incoming inspection on parts and supplies used for the manufacture of products, First Article Inspection, and final product verification. WHO WE ARE Founded in 1964, Tech Etch specializes in manufacturing precision-engineered components and flexible printed circuits in the Aerospace and Defense, Medical Devices, and Electronics and Telecommunications industries.
Director, Clinical Quality Control Disc Medicine IncDirector, Clinical Quality ControlMA$198,000–$242,000 / yearAct as the team leader to ensure alignment and effective communication among cross-functional areas, including analytical development, process development, formulation development, manufacturing, supply chain, regulatory, quality assurance, and other internal and external partners. Ability to work both independently and collaboratively with project teams and cross-functionally, to build productive relationships with internal and external partners, to influence decision-making, and to engage in conflict resolution.
Quality Control (QC) Chemist Inhalation Products (MDI Focus) Aequor Technologies LLCQuality Control (QC) Chemist Inhalation Products (MDI Focus)Fall River, MA$65,000–$105,000 / yearAs a QC Chemist specializing in inhalation products, you’ll play a vital role in ensuring the safety, quality, and performance of metered dose inhalers (MDIs) and related dosage forms that patients rely on every day. This is not your average QC role—here, you’ll work on complex aerosol and particle-based delivery systems, applying advanced analytical techniques to confirm product integrity and regulatory compliance in a highly controlled cGMP environment.
Associate Director, Analytical Development & Clinical Quality Control Disc Medicine IncAssociate Director, Analytical Development & Clinical Quality ControlMA$158,000–$193,000 / yearAct as the team leader to ensure alignment and effective communication among cross-functional areas, including analytical development, process development, formulation development, manufacturing, supply chain, regulatory, quality assurance, and other internal and external partners. Ability to work both independently and collaboratively with project teams and cross-functionally, to build productive relationships with internal and external partners, to influence decision-making, and to engage in conflict resolution.
Director, Quality Control Dyne Therapeutics IncDirector, Quality ControlWaltham, MA$190,000–$230,000 / yearRole Summary: The Director, Quality Control leads global Quality Control activities, including oversight of external laboratories supporting analytical testing, release, and stability programs across clinical and commercial stages. The company is advancing clinical programs for Duchenne muscular dystrophy (DMD) and myotonic dystrophy type 1 (DM1) as well as a preclinical programs for facioscapulohumeral muscular dystrophy (FSHD) and Pompe disease.
Director, Quality Control Oruka Therapeutics IncDirector, Quality ControlWaltham, MA$213,000–$240,000 / yearRole Overview: The Director, Quality Control - Combination Products will provide strategic and operational leadership for the Quality Control function supporting late-stage clinical development, analytical testing oversight for clinical drug substance and drug product, process performance qualification (PPQ), regulatory submissions, and commercial launch readiness for monoclonal antibody drug products and combination products, including pre-filled syringes and autoinjectors. Strong knowledge of cGMP regulations and global regulatory expectations, including 21 CFR Parts 210, 211, and 4. Hands-on experience supporting combination products such as pre-filled syringes, autoinjectors, or related delivery systems.
Senior Scientist, CMC Quality Control City TherapeuticsSenior Scientist, CMC Quality ControlCambridge, MassachusettsThe current focus will be on release and stability management of oligonucleotide drug substances, drug products, and process intermediates (e.g., siRNA and conjugates). Your actual base salary will be based on several factors, including relevant skills, experience, internal equity, relevant education or training and market dynamics.
Senior / Executive Director, Analytical Sciences & Quality Control Arrivent Biopharma IncSenior / Executive Director, Analytical Sciences & Quality ControlMAThis role will lead Analytical Sciences and Quality Control across small molecule and large molecule programs, supporting development from early-stage through commercialization, with a focus on late-stage ADC assets. You will own end-to-end analytical strategies, including product characterization, control strategy, and method lifecycle management, ensuring readiness for global regulatory submissions and commercial supply.
Scientist/Senior Scientist, Analytical Development and Quality Control Terrestrial Bio IncScientist/Senior Scientist, Analytical Development and Quality ControlCambridge, MAScientist/Senior Scientist, Analytical Development and Quality Control - Vaxess Technologies Inc.
Quality Control Laboratory Specialist (Hematology) American Red Cross Blood ServicesQuality Control Laboratory Specialist (Hematology)Dedham, MA$2.25–$5 / hourAmeriCorps, the federal agency that brings people together through service, and its partners - the Peace Corps, AmeriCorps Alums, National Peace Corps Association, and the Service Year Alliance - launched Employers of National Service to connect national service alumni with opportunities in the workforce. Key Responsibilities: Perform moderate to high complexity laboratory testing procedures and interpret various testing procedures on donor specimens, and blood products; Identify and quarantine products/samples that don't meet quality requirements.
Sr. Director Global Quality Control Scholar Rock Holding CorpSr. Director Global Quality ControlCambridge, MA$245,000–$335,000 / yearProvide strategic oversight of stability programs, including protocol design, pull schedule governance, data review, and trending, shelf-life support, comparability assessments, and post-approval stability commitments. Lead the companys global QC function across a fully outsourced model with end-to-end oversight of external QC laboratories, CMOs, and other testing partners supporting clinical and commercial programs.
Director, Quality Control Sebela PharmaceuticalsDirector, Quality ControlHolbrook, MassachusettsThis position is responsible for leading Quality Controls Laboratory operations at the Holbrook site including the development, implementation and maintenance of quality control systems and activities to support commercial manufacturing and new product introductions. Strong organizational, prioritization, and time management skills, coupled with strong critical-thinking abilities to evaluate complex challenges, solve problems effectively, and drive continuous improvement.
Senior Scientist I, Quality Control Candel TherapeuticsSenior Scientist I, Quality ControlNeedham, MAFull timeThis position collaborates with external manufacturing and tech transfer and is focused on Adenovirus and Herpesvirus vectors, associated cell-based potency assays, as well as performing training of new technical staff and troubleshooting and validation of new and established assays. A strong background in one or more analytical techniques such as various HPLC based methods, microplate UV/Vis/Luminescent assays, cell-based assays including virus quantification and potency, qPCR, electrophoresis, sizing techniques such as DLS, etc. .
Quality Control Inspector (Braintree, MA) Consolidated Precision ProductsQuality Control Inspector (Braintree, MA)Braintree, MAFull timecomponents and sub-assemblies, supplying the commercial aerospace, military, and industrial markets with small-to-large "function critical" products. CPP provides its customers with a "total solution" source, taking them from concept to finished product with one of the broadest and most diverse product offerings in the industry.
Quality Control Inspector Consolidated Precision ProductsQuality Control InspectorBraintree, MAcomponents and sub-assemblies, supplying the commercial aerospace, military, and industrial markets with small-to-large “function critical” products. CPP provides its customers with a “total solution” source, taking them from concept to finished product with one of the broadest and most diverse product offerings in the industry.
NewQuality Control Inspector WP CPP Holdings LLCQuality Control InspectorBraintree, MAcomponents and sub-assemblies, supplying the commercial aerospace, military, and industrial markets with small-to-large "function critical" products. CPP provides its customers with a "total solution" source, taking them from concept to finished product with one of the broadest and most diverse product offerings in the industry.
Quality Control Technician North Coast SeafoodsQuality Control TechnicianBoston, MAThe QC Technician will participate in the inspection and grading of Grade-A products, perform moisture analysis, produce written reports, verify inventory, quality, and usability of products. They will test products across three stages of production (before, in-process, and final) to ensure that the final product is safe to release for sale or distribution and report findings back to management.
Quality Control (QC) Chemist Cipla LtdQuality Control (QC) ChemistFall River, MA$65,000–$105,000 / yearAbout InvaGen Pharmaceuticals, a Cipla subsidiary InvaGen Pharmaceuticals, Inc. is engaged in the development, manufacture, marketing, and distribution of generic prescription medicines with focus on a range of therapeutic areas, including cardiovascular, anti-infective, CNS, anti-inflammatory, anti-diabetic, and anti-depressants. Over the last eight decades, we have strengthened our leadership in India's pharmaceutical industry and fortified our promise of strengthening our global focus by consolidating and deepening our presence in the key markets of India, South Africa, the U.S., and other economies of the emerging world.
Quality Control Technician Prysmian SpAQuality Control TechnicianTaunton, MAWith Diversity, Equity, and Inclusion (DE&I) as part of our Social Ambition 2030 and a strategic pillar of our Company culture, Prysmian is committed to the development of an organization that prioritizes talent, where people feel respected, included, and free to fully express their potential just as they are. Prysmian is the world leader in solutions for energy and digital connections, developing resilient, high-performing, sustainable, and innovative cable systems for the transmission, power grid, electricity and digital solutions.
Quality Control Lab Tech Amrize LtdQuality Control Lab TechRockland, MAWe're seeking a Quality Control Lab Tech who's ready to be part of a company committed to formulating everyday success for every customer through innovative, reliable products used to adhere, seal, and protect at every level of the building envelope. Personal ability to be comfortable in the Quality role knowing that you are responsible for presenting accurate data and are not authorized to make decisions on the disposition of nonconforming product.
Contractor, Manager Quality Control StratAcuity Staffing Partners IncContractor, Manager Quality ControlWaltham, MA$75–$82 / hourIn terms of professional development, Everforth Apex hosts an on-demand training program, provides access to certification prep and a library of technical and leadership courses/books/seminars once you have 6+ months of tenure, and certification discounts and other perks to associations that include CompTIA and IIBA. Everforth Apex also offers a HSA (Health Savings Account on the HDHP plan), a SupportLinc Employee Assistance Program (EAP) with up to 8 free counseling sessions, a corporate discount savings program and other discounts.
New3rd Shift - Quality Control Sr. Associate/Sr. Specialist (contract) 29622 Vertex Pharmaceuticals3rd Shift - Quality Control Sr. Associate/Sr. Specialist (contract) 29622Boston, Massachusetts$42–$52 / hourFull timeAgreeing to the Atrium Terms and Conditions, includes permission to use the email address and mobile phone number you provide during the application process or throughout the duration of your prospective or actual employment to notify you of job openings, profiles, articles, news, and other employment-related information, as well as to notify you of special promotions or additional products and services offered by us or our affiliates and partners. Job Description: The Vertex Cell and Gene Therapy (C>) Quality Control (QC) team is responsible for the routine testing of samples and associated workflows for our internally manufactured stem-cell based T1D and genetically modified Casgevy programs.
2nd Shift - Quality Control Sr. Associate/Sr. Specialist (contract) 29531` Vertex Pharmaceuticals2nd Shift - Quality Control Sr. Associate/Sr. Specialist (contract) 29531`Boston, Massachusetts$40–$44 / hourFull timeAgreeing to the Atrium Terms and Conditions, includes permission to use the email address and mobile phone number you provide during the application process or throughout the duration of your prospective or actual employment to notify you of job openings, profiles, articles, news, and other employment-related information, as well as to notify you of special promotions or additional products and services offered by us or our affiliates and partners. Job Description: The Vertex Cell and Gene Therapy (C>) Quality Control (QC) team is responsible for the routine testing of samples and associated workflows for our internally manufactured stem-cell based T1D and genetically modified Casgevy programs.
Senior Director, Quality Control Solid Biosciences IncSenior Director, Quality ControlMA$245,878–$262,676 / yearSolid Biosciences is a precision genetic medicine company focused on advancing a portfolio of gene therapy candidates targeting rare neuromuscular and cardiac diseases, including Duchenne muscular dystrophy (Duchenne), Friedreich's ataxia (FA), catecholaminergic polymorphic ventricular tachycardia (CPVT), TNNT2-mediated dilated cardiomyopathy, BAG3-mediated dilated cardiomyopathy, and additional fatal, genetic cardiac diseases. The ideal candidate has direct experience in preparation and execution of a QC strategy for registrational stage programs (PPQ/BLA readiness), demonstrated success as a people manager, and a solid technical background, including hands-on experience leading and supporting assay qualification/validation of analytical methods, tech transfer, comparability studies, quality systems, regulatory filings and CMC activities.
Quality Control Whirlpool CorpQuality ControlFall River, MAThis role involves performing hands-on, detailed inspections, testing, and visual audits of products and components, leading root cause analysis of quality issues, managing rework operations and field service activities, and maintaining critical quality documentation like Control Plans. Manages post-production quality assurance and rework, including providing guidance for the Rework Crew, processing hold orders (tracking, closing, editing) in systems like QIM/SAP, and performing safe launch testing of new models.
Quality Control Microbiologist RD PartnersQuality Control MicrobiologistNorton, Massachusetts£74,880–£93,600Perform routine/non-routine analytical (HPLC/UPLC) and/or microbiological assays for raw materials, in-process samples, product release, and stability studies following SOPs. R&D Partners is a global functional service provider and strategic staffing resource specializing in scientific, clinical research & engineering.
Quality Control Senior Associate (Contract) 28655 Vertex PharmaceuticalsQuality Control Senior Associate (Contract) 28655Boston, Massachusetts$35–$37 / hourFull timeAgreeing to the Atrium Terms and Conditions, includes permission to use the email address and mobile phone number you provide during the application process or throughout the duration of your prospective or actual employment to notify you of job openings, profiles, articles, news, and other employment-related information, as well as to notify you of special promotions or additional products and services offered by us or our affiliates and partners. Typical test methods performed include flow cytometry, qPCR (MycoTOOL), ELISA, cell counts, sterility (BACT), gram stain and endotoxin (LAL) testing.
Associate Director, Analytical Development and Quality Control Kailera Therapeutics, Inc.Associate Director, Analytical Development and Quality ControlWaltham, MassachusettsThe individual will provide technical expertise and will work closely with cross-functional stakeholders to ensure end-to-end drug development and manufacturing activities are executed seamlessly and in alignment with the company’s integrated development plans and program timelines. Maintain current knowledge in analytical methods and control strategies supporting a variety of molecule platforms and dosage forms.
Quality Control Inspector nex MasTec IncQuality Control Inspector nexMAWith a genesis in construction and a skilled team of multidiscipline engineers and project management professionals, the company delivers best-in-class infrastructure solutions, including design, asset integrity management, feasibility studies, surveys, constructability reviews, turnkey delivery services, and more. Physical Demands and Work Environment This position may require significant time standing or walking on uneven ground, possible climbing of ladders or being in high places, working in tight spaces, lifting up to 50 pounds, and, in general, being overall physically demanding.
Quality Control Inspector Review and Release Nova Biomedical CorpQuality Control Inspector Review and ReleaseWaltham, MA$22–$29 / hourThe physical requirements for this role include: • Ability to pay attention to detail • Ability to multi-task • Math skills and ability to use a calculator • Basic to advanced computer knowledge and use • Ability to follow written protocols or procedures in the execution of daily assigned work and working in a Quality System Regulated (QSR) FDA regulated industry. You will be self-motivated and responsible for performing the following tasks: • Real Time Inspection of the Reagent Department filling and packaging • Review of Device History Records (DHR) • Inspection of labels / final products • Performance of line clearances • Processing of Non-Conforming Materials in support of Manufacturing's schedule.
Director, Quality Control TScan TherapeuticsDirector, Quality ControlWaltham, MA$210,000–$220,000 / yearThe submission of unsolicited resumes by recruitment or staffing agencies to TScan Therapeutics or its employees is strictly prohibited unless contacted directly by TScan Therapeutics’ internal Talent Acquisition team. Reporting to the Associate Vice President of QC and AD, the ideal candidate should have relevant experience in compendial, cellular, molecular, and environmental monitoring in a cGMP facility, and enjoy fast-paced, collaborative, and vibrant culture.
Principal Business Consultant - Quality Control Veeva Systems IncPrincipal Business Consultant - Quality ControlBoston, MA$120,000–$250,000 / yearYou will focus on transforming our customer's laboratory network with Veeva's disruptive LIMS software, including reshaping operating models, driving organizational change, and measuring tangible business value. As a Principal Business Consultant focused on Quality Control in our Quality Practice, you will help customers bring treatments to patients faster by transforming how they work with Technology, Data, and AI.
Quality Control Technician CRH AmericasQuality Control TechnicianAcushnet, MA$23–$25 / hourOur modern facilities, veteran paving crews, experienced construction management team and large investment in plants and equipment make us one of the largest and most efficient producers in the state of Massachusetts as well as one of only two RIDOT approved stone suppliers in the state of Rhode Island. Responsible for collecting, measuring and testing of materials for construction projects including hot mix asphalt, soils sampling, aggregate sampling, core sampling, nuclear density testing, laboratory testing and mix design.
Quality Control Finish Line Staffing ServicesQuality ControlMansfield, MAWe are hiring on behalf of our client for a detail-oriented Quality Control Inspector to support incoming, in-process, and final inspections within a medical device manufacturing environment. Perform incoming, in-process, and final inspections following work instructions and inspection plans.
Director, Quality Control TScan Therapeutics IncDirector, Quality ControlWaltham, MA$210,000–$220,000 / yearThe submission of unsolicited resumes by recruitment or staffing agencies to TScan Therapeutics or its employees is strictly prohibited unless contacted directly by TScan Therapeutics internal Talent Acquisition team. Reporting to the Associate Vice President of QC and AD, the ideal candidate should have relevant experience in compendial, cellular, molecular, and environmental monitoring in a cGMP facility, and enjoy fast-paced, collaborative, and vibrant culture.
Quality Control Lab Technician II Waters CorpQuality Control Lab Technician IITaunton, MAOperating laboratory instruments and software including:Thermogravimetric Analyzer, Carbon/Nitrogen Analyzer, Nitrogen Sorption Analyzer (Surface Area), Density Meter, pH Meter, Automatic Titrator, Moisture Analyzer, Particle Size Analyzer, UV/VIS, Conductivity Meter, ICP‑AES, and other tools used for chromatographic particle analysis. We collaborate with customers around the world to advance the release of effective, high-quality medicines, ensure the safety of food and water, and drive better patient outcomes by detecting diseases earlier, managing routine infections, and combating antibiotic resistance.
Sr Quality Control Lab Technician Waters CorpSr Quality Control Lab TechnicianTaunton, MAConduct testing using instruments such as TGA, Carbon/Nitrogen Analyzer, Surface Area Analyzer (Nitrogen Sorption), Mercury Porosimeter, Density Meter, pH Meter, Automatic Titrator/Moisture Analyzer, Particle Size Analyzer, SEM, UV/VIS, Conductivity Meter, ICP-AES, and other chromatographic particle analysis tools. We collaborate with customers around the world to advance the release of effective, high-quality medicines, ensure the safety of food and water, and drive better patient outcomes by detecting diseases earlier, managing routine infections, and combating antibiotic resistance.