Sr. QA Specialist - Supplier Quality
PCI Pharma Services
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.JOB DESCRIPTION:Position Title: Sr. QA Specialist – Supplier QualityLocation: Bedford, New HampshireDepartment: Quality AssuranceReporting To: QA Dir, Quality Systems & ComplianceResponsible For (Staff): NoThis position is part of PCI’s Quality Compliance team responsible for the quality aspects of supplier quality management for suppliers that provide raw materials, components, contract test labs and services for GMP operations. The position is responsible to ensure all aspects of the Supplier Qualification program are successfully executed across all PCI facilities.ESSENTIAL DUTIES AND RESPONSIBILITIES:Responsible for compliance relative to the overall Supplier Qualification Program by performing supplier audits to evaluate compliance to standard operating procedures, quality and regulatory standards and is responsible for creating and issuance of audit reportsResponsible for follow up and tracking of supplier audit observations to assure timely closureMonitor and communicate supplier change notifications and manage supplier non-conformance and complaint handlingResponsible for reviewing all audit responses to assure non-recurrence of deficienciesMaintain, trend, analyze and report quality metrics as it relates to supplier audits and performanceDrafting, review and management of supplier quality assurance agreements (QAA’s) and non-disclosure agreementsProvide support for Quality Council meetingsProvides support during FDA and other regulatory agency inspectionsComplete assignments and works independently without appreciable directionWrites and revises QA Standard Operating Procedures (SOP)Support continuous improvement initiativesPerforms other duties as assigned.QUALIFICATIONS:Required:Bachelor of Science Degree preferred with 15+ years’ in a QA GMP environment; alternatively, Master’s Degree with 10+ years’ experience in a QA GMP environment. (High School diploma with 20+ years’ of progressive experience in QA GMP environment).Exceptional organizational skillsExcellent interpersonal skills and the ability to communicate well orally and in writingProficiency in MS Office including Word, Excel, Access and VisioExcellent verbal and written communication skills requiredExperience with GMP quality systems in a pharmaceutical/biotech/medical device environment is a mustThorough knowledge of FDA regulations (i.e., 21CFR Part 210, 211 & 820) Guidance’s, and ICH is required; EMEA and other agency regulationsPreferred:Auditing certification preferred (i.e., ASQ, CQA or similar)Experience working with cross-functional teams, including giving training and/or presentations to large groupsDetail oriented and a results driven team playerAbility to work in a dynamic, fast paced work environmentHonesty, integrity, respect and courtesy with all colleagues Creative with the ability to work with minimal supervision and balanced with independent thinkingResilient through operational and organizational change#LI-RS1Join us and be part of building the bridge between life changing therapies and patients. Let’s talk futureEqual 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.SummaryLocation: Bedford, NH, USAType: Full time
- ...our global network to pioneer and shape the future of PCI.JOB DESCRIPTION:Position Title: Sr. QA Specialist - Supplier QualityLocation: Bedford, New HampshireDepartment: Quality AssuranceReporting To: QA Dir, Quality Systems & ComplianceResponsible For (Staff): NoThis...QualitySeniorFull timeContract work
- ...the future of PCI.This position is part of PCI’s Quality Compliance team responsible for the quality aspects of supplier quality management for suppliers that provide... ...of Science Degree preferred with 3+ years’ in a QA GMP environment; High School diploma with 5+ years...QualityFull timeContract work
- ...across our global network to pioneer and shape the future of PCI.Job DescriptionPosition Title: QA Specialist II OperationsLocation: Bedford, New HampshireDepartment: Quality AssuranceReporting To: QA Manager / QA DirectorResponsible For (Staff): NoThe QA Specialist II...QualityFull timeWeekend work
- ...building teams across our global network to pioneer and shape the future of PCI.Position Title: QA Specialist II - Document ControlLocation: Bedford, New HampshireDepartment: Quality Assurance, Document ControlReporting To: Supervisor, Document ControlResponsible For (Staff...QualityFull time
- ..., 2026Application Deadline:August 25, 2026Wage Level:SalaryJOB DESCRIPTION:Position Title: QA Specialist II - Ops/Floor SupportLocation: Bedford, New HampshireDepartment: Quality Assurance OperationsReporting To: QA Supervisor or aboveResponsible For (Staff): YesThe QA...QualityFull timeImmediate start
- ...that will play a crucial part in bringing innovative and life changing products to life. Position Summary The Senior Supplier Quality Engineer (Sr. SQE) is responsible for leading supplier quality activities across both New Product Introduction (NPI) and sustaining...QualitySeniorFull timeContract workRemote work
- ...company that will play a crucial part in bringing innovative and life changing products to life. Position Overview: The Supplier Quality Manager is responsible for leading the Supplier Quality Engineering (SQE) function and serving as the management representative...QualityFull timeContract work
- ...position provides senior leadership and strategic direction for Quality Control (QC) operations across the NH Development and... ...robustness, and data integrityProvide strategic oversight for supplier and contract laboratory quality, ensuring appropriate governance...QualitySeniorFull timeContract work
- ...support contracts, and work closely with the Quality and Validation teams to ensure these... ...details and execute to solve problems. The Sr. Automation Engineer possess expertise in... ...s and solicit quotations from automation suppliers.Design the layout of equipment and...QualitySeniorFull time
$132.96k - $226.04k
...Supplier Quality ManagerOur employees work on the world's most advanced electronics – from detecting threats for F-35 pilots to illuminating the night for soldiers. Spanning air, land, sea, and space, we are developing the technology of tomorrow, delivered today. Drawing...QualityFull timeLocal areaWorldwideFlexible hoursNight shift- ...mix, low-to-medium volume production , delivering precision, quality, and on-time performance on custom-engineered products. Our capabilities... ...complex AS9100, NAVSEA, customer, internal, and external (supplier) audits. Reviews and approves final documentation packages....QualitySeniorContract workWork at officeLocal areaFlexible hours
- ...Quality Assurance Associate Are you meticulous, technically-minded, and committed to high standards? Become a quality assurance associate with a highly flexible schedule. We offer short-term mandates in high-quality manufacturing and distribution, allowing you to apply...QualityTemporary workImmediate startFlexible hours
- Gentex Corporation seeks a Sr. Mechanical Engineer for our Defense & Aerospace Engineering & Design team. You will lead mechanical... ...Collaborate closely with electrical, software, manufacturing, and quality teams to ensure innovative, reliable, and cost‑effective designs...QualitySenior
- ...Quality Inspector The Quality Inspector must be a quick-thinking, self-motivated individual with knowledge on all aspects of inspection... ...accurately respond to questions from team members, internal suppliers, and customers. Communicate non-conformances and work with...QualityPermanent employmentShift work
- ...Quality ManagerThe Lead Quality Manager is responsible for the effectiveness of the Quality Management System for the Lincoln facility... ...adherence.Preparing for and leading registrar, customer, internal, supplier, and external audits; ensuring findings are addressed with...Quality
- ...in designing military equipment a plus ABOUT THE JOB! The Sr. Mechanical Engineer will join the New Product Development team... ...tasks. Review designs and models for performance, DFM, DFA, and quality. Apply lean design and six sigma design for manufacturing plastic...QualitySenior
- ...diversified manufacturer with a commitment from our team to proudly provide pure precision solutions to our customers, delivering superior quality, value, and service.Ferrotec (USA) Corporation is a technology company with a worldwide presence in a broad array of end products,...QualitySeniorFull timeTemporary workLive inWork at officeLocal areaRemote workWorldwide
- ...Quality Systems SpecialistDEKA R&D, on behalf of Millyard Advanced Medical Products, is looking for a Quality Systems Specialist to work in a dynamic Medical Device Research and Development environment... ...QMS awareness to non-QA departments throughout DEKASkills...QualityContract workWork at office
- ...including cleanrooms, component preparation, sanitization, filling, and packaging activities.Work closely with Validation, Facilities, Quality, and Project Management teams to ensure operational efficiency and regulatory readiness.Additional ResponsibilitiesSupport audits...QualitySeniorFull time
$159.43k
...make a difference and change the world. Job Description Job Duties: • Develop, implement, and maintain the project-specific Quality Assurance Surveillance Plan (QASP) in compliance with Federal Acquisition Regulations (FAR), Construction Quality Management (CQM)...QualityContract workFor contractorsWork experience placementFor subcontractorH1bImmediate startFlexible hours- ...industrial design, controls, and systems engineers, along with Quality, Regulatory, human factors, safety testing, and external vendors... ...Modeling, selecting materials and processes, interacting with suppliers and manufacturers, and documenting the design input/output, and...QualitySenior
- ...innovative medical device and disposable designs into scalable, high-quality, and regulatory-compliant manufacturing solutions. You’ll work... ...on DFMEA/PFMEA, managing prototype builds, and optimizing supplier strategies, to developing ROI-backed launch plans and driving continuous...QualitySenior
- ...Job Description Job Description Job Description: Quality Manager Location: Manchester, NH Department: Quality Reports... ...provide timely and thorough responses or actions to customers and suppliers. With an expanding facility and increased production volume,...QualityWork experience placement
- ...PROILE: We are currently seeking a Senior Mortgage Operations Specialist to join the Pinnacle Mortgage Corp. team. The Senior Mortgage... ...System (LOS) and supporting platforms. • Support quality control reviews, audits, and regulatory examinations. • Ensure...QualitySeniorFull time
- ...Senior CAD Designer contributes design modifications to improve the quality and function of the product and may be responsible for the... ...other documented information furnished by Design Engineers or from suppliers. Creating drawings by planning arrangement of a product...QualitySenior
- ...Position Summary The Quality System Specialist – CAPA is responsible for supporting and maintaining the Quality Management System (QMS) in compliance with ISO 13485 and applicable regulatory requirements for medical device operations. This role is primarily focused...QualityFull timeWork at office
- ...impact. The Impact That You Will MakeThe Sr. Buyer is critical to the evolution of ARMI... ..., placing orders, tracking status, supplier follow up, invoice reconciliation and order... ...seamless relationship with Operations Support, Quality Assurance, Quality Control, Project...QualitySeniorContract workShift work
- ...best solution based on cost, engineering quality, or availability of materials. Uses historical... ...(accurate) information on prices from suppliers Reviews all pricing with the Director... ...disciplines, cost control systems, and QA/QC. ~ Advanced math and computer skills...QualitySeniorFor subcontractor
- ...Job Description Job Description POSITION SUMMARY The Quality Engineering Manager is responsible for overseeing all manufacturing... ...) per AS9102 requirements. Develop and manage the Approved Supplier List (ASL). Conduct supplier audits and performance evaluations...QualityFlexible hours
- ...Supplier Quality EngineerThe Supplier Quality Engineer is responsible for leading supplier quality activities during design transfer and process/product validation. This role ensures supplier compliance to applicable requirements, including 21CFR, ISO 13485, and drives...QualityContract work
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