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
- ...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
- Travere Therapeutics is seeking a Senior Specialist in Quality Assurance Technical to support qualification/validation activities for solid oral... ...from vendors meet Travere standards. A strong background in GMP QA, QMS, and regulatory knowledge is essential for success. #J-...QualitySeniorRemote job
$95k - $124k
Department: 107100 Quality Location: San Diego, USA- Remote Be a part of a global team that is inspired to make a difference in the... ...Auditing is responsible for executing GMP and GDP audits, supporting supplier qualification, compliance oversight, and inspection readiness...QualitySeniorContract workTemporary workRemote work- ...Senior Supplier Quality Engineer The Senior Supplier Quality Engineer (Sr. SQE) is responsible for leading supplier quality activities across both New Product Introduction (NPI) and sustaining manufacturing operations. This role ensures supplier compliance to applicable...QualitySeniorContract workRemote work
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- ...QA Specialist Compliance Life changing therapies. Global impact. Bridge to thousands of biopharma companies and their patients. Our... ...and shape the future of PCI. Reporting to the Director of Quality Systems & Compliance, the QA Specialist Compliance is responsible...QualityWeekend work
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- ...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
- Travere Therapeutics in San Diego, CA, seeks a Senior Quality Assurance Associate - GMP/GDP Auditing to execute audits, support supplier qualification, and drive inspection readiness across our external partner network. This role partners with Technical Operations, Supply...QualitySeniorRemote job
- ...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
$95k - $124k
Department: 107100 Quality Location: San Diego, USA- Remote Be a... ...Position Summary The Senior Specialist, Quality Assurance Technical,... ...Change Controls related to supplier changes Manufacturing and Laboratory... ...job performance. Support QA with various technical...QualitySeniorContract workTemporary workInterim roleRemote work- ...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
- ...transforming innovative medical device 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
- ...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
- ...allocation in complex products(acoustic) • Provide project support to resolve issues, reduce program risk, and facilitate the delivery of quality products to our customers • Prepare and present technical briefings to peers, management, and customer community. • Align key...QualitySeniorFull time
- ...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
- ...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
- ...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
- ...facilities. This position is location flexible in the U.S. You'll provide design work, contribute to team technical collaboration, perform quality reviews of design packages, and assist directly with other portions of the design process. You may also interact directly with the...QualitySeniorFor contractorsWork at officeFlexible hours
- ...vendors, size and select equipment, and preparing construction design packages. You'll be accountable for the schedule and technical quality of challenging engineering tasks as you gain familiarity with the client's expectations, scope, budget, and schedule. You'll work...QualitySeniorRemote work
- ...united by a unique culture and commitment to provide the highest quality products to those who serve. POSITION PROFILE: The... ...variety of product platforms. Routinely interact with vendors / suppliers and demonstrate awareness of industry resources/ standards...QualitySeniorPermanent employmentTemporary workRemote work
- ...The Impact That You Will Make The Sr. Buyer is critical to the evolution of ARMI... ...requests, placing orders, tracking status, supplier follow up, invoice reconciliation and order... ...relationship with Operations Support, Quality Assurance, Quality Control, Project Management...QualitySeniorContract workShift work
- ...manufacturing process and equipment improvements to advance safety, quality, delivery, and efficiency. Design tooling, fixtures, and... ...Specify and procure new capital equipment working with outside suppliers. Lead projects and solve complex problems in a dynamic team...QualitySeniorWork at office
- ...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...QualitySenior
- ...PROILE: We are currently seeking a Senior Mortgage Operations Specialist to join the Pinnacle Mortgage Corp. team. The Senior Mortgage... ...Loan Origination System (LOS) and supporting platforms. Support quality control reviews, audits, and regulatory examinations. Ensure...QualitySeniorFull time
$77.1k - $100.2k
...content creation, and production. Review new and existing content and update plans against the editorial team strategy, Cengage's quality learning standards, research-based insights, and established protocols. Ensure alignment, consistency, and appropriateness across...QualitySeniorFull timeWork experience placementFreelanceLive inWork at officeLocal areaRemote workWorldwide- ...with a unique combination of skill + passion. If you have the qualities and drive to lead yourself or teams, there are roles ready to... ...compliance, inbound receipts, kitting, processing orders, procuring suppliers, managing inventory, staffing, facility inspections, employee...QualitySeniorPermanent employment
- ...behalf of Millyard Advanced Medical Products, is looking for a Quality Systems Specialis t to work in a dynamic Medical Device Research... ...training as required to DEKA personnel Promote QMS awareness to non-QA departments throughout DEKA Skills needed to be successful: 2+...QualityContract workWork at office
$88k - $132k
...Accounting teams. This role partners closely with IT to ensure data quality, integrity, and seamless integration across Salesforce CPQ,... ...implement solutions Participate in all stages of the SDLC, including QA and UAT, for Zuora-related changes and dependent system impacts...QualitySeniorRemote workHome office
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