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
- ...Summary of Objective: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 5+ years’ in a QA GMP environment; High School diploma with 10+...QualityFull 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
- ...PCI Pharma Services seeks a QA Specialist II to oversee supplier qualification and compliance programs across GMP operations. The role involves conducting... ...supplier audits to evaluate compliance with SOPs, quality and regulatory standards Track supplier audit observations...Quality
- ...teams across our global network to pioneer and shape the future of PCI.Position Title: Sr. QA Operations Specialist - Visual InspectionLocation: Bedford, New HampshireDepartment: Quality Assurance,Reporting To: Sr. Director, QualityShift: 1st M-F (8:30am - 5:00pm) The Sr....QualitySeniorFull time
- ...Senior QA Operations Specialist responsible for overseeing visual inspection activities, product sampling, and packaging operations at a pharmaceutical... ...while coordinating with cross-functional teams on quality assurance and continuous improvement initiatives. Responsibilities...QualitySeniorWork at office
- ...teams across our global network to pioneer and shape the future of PCI.JOB DESCRIPTION:Position Title: QA Specialist ILocation: Bedford, New HampshireDepartment: Quality AssuranceReporting To: QA Supervisor, External QAResponsible For (Staff): NoThe QA Specialist will...QualityFull time
- ...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
- ...seeking to commercialize enabling technologies that will grow the industry's impact. The Impact That You Will Make Quality Assurance Specialists/Senior Specialists are critical to our success. In this role, you will support quality system initiatives, ensuring...QualitySeniorWork experience placement
- ...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
- ...our global network to pioneer and shape the future of PCI.Position Title: QA Operations Specialist I - Floor SupportLocation: Bedford, New HampshireDepartment: Quality Assurance,Reporting To: Sr. Director, QualityResponsible For (Staff): NoThe QA Operations Specialist...QualityFull timeImmediate startFlexible hoursShift work
- ...Electrical Engineering EXPERIENCE: • 8+ years of previous experience with quality concepts, metrics and problem-solving methodologies, including but not limited to Supplier Quality, Manufacturing Quality, Auditing, SPC, CAPA processes (internal/supplier/...QualitySeniorFull timeContract workWork at office
$116k - $154k
...Job Description Summary The Senior Supplier Quality Engineer will be responsible for driving quality for assigned suppliers, including quality plan implementation for structural casting suppliers. You will select suppliers through qualification processes, own supplier...QualitySeniorPermanent employmentContract workRemote workRelocation package- Micross in Manchester, NH is seeking a Quality Assurance Technician to support QA administrative tasks, including creating First Article Inspection reports using web systems and Excel, gathering records, and inspecting sample components. You will review Quality Assurance...Quality
- Job Title: Associate Manager, Quality Engineering (Supplier Quality)Job Code: 45370Job Location: Londonderry, NHJob Schedule: 9/80: Employees work 9 out of every 14 days- totaling 80 hours worked- and have every other Friday offJob Description:The Associate Supplier Quality...QualityShift work
- ...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...QualitySeniorContract workRemote work
- ...systems are in an inspection ready state. The Sr. Automation Engineer possesses expertise... ...s and solicit quotations from automation suppliers. Evaluate supplier quotations to... ...have an uncompromising focus on providing quality and operational excellence and providing...QualitySeniorLocal areaShift work
- ...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
- ...QA Specialist I will oversee batch record reviews, lot disposition, and quality system administration for clinical and commercial pharmaceutical products. The role involves deviation management, investigation oversight, CAPA coordination, and cross-functional collaboration...Quality
- ...Quality Assurance Specialist supporting clinical and commercial pharmaceutical manufacturing at a contract manufacturing organization in Bedford,... ...documentation Lead quality improvement projects and serve as QA representative on cross-functional teams Interface with...QualityContract work
- ...PCI Pharma Services seeks a QA Specialist II for Document Control in Bedford, New Hampshire to manage cGMP documentation, procedures, and... ...The role involves coordinating document workflows, maintaining quality management systems, and leading continuous improvement initiatives...Quality
- ...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
- ...Overview PICA Manufacturing Solutions is seeking an experienced Quality Manager to lead and continuously improve our Quality Management... ...ITAR requirements while driving operational excellence through supplier quality, manufacturing quality, customer quality, and...QualityRemote jobFlexible hours
- ...coordination using Navisworks and Revizto. Post deliverables utilizing the Autodesk Construction Cloud (ACC) platform. Assist in model quality checking, digital close-out and asset data encoding for handover. Work with point clouds in design software. Process &...QualitySeniorWork at office
- ...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
- ...better.We're committed to bringing safety, quality, and customer focus to the business of... ...TitleSr. Automation/Controls EngineerAs the Sr Automation/Controls Engineer, you will... ...controls specifications, evaluating equipment suppliers and system integrators, supporting...QualitySeniorFull timeRemote work
- ...experience with hyperscale data center projects ~ Ability to lead teams to deliver commitments on schedule and on budget while meeting quality and client expectations #LI-TD1 Jacobs is an Equal Opportunity/Affirmative Action Employer. All qualified applicants will...QualitySeniorRemote work
- ...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
- ...PCI Pharma Services seeks a QA Operations Specialist I to support visual inspection and final product sampling, packaging, and shipment activities... ...-functional teams, and driving continuous improvement in quality assurance processes. Responsibilities Provide QA...Quality
$26 - $28 per hour
Innova Solutions is seeking a Quality Inspector for a 12-month, full-time contract in Londonderry, NH (on-site). The role involves precision... ...available. Qualified candidates will maintain records, support supplier audits, and collaborate with engineers and program leadership....QualitySeniorFull timeContract workDay shift- ...PCI Pharma Services seeks a QA Operations Specialist II to oversee visual inspection activities, final product sampling, and quality compliance at its Bedford, New Hampshire manufacturing site. The role involves coordinating cross-functional teams, maintaining inspection...QualityWork at office
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