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PCI Pharma Services

Pharmaceutical packaging and contract services

QA Specialist 1 - Supplier Quality

Regulatory & Quality (Life Sciences)Confirmed live in the last 24 hours
Full-timeBedford, NH, USANo salary listed

About the Job

Requirements

  • A Bachelor of Science degree is preferred, along with 3 or more years of experience in a quality assurance good manufacturing practice environment; a high school diploma with 5 or more years of progressive quality assurance good manufacturing practice experience is also considered.
  • Ability to articulate and comprehend industry-related technical subject matter.
  • Proficiency in Microsoft Office, including Word and Excel.
  • Experience with good manufacturing practice quality systems in a pharmaceutical, biotechnology, or medical device environment is preferred.
  • Familiarity with regulatory guidance, including FDA 21 CFR Parts 210, 211, and 820; the European Medicines Agency; and the International Council for Harmonisation is preferred.
  • Experience working with cross-functional teams.
  • Ability to maintain organization of assigned tasks and meet deadlines.
  • Ability to think strategically and tactically.
  • Frequent reading, writing, and verbal communication.
  • Ability to work in a highly complex and regulated environment.
  • Ability to translate ideas into concepts and processes.

Responsibilities

  • Follow up on and track supplier audit observations to ensure timely closure.
  • Monitor and communicate supplier change notifications, and manage supplier non-conformance and complaint handling.
  • Review audit responses to assure non-recurrence of deficiencies.
  • Draft, review, and manage supplier quality assurance agreements and non-disclosure agreements.
  • Collaborate with Corporate Supplier Quality team members to align on Supplier Qualification program initiatives and report the status of site-specific Supplier Qualification actions.
  • Support Supplier Risk Assessments.
  • Support Annual Product Quality Reviews.
  • Support Quality System events impacting the Supplier Quality program.
  • Request, reconcile, and file Supplier Qualification documentation.
  • Provide support for Quality Council meetings.
  • Write and revise Standard Operating Procedures.
  • Support continuous improvement initiatives.
  • Perform other duties as assigned.

Desired Qualifications

  • Bachelor of Science degree.
  • Experience with good manufacturing practice quality systems in a pharmaceutical, biotechnology, or medical device environment.
  • Familiarity with regulatory guidance, including FDA 21 CFR Parts 210, 211, and 820; the European Medicines Agency; and the International Council for Harmonisation.

About the Company

PCI Pharma Services

Pharmaceutical packaging and contract services

PCI Pharma Services provides end-to-end pharmaceutical packaging and related services, including folding cartons, labels, contract packaging, clinical services, and brand protection, acting as a one-stop source for healthcare product development and commercialization. It handles packaging operations from cartons and labels to contract packaging and labeling, plus clinical packaging and brand protection, with processes built on cGMP and ISO compliance, lean manufacturing, and ongoing R&D, supported by mandatory training and strict security, hygiene, and inspections. It differentiates itself with eight decades of experience and a broad, integrated service suite under one roof, reducing risk and handoffs for clients. Its goal is to be a trusted packaging partner that delivers reliable, compliant, and scalable solutions so healthcare brands stay protected and clients can focus on their core business.

Company size
1-10
Company stage
Debt Financing
Total funding
$4B
Headquarters
Burlington, Canada
Founded
1971

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