Unknown Company

Associate Director, Quality Assurance

pa • Posted 1 weeks ago
Onsite Contract Quality Management & Operations

Primary Responsibilities:

  • Facilitate communication and alignment with key stakeholders.
  • Execute and close global GLP QA audit activities (domestic/international sites and contract facilities) and ensure compliance with FDA GLP/OECD guidance, company policies, procedures, and QA SOPs.
  • Conduct GLP and regulated Bioanalysis/Bioequivalence/Vaccine Clinical Assay audits using QA risk-based processes.
  • Lead liaison for QA activities supporting regulated work across sites.
  • Independently function as a lead auditor; provide regulatory perspective/quality advice.
  • Plan, prioritize, schedule, monitor, document/track audits/inspections, ensure timely resolution of findings, and report findings to appropriate personnel.
  • Maintain expertise in applicable worldwide regulations; interpret and distribute regulatory guidance as needed.
  • Develop and deliver compliance training; mentor less experienced QA staff; participate in committees.
  • Manage multiple/moderately complex projects; lead escalation and support CAPA/root-cause assessment.
  • Serve as key point person for inspection management; represent GLP QA/QA on cross-functional teams.

Education:

  • Bachelor’s degree in an appropriate Science, IT, or Engineering discipline.

Required:

  • 8+ years of audit experience in regulated pharma/biopharma/biologics.
  • Extensive FDA and OECD GLP knowledge; experience leading audits.
  • Leadership; cross-functional teamwork; electronic quality systems experience.
  • Strong attention to detail; Microsoft PowerPoint/Excel/Word; excellent written/verbal communication; manage competing priorities.

Preferred:

  • Experience with Pristima, electronic laboratory notebooks, Veeva, LIMS, Empower.
  • Experience leading/supporting US/EU health authority inspections.
  • Superior collaboration.

Skills:

  • Audit Management, Collaborative Leadership, Project Leadership, Quality Assurance Systems, Quality Oversight, Regulatory Compliance

Benefits (explicitly stated):

  • Medical/dental/vision insurance, retirement (401(k)), paid holidays/vacation, compassionate and sick days.

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Associate Director, Quality Assurance in pa at Unknown Company

This position is listed as contract and onsite.

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