Quality Assurance Manager, Finished Goods

in Healthcare + Life Sciences Contract

Job Detail

  • Experience Level Mid Level
  • Degree Type Bachelor of Science (BS)
  • Employment Contract
  • Working Type Hybrid
  • Job Reference 0000015369
  • Salary Type Hourly
  • Industry Pharmaceuticals
  • Selling Points

    Lead impactful quality assurance initiatives for finished goods operations. Collaborate with global teams in a hybrid work environment. Enhance compliance and operational effectiveness through continuous improvement.

Job Description

Overview

  • Manage quality assurance for commercial finished goods and external manufacturing partners in a hybrid work environment.
  • Ensure compliance with internal standards and regulatory requirements for global commercial supply operations.
  • Collaborate with internal teams and external contract manufacturers to oversee production quality aspects.
  • Review and approve manufacturing documentation, including BOMs, MPRs, and product specifications.
  • Archive manufacturing partner documentation in the client’s document management system.
  • Manage quality records such as deviations, CAPAs, and change controls related to finished goods operations.
  • Identify and recommend continuous improvement opportunities to mitigate risks and enhance operations.
  • Support business needs by maintaining effective quality assurance processes and practices.

Key Responsibilities & Duties

  • Act as QA representative for commercial finished goods and external manufacturing partners.
  • Represent Finished Goods Quality Operations in internal and external meetings.
  • Oversee quality aspects of specifications, validation, and packaging operations at CMOs.
  • Review and approve manufacturing partner and client label and pack documents.
  • Ensure proper archival of manufacturing partner documentation in the document management system.
  • Manage quality records, including deviations, CAPAs, and serialization excursions.
  • Recommend and implement continuous improvement initiatives to support operational effectiveness.
  • Train and lead teams in root cause analysis and effective investigation practices.

Job Requirements

  • Bachelor’s degree in life sciences, engineering, or related field.
  • Minimum of 5 years of experience in pharmaceutical or biopharmaceutical industries.
  • Proficiency in finished goods assembly, labeling, and packaging operations.
  • Strong organizational, communication, and interpersonal skills.
  • Experience managing quality records and ensuring compliance with regulatory standards.
  • Ability to recommend and implement continuous improvement initiatives.
  • Proven ability to lead and train teams in investigation practices.
  • Familiarity with document management systems and quality assurance processes.
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