Bristol Myers Squibb logo

Senior Manager, Quality Assurance - Lab Operations

Bristol Myers Squibb
Full-time
Remote friendly (Devens, MA)
United States
Operations

Want to see how your resume matches up to this job? A free trial of our JobsAI will help! With over 2,000 biopharma executives loving it, we think you will too! Try it now — JobsAI.

Role Summary

The Senior Manager, Quality Assurance - Lab Operations oversees QA for GMP laboratory operations, including testing, method validation, and stability programs in a biotech manufacturing environment. Ensures compliance with regulations and internal procedures, maintains data integrity, supports regulatory inspections, and drives continuous improvement across quality control laboratories.

Responsibilities

  • Provide strategic and operational QA oversight for GMP laboratory operations, including QC testing, method validation, and stability studies.
  • Lead QA review and approval of laboratory documentation such as test records, method validation protocols/reports, and stability data.
  • Ensure compliance with cGMP, GLP, and data integrity standards across all lab operations.
  • Collaborate with QC, Analytical Development, and Regulatory Affairs to support product release and regulatory submissions.
  • Manage and mentor a team of QA professionals supporting lab operations.
  • Lead or support investigations related to laboratory deviations, OOS/OOT results, and laboratory incidents.
  • Participate in internal audits and regulatory inspections as a QA representative and subject matter expert.
  • Drive continuous improvement initiatives to enhance lab compliance, efficiency, and quality culture.

Qualifications

  • Experience with electronic laboratory systems (e.g., LIMS, Empower, LabWare).
  • Strong leadership, communication, and interpersonal skills.
  • Ability to manage multiple priorities in a fast-paced environment.
  • Experience supporting regulatory inspections (FDA, EMA, etc.).
  • Bachelor's or Master's degree in Life Sciences, Chemistry, or a related field.
  • 8+ years of experience in Quality Assurance or Quality Control in a GMP-regulated biotech or pharmaceutical environment.
  • 3+ years of leadership or management experience.
  • Strong understanding of analytical testing, method validation, and stability programs for biologics.
  • In-depth knowledge of cGMP, GLP, ICH guidelines, and data integrity principles.

Skills

  • QA leadership and team management
  • Laboratory data integrity and regulatory compliance
  • Documentation review and approval
  • Investigations into deviations and OOS/OOT
  • Internal audits and regulatory inspections

Education

  • Bachelor's or Master's degree in Life Sciences, Chemistry, or a related field

Additional Requirements

  • None
Apply now
Share this job