QC Stability Manager

2 weeks ago


Monroe, North Carolina, United States Glenmark Pharmaceuticals Inc., USA Full time
Job Title: QC Stability Manager

Glenmark Pharmaceuticals Inc., USA is seeking a highly skilled QC Stability Manager to join our team. As a key member of our Quality Control department, you will be responsible for ensuring the stability of our pharmaceutical products.

Key Responsibilities:
  • Develop and implement stability programs to ensure compliance with regulatory requirements.
  • Manage and oversee the stability testing process, including sample management and data evaluation.
  • Collaborate with cross-functional teams to ensure stability programs are aligned with business objectives.
  • Develop and maintain SOPs and technical documents related to stability programs.
  • Ensure compliance with Good Manufacturing Practices (GMP), Good Laboratory Practices (GLP), and Good Documentation Practices (GDP).
Requirements:
  • Master's degree in Pharmacy, Pharmaceutics, or Biotechnology.
  • 5+ years of experience in pharmaceutical quality control laboratory environment, including experience with conducting stability studies.
  • Minimum 4 years of laboratory managerial experience, including involvement with regulatory audits.
  • Strong understanding of GMP, GLP, GDP, cUSP, and ICH Q1A (R2).
  • Experience with electronic systems such as Trackwise, SAP, and/or other relevant QMS systems.
What We Offer:
  • Competitive salary and benefits package.
  • Opportunities for professional growth and development.
  • Collaborative and dynamic work environment.

Please visit our career site website at https://glenmarkpharma-us.com/careers-at-glenmark/career-search/ to create a profile and submit a resume. Job#20240106



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