Regulatory Compliance Project Lead

2 days ago


New Brunswick, New Jersey, United States PSC Biotech Full time

PSC Biotech is a dynamic life sciences company that provides innovative solutions to ensure the quality and safety of healthcare products.

Job Requirements

We are seeking a highly experienced Validation Project Manager to join our team. The ideal candidate will have 10+ years of experience in CQV in a regulated GMP environment. Responsibilities include planning, executing, and managing CQV projects, managing vendors, and providing technical execution review.

  • Develop and manage project plans, schedules, and budgets.
  • Evaluate potential risks and issues and escalate to upper management as necessary.

Requirements:

  • Bachelor's degree in engineering or related technical field.
  • 10+ years of CQV experience in a regulated GMP environment.
  • Strong understanding of regulatory requirements (FDA, EMA, ICH, etc.) and industry standards (GMP, GLP, GAMP, etc.).
Salary Range

The estimated salary for this position is $120,000 - $150,000 per year, depending on experience.



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