Quality Management System Specialist

1 week ago


Piscataway, New Jersey, United States Global Life Science Hub Full time

We are seeking a Quality Management System (QMS) Specialist to join our client's team in New Jersey. In this role, you will play a vital part in ensuring product integrity and regulatory adherence throughout the manufacturing process.

Job Responsibilities:
  • Support the development and execution of QMS procedures and processes to uphold GMP compliance.
  • Assist in the review and management of quality documentation, including SOPs, deviation reports, and CAPAs.
  • Conduct internal audits and participate in regulatory inspections to support quality standards.
  • Collaborate with cross-functional teams to promote continuous improvements in quality processes and ensure accurate record-keeping.

In this pivotal role, you will contribute directly to quality and compliance as the company expands through 2030. You will work collaboratively in a team-focused environment, utilizing your strong attention to detail and excellent organizational skills.

Qualifications:
  • Bachelor's degree in a scientific field or equivalent experience.
  • Minimum of 2 years of experience in a GMP-regulated environment, preferably within the pharmaceutical or biotech industry.
  • Familiarity with quality systems, documentation practices, and basic GMP compliance requirements.

This is an exceptional opportunity to join a pioneering biotech company in New Jersey, offering a competitive salary range of $80,000 - $110,000 annually, commensurate with experience.



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