Quality Assurance Investigator

5 days ago


Saddle Brook, New Jersey, United States Lynkx Staffing LLC Full time
About the Position

This Manufacturing Regulatory Expert role at Lynkx Staffing LLC offers a challenging opportunity to work in the Pharmaceutical industry. As part of our team, you will be responsible for ensuring compliance with regulatory requirements, including Good Manufacturing Practices (GMP), Good Documentation Practices (GDP), and Good Laboratory Practices (GLP).

Responsibilities
  • Support internal and external audits, which may include interaction with Health Authorities and clients.
  • Prepares and issues change control as necessary.
  • Adheres to all compliance regulations as required by regulatory agencies and per the Company's processes and procedures.
  • Ensures appropriate CAPAs are generated to increase compliance and prevent repeat occurrences of deviations.

The ideal candidate will have a B.S in biological sciences or other relevant field of study and minimum 5 years' experience in QA in a life sciences company. Experience in authoring, reviewing, and/or approving cGMP/cGTP related documents is required.

The estimated annual salary for this position is $90,000 - $120,000, depending on experience.



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