Pharmaceutical Quality Expert

7 days ago


Bridgeport, Connecticut, United States Siegfried AG Full time

Siegfried AG, a premier Custom Development and Manufacturing Organization (CDMO), is seeking a highly skilled Pharmaceutical Quality Expert to join our team in Pennsville, New Jersey, USA. The ideal candidate will have extensive experience in quality assurance, regulatory affairs, and cGMP compliance.

About the Opportunity

This is a unique chance to work with a global leader in the pharmaceutical industry, where you will be responsible for ensuring the highest level of quality in our products. You will collaborate with cross-functional teams to develop and implement quality systems, review processes, and procedures.

The successful candidate will have a Master's degree in a relevant field, 7+ years of experience in a similar role, and exceptional knowledge of US FDA and international regulations. A competitive salary of $110,000 per annum, a dynamic work environment, and opportunities for career growth and development await the right candidate.

Key Responsibilities
  • Develop and implement quality systems, review processes, and procedures.
  • Ensure cGMP compliance of assigned manufacturing operations/areas.
  • Collaborate with cross-functional teams to achieve quality goals.


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