Job Summary
A company is looking for a Sr. Principal Associate - Global Compendial Affairs.
Key Responsibilities
- Monitor and evaluate proposed changes to pharmacopoeia requirements affecting products and practices
- Provide technical support and oversight for compliance with global compendial requirements for excipients and raw materials
- Coordinate communication and responses to pharmacopoeias, ensuring compliance across global sites
Required Qualifications
- Bachelor's or Master's degree in Biology, Chemistry, Biochemistry, Pharmacy, Pharmaceutical Science, or related field
- 7 or more years of experience in the pharmaceutical industry
- Strong technical knowledge of analytical testing methods and pharmacopoeias
- Experience working within a GMP Analytical laboratory
- Project management skills with the ability to coordinate schedules and meet deadlines
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