Regulatory Compliance Change Assessor - Sr. Associate

Roles & Responsibilities:

Key responsibilities of the Regulatory Sr Associate include:

• Reviews change records to evaluate impact of the change with respect to reportability and product restrictions for any product in scope.
• Defines and documents the reporting and product distribution restriction requirements for the change within the change control management system.
• Liaise with other functions, including Process Development, Operations, Quality and Supply Chain to ensure alignment of regulatory strategies

What we expect of you

We are all different, yet we all use our unique contributions to serve patients. The professional we seek is a type of person with these qualifications.

Basic Qualifications:

• Masters degree OR
• Bachelors degree and 2 years of manufacture, QA/QC, or regulatory CMC in the Pharmaceutical/Biotechnology industry OR
• Associates degree and 6 years of manufacture, QA/QC, or regulatory CMC in the Pharmaceutical/Biotechnology industry OR
• Diploma and 8 years of manufacture, QA/QC, or regulatory CMC in the Pharmaceutical/Biotechnology industry

Preferred Qualifications:

• Degree in Life Science discipline
• Regulatory CMC specific knowledge & experience
• Understanding and application of principles, concepts, theories and standards of scientific/technical field
• Experience in manufacture, testing (QC/QA or clinical), or distribution in Pharmaceutical/Biotech industry.