Rapidly growing Biotech Firm who manufactures injectables is now seeking a Quality Specialist responsible for supporting GMP manufacturing of raw materials and sterile drugs for clinical trials.

Summary of position
Quality Assurance Specialist supports GMP manufacturing of raw materials and sterile drugs for clinical trials. The individual in this role will review documentation related to raw materials, components, and completed batch records.  Individual will disposition raw materials, components, and products.  Assist with quality systems improvements.
Duties and responsibilities

Specific skills

Able to easily switch between multiple ongoing projects and adjust priorities based on business needs.

This job description is a complete list of all desired skills but not all are required. We strongly encourage candidates who have some of the skills to apply. We look forward to a conversation to learn more about you!