Quality Control Associate
On-site · United States
Core
Perform specialized technical tasks in laboratory testing and deviation management to manufacture medicines to the highest quality and safety standards.
Role type
Quality Control Associate (Laboratory/Deviation Management)
Builds
Medicines manufactured to cGMP standards
Domain
Life Sciences / Pharmaceutical Manufacturing
Required skills
Laboratory testing, Deviation management, cGMP compliance, Cell based assays, ELISA, Potency methods
Preferred skills
Effective communication, Information analysis, Adaptability, Prioritization
Technologies
cGMP, EHS, Lonza standards
Responsibilities
Perform operational roles such as laboratory testing; Execute duties in alignment with Quality Control policies and cGMP requirements; Conduct work to meet customer commitments.
Seniority
Mid-Senior level (5-10 years experience)