Opportunity to work with a specialty pharmaceutical CDMO where quality, compliance and execution drive success for our partners’ healthcare programs worldwide.
Bachelors degree in a science-related field such as Pharmacy, Chemistry, Biological Sciences, or related Life Sciences. GMP experience, with experience in pharmaceutical laboratory quality assurance, quality control, or laboratory operations in a dry product or solid oral dosage form environment. Lilly
To perform Pharmacovigilance activities per project requirement including but not limited to, collecting and tracking incoming Adverse Events(AE)/endpoint information
The Team Leader will report to the Team Manager or Manager – Operations and will play a key role in people leadership, process excellence, and client delivery.