Quotient Sciences is a leading drug development and manufacturing accelerator, helping biotech and pharma companies bring new medicines to patients faster. The company provides Drug Product (CDMO) and Clinical (CRO) services across the entire development pathway.
Requirements
- Weighing and manufacturing of GMP, R&D, clinical and commercial batches
- Operating, cleaning, and sanitizing equipment and production rooms
- Performance verification of scales and balances prior to use
- Preparing documentation and submitting samples collected during manufacturing
- Assuring manufacturing department is always neat and clean
- Participating in process and cleaning validation activities
- Notifying the GMP Coordinator or Supervisor to ensure supplies are kept in stock
- Following all GMP rules and executing GMP, R&D and Clinical batch records with minimal or no supervision
- Ensuring training is within compliance for all activities assigned prior to execution of any assigned tasks
- Adhering to schedule to support deadlines and willingness to work outside of normal shift (overtime) as needed
Benefits
- Professional development opportunities
- Diverse and inclusive work environment
- Opportunity to work in a fast-paced and dynamic industry