Summary:
A rapidly growing global pharmaceutical company that focuses on assisting in treatments for patients is looking for a quality professional to join their thriving team. They emphasize on providing patients access to affordable medicines to help with their treatments. Their R&D team focuses on developing innovative medicines and drug delivery systems.
Responsibilities:
- Developing and validating methods for drug product programs for external clients
- Contribute to SOPs and protocols by writing, reviewing, and revising reports
- Maintain the analytical instruments through routine testing and troubleshooting
- Uphold Good Manufacturing Practices in the lab and develop understanding EMEA regulations
- Performing experiments using analytical techniques of HPLC, Mass Spectrometry, and GC independently
- Mentoring junior scientists
Qualifications:
- BS with 6+ years of experience, MS with 4+ years of experience, OR PhD with 0-2 years of relevant industry experience
- Extensive experience with small molecules in an FDA regulated environment
- Ability to communicate well and work independently
- Experience with developing validation-ready methods for Quality Control
Benefits:
- Competitive salary and annual bonus
- PTO plus holidays