Sr. Associate, Manufacturing
2 weeks ago
- Author and execute CAPA plans, deviations, and change controls.
- Lead investigations for deviations from procedures (quality events).
- Review batch-related documentation and ensure resolution of issues to release product.
- Assist in implementing improvement ideas.
- Additional responsibilities as assigned.
- BS in life sciences, engineering, or other relevant discipline with 1 to 4 years of relevant experience.
- Strong oral, written and interpersonal communication skills
- Previous experience in pharmaceutical, biotech, or biologics cGMP regulated manufacturing environment is preferred but not required.
- Experience conducting compliance investigations is preferred.
- Strict attention to detail and safety.
- Proficiency in MS word, Excel, Power Point, Microsoft Office 365, and other applications
- Must possess effective interpersonal, verbal, and writing skills, patience, professionalism, and the ability to effectively interact and communicate with internal staff and management.
- Ability to thrive in a fast-paced, patient-focused manufacturing environment with minimal direction and able to adjust workload based on changing priorities.
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