A well-funded pharmaceutical company is looking to bring on a Quality Assurance/Systems Professional to join their clinical manufacturing team. Here, you will be responsible for supporting quality system functions to support GMP operations.
Responsibilities:
The Quality Specialist will provide oversight of quality systems including deviations, CAPAs, Change Controls, Training, Internal Auditing.
Qualifications:
- B.S. or BA preferred
- 3-5 years in industry with GMP quality assurance/systems
- Experience in Quality assurance and/or manufacturing
- Experience with Quality Systems governance for Deviations, CAPAs, Change Control and Internal Auditing.
- Review and approve proposed changes to systems, procedures and methods.
Benefits
- Health Benefits (Dental, Vision, Medical)
- 401K
