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- Liaise with the Production team for the review of executed Production Records
- QA on the floor to support manufacturing (Gowning qualification required)
- Review SOPs, logbooks, and other documentation related to daily QA activities
- Assist in internal audits of GMP operations
- Provide support for external regulatory or partner GMP audits
- Ensure implementation of quality system procedures
- Other duties as assigned.
- HS diploma with 0-1 years of QA experience in the pharmaceutical bio industry (certificate work in pharmaceutical bio industry could be in lieu of experience)
- Highly interested in quality assurance work
- General understanding of quality assurance
- Effective communication (verbal and written), interpersonal, and teamwork skills
- An ability to be productive and successful in an intense work environment
- MS Office working experience (excel, Word, PowerPoint)
- Associate degree with 0-1 years of QA experience in the pharmaceutical bio industry
- Previous experience in CDMO industries is desirable
- Experience in working with GMP compliant/quality-controlled procedures is desirable
- Multilingual (Chinese speaking desired)
- Able to stand for 5-6 hours
Quality Assurance Technician - Germantown, United States - uBriGene Biosciences
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Description
Job Description
Quality Assurance Technician
Qualifications:
Additional Preferred Capabilities