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Quality Operations Drug Product: Associate
Company Name
Pfizer
Job Overview
This role supports quality operations for GMP clinical drug product manufacturing and disposition in Groton, CT.
Responsibilities
- Quality touchpoints in cleaning validation
- Batch records
- Investigations
- Compliance
- Documentation lifecycle activities
Requirements
- Bachelor's degree with 0+ years of experience
- Associate's degree with 4 years of experience
- High school diploma with 6 years of relevant experience
Skills
- Strong communication skills
- Organizational skills
- Learning agility