Join a leading GMP regulated manufacturing environment supporting quality compliance and microbiology operations
Role Summary
Looking for professionals with hands on experience in Quality Assurance and Environmental Monitoring within pharma or CDMO settings
Key Responsibilities
- Batch record review and release support
- Document control archival logbook and SOP management
- Raw materials review and GMP documentation
- Environmental monitoring including viable and non viable
- Microbiological sampling incubation and plate reading
- Ensure compliance with GMP GDP and cleanroom standards
Required Skills
- GMP Quality Assurance
- Batch Review and Release
- Document Control and GDP
- Aseptic Techniques and Cleanroom Compliance
Ideal Candidate
- Detail oriented and compliance driven
- Experience in regulated manufacturing environments
Note : This opportunity is open for W2 candidates only
If interested or know someone suitable feel free to reach out referrals are welcome