Job Title: QC Microbiology Analyst
Location:San Diego CA
Duration: Long Term Contract
Responsibilities:
- Perform finished product testing environmental monitoring and sterility QC evaluations.
- Document results accurately and escalate non-conformances or deviations as required.
- Support investigations for deviations OOS/OOT/OOE CAPA activities and Change Control updates.
- Complete all required training (SOPs aseptic methods HSE gowning testing procedures).
- Prepare and maintain cGMP-compliant documentation and batch records.
- Assist during internal and external audits as needed.
Must Have:
- Bachelors in Microbiology Chemistry or related scientific field.
- 0 2 years in a cGMP or aseptic manufacturing environment (preferred).
- Knowledge of cGMP FDA guidelines and aseptic techniques.
- Hands-on experience with microbiological testing environmental monitoring and QC assays.
- Familiarity with method/equipment validation principles.
- HPLC experience required.
- Understanding of HSE practices and QC sampling/testing.
Job Title: QC Microbiology Analyst Location:San Diego CA Duration: Long Term Contract Responsibilities: Perform finished product testing environmental monitoring and sterility QC evaluations. Document results accurately and escalate non-conformances or deviations as required. Support investigati...
Job Title: QC Microbiology Analyst
Location:San Diego CA
Duration: Long Term Contract
Responsibilities:
- Perform finished product testing environmental monitoring and sterility QC evaluations.
- Document results accurately and escalate non-conformances or deviations as required.
- Support investigations for deviations OOS/OOT/OOE CAPA activities and Change Control updates.
- Complete all required training (SOPs aseptic methods HSE gowning testing procedures).
- Prepare and maintain cGMP-compliant documentation and batch records.
- Assist during internal and external audits as needed.
Must Have:
- Bachelors in Microbiology Chemistry or related scientific field.
- 0 2 years in a cGMP or aseptic manufacturing environment (preferred).
- Knowledge of cGMP FDA guidelines and aseptic techniques.
- Hands-on experience with microbiological testing environmental monitoring and QC assays.
- Familiarity with method/equipment validation principles.
- HPLC experience required.
- Understanding of HSE practices and QC sampling/testing.
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