--Must See--
BSc Microbiology Jobs Panacea Biotec – BSc/MSc Biotech & Microbiology Apply
Scientific Officer – QC (Micro Section)
Baddi, Himachal Pradesh, India
About the job
Key Responsibilities:
- Environmental Monitoring: Conduct routine environmental monitoring of Quality Control, Production, and Warehouse areas, including but not limited to, viable and non-viable particle counting, surface sampling, and air sampling, all in strict adherence to approved procedures.
- Sampling: Perform accurate and timely sampling of Active Raw Materials (ARMs) and Inactive Raw Materials (IRMs), as well as final lot samples of finished products, according to established protocols.
- Microbiological Analysis: Execute microbiological analysis of various samples, including environmental swab samples and compressed air samples, utilizing validated methods.
- Trend Analysis & Reporting: Prepare and submit comprehensive monthly and annual microbiological trend summary reports for environmental monitoring procedures, identifying any deviations or critical trends.
- Documentation & Compliance: Maintain meticulous logbooks within the Quality Control department, review generated reports for accuracy and completeness, and actively participate in the preparation and revision of Standard Operating Procedures (SOPs).
- Media Fill Support: Participation in media fill, sample incubation and perform diligent vial observation to assess aseptic processing performance.
- Team Collaboration: Collaborate effectively with cross-functional teams and proactively take on any additional responsibilities assigned by the Head of Department to support overall QC operations.
Qualifications:
- Bachelor’s or Master’s degree in Microbiology, Biotechnology, or a related scientific discipline.
- 1-5 years of experience in Quality Control Microbiology, preferably within a pharmaceutical, vaccine, or sterile manufacturing environment.
- Proficient in environmental monitoring techniques, microbiological testing, and aseptic practices.
- Strong understanding of cGMP guidelines and regulatory requirements for pharmaceutical manufacturing.
- Excellent data analysis, report writing, and documentation skills.
- Ability to work independently and as part of a team in a fast-paced environment.
- Detail-oriented with a strong commitment to quality and compliance.
Keywords: Please ensure you are subscribed to the Biotecnika Times Newsletter and our YouTube channel to be notified of the latest industry news. Follow us on social media like Twitter, Telegram, Facebo
