Location: Neemrana, Rajasthan (Sterile Facility)
Open Positions: Executives & Officers
Qualifications Required:
- B.Pharma
- M.Pharma
- M.Sc (Microbiology, Chemistry, Biotechnology)
Experience:
1 to 5 years in Sterile Manufacturing
Available Departments & Skills Required
1. Sterile Manufacturing (Production)
Key Responsibilities:
- Expertise in sterile compounding processes including CIP/SIP systems, component preparation, and sterilization.
- Hands-on experience with aseptic operations, media filling, and sterilization processes.
- Proficiency in area monitoring and troubleshooting challenges in aseptic manufacturing environments.
2. Quality Assurance (QA)
Key Responsibilities:
- Risk assessment, investigations, and CAPA implementation with effectiveness checks.
- Knowledge of SOPs, change control, and compliance monitoring for sterile environments.
- Strong experience in handling deviations, internal/external audits, and ensuring GMP adherence.
- Expertise in record reviews, protocol batch preparation, and regulatory compliance.
3. Quality Control (QC)
Key Responsibilities:
- Strong understanding of analytical and microbiological testing in sterile manufacturing.
- Proficiency in analytical techniques such as HPLC, UV, and DC for product quality and regulatory compliance.
- Expertise in environmental monitoring, bioburden testing, and sterility testing.
- Knowledge of stability studies, release testing, and pharmacopoeia requirements for sterile products.
Why Join Puerto Life Sciences Pvt. Ltd.?
- Be part of a state-of-the-art sterile facility.
- Work in an environment that prioritizes innovation and compliance.
- Grow your career with a team of professionals dedicated to excellence in sterile manufacturing.
How to Apply
Share the following details:
- Your Updated Resume
- Current CTC
- Notice Period
Email: hr@puerto.in
