Job Title: Senior Officer / Officer – QC Microbiology (Injectables)
Location: Udaipur, Rajasthan
About Cadila Pharmaceuticals Limited:
Cadila Pharmaceuticals Limited, a leading and rapidly growing pharmaceutical company in India, is seeking a highly motivated and skilled Senior Officer or Officer to join our Quality Control Microbiology team at our state-of-the-art manufacturing facility in Udaipur, Rajasthan. This is an exceptional opportunity to contribute to the production of high-quality sterile injectable products and advance your career within a dynamic and innovative organization. If you are passionate about microbiology, possess relevant experience in sterile injectable testing, and are seeking a challenging yet rewarding role, we encourage you to apply.
Job Summary:
We are looking for a dedicated and detail-oriented QC Microbiology professional to support the quality control operations for our sterile injectable manufacturing facility. The ideal candidate will be responsible for performing a variety of microbiological tests, ensuring compliance with regulatory requirements, and maintaining the integrity of our cleanroom environment. This role offers a unique opportunity to work with advanced QC instruments, contribute to the continuous improvement of our processes, and grow professionally within a leading pharmaceutical company.
Responsibilities:
- Perform microbial limit testing (MLT), sterility testing, bacterial endotoxin testing (BET/LAL test), and environmental monitoring of clean rooms (Grade A to D) for injectable products according to established procedures and regulatory guidelines.
- Conduct water testing, bioburden testing, and growth promotion tests in compliance with USP/EP/IP pharmacopoeial standards.
- Prepare and sterilize microbiological media, maintain culture collections, and ensure proper storage and handling of microbiological materials.
- Identify microorganisms using conventional and rapid identification methods, interpret results, and document findings accurately.
- Maintain Good Laboratory Practices (GLP) and Good Documentation Practices (GDP) within the QC Microbiology laboratory, ensuring data integrity and compliance.
- Participate in the qualification and validation of laboratory equipment and clean rooms, including the development and execution of protocols.
- Investigate Out-of-Specification (OOS) and Out-of-Trend (OOT) results, as well as microbial deviations, and implement corrective and preventive actions (CAPA) effectively.
- Prepare, review, and revise Standard Operating Procedures (SOPs), protocols, and trend analysis reports to ensure accuracy, clarity, and compliance.
- Contribute to the training and development of junior team members.
- Collaborate with other departments to resolve quality-related issues and ensure product quality.
Qualifications and Experience:
- M.Sc in Microbiology or Biotechnology.
- Minimum of 1 to 6 years of relevant experience in QC Microbiology, specifically within a sterile injectable manufacturing environment.
- Hands-on experience with sterility testing, bacterial endotoxin testing (BET/LAL test), microbial limit testing (MLT), and environmental monitoring techniques.
- Thorough knowledge of current Good Manufacturing Practices (cGMP), 21 CFR Part 210 and 211, and Schedule M requirements.
- Familiarity with USP, EP, and IP pharmacopoeial standards.
- Strong analytical and problem-solving skills.
- Excellent communication and interpersonal skills.
- Ability to work independently and as part of a team.
- Immediate joiners or candidates with a short notice period will be given preference.
- Apprentices with relevant injectable microbiology project experience may also be considered.
Benefits Offered:
- Competitive salary package with performance-based incentives.
- Subsidized food and transportation facilities.
- Comprehensive group mediclaim and personal accident insurance coverage.
- Provident Fund and gratuity benefits.
- Exceptional learning and career growth opportunities within sterile manufacturing.
- A modern and well-equipped work environment with advanced QC instrumentation.
How to Apply:
If you meet the qualifications and are enthusiastic about this opportunity, please submit your updated resume to [email protected]. Please include the subject line: “Application for Sr Officer / Officer – QC Microbiology (Injectables) – Udaipur.”
Only shortlisted candidates will be contacted for an interview. We appreciate your interest in Cadila Pharmaceuticals Limited.