IPCA Laboratories Ltd., a leading pharmaceutical company with a strong presence in Dewas, is currently seeking highly motivated and skilled individuals to join our dynamic Quality Control – Microbiology department. We offer excellent career growth opportunities within a thriving, innovative environment. This is an exceptional chance to contribute to the production of high-quality pharmaceutical products and advance your career in a respected organization.
About IPCA Laboratories Ltd. Dewas
IPCA Laboratories Ltd. is a renowned pharmaceutical company with a long-standing commitment to quality and innovation. Our Dewas facility plays a crucial role in our manufacturing operations, adhering to the highest industry standards and regulatory requirements. We are a team of dedicated professionals who are passionate about delivering high-quality medicines to patients worldwide. Our commitment to employee development ensures a supportive and enriching work environment.
Job Overview: QC Microbiology Officer/Sr. Officer
We are looking for experienced and qualified candidates for the position of QC Microbiology Officer/Sr. Officer at our Dewas facility. The ideal candidate will be a meticulous and detail-oriented individual with a strong understanding of microbiological techniques and quality control procedures within the pharmaceutical industry.
Responsibilities:
The successful candidate will be responsible for a range of key tasks, including:
- Equipment Operation and Calibration: Performing routine operation and calibration of critical laboratory equipment such as top-pan and analytical balances, ensuring accuracy and reliability of measurements. This involves maintaining detailed calibration logs and adhering to strict calibration schedules.
- Sterilization and Media Preparation: Managing the decontamination process using vertical autoclaves, meticulously following sterilization protocols to ensure the sterility of media and equipment. Preparing various culture media for routine microbiological analysis, adhering to strict aseptic techniques and quality control checks.
- Environmental Monitoring: Conducting comprehensive environmental monitoring of the production areas to identify and mitigate potential contamination risks. This includes performing settle plate, air sampling, and contact plate tests, analyzing results, and generating reports. Maintaining accurate and detailed records of all monitoring activities is crucial.
- Water Sampling and Analysis: Following established schedules for collecting and analyzing raw, potable, and purified (DM) water samples. Performing microbiological tests to ensure the water quality meets required pharmaceutical standards. Maintaining detailed documentation and tracking of water quality parameters.
- Data Recording and Documentation: Meticulously recording and maintaining accurate records of temperature, relative humidity (RH), and differential pressure (DF) monitoring data. This ensures compliance with regulatory requirements and assists in identifying any potential deviations from established parameters. Precise and accurate record-keeping is paramount.
- Adherence to GMP: Maintaining a thorough understanding and strict adherence to Good Manufacturing Practices (GMP) guidelines and relevant regulatory requirements. This encompasses all aspects of the role, from sample handling and testing to documentation and record-keeping.
Qualifications and Experience:
- Master of Science (M.Sc.) in Microbiology: A minimum of an M.Sc. degree in Microbiology is required.
- Experience: 1-4 years of relevant experience in a pharmaceutical or related industry quality control laboratory is preferred.
- Technical Skills: A strong understanding of microbiological techniques, including aseptic techniques, media preparation, environmental monitoring, and water quality testing. Proficiency in operating and maintaining laboratory equipment is essential.
- Analytical Skills: Excellent analytical and problem-solving skills are crucial for accurately interpreting results and identifying potential issues.
- Documentation Skills: Meticulous attention to detail and exceptional record-keeping skills are essential for maintaining accurate and compliant documentation.
- Compliance: A comprehensive understanding of GMP regulations and their application in a pharmaceutical manufacturing environment.
Benefits of Working at IPCA Laboratories Ltd.:
- Competitive salary and benefits package.
- Opportunities for professional development and career advancement.
- A collaborative and supportive work environment.
- Contribution to the production of life-enhancing pharmaceuticals.
To Apply:
Interested and qualified candidates are encouraged to submit their resumes to gautam.anand@ipca.com. Please clearly state “QC Microbiology Officer/Sr. Officer Application” in the subject line of your email. We look forward to hearing from you.
