Job Description

• Setting the analysis priorities based on the production planning in microbiology section.
• Analysis of Water, Raw Materials, Finished products and Crossover Studies in microbiology section (If, required).
• Responsible for the environmental monitoring, daily verification of equipment's as per the schedule.
• Responsible for the online completion of Analyst Hard books, Analytical Raw Data, Equipment usage log books, Protocols and Reports etc.
• Maintenance of Media preparation/reconciliation data, Culture etc.
• Responsible for daily balance verification, pH Meter daily calibration, daily temperature and relative humidity monitoring records.
• Responsible for planning of Calibrations and Preventive Maintenance activities for Autoclaves, Incubators, Laminar Air Flow, Microscopes, Analytical Balances, Ovens, TOC analyzer and pH Meter etc. as per the schedule in microbiology section.
• Responsible for intimation of any deviations/ out of specifications in microbiology section.
• Ensure Safe working conditions and clean environmental practices in microbiology section.
• Responsible for the preparing/reviewing of trending reports for water and environmental and others.
• Responsible for periodic validation activities for ovens, autoclave, incubators, LAF and air samplers.
• Responsible for analysis of chemical water analysis.
• Responsible for the preparation of Protocols, Reports, SOP's, Spec & STP's and other documents related to microbiology section.
• Observe unsafe acts / conditions and take Corrective & Preventive actions immediately in the section.
• Impart SHE training to all respective persons and report any incident / accident / near miss / illness to the respective superiors in the microbiology section.
• Responsible for revision of documents updated as per the changes made to the pharmacopeias/regulatory documents.
• Responsible for crossover/method transfer activities and its closures.
• Identify unsafe conditions and unsafe acts and report to superiors.
• To sign all the documents connected with the activities under his/her control.
• In the absence of Superior, he/she is responsible for his / her activities / responsibilities
• He/She should be familiar with the trouble shooting techniques in microbiology section.


In the three decades of its existence, Piramal Group has pursued a twin strategy of both organic and inorganic growth.
Driven by its core values, Piramal Group steadfastly pursues inclusive growth, while adhering to ethical and values-driven practices.



Equal employment opportunity Piramal Group is proud to be an Equal Employment Opportunity and Affirmative Action employer. We do not discriminate based upon race, ethnicity, religion, color, national origin, gender (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity, gender expression, age, status as a protected veteran, status as an individual with a disability, genetics, or other applicable legally protected characteristics.



We base our employment decisions on merit considering qualifications, skills, performance, and achievements. We endeavor to ensure that all applicants and employees receive equal opportunity in personnel matters, including recruitment, selection, training, placement, promotion, demotion, compensation and benefits, transfers, terminations, and working conditions, including reasonable accommodation for qualified individuals with disabilities as well as individuals with needs related to their religious observance or practice.

Piramal Pharma Solutions (PPS) is a Contract Development and Manufacturing Organization (CDMO) offering end-to-end development and manufacturing solutions across the drug life cycle. We serve our customers through a globally integrated network of facilities in North America, Europe, and Asia. This enables us to offer a comprehensive range of services including drug discovery solutions, process & pharmaceutical development services, clinical trial supplies, commercial supply of APIs, and finished dosage forms. We also offer specialized services such as the development and manufacture of highly potent APIs, antibody-drug conjugations, sterile fill/finish, peptide products & services, and potent solid oral drug products. PPS also offers development and manufacturing services for biologics including vaccines, gene therapies, and monoclonal antibodies, made possible through Piramal Pharma Limited's investment in Yapan Bio Private Limited. Our track record as a trusted service provider with experience across varied technologies makes us a partner of choice for innovators and generic companies worldwide.