
Asst. Manager- QC (Micro) Jobs in Indoco Remedies Limited - Chhatrapati Sambhaji Nagar,Mumbai
Indoco Remedies Limited
Chhatrapati Sambhajinagar, Maharashtra, India
Posted on 29-01-2026
1 Vacancy
Description
- Job Title: Asst. Manager- QC (Micro)
- Qualification: BSc/MSc
- Location: Indoco Remedies Limited - Chhatrapati Sambhaji Nagar,Mumbai
- Work Experience: 8 to 12 Years
Job Description
- Oversee and execute routine microbiological testing as per approved specifications.
- Manage environmental monitoring of clean rooms, utilities, and controlled areas.
- Ensure compliance with cGMP, GLP, and regulatory guidelines.
- Review and approve microbiology test results, logbooks, and reports.
- Investigate OOS, OOT, deviations, and implement CAPA.
- Perform and review method validation, media validation, and revalidation.
- Monitor water systems (PW/WFI) and trend analysis.
- Handle internal, customer, and regulatory audits (USFDA, WHO, EU-GMP).
- Prepare, review, and control SOPs and microbiology documentation.
- Train and supervise QC Microbiology team.
- Ensure proper calibration, maintenance, and qualification of instruments.
- Maintain data integrity and laboratory safety compliance.
Take this opportunity to join Indoco Remedies Limited - Chhatrapati Sambhaji Nagar, Mumbai as a Asst. Manager- QC (Micro) in Chhatrapati Sambhaji Nagar, Mumbai and build a successful career in the healthcare industry. Apply today for this job opportunity and grow with a leading healthcare organization.
Category
Pharmaceuticals
Functional Area
Pharma Quality Control (QC)
Preferred Education
Key Skills
About Organization
Indoco Remedies Limited, Chhatrapati Sambhaji Nagar (Aurangabad), Maharashtra, is a well-established pharmaceutical company known for its strong manufacturing capabilities and quality-driven culture. The company is strengthening its Quality Control (Microbiology) function and invites applications for the position of Asst. Manager – QC (Micro). The role involves overseeing microbiological testing of raw materials, in-process samples, finished products, water systems, and environmental monitoring, ensuring compliance with GMP, regulatory guidelines, and internal SOPs. Responsibilities include review and approval of microbiology data, investigations and CAPA for OOS/OOT, method validation and verification, audit support, training of team members, and coordination with QA, Production, and Regulatory teams. This opportunity offers hands-on exposure to regulated pharma operations, leadership responsibilities, professional growth, and long-term career development in a structured and compliant manufacturing environment.
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