Microbiologist Jobs in Meck Pharmaceuticals & Chemicals Pvt. Ltd - Sanand, Gujarat
Meck Pharmaceuticals & Chemicals Pvt. Ltd
Sanand, Gujarat, India
Posted on 29-01-2026
1 Vacancy
Description
- Job Title: Microbiologist
- Qualification: BSc/MSc
- Location: Meck Pharmaceuticals & Chemicals Pvt. Ltd- Sanand, Gujarat
- Work Experience: 0 to 1 Years
Job Description
- Perform and supervise microbiological testing of clinical samples.
- Interpret and validate culture & sensitivity reports.
- Ensure compliance with biosafety and quality standards.
- Support infection control activities and hospital surveillance.
- Coordinate with clinicians for appropriate diagnosis & treatment.
- Maintain quality control, calibration, and documentation.
- Participate in NABL / NABH audits and accreditation.
- Supervise lab technologists and ensure SOP adherence.
- Monitor antibiotic resistance trends and prepare reports.
- Handle outbreak investigations and infection alerts.
- Ensure proper waste disposal and lab safety practices.
Take this opportunity to join Meck Pharmaceuticals & Chemicals Pvt. Ltd - Sanand, Gujarat as a Microbiologist in Sanand, Gujarat and build a successful career in the healthcare industry. Apply today for this job opportunity and grow with a leading healthcare organization.
Category
Doctor / Surgeon
Preferred Education
Key Skills
About Organization
Meck Pharmaceuticals & Chemicals Pvt. Ltd., Sanand, Gujarat, is a well-established pharmaceutical manufacturing company known for its strong quality systems and compliance with regulatory standards. The company is expanding its Quality Control function and invites applications for the position of Microbiologist. The role involves performing routine microbiological analysis of raw materials, in-process samples, finished products, water systems, and environmental monitoring in accordance with GMP and internal SOPs. Responsibilities include media preparation and validation, microbial limit tests, sterility testing, documentation and data review, handling OOS/OOT investigations with CAPA support, and coordination with QA and Production teams. This opportunity offers hands-on exposure to regulated pharmaceutical operations, professional skill development, and long-term career growth in a structured and quality-driven manufacturing environment.
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