Emcure Pharmaceuticals is hiring Officer/Executive/AM for QC Microbiology Department Emcure Pharmaceuticals is looking for dedicated and detail-oriented professionals for QC Microbiology team. Details are provided below 1. Position:Officer/Executive / AM 2. Job Location: Sanand, Ahmedabad 3. Experience: 2 to 8 Years 5. Department: QC Micro 6. Qualification: B.Sc./M.Sc. Microbiology (or) B.Pharm / M.Pharm 7. Key areas of Work : -Water Testing: Perform analysis of purified-water, WFI, potable water and water for injection as per IP/USP/EP guidelines. -Sterility Testing: Perform sterility testing of pharmaceutical products, raw materials and components as per IP/USP. -Microbial Limit Testing (MLT): Conduct microbial limit tests of raw materials, in-process and finished products. -Environmental Monitoring (EM): Perform monitoring of viable and non-viable particles in clean areas as per SOP -Media & Reagent Preparation: Prepare, sterilize and per...
Indus Pharma Private Limited is hiring for QC GLP Officer
Details are provided below
1. Position Title: QC GLP Officer (Liquid Injectable Only)
2. Department: Quality Control
3. Location: A-181, Riico Industrial Area, Ghiloth, Neemrana, Rajasthan-301705
4. Reporting To: QC Head
5. Job Summary:
-To ensure all Quality Control laboratory activities are performed in compliance with GLP (Good Laboratory Practices), regulatory guidelines, and company SOPs.
-The QC GLP Officer is responsible for documentation review, laboratory compliance monitoring, instrument qualification support, and internal audits.
6. Key Responsibilities:
-Monitor QC laboratory activities to ensure adherence to GLP, cGMP, and regulatory standards.
-Conduct routine checks for data integrity, traceability, instrument cleanliness, and analyst practices.
-Ensure proper documentation practices (ALCOA+). Review laboratory logbooks, instrument usage logs, and calibration records.
-Review and maintain QC
documents, including raw data, worksheets, test records, and analytical reports.
- Assist in preparation, revision, and implementation of SOPs related to QC and GLP compliance.
-Ensure all entries in laboratory records are accurate, complete, and timely.
-Participate in internal audits and external regulatory inspections.
-Support in CAPA preparation, deviation investigations, and OOS/OOT documentation review.
-Perform self-inspections of the QC laboratory.
-Support IQ/OQ/PQ activities for laboratory instruments.
-Ensure all instruments used for analysis are calibrated and maintained as per schedule.
-Monitor instrument controls, system suitability checks, and preventive maintenance records.
-Provide GLP training to QC analysts and new joiners.
-Promote continuous improvement and compliance culture within QC.
-Ensure proper handling, labeling, storage, and disposal of samples and reagents.
-Verify environmental conditions (temperature, humidity) for sample retention and storage.
7. Required Qualifications
B.Sc. / M.Sc. in Chemistry /Biotechnology / Microbiology or equivalent.
8. Experience Required:
1-4 years' experience in QC, preferably in a GLP-focused environment in a pharma injectable company.
Knowledge of GLP, GMP, GDP, ALCOA+, OOS/OOT handling, and regulatory guidelines (WHO, USFDA, MHRA).
Familiarity with analytical instruments (HPLC, GC, UV, IR, Dissolution, etc.).
9. How to Apply:
Share your CV on
hr@infuapharmaindia.com
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