CSIR-NEERI Recruitment 2026: Technical Assistant and Technical Officer – 13 Vacancies Organization: CSIR–National Environmental Engineering Research Institute (CSIR-NEERI), Nagpur, Maharashtra CSIR-NEERI, a constituent laboratory of the Council of Scientific and Industrial Research (CSIR), has announced recruitment for Technical Assistant and Technical Officer positions under Advertisement No. CSIR-NEERI/1/2026 . Candidates from Science, Life Sciences, Engineering, and Management backgrounds can explore this opportunity, subject to the post-wise eligibility criteria specified in the official notification. 1. Recruitment Overview Organization: CSIR–National Environmental Engineering Research Institute (CSIR-NEERI) Advertisement Number: CSIR-NEERI/1/2026 Job Location: Nagpur, Maharashtra Total Vacancies: 13 Application Mode: Online 2. Vacancy Details Post Name Vacancies Pay Level Pay Mentioned in Advertisement Technical Assistant 1 Level 6 ₹6...
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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