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Quality Control, Pharma Industry, R and D, CSIR, Food Industry, Pathology, Medical Writing, coding

Required Junior Research Fellow - B.S. 4 years programme/BPharm/MBBS/Integrated BS-MS/MSc/BE/BTech or equivalent degree, with 55% marks and passing of NET/GATE test- Fellowship Junior Research Fellow (JRF)- Rs.37,000/-p.m.

Nirma University, Institute of Science is hiring Junior Research Fellow  ADVERTISEMENT FOR JRF POSITION Date: 02/05/2026 Applications are invited from interested and motivated candidates for the post of Junior Research Fellow (IRF) in a time-bound research project under CSIR-HRDG sponsored research support scheme [project file no: 37WS (0038)-2023-24/EMR-IL/ASPIRE] for a temporary period, purely on a contractual basis as per the following details 1. Position: Junior Research Fellow (JRF) 2. Number of Vacancy: 01 3. Project Title: Profiling of interferon-alpha for early detection of maternal anaemia during pregnancy 4. Principal Investigator: Dr. Aarthi Sundararajan Assistant Professor Institute of Science, Nirma University Ahmedabad-382481 5. Department: Institute of Science  6. Project Tenure : 15 Months  7. Job Description: JRF responsibilities will include conducting research activities, maintaining proper data records, keeping track of consumables, assisti...
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Require Officer/Sr. Officer/Executive for Quality Control Department - B.Sc / M.Sc. / B.tech (Biotechnology)

Job Opening:

INDUS PHARMA PVT. LTD.
Vacancy for Manufacturing Plant located at Riico Industrial Area, Ghiloth, Neemrana, Rajasthan

Department: Quality Control
Designation: Officer/Sr. Officer/Executive
Experience: 03 Yrs – 06 Yrs
Qualifications: B.Sc / M.Sc. / B.tech (Biotechnology)
Job Responsibilities:-
1. Sample Analysis
Analyze raw materials, in-process samples, finished products, and stability samples to ensure compliance with specifications.
Perform chemical and physical testing, including pH, viscosity, osmolality, sterility, particulate matter, and assay of active pharmaceutical ingredients (APIs).
2. Method Development and Validation
Develop, optimize, and validate analytical methods (e.g., HPLC, GC, UV-Vis Spectroscopy) to ensure reproducibility and reliability.
Troubleshoot and maintain analytical methods as needed.
3. Documentation
Maintain accurate and detailed records of testing, analysis, and calibration in compliance with Good Documentation Practices (GDP).
Prepare and review Certificates of Analysis (COAs), test reports, and deviation reports.
4. Regulatory Compliance
Ensure adherence to regulatory requirements, including Good Manufacturing Practices (GMP) and International Council for Harmonisation (ICH) guidelines.
Support audits and inspections by regulatory agencies (e.g., FDA, EMA).
5. Equipment Management
Operate, calibrate, and maintain laboratory instruments like HPLC, GC, UV-Vis spectrophotometers, FTIR, and more.
Ensure proper validation and qualification of laboratory equipment.
6. Microbiological Oversight (if applicable)
Collaborate with microbiology teams to ensure sterility and endotoxin testing of injectable products.
Participate in environmental monitoring programs for sterile production areas.
7. Quality Assurance Support
Assist in investigating Out-of-Specification (OOS) and Out-of-Trend (OOT) results.
Participate in root cause analysis and corrective/preventive actions (CAPA).
8. Stability Studies
Conduct stability testing of products to determine shelf life and storage conditions.
Monitor stability chambers and ensure samples are tested as per the stability protocol.

Please share your CV on :-
hr@induspharmaindia.com
+91-9990334200 (Only WA)

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