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Required Drug Substance (Viral Vaccine Experience)- Upstream /Downstream Processing of viral vaccines

Job Opportunity - Drug Substance (Viral Vaccine Experience) Bharat Biotech is looking for skilled professionals with hands-on experience in Drug Substance manufacturing for Viral Vaccines. Details are provided below  1. Location: Hyderabad 2. Experience: 2-6 Years 3. Key Skills & Experience Required a. Experience in Upstream /Downstream Processing of viral vaccines b. Operation and handling of bioreactors, fermenters, centrifuges, chromatography systems, filtration units c.  Knowledge of cell culture techniques (mammalian/avian cell lines)  d. Familiarity with aseptic techniques, GMP documentation, batch records e. Understanding of process optimization, scale-up, and technology transfer f. Exposure to in-process testing, troubleshooting, and equipment cleaning/sterilization g. Ability to work in a regulated, fast-paced manufacturing environment 4. How to Apply Interested candidates can share their updated CV to kiran4978@bharatbiotech.com Mention subject line as: Appl...
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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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