ICHOR Biologics Pvt. Ltd is a specialty plasma derived biopharmaceuticals company committed to innovate, develop and commercialize high-quality plasma derivatives to save lives and enhance the quality of life for the people. Ichor operates through an integrated platform of safe and reliable collection of high-quality human plasma, a state-of-the-art fractionation facility capable of producing life-saving therapies in conformance with the most stringent international standards that is supported by a cross functional team of scientists.
Inviting Candidates for a Walk-In Interview for QA-IPQA on 28th & 29th August, 2023, from 09:00 hrs. to 16:00 hrs. @ ICHOR BIOLOGICS Pvt. Ltd, Hyderabad (Shameerpet).
Interested candidates can walk-in for an interview with their updated CVs along with the current CTC details.
- Department: Quality Assurance – IPQA
- Experience: 4-8 yrs
- Role: Executive
- Qualification: M.Sc / B.Pharm / M.Pharm
- Note: Candidates should have experience in experience in Sterial Operations/ Biological Process-Preferable Biotechnology Companies.
- Location: Sy. No: 222P, Thurkapally Shamirpet Manda Hyderabad, Telangana 500078
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Walk-In Interview Details:
- Interview date: 28th & 29th August, 2023
- Timings: 09.00am to 4.00pm
- Interview & Work Location: ICHOR BIOLOGICS Pvt. Ltd,Sy. No: 222P, Thurkapally (V), Shameerpet (M), Hyderabad.
- Submit your CV at hr@ichor.in
Documents to be Carried:
- Updated Resume / CV
- Last 3 Months Pay slips
- Aadhaar & Pan Card
- Latest Appraisal salary break up
- All Educational Documents Xerox Copies.
Similar Jobs: Shodhana Laboratories – Hiring Freshers & Experienced B.Sc, M.Sc, B.Pharm, M.Pharm Candidates for QC / AR&D Departments – Apply Now
Require Skills:-
- Preparation, review and approval of In-Process quality assurance standard operating procedures.
- Perform and monitor IPQA activities at shop floor level in each and every stage
of Bio Process (Down Streem) - Review and monitoring of In-Process quality checks in manufacturing area.
- Responsible to review of Production-API and Production formulation activities and line clearance of in-process activities.
- To prepare, review and approval of process validation protocols and reports.
- In-Process and Bulk Sample collection, Submission and review of the results.
- Responsible to prepare and compilation of documents with related to regulatory agencies.
- Responsible to review of plasma sampling and Quality control analytical repts Responsible to monitoring of control samples.
- Immediate reporting to superior for any deviation, OOS observed at shop floor level
