Medreich is a pharmaceutical company that has been in existence since 1976, manufacturing generic and branded drugs in several therapeutic areas. With more than 2900 employees worldwide, exceptional quality standards and a client base that is spread across 54 countries, Medreich has built a reputation for raising the bar on product superiority with every undertaking. Medreich’s Research & Development and manufacturing facilities have received the seal of approval from leading global regulatory bodies such as -UK MHRA, Australia TGA, SA MCC, Health Canada, French FDA. The company produces drugs for leading, global pharmaceutical companies such as GSK, Pfizer, Sanofi Aventis, Wyeth, Merck, among others. Medreich has 8 manufacturing facilities built to comply International regulatory standards. Two newly added facilities are State of the art technology driven plants. One among them has the capacity to produce 9 billon tablets and capsules per annum.
Medreich Limited – Walk-In Interviews for Freshers & Experienced in Production / QA / QC / Engineering / Technology Transfer on 3rd Dec’ 2022
- Experience: 0-6 yrs
- No of Openings: 32
- Qualification: B.Pharm / M.Pharm / B.E / B.Tech
- Designation: Officer / Executive
Production:
- Monitoring of shop floor Production Activities with respect to Granulation, Compression, Coating & Packing.
- Handling BMR or BPR
- Candidates should be flexible to work in shift
Quality Assurance:
- Handling of IPQA activities like Line Clearance, Process and Cleaning validation sampling, Qualification, Intermediate, bulk & FG sampling.
- Review of BMR & BPR and In-process checks
- QMS activities like Change Control, Deviations and APQR knowledge
Quality Control:
- Wet Analysis like UV, IR & Dissolution knowledge
- HPLC, GC Experience & Documentation Exp
- GLP & Documents Review and Audit compliance
Engineering:
- Handling of Process equipment (OSD)
- PPM, Utility knowledge
- should be able to handle individual task assigned
Technology Transfer (TT):
- Tech transfer of new products, Site transfer from inter-units/customers sites
- R & D trials and Engineering Batches.
- QMS, validation & trials batch documents preparation
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