Job for M.Pharm, M.Sc, B.Pharm, B.Sc at Coral Drugs

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Coral Drugs, headquartered in New Delhi, India, is an integrated, research-based international pharmaceutical company that produces a wide range of high-quality, affordable active drug ingredients. With a team of dedicated scientists, Coral's R&D department provides efficient processes for off-patent products. Our goal is to maximize on the production of active ingredients by discovering new ways to manufacture, without compromising quality. Having clients all over the world, we assume a great level of corporate responsibility. Adhering to quality production standards across the globe, Coral Drugs takes pride in being a true international supplier of high-quality pharmaceuticals.

M.Sc/ B.Pharma/B.Sc. Should have knowledge of Change Control, OOS, Deviation handling, APQR, BPR, SOP. Should have working experience in API Plant.
Desirable: 2 to 5 year working experience.

Executive - QC
M.Sc/ B.Pharma/B.Sc. Candidate should have good knowledge of GC, Wet lab and HPLC.
Desirable: 2 to 5 year working experience.

Asst. Manager - QC
Candidate should have good knowledge of GC, Wet lab and HPLC, can handle team of 10 to 15 persons. Good knowledge of SOP's and documentation.
Desirable: 7 to 10 year working experience.


Officer – Quality Assurance
Preferable candidate from Bulk (Active Pharmaceutical Ingredients (API)
1. To Handle Change Control, Deviation, OOS, OOT & CAPA.
2. Must have knowledge regarding Process Validation, Cleaning Validation, SOP Preparation, Closed the observation.
3. Review of BPR & Protocol
4. Quality Control documentation review
Desirable: Minimum 02 years working experience post B.Sc./M.Sc.
Location: Murthal, Sonepat.

Manager – Quality Control
1. Budgeting, forecasting & projection for the departmental goals & targets.
2. Provide strategic and tactical workforce planning & staffing strategy in alignment with the production plan.
3. Overall planning, supervision & control on the QC activities.
4. Effective management of all the sections HPLC/GC/WET/Micro etc.
5. Method verification & validation on HPLC & GC. 6. Ensuring smooth implementation and execution of cGMP, GLP guidelines.
7. To support Regulatory Filings. Candidate must have faced Regulatory audits like USFDA, EU-GMP, WHO etc.
Desirable: Minimum 10 years working experience post M.Sc./ B.Sc./ M. Pharma / B. Pharma.
Location: Murthal, Sonepat.

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