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Encube Ethicals – Openings for Quality Assurance Department


 Encube Ethicals is an integrated pharmaceutical company dedicated to topical formulations with 23+ years of experience in contract development and manufacturing. Our manufacturing facility in Madkaim – Goa, India is the largest single-site topical manufacturing facility in the world, dedicated to prescription and OTC pharmaceuticals, and cosmetic semisolid dosage forms. Encube’s R&D Centre in Mumbai, India houses a team of 150+ scientists working for the formulation development of topical products.


We at Encube are looking for Officer – Quality Assurance Department. The job will be based in Goa location.

We are Hiring!!!!!

  • Job Title:  Officer – Quality Assurance (Validation)
  • Department:   Quality Assurance
  • Experience: 2- 8 Yrs.
  • Qualification: B.Pharm/M.Pharm
  • Location: Ponda (Goa)


Job Description:
1. Prepare / review documents like SOPs, Periodic Process Validation & Report, Filling Validation Protocol & Report, Process Validation/Verification/Assessment Protocol & Report, Hold Time Study Protocol & Report, Cleaning validation/verification Protocol & Report, Study Protocol & Report.
2. Keep track of validation, periodic process validation or activities pertaining to validation, hold time study, cleaning validation, Computer system validation etc. and communicating the same.
3. Maintaining logs or other documentation required for qualification / validation / CSV activities as defined in respective SOPs.
4. Monitor pre-exhibit, Exhibit and Commercial validation batches manufacturing, filling and packing.
5. Perform / review qualification and validation documents, other Master documents (e.g. Master Formula Records, Batch Manufacturing Records and Batch Packing Records etc.) and CSV documents.
6. Review QMS documents (e.g. Change control, Deviation CAPA, Investigation etc.).
7. Responsible for ensuring that computerized system is supported and maintained in accordance with applicable SOP and for executing data governance enhancement program.
8. Responsible for preparation and review of CSV lifecycle documents of laboratory instruments and process equipment’s.
9. Perform activities related to eBRM and DMS as applicable.


· Male candidates will be prepared
· Candidates wish to relocate Goa can apply.
Mail your Resume on –


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