Gracure Pharmaceuticals Urgent Hiring for Manager/Sr. Manager – QA in Bhiwadi, Rajasthan

Gracure Pharmaceuticals Recruitment Notification

Gracure Pharmaceuticals Ltd., a leading pharmaceutical manufacturer specializing in tablets, capsules, dry syrups, ointments, and syrups, is urgently hiring for the position of Manager/Sr. Manager – QA. This role is based at our major manufacturing unit in Bhiwadi, Rajasthan, which boasts 100% exports and prestigious certifications including WHO-GMP and EU-GMP. We are looking for experienced professionals with a strong background in the pharmaceutical industry to join our team.

Company Profile

Gracure Pharmaceuticals Ltd. is renowned for its high-quality pharmaceutical products and adherence to stringent regulatory standards. Our Bhiwadi unit, a major hub for our operations, has received EU-GMP approval, along with waivers for Ukraine and Australian TGA. Additionally, we hold Tanzanian GMP and Ethiopian GMP certifications, reflecting our commitment to excellence and global standards.

Job Location

  • Location: Bhiwadi, Rajasthan, India

Position Details

  • Position: Manager/Sr. Manager – QA
  • Experience: 10-18 years (Only candidates with pharmaceutical industry experience will be considered)
  • Qualification: M.Sc/M.Pharm

Key Responsibilities

  • Experience in Regulatory (MHRA, EU-GMP, USFDA, TGA.)Audits & Documentation as per cGMP.
  • Monitored & ensured that batch production records are executed and reviewed in accordance with established SOPs and cGMP regulations.
  • o monitor the line clearance and in-process checks at the different stages of batch manufacturing and packing & Compliance of Mfg. & Pkg. process activities as per approved BMR/BPR.
  • Assessing & approving the equipment qualification protocols and reports for accuracy, completeness and traceability as well as adherence to the protocol /procedures.
  • Capable to handling the team of 15 to 20 persons.
  • To do Impact and Risk Assessment in the change controls & Preparation of Risk Assessment Protocols/Reports.
  •  Preparation of Investigation Reports & Review of QMS documents such as Events, Investigation reports, OOS, Annual product quality review, Site master file and validation master file etc.

Application Details

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