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Walk In Drive in Production and QC Department at Ajanta Pharma- 09th Feb 2025

Ajanta Pharma
Pharmacareer

Website Ajanta Pharma

Join Ajanta Pharma – A Leader in Specialty Pharmaceuticals

About Ajanta Pharma:

Ajanta Pharma is a globally recognized specialty pharmaceutical company dedicated to the development, manufacturing, and marketing of high-quality finished dosage forms. Our commitment to serving healthcare needs worldwide is reflected in our comprehensive range of innovative, first-to-market products in specialized therapeutic segments.

We are seeking skilled professionals for our Formulation Facility in Dahej, Gujarat. If you are passionate about pharmaceutical manufacturing and quality control, we invite you to join our team.

Walk-in Interview Details

  • Date: Sunday, February 9, 2025
  • Time: 09:00 AM to 04:00 PM
  • Venue: Hotel Silver Leaf, Hexzone Arcade, Next to Jaya Ben Modi Hospital, GIDC, Ankleshwar, Gujarat 393002

Open Positions

1. Production – Officer / Senior Officer

  • Qualification: B.Pharm / M.Pharm
  • Experience: 2 to 8 years
  • Key Responsibilities:
    • Experience in OSD Manufacturing Operations including Granulation, Compression, Pellet Coating, Capsule Filling, and Packing (Primary & Secondary).
    • Knowledge of e-BPR and e-Log will be an added advantage.

2. Production – Associate / Operator

  • Qualification: 10th / 12th + I.T.I / Diploma / D.Pharm
  • Experience: 2 to 10 years
  • Key Responsibilities:
    • Hands-on experience in OSD Manufacturing Operations such as Granulation, Compression, Pellet Coating, Capsule Filling, and Packing (Primary & Secondary).
    • Familiarity with e-BPR and e-Log will be beneficial.

3. Quality Control – Officer / Senior Officer

  • Qualification: B.Pharm / B.Sc / M.Sc
  • Experience: 2 to 8 years
  • Key Responsibilities:
    • Conduct analysis of Solid Oral – FP, In-process, and Stability Samples.
    • Expertise in operating HPLC, UV Spectrophotometer, and Dissolution Tester.
    • Experience in Analytical Method Validation/Transfer for Solid Oral formulations.
    • Knowledge of GC, ICPMS, and LCMS operations is desirable.

Eligibility Criteria

  1. Candidates with experience in regulatory-compliant manufacturing units adhering to cGMP/GDP standards will be preferred.
  2. Applicants currently employed in USFDA/MHRA-approved facilities are encouraged to attend.
  3. Please bring the following documents:
    • Updated CV
    • Current CTC structure
    • Last three salary slips
    • Educational qualification certificates
    • Experience certificates from previous employers
  4. Candidates who have attended an interview in the last six months are not eligible.

Join us and be part of a dynamic team that is making a global impact in healthcare.