Gland Pharma Ltd – Urgent Vacancy for QA/ FR&D departments

Gland Pharma - Pharmawalks
Dear Aspirents,
Greetings from Gland Pharma Ltd..!!!
We are hiring Quality Assurance, FR&D departments. Please find the details attached below.

Training – Quality Assurance

Experience: 1 to 4 Years (Injectable Experience)
Openings: 05
Job Description:
  • To conduct induction and orientation programme for new recruits.
  • To conduct General training programmes like behavior, hygiene and documentation practices, line clearance procedures etc., shall be provided and basic GMPs during routine training schedules.
  • To facilitate the identification of training needs with coordination of respective HODs/Incharges
  • Preparation of training schedules, presentations and maintain the assets of the Training division.
  • Preparation and evaluation of questionnaires.
  • To co-ordinate for continual focus on cGMP, design and train individuals in their relevant Operation.
  • To co-ordinate for refresher training for the qualification of personnel activity as and when recommended by department Incharge.
  • To co-ordinate for On the job activities of personnel whose activities could affect the quality of product.
  • To coordinate with respective departments HODs/Incharges and conduct the Schedule trainings, new or revised SOP trainings and etc.

  • To Handle the Training Management system (Electronic) through Software
  • Preparation of power point presentations.
Interested Candidates, please share us your updated profile (with Plhoto) along with CTC Letter to &

Quality Assurance (AQA)

Qualification: B.Pharm, M.Pharm / M.Sc
Experience: 2-5 years
Openings: 06
Job description:
  1. Review of analytical raw data and reports of raw materials, packing materials, in process (bulk), finished products and stability studies.
  2. Review of analytical raw data and reports of submission batches, process validation batches, equipment / instrument calibrations and working standard qualifications.
  3. Participating in the Regulatory & Various customer audits.
  4. Check the audit trails for instruments and equipment’s in quality control lab.
  5. Review of preliminary investigations for in process (bulk) and finished product OOT in quality control lab.
  6. Review of preliminary investigations for OOS’ in Quality control lab.
  7. Review of stability OOT in Quality control lab.
  8. Verification of CAPA effectiveness in Quality control lab.
  9. Review on Lab solutions must.
Interested Candidates, please share us your updated profile (with Plhoto) along with CTC Letter to &

Formulation R&D

Experience: 1 to 3 Years (Injectable Experience)
Qualification: B.Pharm / B.Sc / M.Pharm / M.Sc
Openings: 10
Job Description:
  • Formulation Development of Sterile Dosage Forms for Regulatory market which included parenteral dosage forms.
  • Developed parenteral formulations and transferred into commercial manufacturing.
  • Also initiated development work on lyophilized products.
  • Conduct Pre-formulation studies (drug- excipient compatibility studies, forced degradation studies, Solubility studies, Filter compatibility studies, Stopper compatibility studies and container closer compatibility studies).
If you are interested please share us the below details along with updated profile to
Total Experience-
Current Ctc-
Expected Ctc-
Notice Period-

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