Gland Pharma Limited - Multiple Openings in FR&D / Quality Assurance (AQA / Training) - Apply Now

 Urgent Requirement for - FR&D

Greetings from Gland Pharma Limited!!

We have an urgent Requirement for FR&D Department .In case if you are interested please share us the below details along with updated profile to durgabhavani.ancha@glandpharma.com.

Total Experience-

Current Ctc-

Expected Ctc-

Notice Period-
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).

Experience: 1 to 3 Years (Injectable Experience)

Openings: 10

Qualification: B.Pharm / B.Sc / M.Pharm / M.Sc

Urgent requirement for QA (AQA)

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.

Qualification: B.Pharm, M.Pharm / M.Sc

Experience: 2-5 yrs

Openings: 06

Urgent requirement for - QA Training

Greetings from Gland Pharma Limited!!
Interested Candidates, please share us your updated profile (with Photo) along with CTC Letter to hrd.pmy@glandpharma.com & hanumanthrao.rasike@glandpharma.com

Description:

1. To conduct induction and orientation programme for new recruits.

2. 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.

3. To facilitate the identification of training needs with coordination of respective HODs/Incharges

4. Preparation of training schedules, presentations and maintain the assets of the Training division.

5. Preparation and evaluation of questionnaires.

6. To co-ordinate for continual focus on cGMP, design and train individuals in their relevant Operation.

7. To co-ordinate for refresher training for the qualification of personnel activity as and when recommended by department Incharge.

8. To co-ordinate for on the job activities of personnel whose activities could affect the quality of product.

9. To coordinate with respective departments HODs/Incharges and conduct the Schedule trainings, new or revised SOP trainings and etc.

10. To Handle the Training Management system (Electronic) through Software

11. Preparation of power point presentations.

Experience: 2 to 4 Years.

Openings: 06

Urgent requirement for - QA Training

Greetings from Gland Pharma Limited!!
Interested Candidates, please share us your updated profile (with Photo) along with CTC Letter to hrd.pmy@glandpharma.com & hanumanthrao.rasike@glandpharma.com

Description:

1. To conduct induction and orientation programme for new recruits.

2. 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.

3. To facilitate the identification of training needs with coordination of respective HODs/Incharges

4. Preparation of training schedules, presentations and maintain the assets of the Training division.

5. Preparation and evaluation of questionnaires.

6. To co-ordinate for continual focus on cGMP, design and train individuals in their relevant

Operation.

7. To co-ordinate for refresher training for the qualification of personnel activity as and when recommended by department Incharge.

8. To co-ordinate for On the job activities of personnel whose activities could affect the quality of product.

9. To coordinate with respective departments HODs/Incharges and conduct the Schedule trainings, new or revised SOP trainings and etc.

10. To Handle the Training Management system (Electronic) through Software

11. Preparation of power point presentations.

Experience: 1 to 4 Years (Injectable Experience)

Openings: 05