Saga Lifesciences – Urgent Vacancy for Regulatory Affairs / Production

Saga Laboratories is an Indian Pharmaceutical company based in Ahmadabad, India which was established in 1981. It is a very progressive company having global presence and dominance. Saga Labs is a privately owned company manufacturing and supplying finished pharmaceutical products and is one of the largest suppliers of medicines. The satisfaction of the customers and providing good service to them are some of the motives of the company which it constantly wishes to fulfil.

The company is unwavering in its determination to attain excellence in all that it does and sets the highest standards for itself in the areas of health, safety, quality, cost and research and development programs. It has a philosophy which involves continuous improvement. Releasing the potential of the company and where it stands in the market always helps. More

Vacancy Details

Regulatory Affairs – officer/Executive

• Post: Regulatory Affairs – officer/Executive
• Qualification: B.Sc, M.Sc, B.Pharm, M.Pharm
• Experiences: 01 to 04 years
• Location: Prahaladnagar, Ahmedbad

Job Description – Regulatory Affairs – officer 
1. Prepare & compile registration dossier of ACTD, CTD & Regional as per the guidelines and checklist for submission to Regulatory authorities.
2. Co- ordinate with various departments to obtain essential documents required to send query responses & review and compile error free responses to query letters.
3. Must have knowledge regarding Analytical Method validation preparation and review
4. Distribution and Execution of the regulatory work plans.
5. Artwork checking as per country guideline
6. FDCA work (COPP, FSC, product permission) & CDSCO Sugam application
Interested candidates can apply on hr@sagalifesciences.com or 8347011134/21/23

 Production Officer 

• Qualification: B.Sc, M.Sc / B.Pharmacy ,M.Pharmacy
• Experience: 01 to 03  years
• Location: Ahmedbad, Gujarat

Job Description:
1. Approval in tablet & capsules most preferred.
2. Knowledge of granulation, compression & coating.
3. BRM, CGMP Practices.
4. Audit knowledge of GMP, MHRA & EU
5. Shifting scheduling, Batch Manufacturing, line clearness, production planning.
6. Materials management(RM & PM) both
7. Manpower planning and allocations.
8. Knowledge of Tablet Capsule, Coating, Compression, Granulation,)
9. Issue of Batch from quarantine area for compression, coating, capsule and Granulation.
10. Carry out in process parameter checking activity during compression, coating, capsule and Granulation activity.
11. Allocation of work to operator and helpers.
12. Performing production activities as per daily production plan.
13. Ensure environmental condition and pressure differential in production area.
14. Ensure all SOP’s of respective equipment are followed during production.
15. Transfer of production Batch to quarantine area and completion and reconciliation of Batch.
Interested candidates can apply on hr@sagalifesciences.com or 8347011134/21/23