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
- Qualification: B.Sc, M.Sc, B.Pharm, M.Pharm
- Experiences: 01 to 03 years
- Salary: Depend on Personal Interview
- Location: Ahmedbad
- Prepare & compile registration dossier of ACTD, CTD & Regional as per the guidelines and checklist for submission to Regulatory authorities.
- Co- ordinate with various departments to obtain essential documents required to send query responses & review and compile error free responses to query letters.
- Must have knowledge regarding Analytical Method validation preparation and review
- Distribution and Execution of the regulatory work plans.
- Artwork checking as per country guideline
- FDCA work (COPP, FSC, product permission) & CDSCO Sugam application
Interested candidates can mail or contact on hr@sagalifesciences.com