Ind Swift Limited – Hiring for Officer & Executive – Formulation Development And Regulatory Affairs

Swift is the fastest flying bird on earth. It is the philosophy behind the genesis of the name Ind-Swift Ltd. Incepted in 1986 when three visionaries the Mehtas, the Munjals and the Jains, all 1st generation entrepreneurs visualized the business.Even with limited resources, the vision was to develop a Pharma enterprise with its body spread internationally and soul rooted in ethics. Today with strong business acumen, apart from pharmaceutical business Ind-swift has also progressively forayed in diversification into multifarious fields viz Infrastructure, Printing, Packaging & Stationary, Education, and Media Publication with its every unit as an independent profit earning centre.It is indeed a proud moment for us today, starting as a small domestic company in 1986 we have transformed into a truly global organisation with its operations and product range in more than 50 countries.

Vacancy Details

1. Department – Formulation Development / Regulatory Affairs
2. Role – Officer & Executive
3. Education – B. Pharma / M. Pharma
4. Experience – 02 to 05 Years
5. Location – Dera Bassi
6. Salary – ₹ 2,00,000 – 6,00,000 P.A.

Department – Formulation Development

Roles and Responsibilities :

1. Should have experience of 3-6 years (of reputed companies) with least master degree.

2. Candidates are required to have research formulation development experience of regulated market US, EU and Japan markets..

3. Candidates should be well versed with solid oral dosage forms, formulation development with QbD approach.

4. Should have experience of MUPs, pellet technology.

5. Should have expertise experience of product development report preparation with DOE, QbD, FMEA,

6. Should have experience of regulatory queries response.

7. Should be able to understanding of stability study interpretation.

Department – Regulatory Affairs

Roles and Responsibilities :

1. Preparation and submission of dossier as Per format CTD, ACTD, country specific, preparing SOP related Department.

2. Good working hand on clinical research Regulatory Affairs.

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