Openings for Production in Marksans pharma and Regulatory affairs in Biological e

Openings for Production in Marksans pharma and Regulatory affairs in Biological e


About the Company :

The firm is one of the major contributor of medicines in India, established in the year 1968 by the professor of chemistry. This MNC located in several locations like Mumbai and Maharashtra in India, it is the 8th biggest among the generic revenue companies. 
The company has the products like pediatric, anti-tubercular, diabetic, cardiovascular, anti-infectives. The company has 28 products with the offices and labs distributed globally. like USA, Europe, south Africa, Japan, Philippines, Mexico and Latin America.
The firm also focused on the biotechnological projects, there by delivering high standard medicines to man kind.

About the Job :

Openings for Production:

Urgent Requirement

For Marksans Pharma Ltd

Location : Goa

For Softgel Production Department

Qualification : Bpharm/Mpharm/Bsc/MSc

Experience - 7 - 12 Years

Candidates need to handle volumes, should have worked in a regulated company, Expertise in all areas of Softgelatin manufacturing and Manpower handling, Knowledge of handling QMS related activities relating to Softgel.

Interested may kindly email their CV on:

[email protected]

Regulatory affairs: 


Department: Regulatory affairs (Injectable formulations)

Designation: assistant manager

Qualification Masters in pharmacy or bachelors in pharmacy with 7 to 10 years of experience 

Work location Hyderabad

required job skills

knowledge on drug device combination products complex products

good regulatory work experience in sterile injectable formulations for global markets like USA Europe and Canada

Good communication and drafting skills

Ability to work with minimum guidance

Required to have knowledge on product development support like meeting package strategy preparation

dossier publishing using lifecycle management and post approval dossier review and compilation for global markets


Required good regulatory experience in sterile injectable formulation with 10 to 12 years of experience

Qualification: Masters or bachelors in pharmacy

department :emerging markets of regulatory affairs

Coordination with CFD for regulatory requirements and review of master documents for submission

Knowledge on labelling preparations work experience in regulatory and emerging markets is more desirable

interested candidates can share the resume before 7th of April to [email protected]

mention subject as "RA-712"