MSN Group is the fastest growing research-based pharmaceutical company based out of India. Founded in 2003 with a mission to make health care affordable, this Hyderabad-based venture has Fifteen API and Six finished dosage facilities established across India & USA.
The group has an integrated R&D center for both API and formulation under one roof, dedicated to research and development of pharmaceuticals to make them more accessible. With core focus on speed and consistency in delivery, MSN has achieved the following:
- More than 900+ national and international patents
- Product portfolio featuring over 450 + APIs
- 300+ Formulations, covering over 35 major therapies
- Won the trust of more than 40 Million patients across 80+ countries globally
Innovation and speed form the crux of our business strategy. Backed by a dedicated and experienced team of over 14,000 the organizational environment at MSN integrates multiple disciplines and functions by effective implementation of goals and objectives through technology, coupled with Integrity, Imagination and Innovation.
DATE AND TIME:
- Date: 13th December 2024 (Friday)
- Time: 9:00 AM to 2:00 PM
- Venue:
MSN Laboratories Pvt. Ltd.,
MSN R&D Center,
Pashamylaram, Isnapur, Patancheru,
Sangareddy, Telangana - Contact: 040-30438786
Apply
Walk in with your documents on the interview date. Alternatively, you can share your CV with Dinesh Baratham at dinesh.baratam@msnlabs.com.
- Qualification:
- M.Sc. in a relevant field.
- Experience:
- 1-3 years in the pharmaceutical API industry.
- Candidates from R&D, AR&D, QA, and QC departments with less than 3 years of experience are also eligible.
- Note: Candidates with more than 3 years of experience are not eligible
Responsibilities
- Regulatory Submissions: Prepare and manage regulatory filings for API products, ensuring compliance with applicable regulations.
- Documentation: Maintain and update regulatory documents, such as DMFs and technical files.
- Compliance: Monitor regulatory changes, assess impacts, and ensure alignment with guidelines.
- Communication: Liaise with regulatory authorities, addressing inquiries and managing inspections.
- Collaboration: Partner with R&D, QA, and production teams for regulatory support.
- Quality Standards: Ensure compliance with GMP and other quality regulations.
- Strategic Input: Contribute to regulatory strategies for product development and lifecycle management.Updated Resume
- Valid Photo ID
- Copies of Educational and Experience Certificates
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