Jobs Scan

Jobs Scan

Sun Pharma – Urgent Openings for Regulatory Affairs / R&D – Apply Now

Sun Pharmaceutical Industries Limited is the largest specialty generic pharmaceutical company in the world. We provide high quality, affordable medicine trusted by healthcare professionals and patients in over 150 countries. It is also India’s largest, most trusted and most valuable pharmaceutical company by market capitalization. To keep pace with our growth plan we require young and energetic professionals of our plant at Baroda.


Sun Pharmaceutical Inds Limited
Opening in Regulatory Affairs – Branded

  • Qualification:   M.Pharm / M.Sc in Biotech
  • Grade: Executive / Sr. Executive
  • Job Location: Baroda / Mumbai / Gurgoan

1) This position will support and manage the regulatory activities associated with the Chemistry, Manufacturing and Controls for licensed biologic products across globe. Regulatory activities focus on filing activities/query responses/post approval changes as suggested across globe.
2) Incumbent will be responsible for assuring the established regulatory strategy is aligned with Health Authority requirements from a global perspective and assuring that regulatory submissions are on time and high quality.
3) Understanding country specific requirements, particularly for EM, and sharing additional data generation/gap assessments with CFT
4) Closely work with consultants, partners and local regulatory colleagues to understand regional requirements.
5) Preparation of Agency consultation packages, briefing book and required presentations and engage with Agency for consultations
6) Provide CMC support for other branded projects as needed.
7) Additional duties include coordination with our global manufacturing sites, integration of regulatory strategy with those sites and communication to senior management.
8) Responsible for preparation of IND and IMPD documents
9) Providing consistent support to commercial and clinical teams.
Send in your resume to :

Sun Pharmaceutical Inds Limited – Baroda:
Opening in R&D – Biotechnology – Upstream Process

  • Grade : Manager / Sr. Manager
  • Qualification : M.Tech / M.Sc / PhD – Biotechnology or Biochemistry
  • Job Location : Baroda

Brief JD :
1) Planning of lab scale studies for development, optimization and characterization of upstream process.
2) Exposure to Global market requirements related to biosismilars.
3) Participating in project planning, including timelines and resources for internal and CDMO projects.
4) Supporting GMP manufacturing during scale-up, technology transfer and through process investigations, deviations and change control assessments.
5) Seeking and identifying improvement and optimization of the process with regards to technical as well as economic aspects.
6) Collaboration with DSP, analytical, PM, QA/QC, Regulatory, IP and external CDMO clients in order to achieve results.
7) Supporting all activities related to setting up process development lab with good laboratory practices and organizational and safety standards.
8) Good exposure for CMC support for global biotech product filing.
9) Upstream MSTG experience is desirable.
Send your resume to :
Freshers need not apply



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