Sun Pharma Hiring Analytical Development Executive | Apply Now

Sun Pharma Walk-in Interview for Regulatory Affairs: Exciting Career Opportunities

Sun Pharma Recruitment Notification

Sun Pharma is hiring for the position of Analytical Development Executive at their Tandalja – R&D location. This is a fantastic opportunity for professionals with a strong background in analytical chemistry, method development, and regulatory affairs.

Job Overview

As an Analytical Development Executive at Sun Pharma, you will be responsible for a variety of crucial tasks, including drug substance and product analysis, specification preparation, and support for regulatory submissions. This role requires a deep understanding of analytical techniques and regulatory compliance to support the development and lifecycle management of pharmaceutical products.

Key Responsibilities

  •  Specification & ATP preparation, review and approval for drug substance, drug product, excipient & packaging material for new product for all markets.
  • Analytical activities related to  Extractable & leachable method development & stability analysis of drug product on LC-MSMS, GC-MSMS, ICP-MS, ICP-OES etc..
  • Drug substance & drug product support for Life cycle management related to documentation for all markets.
  • Provide support to respond the regulatory query.
  • Support to plant location for documentation related work.
  • Specification finalization meeting for drug substance and drug product.
  • Co-ordination with development team, non-oral group leads and PMO’s for documentation related activities on requirement basis.
  • Responsible for review of analytical documents in terms of Technical reports and Justification reports, which are submitted to various agencies.
  • Review of out source drug master file related documents.
  • Responsible for smooth functioning and co-ordination across various sites for harmonization and simplification.
  • Support for the filling related activities on requirement basis.
  • SOP review on requirement basis. (LIMS, LMS training)
  • Technical report/MFF/Monograph/gape/Harmonization code related activities.
  • Support for the Pharmacopoeial Compliance related activities on requirement basis.
Sun Pharma Job Opportunity for Manufacturing (OSD / Tablet) Roles
Sun Pharma Job Opportunity for Manufacturing (OSD / Tablet) Roles

Qualifications and Experience

To be considered for this role, candidates must meet the following qualifications:

  • Educational Background: A Bachelor’s or Master’s degree in Pharmacy, Analytical Chemistry, or a related field.
  • Experience: A minimum of 3-5 years of relevant experience in analytical development, method validation, or regulatory affairs within the pharmaceutical industry.
  • Skills: Strong proficiency in using analytical techniques such as LC-MSMS, GC-MSMS, ICP-MS, ICP-OES, and others relevant to method development and analysis.
  • Documentation: Hands-on experience with technical reporting, regulatory submission documentation, and compliance activities.

Location

This position is based at Sun Pharma’s R&D facility in Tandalja

How to Apply

If you are a skilled Analytical Development Executive with the qualifications mentioned above, Sun Pharma invites you to apply. Click the link below to submit your application:

Apply Here

To apply for this job please visit careers.sunpharma.com.

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