Sun Pharma Hiring Analytical Development Executive | Apply Now
- Sun Pharma Recruitment Notification
- Job Overview
- Key Responsibilities
- Qualifications and Experience
- Location
- How to Apply
- Apply Here
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.
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.