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
- To work as per cGMP and ensure its compliance as per current guideline and SOPs.
- Responsible to take training before execution of allotted work & maintaining the training file.
- Responsible to follow safety precaution as per laboratory procedure.
- Responsible to escalate any issue / incident to reporting manager for prompt corrective action.
- Responsible for method development studies of API, Drug Product & In process Material preferably Peptide molecules
- Responsible for method Validation studies of API, Drug Product & In process Material preferably Peptide molecules
- Responsible for routine and stability studies of API, Drug Product & In process Material preferably Peptide molecules
- Responsible to perform the pharmacopeial evaluation study as per requirement.
- Responsible to align with organization goal.
- Other responsibilities assigned by reporting authority.
- Responsible to follow Quality Management Document procedure.
- Responsible to perform the calibration of instrument.
- Responsible to prepare Study Protocol and Study Reports.
- Responsible to maintain instrument/equipment as per SOPs.
- Responsible for timely archival of documents as per SOP.
- Responsible to follow safety precaution as per laboratory procedure.
- Responsible to ensure proper Handling and Disposal of waste.
- Responsible to qualification reference standard / working standard/chemical reference standard samples as per approved and valid procedure.

Qualifications and Experience
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📱 Join Click HereTo 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.