Sun Pharma Careers: Senior Executive Jobs | MSc Chemistry Graduates Apply Now
Are you looking for Senior Executive jobs in Analytical Development with a leading pharmaceutical company? Sun Pharma Careers offers an excellent opportunity for professionals seeking MSc Chemistry jobs in Gurgaon R&D. This Executive / Senior Executive – Analytical Development role allows you to work on regulatory queries, pharmacopoeial compliance, and analytical support while growing your career at Sun Pharma.
About Sun Pharma
Sun Pharmaceutical Industries Ltd is India’s largest pharmaceutical company and a global healthcare leader. Sun Pharma Careers provides excellent opportunities for professionals seeking Senior Executive jobs, Analytical Development roles, and MSc Chemistry jobs, offering a culture driven by innovation, regulatory excellence, and continuous career growth.
- Job Title: Executive/ Senior Executive – Analytical Development
- Location: Gurgaon – R&D
- Job Grade: G12A/11B
- Educational Qualification: M.Pharm/M.Sc
- Experience: Tenure: 3 to 8 years
Regulatory Queries:
- To coordinate for Analytical queries received for the US/OAM/EM markets from regulatory agencies.
- Ensure a timely response from Analytical to the Regulatory team for responding to the Regulatory agency.
- To revise the specs /STP for changes related to query response.
Pharmacopoeial Compliance of Excipients:
- Responsible for the timely review of pharmacopoeial updates as appeared in different pharmacopoeias, IP/USP/BP/EP.
- To share gap assessments for the changes that appeared in the pharmacopoeia.
- To ensure the evaluation of changes that appeared in the pharmacopoeia and the revision of corresponding specs /STP.
Excipient Review for New Projects and LCM Projects (Market Extension):
- To manage and ensure review and release of excipient specs/STP for new development, LCM, and filing projects.
Creation of Specs /ATP:
- To provide analytical support to FRD/RA/ AD and the plant by preparing specifications (specs) and Standard test procedures (STPs) as a creator related to:
- New Drug products/APIs/vendor addition and vendor updates/Pharmacopeia updates.
- Life cycle updates.
- To review the vendor documents in case of outsourced APIs.
- To keep a track of multiple tasks that are under review/approval with other stakeholders for timely release.
