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Senior Executive

Sun Pharma
Sun Pharma
0-2 years
Not Disclosed
10 April 30, 2025
Job Description
Job Type: Full Time Education: B.Sc./M.Sc/B.Pharm/M.Pharm/Life Science Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Job Title:

Senior Executive – R&D


Company:

Sun Pharmaceutical Industries Ltd


Location:

Tandalja – Research & Development (R&D) Facility


Posting Date:

April 21, 2025


Job Summary:

The Senior Executive at Sun Pharma’s R&D center in Tandalja will be responsible for end-to-end activities related to product development, including regulatory documentation, procurement coordination, formulation, analytical testing, and tech transfer. This role supports new product development for global markets.


Key Responsibilities:

  • Generate and request codes (RM, project, product).

  • Apply for licenses related to API imports and manufacturing for analysis/testing.

  • Coordinate procurement of raw materials, excipients, packaging, and innovator samples.

  • Execute pre-formulation, prototype, stability, and method development/validation batches.

  • Record experimentation details in laboratory notebooks (Log book/ELN).

  • Prepare and execute development protocols and study reports.

  • Initiate testing requests for raw materials and drug products.

  • Develop and submit stability protocols and place samples on stability.

  • Prepare tech transfer documents (Sheet II, MF, RA, FMEA, SDS, etc.).

  • Supervise scale-up, exhibit, and clinical batches at plants or CMOs.

  • Contribute to regulatory submissions and draft responses to regulatory queries.

  • Propose specifications for in-process and finished products.

  • Handle documentation for narcotics/psychotropics (if applicable).

  • Draft SOPs for lab instruments/equipment.

  • Participate in qualification of new instruments/equipment and document the process.

  • Utilize IT systems and platforms introduced by management.

  • Participate in process improvement and operational excellence initiatives (e.g., PACE, Kaizen).


Required Skills and Attributes:

  • Strong understanding of pharmaceutical product development and regulatory requirements

  • Experience with documentation for international markets

  • Familiarity with ELN systems and IT tools

  • Detail-oriented with strong organizational and reporting skills

  • Proactive in process optimization and quality compliance