Sun Pharma Hiring Formulation Development (Orals) Executives

Sun Pharma Formulation Development (Orals) Executive/Sr. Executive Job Vacancies

Are you passionate about formulation development and looking to grow your career in the pharmaceutical industry? Sun Pharmaceutical Industries Ltd, one of the world’s largest specialty generic pharmaceutical companies, is hiring for the position of Executive/Sr. Executive – Formulation Development (Orals) at its R&D facility in Tandalja, Baroda.

This role is ideal for candidates with a Master’s degree in Pharmacy (M.Pharm) and 2 to 5 years of relevant experience in formulation development, regulatory compliance, and document management.

Sun Pharma Recruitment Notification

Sun Pharma’s recruitment drive for this position offers a fantastic opportunity to contribute to a team dedicated to ensuring product robustness, regulatory compliance, and technical excellence. This could be the perfect next step in your career if you possess the required qualifications and expertise.

Position Overview

Position: Executive/Sr. Executive – Formulation Development (Orals)
Location: Tandalja – R&D Facility, Baroda
Experience: 2 to 5 years
Education: M.Pharm

As a member of the Product Robustness Review and Compliance Team, you will play a pivotal role in reviewing technical documents, assessing product robustness, and supporting compliance-related activities for regulated markets.

Key Responsibilities

• Review of technical documents for adequacy, raw data and quality of documents within defined SLA for regulated markets.
• Product Robustness Assessment.
• To perform and review statistical assessment using statistical tools such as JMP, Minitab for S1/S2 probability assessment, shelf life extrapolation, inverse extrapolation, DOE etc.
• Prepare, revise and review internal/ harmonised SOPs and guideline.
• Document Management- Provide document numbering and keep a record of the same as per SOP/guideline, issuance, archival and retrieval of documents & LNBs, inventory management for LNBs. Share historical data available in database with the team whenever required.
• Manage and provide inputs in Laserfische scanning of documents for EDAMS archival.
• Train the trainer activities.
• QMS related activities in track wise.
• EDMS related support

Qualifications and Skills

Candidates must meet the following criteria to apply for the role:

• Education: Master’s degree in Pharmacy (M.Pharm).
• Experience: 2 to 5 years of relevant experience in formulation development and regulatory compliance.
• Technical Skills:
  • Proficiency in statistical tools like JMP and Minitab.
  • Strong knowledge of formulation development processes and regulatory guidelines.
• Soft Skills:
  • Excellent organizational and communication skills.
  • Ability to manage and maintain technical documents effectively.

Application Process

Interested Candidates Apply online through the official Sun Pharma careers portal. Click here to start your application:
Apply Now.

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