MSTG Scientist

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Sun Pharma is the world’s fourth largest generics company with presence in Specialty, Generics and Consumer Healthcare products. Supported by more than 40 manufacturing facilities, we provide high-quality medicines, trusted by healthcare professionals and patients, to more than 100 countries across the globe. Over the last two decades, Sun Pharma has established itself as a leading player in the generics market in the U.S., and we are rapidly ramping up our presence in the specialty branded market with a focus on dermatology, ophthalmology and onco-dermatology.

Are you a scientist who enjoys turning data into solutions and driving products from development through validation and commercial readiness? We are seeking a MSTG
Scientist I to support process development, exhibit batch execution, process qualification activities, and manufacturing support within a fast-paced pharmaceutical environment.

This role offers an excellent opportunity to work cross-functionally with Manufacturing, Quality, and Technical Services teams while contributing to the development, optimization, validation, and successful transfer of solid dosage pharmaceutical products.

• Design and execute Design of Experiments (DOE), process optimization studies, and process qualification batches.
• Compile, analyze, and interpret process data using statistical tools to support process development and continuous improvement initiatives.
• Support product development projects from conceptual studies through process characterization and qualification activities.
• Participate in cleaning validation studies and related process development initiatives.

• Develop and maintain comprehensive technical documentation throughout various stages of product development.
• Prepare and review:
  • Master Batch Records (MBRs)
  • Exhibit Batch Protocols
  • Pre-Validation Documentation
  • Process Validation Protocols
  • Validation Reports
  • Technical Study Reports
• Ensure all documentation meets cGMP and regulatory requirements.

• Provide technical troubleshooting support to manufacturing operations.
• Investigate process challenges and recommend scientifically sound solutions to improve product quality and operational efficiency.
• Support technology transfer, scale-up, and validation activities as needed.
• Collaborate with Manufacturing and Quality teams to support successful production and compliance outcomes.

• Lead and support compliance-related investigations.
• Assist with Corrective and Preventive Actions (CAPA), commitments, and Change Control activities.
• Participate on cross-functional teams to address technical challenges, improve processes, and strengthen collaboration across departments.
• Support continuous improvement initiatives that enhance efficiency, compliance, and product quality.

• Bachelor's degree in:
  • Pharmacy
  • Pharmaceutical Sciences
  • Chemical Engineering
  • Chemistry
  • Other relevant scientific discipline
• Minimum four (4) years of relevant pharmaceutical industry experience.
• 1-2 years experience with Solid Oral Dosage (OSD) product development and manufacturing.
• Proficiency with Microsoft Office applications, including:
  • Word
  • Excel
  • Project
  • Power Point
• Strong analytical thinking and problem-solving abilities.
• Excellent technical writing, documentation, and reporting skills.
• Strong verbal and interpersonal communication skills.
• Self-motivated individual with a hands-on approach and a proactive mindset.
• Intermediate English proficiency (CEFR B1+ or equivalent).

• Master's degree in a relevant scientific discipline.
• Knowledge of process validation, cleaning validation,…