MSTG Scientist I: Process Development & Validation

Sun Pharmaceutical Industries, Inc.

New Brunswick (NJ)

On-site

USD 76,000 - 86,000

Full time

7 days ago
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Job summary

Sun Pharma is seeking a MSTG Scientist I to support process development, exhibit batch execution, and manufacturing support within a fast-paced pharmaceutical setting. You will work with Manufacturing, Quality, and Technical Services to drive development, validation, and transfer of solid dosage products.

The role emphasizes design of experiments, data analysis, and robust technical writing to ensure cGMP compliance and successful product transfers.

Qualifications

  • Bachelor's degree in a relevant science field.
  • Minimum four (4) years of pharma industry experience.
  • 1–2 years experience with Solid Oral Dosage (OSD) product development and manufacturing.
  • Proficiency with MS Office applications: Word, Excel, Project, PowerPoint.

Responsibilities

  • Design and execute DOE, process optimization studies, and process qualification batches.
  • Compile, analyze, and interpret process data to support development and continuous improvement.
  • Prepare and maintain Master Batch Records, Exhibit Batch Protocols, and Validation documents.
  • Provide technical troubleshooting and support to manufacturing operations; support tech transfer and scale-up.

Skills

Analytical thinking
Problem solving
Technical writing
Verbal communication
Interpersonal communication
CEFR B1+ English

Education

Bachelor's degree in Pharmacy
Bachelor's degree in Pharmaceutical Sciences
Bachelor's degree in Chemical Engineering
Bachelor's degree in Chemistry
Other relevant scientific discipline
Master's degree (preferred)

Tools

Word
Excel
Project
PowerPoint

Job description

Sun Pharma is seeking a MSTG Scientist I to support process development, exhibit batch execution, and manufacturing support within a fast-paced pharmaceutical setting. You will work with Manufacturing, Quality, and Technical Services to drive development, validation, and transfer of solid dosage products.

The role emphasizes design of experiments, data analysis, and robust technical writing to ensure cGMP compliance and successful product transfers.

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