Senior Process Development Scientist

Sun Pharmaceutical Industries LtdBillerica, MA
Hybrid

About The Position

Lead new product formulation, process development, transfers into manufacturing, and continuous improvement of existing processes.

Requirements

  • Minimum B.S. in related scientific field required
  • Minimum 7-10 years related experience preferred
  • Able to work with external contractors to find new technology, equipment or solutions to process issues
  • Process validation experience
  • Cleaning validation experience
  • Analytical hands-on experience with techniques such as HPLC, Karl Fischer, DSC, and spectroscopic techniques
  • Experience working in a cGMP environment
  • Process development experience and manufacturing process investigation skills
  • Strong technical writing skills and resourceful problem solving skills
  • Ability to work independently and as a member of a cross functional team
  • Excellent verbal, written and interpersonal communications skills
  • Strong attention to detail and ability to manage multiple assignments concurrently
  • Able to lead cross functional teams to design experiments and address process issues

Nice To Haves

  • Experience with parenteral formulation, lyophilization and sterilization techniques preferred
  • Experience with aseptic techniques in a clean room environment is highly beneficial
  • Understanding of Quality by Design principles and statistics is preferable

Responsibilities

  • Manage tasks at independent level and contribute to cross-functional project management teams
  • Design experiments using Quality by Design principles, execute and author reports in support of: Formulation, aseptic filling and lyophilization development of new products; Continuous improvement, troubleshooting and investigations of existing processes and products; Process transfers into manufacturing
  • Perform analytical testing in support of product development studies
  • Prepare cGMP documents such as SOPs, batch records and protocols
  • Design, execute and write technical reports to support FDA filings
  • May direct the work of junior Process Development staff
  • Other duties as assigned
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