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Associate Scientist / Production Chemist


Summary: cGMP and non-GMP manufacture contracted to CMO.


Purpose of Job:  To manufacture and adequately document Active Pharmaceutical Ingredients (APIs), Intermediates, regulatory starting materials and other chemicals according to approved batch records (or other laboratory records) under close supervision.


Essential Duties/Responsibilities: 

  • Manufacturing APIs, intermediates, and regulatory starting materials according to approved batch production records
  • Assisting in the development and approval of cGMP batch records and other cGMP process documentation
  • Setup, use and cleaning of process equipment and maintenance of corresponding equipment logs, as applicable
  • Ensuring a secure supply of raw materials from reliable and qualified vendors
  • Dispensing and use of raw materials, and maintenance of corresponding material logs, as applicable
  • Maintaining schedule of manufacture activities
  • Participating in research and development activities under close supervision
  • Scaling up development processes for cGMP or non-GMP manufacture
  • Maintaining accurate cGMP records and R&D lab records
  • Preparing project reports and/or data summaries, as needed
  • Understanding of and compliance with appropriate SOPs
  • Ensuring safety and cleanliness of laboratory work areas
  • Cleaning glassware
  • Helping create a positive work environment
  • Other reasonable duties may be assigned as necessary


Qualification Requirements: 

  • Bachelor’s degree in chemistry or equivalent formal training
  • Ability to scale-up processes
  • Knowledge of synthetic and purification techniques
  • Appropriate knowledge of cGMP regulations


Physical Demands/Work Environment: 

  • Ability to work with large glassware
  • Ability to safely handle hazardous materials
  • Ability to move/lift 50 pounds
  • Ability to bend to reach floor level
  • Ability to wear a respirator


‚ÄčIf interested, please send your resume and cover letter to

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