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Scientist Formulation Development

2 weeks ago

Montreal, Quebec, Canada Core Healthcare Full time

Primary Duties

  • Design and develop oral dosage forms, including both solid and liquid preparations.
  • Carry out early-stage research on active ingredients, excipients, comparator products, and applicable patents.
  • Apply Quality-by-Design methodologies to refine formulations and improve manufacturing processes.
  • Lead scale-up activities, feasibility work, proof-of-concept batches, and registration-stage manufacturing; prepare all associated technical and regulatory documents.
  • Work closely with analytical labs, warehousing, regulatory affairs, and technology-transfer groups to ensure smooth project execution.
  • Maintain full compliance with GMP requirements, internal SOPs, and safety regulations; serve as a subject-matter expert during internal and external audits.
  • Review, approve, and sign off on batch records; participate in internal audits and continuous-improvement (Lean Six Sigma) projects.
  • Organize and track development data, manage material requests, and maintain comprehensive technical files.
  • Provide scientific guidance to contract research partners and assist with equipment evaluation, upgrades, and new technology implementation.

Core Skills & Expertise

  • Demonstrated experience in developing either solid oral products or liquid pharmaceutical formulations.
  • Strong working knowledge of GMP, QbD, regulatory filing requirements in Canada/US/EU, and patent and literature research.
  • Hands-on experience with technology transfer, technical writing, and maintaining audit readiness.
  • Solid understanding of pharmaceutical equipment, manufacturing workflows, and industry standards.

Education & Experience

  • Bachelor's degree in Science, Pharmacy, or a related technical field (or equivalent diploma), along with a minimum of 3–5 years of relevant experience in the pharmaceutical industry.

Job Type: Full-time

Work Location: In person