Job Description

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