R&D Formulation Specialist responsible for innovative, high-quality formulations at Medisca. Collaborating throughout the product lifecycle, from ideation to launch and scale-up across pharmaceutical disciplines.
Responsibilities
New product development
Generate new ideas leading to innovative, differentiated and potentially patentable products and formulations by applying scientific expertise and monitoring emerging pharmaceutical trends, including personalized medicine
Lead or support formulation/reformulation projects from concept through product launch, including scale-up and commercialization, ensuring technical feasibility and manufacturability
Design and execute experiments to develop new and optimized formulations
Conduct literature reviews, perform market research and monitor emerging technologies relevant to compounding and related industries
Perform product testing to evaluate and identify opportunities for improvement and innovation
Conduct preliminary intellectual property and patent assessments and support invention disclosures and patent development activities
Collaborate with external partners on potential co-development projects
Work with raw material suppliers to source and evaluate materials for new, existing or reformulated products
Collaborate with process engineers to successfully scale formulations from the laboratory to pilot and commercial production
Maintain GMP-compliant documentation and provide quality control support across product ranges
Participate in investigations related to out-of-specification (OOS) results, deviations and customer complaints using root cause analysis and continuous improvement principles
Contribute to training efforts and the development of educational materials
Provide internal and customer-facing R&D technical support, including troubleshooting and formulation advice
Requirements
Master's degree or higher in pharmaceutical sciences, chemistry, chemical engineering or a related field
More than 5 years of experience in pharmaceutical formulation development with demonstrated experience scaling products from the laboratory to commercial manufacturing (experience in compounding is an asset)
Proven experience developing innovative or differentiated formulations, ideally with measurable technical or commercial impact
Experience developing formulations across multiple dosage forms and delivery technologies
Experience supporting intellectual property development (e.g., patent drafting, invention disclosures or patent filings) is considered a major asset
Experience identifying and executing projects eligible for the SR&ED (RS&DE) program and contributing to SR&ED claims is considered a significant asset
Strong regulatory knowledge and understanding of GMP, USP, NAPRA, FDA, DEA, Health Canada, TGA, ISO and ICH guidelines
Proficiency with Microsoft Office (Word, Outlook, Teams and Excel) required
Fluency in English (spoken and written) required
Demonstrated project management, document control, organizational, administrative and collaborative skills
Demonstrated problem-solving ability, Quality by Design (QbD) approach, process-oriented mindset, attention to detail and strong team spirit
Benefits
Work-life balance — 37.5-hour workweek with early-finish Fridays year-round, paid leave and vacation policy
Invest in your health — Choice of modular plans, a health spending account and free telemedicine
Your wellbeing matters — Employee wellness program offered
Flexible work environment — Hybrid work schedule with a home-office reimbursement program
Your future is promising — Learning and career advancement opportunities within Medisca
Save for your future — Medisca contributes to a Deferred Profit Sharing Plan (RPDB) when you contribute to RRSPs
Help us grow — Employee referral program
A central location — Free parking and public transit access; shopping center within walking distance for lunch or groceries
We like to have fun — Company events throughout the year
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