Senior Development Chemist

Job Title: Senior Method Development Chemist
Cambridge, ON (In-Office)
Position Type: Full-time Fixed Term (18 Months Contract)
Vacancy Status: This contract position will become vacant in May 2026
AI Disclosure in Hiring: We do not use artificial intelligence to screen, assess, or select applicants
The Senior Method Development Chemist is responsible for developing and validating robust methods for the analysis of new products in support of new product registrations for global markets. The Senior Method Development Chemist serves as a technical expert who: supports new product application submissions, new product method improvements and cost savings initiatives.
Develops analytical procedures and methods for raw material and/or finished product using up-to-date knowledge in various analytical techniques and ICH/VICH guidelines.
Ensures that all work is carried out in compliance with company Safety policies, Good Manufacturing Practices (GMP/GLP) and Standard Operating Procedures (SOPs).
Creates Project Timelines in accordance with marketing priorities, sets milestones/critical path and ensures on time project completion.
Is able to think critically and respond to issues in a timely manner with little supervision.
Responsible for executing stability studies on new products under development and analyzing/reporting stability trends.
Prepares product registration documentation and product chemistry packages to meet regulatory requirements.
Participates in team driven activities to new product development projects.
CRITICAL THINKING – is the ability to be thoughtful and draw pertinent conclusions after a discussion or meeting;
global performance. help facilitate sharing of information between people. data and facts. Minimum B.Sc in technical field or scientific discipline (Biology, Biochemistry, Chemistry) is required.

Technical
~ HPLC and GC techniques, wet chemistry techniques.

5 years pharmaceutical industry experience.

• Strong working knowledge of FDA regulations and requirements with the ability to integrate into projects.
• Strong technical writing and editing skills.

Sc, PhD,) Microbiology, Biochemistry, Biology or PharmD is preferred.

Technical
~ Advanced knowledge in HPLC and GC, techniques; extensive experience with analytical method development. Strong understanding of cGMP guidelines and FDA regulations related to the pharmaceutical industry.

Should possess a well-defined sense of diplomacy, including solid negotiation, conflict resolution, and people skills.
Able to build and maintain lasting relationships with corporate departments and key business partners.
13 paid holidays.

• Medical, dental & vision.
• Employee Assistance Program.
• Bimeda is a leading global innovator, manufacturer and marketer of veterinary pharmaceuticals and animal health products and has over half a century’s experience in providing science-driven solutions to optimize the health, wellbeing and productivity of the world’s animals.

Bimeda’s global innovation program sees eight state-of-the art R&D centers across four continents collaborate on an enviable product development pipeline which anticipates the ever-evolving needs of the animal health industry.
Bimeda’s ten manufacturing facilities across seven countries allow the company to manufacture a broad range of preventative, curative and nutritional products including sterile injectables, vaccinations, nutritional boluses, feed additives, tablets, water-soluble powders, pastes and non-sterile liquids.
Globally, the company focuses on the development, manufacture and commercialization of quality Bimeda-branded products while also being the partner of choice for contract manufacturing and R&D services for prominent companies within the animal health industry.
Accommodations are available upon request.