Senior Method Development Chemist

Job Title: Senior Method Development Chemist Location: 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 Job Summary 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. Role Specific Requirements Develop analytical procedures and methods for raw material and/or finished product using up-to-date knowledge in various analytical techniques and ICH/VICH guidelines. Ensure that all work is carried out in compliance with company safety policies, Good Manufacturing Practices (GMP/GLP), and Standard Operating Procedures (SOPs). Create project timelines in accordance with marketing priorities, set milestones/critical path, and ensure on‑time project completion. Write validation protocols and reports. Think critically and respond to issues in a timely manner with little supervision. Execute stability studies on new products under development and analyze/report stability trends. Establish specifications for new and/or reformulated products. Write necessary documents and reports in a clear and concise manner. Prepare product registration documentation and product chemistry packages to meet regulatory requirements. Participate in team‑driven activities for new product development projects. Other duties as assigned. Competencies required for the role Analytical Thinking / Problem Solving – identify needed information, seek from various sources, tackle problems logically, interpret data, spot patterns, deduce cause and effect. Creativity and Innovation – create, develop, and implement new products, processes or services to improve efficiency, effectiveness or competitive advantage; transcend traditional ideas. Critical Thinking – thoughtful and draw pertinent conclusions after discussion or meeting; support decisions. Fostering Collaboration / Teamwork – work jointly with others, demonstrate ability to lead teams, build partnerships for global performance; respect others. Effective Communication – convey information effectively and efficiently; facilitate sharing of information; express clearly; listen and show respect. Requirements Experience: At least 5 years of drug experience developing microbiological methods in a GMP environment. Experience with the requirements of ANDA, ANADA, IND, and INAD submissions is desirable. Education: Minimum B.Sc in technical field or scientific discipline (Biology, Biochemistry, Chemistry) is required. Technical: HPLC and GC techniques, wet chemistry techniques. Other: Good written and verbal communication skills are required. Good organizational and troubleshooting skills are required. Self‑motivated and committed to a team approach. Strong interpersonal and organizational skills. Desirable Experience: 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. Education: Advanced degree (e.g., M.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. Other: 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. Compensation & Benefits 13 paid holidays. Medical, dental & vision. Employee Assistance Program. Expected Salary Range: $60,000 - $85,000 per year. About Bimeda 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. More info at www.bimedacareers.com Equal Opportunity & Accessibility At Bimeda we are committed to fostering an inclusive, barrier‑free and accessible environment. Part of this commitment includes arranging accommodations to ensure an equitable opportunity to participate in the recruitment and selection process. If you require an accommodation, we will work with you to meet your needs. We are committed to an inclusive and accessible recruitment process. We are an equal‑opportunity employer and assess candidates based on skills and experience. Canadian experience is not required. Recruitment records are retained in accordance with Ontario law. #J-18808-Ljbffr