Senior Method Development Chemist

Bimeda, Inc.; Cambridge; On-site; GBP 44,000 - GBP 64,000; Full time

Job summary

A leading global innovator in veterinary pharmaceuticals seeks a Senior Method Development Chemist to develop and validate methods for analyzing new products in Cambridge, ON. You will play an essential role in supporting new product registrations and driving method improvements while ensuring compliance with regulations. The ideal candidate has at least 5 years of drug experience in a GMP environment, preferably with a B.Sc in a scientific discipline. This position offers competitive compensation and benefits.

Benefits

13 paid holidays

Employee Assistance Program

Qualifications

• Minimum 5 years of drug experience developing microbiological methods in a GMP environment.
• Strong working knowledge of FDA regulations and requirements.
• Good written and verbal communication skills.

Responsibilities

• Develop and validate methods for analysis of new products.
• Ensure compliance with Safety policies, GMP, and SOPs.
• Prepare product registration documentation and chemistry packages.

Skills

Analytical thinking

Creativity and innovation

Critical thinking

Collaboration/teamwork

Effective communication

Education

B.Sc in technical field or scientific discipline (Biology, Biochemistry, Chemistry)

Advanced degree (e.g. M.Sc, PhD) in Microbiology, Biochemistry, Biology or PharmD

Tools

HPLC

GC techniques

Wet chemistry techniques

Job description

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

• 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.
• Writes validation protocols and reports.
• 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.
• Establishes specifications for new and/or reformulated.
• Writes necessary documents and reports in a clear and concise manner.
• Prepares product registration documentation and product chemistry packages to meet regulatory requirements.
• Participates in team driven activities to new product development projects.
• Other duties as assigned.

Competencies required for the role

ANALYTICAL THINKING/PROBLEM SOLVING - is the ability to identify the information needed to clarify a situation, seek that information from various sources and then tackle a problem by using a logical, systematic, sequential approach. Ability to identify and separate the key components of problems and situations. Ability to interpret information from a range of sources to spot patterns and trends in information and to deduce cause and effect from this.

CREATIVITY AND INNOVATION - is the ability to create, develop and implement a new product, process or service with the aim of improving efficiency, effectiveness or competitive advantage. Also, the ability to transcend traditional ideas, rules, patterns, relationships, or the like, and to create meaningful new ideas, forms, methods, or interpretations.

CRITICAL THINKING – is the ability to be thoughtful and draw pertinent conclusions after a discussion or meeting; can eventually support the final outcomes and decisions.

FOSTERING COLLABORATION/TEAMWORK - is the ability to work jointly with others or together especially in an intellectual endeavor; the ability and desire to work cooperatively with others on a team; as a team leader, the ability to demonstrate interest, skill, and success in getting groups to learn to work together. Builds partnerships for global performance. Respects others.

EFFECTIVE COMMUNICATION - Is the ability to convey information to another effectively and efficiently, to listen – help facilitate sharing of information between people. It is about understanding the emotional intention behind the information. The ability to express oneself clearly in conversations, confirm understanding, communicate using data and facts. Exhibit willingness to listen and show respect for oneself and others in interactions with others.

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.
• 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.

Preferred Education

• Advanced degree (e.g. M.Sc, PhD) Microbiology, Biochemistry, Biology or PharmD is preferred.

Advanced 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 (Benefits)

• 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.
• 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.

Bimeda Global Presence

Bimeda is a leading global manufacturer, marketer and distributor of animal health products and veterinary pharmaceuticals. Through ongoing expansion and strategic acquisition, Bimeda has established markets in more than eighty countries worldwide and has R&D, manufacturing and distribution capabilities across Europe, North America, South America, Africa, Asia and Australasia.