Senior Research Chemist (Drug Product) - Eurofins CDMO Alphora, In

Eurofins; Mississauga; On-site; CAD 80,000 - 110,000; Full time

Job summary

A global life sciences company is seeking a Senior Research Chemist to develop and execute analytical methods for drug product development. The ideal candidate has extensive experience in chemistry and a track record of success in multiple projects. This role offers excellent benefits, including health coverage and retirement plans, in a collaborative environment focused on improving patient health.

Benefits

Health & Dental coverage

Life and disability insurance

Paid holidays

RRSP with 3% company match

Qualifications

• Over 10 years of experience in the pharmaceutical-related field or over 5 years with a Ph.D.
• Proven success in multiple projects.
• Ability to work effectively in a multi-disciplinary team.

Responsibilities

• Draft GMP documentation such as test methods and specifications.
• Develop and execute analytical methods for drug product development.
• Conduct investigations for OOT/OOS deviations.

Skills

Drug product development

Analytical development

Project management

Team collaboration

Communication skills

Education

B.Sc. or M.Sc. in Chemistry

Ph.D. in Chemistry

Tools

HPLC

GC

KF

Job description

Overview

Senior Research Chemist (Drug Product) - Eurofins CDMO Alphora, In

Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins works with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labeling is accurate. Eurofins believes it is a global leader in food, environmental, pharmaceutical and cosmetics products testing and in agroscience CRO services. It is also one of the global independent market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, CDMO, advanced material sciences and in the support of clinical studies.

In over 35 years, Eurofins has grown from one laboratory in Nantes, France to 61,000 staff across a decentralised and entrepreneurial network of ca. 900 laboratories in 61 countries. Eurofins companies offer a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products.

In 2024, Eurofins generated total revenues of EUR 6.515 billion, and has been among the best performing stocks in Europe over the past 20 years.

Eurofins CDMO Alphora Inc. develops and manufactures new therapeutics to improve the lives and health of patients. Eurofins CDMO Alphora provides contract research & development services to global pharmaceutical and biotech companies, developing their processes and manufacturing their bulk drug substances (Active Pharmaceutical Ingredients -"API’s") as well as finished dosage products (tablets, capsules, suspensions) for supply to clinical trials and commercial requirements. Eurofins CDMO Alphora provides a rich and technologically challenging environment with a continuing flow of interesting projects. Our employees work in close concert with clients throughout the development process to achieve their program objectives. Eurofins CDMO Alphora Inc. is growing its state-of-the-art organization, with continued investments in modern facilities, equipment, and instrumentation while providing a rich environment for employees to develop their technical skills and careers paths.

Responsibilities

• Draft GMP documentation such as test methods, material/product specifications, protocols, and SOPs as required.
• Develop and execute analytical methods in support of oral drug product development. Methods include but are not limited to Assay, Impurity, Dissolution, Water Content, and Residual Solvent.
• Conduct OOT/OOS/Deviation investigations as required.
• Troubleshoot, maintain and perform equipment qualifications for HPLC, GC, KF and other analytical equipment as required.
• Conduct prototype and GMP stability studies in accordance with ICH or other regulatory guidelines.
• Ensure all work is performed in compliance with applicable SOPs, cGMPs, and GLPs.
• Promote and maintain a safe and healthy working laboratory environment in compliance with established health and safety procedures.
• Other duties as assigned.

Qualifications

• B.Sc. or M.Sc. in Chemistry with >10 years experience or Ph.D in Chemistry with >5 years experience in the pharmaceutical-related field industry
• Strong knowledge of drug product development and hands-on experience in analytical development
• Highly motivated with a proven record of success in multiple projects
• Well organized and able to meet project timeline commitments
• Ability to work effectively in a multi-disciplinary team and possess excellent written and verbal communication skills

Communication and Contacts

Within the Company

• Interact with all staff throughout the company as necessary to implement the business objectives.

Outside of the Company

• Interact with various outsource vendors, clients, contractors, and industry bodies to support the business objectives.

Benefits

At Eurofins we offer excellent full-time benefits including health & dental coverage, life and disability insurance, RRSP with 3% company match, paid holidays, paid time off.

Accommodation: Persons with disabilities who need accommodation in the application process, or those needing job postings in an alternative format, may e-mail a request via the website at www.eurofins.ca.

As a Eurofins employee, you will become part of a company that has received international recognition as a great place to work. To learn more about Eurofins, please explore our website at www.eurofins.ca

We thank all applicants within commuting distance of GTA, Ontario for showing an interest in this position. Only those selected for an interview will be contacted.

This posting is supported by AI technology to assist in screening candidates and resumes.