Research Chemist (Drug Product) - Eurofins CDMO Alphora, Inc.

Eurofins Nederlands Moleculair Diagnostisch Laboratorium B.V; Mississauga; On-site; CAD 60,000 - 100,000; Full time

Job summary

An established industry player is seeking a Research Chemist to join its dynamic team. This role involves supporting laboratory operations and participating in the development of oral dosage forms. The ideal candidate will have a strong background in analytical method development and compliance with GMP and GLP standards. You'll be part of a forward-thinking company dedicated to improving patient health through innovative therapeutics. With a commitment to safety and quality, this position offers a rich environment filled with diverse projects, making it an exciting opportunity for those passionate about science and research.

Benefits

Health & Dental Coverage

Life and Disability Insurance

RRSP with 3% Company Match

Paid Holidays

Paid Time Off

Qualifications

• 3+ years' experience in a pharmaceutical laboratory or manufacturing environment.
• Expertise in GMP, GLP, and Health Canada guidelines.

Responsibilities

• Conduct analytical method development, validation, and sample testing.
• Support Drug Product Operations Team for timely project completion.

Skills

Analytical Method Development

GMP Compliance

GLP Compliance

Sample Testing

Document Preparation

Education

Degree in Chemistry

Degree in Biochemistry

Job description

Research Chemist (Drug Product) - Eurofins CDMO Alphora, Inc.

• Full-time

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 labelling is accurate. Eurofins believes it is a global leader in food, environmental, pharmaceutical and cosmetics products testing and in agroscience CRO services.

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 2023, 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.

The Research Chemist is accountable to the Head of Pre-Formulations. Responsibilities include support for general laboratory operations, equipment on-boarding, equipment set up and operation. The Research Chemist will also participate in analytical method development, validation/transfer and testing to support the development of liquid and solid oral dosage forms.

DUTIES AND RESPONSIBILITIES:

• Conduct work in a safe manner and ensure compliance with established safe work practices and procedures.
• Adhere to the policies and guidelines set out in the Eurofins CDMO | Alphora Employee Handbook.
• Work harmoniously with all fellow employees.
• Provide assistance and support for analytical activities including analytical method development, method validation, method transfer, and sample testing in an R&D and GMP environment.
• Assist in the execution of prototype and GMP stability studies in accordance with ICH or other regulatory guidelines.
• Provide support for document preparation of material specifications, standard operation procedures, and other necessary documentation for Drug Product Operations.
• Ensure that all work is performed in compliance with the applicable SOPs, cGMPs and GLPs.
• Support the Drug Product Operations Team to ensure the timely completion of client projects.
• Perform other related duties as required.

Desired Minimum Qualifications:

• Degree in Chemistry, Biochemistry or related field
• 3+ years' experience in a pharmaceutical laboratory or manufacturing environment
• 2+ years of method transfer/validation
• Expertise in GMP, GLP and other Health Canada guidelines

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.