Analytical Chemist - Eurofins CDMO Alphora, Inc.

Eurofins Humangenetik & Pränatal-Medizin; Oakville; On-site; CAD 60,000 - 95,000; Full time

Job summary

Join a forward-thinking company dedicated to improving lives through innovative therapeutic solutions. As an Analytical Chemist, you will play a crucial role in developing and validating analytical methods for pharmaceutical products. Your expertise in API analysis and proficiency with advanced instrumentation will help drive projects to completion in a state-of-the-art laboratory. With a commitment to quality and safety, you'll collaborate with cross-functional teams to ensure the highest standards in drug development. This is an exciting opportunity to contribute to meaningful advancements in healthcare while enjoying a supportive work environment with excellent benefits.

Benefits

Health & Dental Coverage

Life and Disability Insurance

RRSP with 3% Company Match

Paid Holidays

Paid Time Off

Qualifications

• 5+ years experience in pharmaceutical analysis and method validation.
• Strong technical writing and GMP documentation skills.

Responsibilities

• Develop and author analytical test methods for GMP manufacturing.
• Conduct scientific investigations in support of process development.

Skills

Analytical Method Validation

Communication Skills

Attention to Detail

Problem-Solving Skills

Education

B.Sc. in a related field

Tools

HPLC/UPLC

GC

Ion Chromatography

LCMS

GCMS

Job description

Analytical Chemist - 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.

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.

You possess a high degree of initiative and are a team player with excellent communication abilities. You have a strong understanding of API (active pharmaceutical ingredient) analytical method validation and development. You are comfortable in a modern, state of the art laboratory and are proficient with HPLC/UPLC, GC, IC, KF and various wet chemistry techniques. Proficiency with LCMS and/or GCMS are definite assets. Your attention to detail, a comprehensive understanding of cGMP, strong organizational skills with the ability to drive projects to completion, make you the ideal candidate to become a member of our team.

Description of Department:

The Analytical Services Department is responsible for providing analytical method development and analytical support for Synthetic Process Development.

Description of Major Job Responsibilities:Reporting to the Analytical Chemist Team Leader,

• Work effectively within interdepartmental project teams including analytical, quality assurance, process development and manufacturing.
• Develop and author analytical test methods (raw material, in process control, synthetic intermediate and API) for use in GMP manufacturing.
• Perform analytical method validations and prepare data for review and reports.
• Provide analytical support to both process development and stability.
• Conduct scientific investigations in support of process development and manufacturing.
• Work in accordance with established GMP and safety requirements.

Instrumentation:

• HPLC/UPLC (Empower), GC, GC/Headspace, IR, KF, Ion Chromatography

Qualifications:

• B.Sc. in a related field with a minimum of 5 years relevant experience in pharmaceutical analysis, development and validation.
• Excellent skills in technical writing and GMP documentation.
• Excellent problem-solving, planning and organizational skills coupled with a strong attention to detail.

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.

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.