Senior Analytical Chemist I - Eurofins CDMO Alphora Inc.

Eurofins Scientific; Mississauga; On-site; CAD 60,000 - 95,000; Full time

Job summary

Join a leading international life sciences company as a Senior Analytical Chemist I, where you will play a crucial role in developing and validating analytical methods that ensure the safety and efficacy of new therapeutics. This position offers the opportunity to work in a modern laboratory environment, utilizing advanced techniques and equipment such as HPLC, GC, and various wet chemistry methods. You'll collaborate with interdepartmental teams, contribute to innovative projects, and enjoy a supportive workplace culture that values your expertise. With a strong focus on professional development and excellent benefits, this role is perfect for those looking to make a meaningful impact in the pharmaceutical industry.

Benefits

Health & Dental Coverage

Life Insurance

Disability Insurance

RRSP with 3% Company Match

Paid Holidays

Paid Time Off

Qualifications

• 5-10 years of pharmaceutical experience with B.Sc. or >5 years with MSc/PhD.
• Strong skills in technical writing and GMP documentation.

Responsibilities

• Independently plans and executes analytical method development.
• Conducts stability testing and prepares detailed reports.
• Maintains laboratory in an organized state while adhering to GMP.

Skills

HPLC/UPLC

GC

IC

KF

Wet Chemistry Techniques

LCMS

GCMS

Technical Writing

GMP Documentation

Education

B.Sc. in Pharmaceutical Sciences

M.Sc./PhD in Related Field

Tools

Laboratory Equipment

Analytical Software

Job description

Senior Analytical Chemist I - 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.

The Senior Analytical Chemist Level I is accountable to the Director, Analytical Services for all activities relating to performing either cGMP or non-GMP analytical development work. Responsibilities include performing analytical method development, validations, forced degradation studies, conducting stability testing or R&D support testing as well as preparing the appropriate protocols and reports. You should be comfortable in a modern laboratory and proficient with HPLC/UPLC, GC, IC, KF, and various wet chemistry techniques. Proficiency with LCMS and/or GCMS are definite assets. The Senior Analytical Chemist Level I is also an active member of interdepartmental research teams and can independently plan and carry out investigational work.

Description of Major Job Responsibilities:

• Independently plans and executes analytical method development efforts by developing standard and complex raw material, in-process control, intermediate and API test methods.
• Independently plans and executes investigational work, generating reports subject to regulatory review.
• Researches and applies new technologies/methodologies.
• Prepare method development updates for client review.
• Author analytical test methods and specifications for cGMP use.
• Conduct process development sample analyses.
• Conduct peer review of critical non-GMP analyses of process development samples.
• Plan and prepare analytical method validation protocols, carry out lab-work and prepare reports.
• Plan and prepare stability protocols, carry out lab-work and prepare reports.
• Plan and prepare forced degradation study protocols, carry out lab-work and prepare reports.
• Identify and support the write-up of OOS, OOT, OOC and deviation documents subject to regulatory review.
• Maintain the laboratory in an organized state.
• Work in accordance with established GMP and safety requirements.

Qualifications:

• B.Sc. with 5-10 years of pharmaceutical experience or MSc/PhD with > 5 years of experience in related field.
• 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.
• Assist in project planning and staff training.

Additional Responsibilities:

• Perform instrument calibration/performance verifications.
• Order laboratory supplies and chemicals as required.
• Perform additional duties as required.

COMMUNICATION AND CONTACTS:

• Quality Assurance for documentation approval and corrections.
• Active member of interdepartmental Process Research and Development teams.
• Quality control for the transfer and troubleshooting of new test methods/specifications.
• Engineering for issues relating to facility support of instrumentation.

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

Accommodation: Persons with disabilities who need accommodation in the application process 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.