Analytical Chemist: API Method Dev & Validation

Eurofins-Canada-Biopharma; Mississauga; On-site; CAD 59,000 - 72,000; Full time

Benefits offered by this job

Health & dental coverage

RRSP with 3% company match

Paid holidays

Paid time off

Job summary

Eurofins CDMO Alphora Inc. seeks an Analytical Chemist to join our Analytical Services Department in a state-of-the-art laboratory.

You will develop, validate, and support analytical methods for raw materials, in-process controls, intermediates, and APIs to support process development and GMP manufacturing. The role requires hands-on experience with HPLC, LC-MS, GC, KF and related techniques, plus strong technical writing and GMP documentation skills.

Qualifications

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

Responsibilities

• Develop, validate, and troubleshoot analytical methods for raw materials, in-process controls, intermediates, and APIs.
• Perform analytical method validations, stability studies, and data generation for GMP manufacturing.
• Provide analytical support for process development and collaborate with cross-functional teams.

Skills

Technical writing

GMP documentation

Problem solving

Organizational skills

Communication

Education

B.Sc. in a related field

Tools

HPLC

LC/MS

GC

KF

Job description

Eurofins CDMO Alphora Inc. seeks an Analytical Chemist to join our Analytical Services Department in a state-of-the-art laboratory.

You will develop, validate, and support analytical methods for raw materials, in-process controls, intermediates, and APIs to support process development and GMP manufacturing. The role requires hands-on experience with HPLC, LC-MS, GC, KF and related techniques, plus strong technical writing and GMP documentation skills.