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Eurofins

Analyst II, Analytical Development - Biologics - Eurofins CDMO Alphora, Inc.

Mississauga, ON, Canada

Full-time

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Job details

Job type: Full-time
Posting language: English
Posted: Nov 4, 2026

Original job description

Company Description

Eurofins Scientific is an international network of independent life sciences companies, 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 laboratories work with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate.

The Eurofins network of companies believes that it is a global leader in food, environment, pharmaceutical and cosmetic product testing and in discovery pharmacology, forensics, advanced material sciences and agroscience contract research services. It is also one of the market leaders in certain testing and laboratory services for genomics, and in the support of clinical studies, as well as in biopharma contract development and manufacturing. It also has a rapidly developing presence in highly specialised and molecular clinical diagnostic testing and in-vitro diagnostic products.

In under 40 years, Eurofins has grown from one laboratory in Nantes, France to over 65,000 employees across a decentralised and entrepreneurial network of over 950 laboratories in over 1,000 independent companies across 57 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.

The Eurofins network generated EUR 7.296 billion revenues in FY 2025, and has been one of the fastest growing listed European companies for almost three decades.

________________________________________________________________________________________

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.

Job Description

Join Our Team and Help Shape the Future of Biologics!

Are you passionate about advancing innovative biologic therapies? Do you thrive in a dynamic environment where scientific rigor, collaboration, and problem‑solving are at the forefront?
We’re looking for an Analyst II, Analytical Development to support technology transfer, method development, qualification, and validation activities within our growing biopharmaceutical analytics group.

The Analyst II, Analytical Development, is accountable for supporting technology transfer, method development, qualification, and validation of analytical methods for the characterization and analytical testing of biologics. The successful candidate will play a key role in planning and executing experimental work to generate data and prepare technical reports for early-stage research, preclinical development, or late-stage CMC programs across various drug modalities.

At Eurofins CDMO Alphora Inc., our mission is to harness the power of biotechnology and bioprocessing to create innovative complex medicines that will improve the lives of patients worldwide. With a dedicated team of experienced scientists, motivated technologists, and novel state-of-the-art process development (PD) facility, we are thrilled to be at the forefront of the biopharmaceutical CDMO industry in Canada. Join us on this exciting journey as we push the boundaries of scientific research and provide hope to our most vulnerable.

⭐ What You Will Achieve in This Role

In this position, you will:

Become a key contributor to analytical strategies supporting cutting-edge biologic programs.
Build deep expertise in method development, validation, and the analytical characterization of complex molecules.
Lead analytical activities that directly inform decisions in process development, regulatory submissions, and tech transfers.
Strengthen cross-functional collaboration by working closely with QC, Formulations, Process Development, and external partners.
Help shape best practices, drive continuous improvement, and influence the evolution of Analytical Development capabilities within the organization.
Advance your career through hands-on technical challenge, exposure to diverse modalities, and mentorship opportunities.

This role is perfect for someone who wants to see their work make a measurable impact across the full lifecycle of biologic development.

Core Responsibilities

Apply a strong understanding of analytical methodologies to support the testing and characterization of biopharmaceuticals, including monoclonal antibodies, ADCs, fusion proteins, and recombinant proteins.
Lead and execute analytical method transfers, method development, and validation for drug substance and drug product.
Plan, conduct, troubleshoot, and document laboratory studies independently while ensuring scientific integrity and quality.
Clearly communicate data, insights, and recommendations to project teams and larger audiences; contribute to experimental design discussions.
Develop, optimize, and validate robust analytical separation methods and bioassays to characterize and quantify biologics.
Collaborate with internal and external partners to support biophysical characterization activities.
Adhere to GMP and GDP standards in all analytical work.
Write and review SOPs and work instructions for analytical and lab-related activities.
Work cross-functionally to drive project timelines and deliverables.
Contribute to continuous improvement initiatives and provide technical insight to resolve project challenges.
Mentor junior team members through training, guidance, and feedback.
Follow EHS guidelines, ensuring safe laboratory operations.
Support lab operations including equipment maintenance, supply management, and sample shipments.

⭐ Why You’ll Be a Great Fit

You will excel in this role if you:

Bring strong foundational knowledge in analytical characterization of biologics (e.g., mAbs, ADCs, fusion proteins, recombinant proteins).
Enjoy solving complex scientific problems and designing efficient laboratory strategies.
Communicate clearly and confidently, both in writing and when presenting data to broader teams.
Thrive in a fast-paced environment where adaptability, organization, and attention to detail matter.
Are a collaborative team player who enjoys sharing knowledge, mentoring others, and contributing to a positive lab culture.
Take pride in high-quality documentation and compliance, understanding the importance of GMP/GDP in biologics development.
Are proactive, curious, motivated by continuous improvement, and eager to push projects forward.

If you are someone who enjoys taking ownership, driving innovation, and applying critical thinking to real-world therapeutic challenges, you’ll feel right at home here.

Qualifications

Master's degree in Analytical chemistry, pharmaceutical chemistry, Organic chemistry, Medicinal chemistry, Biochemistry, or biological science with at least 1 year of relevant experience
Bachelor’s degree in Analytical chemistry, pharmaceutical chemistry, Organic chemistry, Medicinal chemistry, Biochemistry, or biological science with at least 3 years of relevant experience understanding of analytical techniques to support the analysis and characterization Comprehensive of biologics.
Good understanding of analytical techniques to support the analysis and characterization of biologics.
Demonstrated experience and technical expertise in the development and validation of separation methods (e.g., HPLC, LC-MS, CE) including proficiency in Empower 3 software is essential.
Hands-on experience in developing and qualifying bioassays, including receptor-binding and cell-based assays is an asset.
In-depth understanding of analytical development strategy to support regulatory filing.
Proven ability to effectively and independently design and plan experiments, prioritize tasks and critically evaluate results under compressed timelines.
Outstanding written and verbal communication skills, with the ability to convey strategies and results to a diverse audience.
Strong interpersonal skills and ability to work collaboratively as a member of a cross-functional team.
Excellent communication, GMP documentation, and organizational skills.
Strong problem-solving skills.

Additional Information

The starting annual base compensation for this position is $65,000 CAD. The actual offer, reflecting the total compensation package plus benefits, will be determined by a number of factors which include but are not limited to the applicant’s experience, knowledge, skills, and abilities.

Disclaimer: Salary information posted on sites other than the official careers page does not reflect the organization’s compensation and may represent estimated ranges provided by third-party job boards. The organization offers competitive wages and a comprehensive total rewards package, which will be discussed during the interview process.

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

At Eurofins CDMO Alphora, we leverage artificial intelligence (AI) technology to support our recruitment process, including preliminary screening of applications and resumes. All hiring decisions are made by human reviewers.

This posting is for a current vacancy and the successful candidate will start as soon as possible.

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.

NO AGENCIES, CALLS OR EMAILS PLEASE

Compensation: up to CAD 65000 - yearly

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More about this job

Responsibilities

The Analyst II will lead and execute analytical method transfers, development, and validation for biologics while ensuring scientific integrity and GMP compliance. They will also collaborate cross-functionally to support characterization activities and mentor junior team members.

Requirements

Candidates must hold a Bachelor's degree with at least 3 years of experience or a Master's degree with at least 1 year of experience in a relevant scientific field. Proficiency in analytical separation methods like HPLC, LC-MS, or CE and experience with Empower 3 software are essential.

Skills

Analytical chemistry
Biologics characterization
Method development
Method validation
HPLC
LC-MS
CE
Empower 3
Bioassays
GMP
GDP
Technical writing
Troubleshooting
Technology transfer
Biochemistry

Benefits

Health coverage
Dental coverage
Life insurance
Disability insurance
RRSP with 3% company match
Paid holidays
Paid time off

Visa sponsorship

Not detected in the job text

Keywords

Analytical Development
Biologics
Monoclonal antibodies
ADCs
Fusion proteins
Recombinant proteins
Method transfer
Method validation
HPLC
LC-MS
CE
Empower 3
Bioassays
GMP
GDP
SOP
Biopharmaceutical
CDMO
Analytical characterization
Regulatory filing
CMC
Preclinical development
Laboratory operations
EHS
Bioprocessing

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