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

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 problemsolving are at the forefront
Were 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 Youll 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 youll feel right at home here.

Qualifications :

• Masters degree in Analytical chemistry pharmaceutical chemistry Organic chemistry Medicinal chemistry Biochemistry or biological science with at least 1 year of relevant experience
• Bachelors degree in Analytical chemistry pharmaceutical chemistry Organic chemistry Medicinal chemistry Biochemistry or biological science with at least 3 years of relevant experience Comprehensive understanding of analytical techniques to support the analysis and characterization 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.

The starting annual base compensation for this position is $65000 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 applicants experience knowledge skills and abilities.

Disclaimer: Salary information posted on sites other than the official careers page does not reflect the organizations 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 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.

Additional Information :

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 .

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 

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

Remote Work :

No

Employment Type :

Full-time