Scientist II (Separation Science), Analytical Development Biologics Eurofins CDMO Alphora, Inc.

We are seeking an experienced and motivated Scientist II (Separation Science) to join our Analytical Development this role you will support the development optimization and validation of analytical methods used to characterize biologics across R&D preclinical and GMP environments. Reporting to the Senior Manager Analytical Development you will play a key role in shaping analytical strategy collaborating across functions and delivering highquality data that enables the successful advancement of diverse biologic programs. This is an excellent opportunity for a scientist who thrives in a dynamic environment enjoys technical problemsolving and wants to contribute meaningfully to innovative therapeutic development.

 The Scientist II Analytical Development is accountable for supporting technology transfer method development qualification and validation of analytical methods for the characterization R&D testing and GMP testing of biologics. The successful candidate will play a key role in planning the analytical strategy and will collaborate with other team members to execute experimental work generate data and prepare technical reports for early-stage research preclinical development or late-stage CMC programs in support of 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 Youll Do

As a Scientist II you will apply your expertise in separation science and biologics characterization to provide technical leadership and drive analytical excellence:

• Apply strong analytical understanding to support the testing and characterization of biopharmaceuticals including monoclonal antibodies ADCs fusion proteins and recombinant proteins.
• Serve as a Subject Matter Expert (SME) in analytical development and testing offering strategic and technical guidance.
• Lead and perform analytical method transfer method development and method validation for both drug substances and drug products.
• Independently plan execute troubleshoot and report laboratory work with minimal supervision.
• Clearly communicate results to internal teams and external clients and actively support the design of subsequent studies.
• Develop optimize and validate robust analytical separation methods to quantify and characterize biologics.
• Manage internal collaborations and external partners responsible for biophysical characterization activities.
• Ensure all analytical activities adhere to GMP and GDP standards with strong documentation practices.
• Write review and approve SOPs and work instructions related to analytical procedures and laboratory operations.
• Lead or participate in quality event investigations (planned and unplanned) recommending effective corrective and preventive actions.
• Collaborate across multidisciplinary teams to advance projects and provide analytical expertise.
• Drive continuous improvement initiatives and contribute to timely resolution of analytical issues or gaps.
• Train mentor and support junior team members through knowledge transfer handson training and clear guidance.
• Support daily laboratory operations including equipment maintenance supply ordering and coordinating shipments of materials or samples.

Why Work Here

Joining our team means becoming part of a collaborative sciencedriven environment where your expertise truly makes an impact. Heres what you can expect:

• Highimpact work: Your analyses directly influence decisionmaking across early research development and CMC stages.
• Meaningful scientific contribution: Youll work on diverse biologic modalities and cuttingedge technologies.
• Growth and development: Exposure to a wide range of analytical techniques mentorship opportunities and crossfunctional project involvement.
• Supportive team culture: Work alongside skilled scientists who value collaboration learning and continuous improvement.
• Autonomy and ownership: You will have the freedom to lead methods drive investigations and shape analytical strategy.
• Commitment to quality: A strong GMP environment where scientific excellence and compliance go hand in hand.

Qualifications :

• Ph.D degree in Analytical chemistry pharmaceutical chemistry Organic chemistry Medicinal chemistry Biochemistry or biological science with at least 3 years of relevant experience
• Masters degree in Analytical chemistry pharmaceutical chemistry Organic chemistry Medicinal chemistry Biochemistry or biological science with at least 5 years of relevant experience
• Comprehensive 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 etc) including proficiency in Empower 3 software are required.
• 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 $85000 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