Scientist I, Downstream Process Development Biologics Eurofins CDMO Alphora, Inc.

We are seeking a motivated and technically driven Scientist I Downstream Process Development to join our growing Process Development this role you will contribute to the design and optimization of purification and bioconjugation processes for a wide variety of therapeutic proteins and novel biologics.

Working closely with senior scientists and crossfunctional partners you will support key laboratory studies involving chromatography tangential flow filtration (TFF) filtration and nanofiltration while also helping scale processes toward largervolume operations. This is an exceptional opportunity for someone early in their career who is passionate about bioprocessing enjoys handson lab work and wants to play a direct role in advancing innovative therapeutics from concept to clinic.

The Scientist I - Downstream Process Development is involved in the development of novel biologics and therapeutics by assuming a crucial role in the design of purification and bioconjugation processes for a wide range of proteins. The successful candidate will play a key role in laboratory studies for the development of a range of downstream processing steps including chromatography tangential flow filtration (TFF) filtration and nanofiltration amongst other steps while being able to communicate progress to internal stakeholders. The ideal candidate will also play key roles in scaling up processes.

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 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 I you will be a key contributor to downstream development activities and process innovation:

• Serve as a Subject Matter Expert (SME) in downstream processing principles and best practices.
• Apply bioprocess engineering and protein chemistry knowledge to design and optimize chromatography TFF and filtration studies.
• Contribute to the design and execution of protein bioconjugation development activities.
• Draft and review technical documents including batch records experimental procedures data summaries and scientific reports.
• Communicate research findings clearly and confidently to internal teams and project stakeholders.
• Support continuous improvement initiatives to deliver robust scalable and costeffective downstream processes for clients.
• Perform handson laboratory execution of planned studies from buffer preparation to purification runs.
• Record raw data in accordance with GDP/GLP standards analyze results and help refine experimental designs.
• Write and review SOPs related to downstream process equipment unit operations and batch record documentation following industry guidelines (GMP HSE IP).
• Collaborate across functional teamsincluding analytical upstream engineering and qualityto advance projects and support equipment qualification activities.
• Independently plan troubleshoot and report on laboratory work with minimal supervision.
• Assist in maintaining a wellrun laboratory by performing basic equipment upkeep and ordering consumables.

Why Work Here

Joining our team gives you the chance to grow contribute and make a real impact in the development of lifechanging biologics:

Meaningful Scientific Impact

Your work directly contributes to developing purification strategies and bioconjugation workflows that enable innovative therapeutics.

HandsOn Technical Growth

Youll gain experience with industryrelevant downstream technologiesincluding chromatography systems TFF skids and advanced filtration techniques.

A Collaborative MentorshipDriven Environment

Work closely with experienced scientists who are invested in your development and ready to support your learning journey.

Ownership & Independence

Youll have the opportunity to plan and execute your own experiments troubleshoot challenges and help shape downstream development strategies.

A Culture of Innovation & Continuous Improvement

We value curiosity new ideas and scientific rigorand we empower you to apply them.

Career Path for Advancement

This role is designed to support your growth toward Scientist II and beyond with exposure to scaleup tech transfer and crossfunctional operations.

Qualifications :

• Minimum Masters degree with 3 years of experience or PhD    
• Working knowledge of protein chemistry and protein purification along with self-directed learning and a willingness to grow ones knowledge.
• Experience with development and execution of chromatography process steps using UNICORN control software.
• Experience with carrying out ultrafiltration and diafiltration studies using TFF.
• Experience in and understanding of aseptic techniques in laboratory setting.
• Knowledge in bioprocess engineering principles underlying effective scale-up design.
• Knowledge of filtration and clarification steps in development and optimization.
• Knowledge of protein bioconjugation (this would be considered an asset).
• Understanding of how to implement Design of Experiments (DoE) and Quality by Design (QbD) in the development of unit operations.
• Understanding of Current Good Manufacturing Practices (cGMP) in biomanufacturing.
• Being a key point of contact and Subject Matter Expert (SME) for scientific studies in the PD lab communicating scientific information succinctly to a range of audiences. 
• 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 $80000 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