SPECIALIST, TECHNICAL SERVICES at Prometic Bioproduction
Laval, QC, Canada -
Full Time


Start Date

Immediate

Expiry Date

08 Nov, 25

Salary

0.0

Posted On

09 Aug, 25

Experience

5 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

No

Skills

Good communication skills

Industry

Information Technology/IT

Description

Making a difference, one role at a time.
Located in the heart of the Cité de la Biotech in Laval, Kedrion Biopharma Canada’s mission is to make rare connections that impact millions of lives. Our team is developing an innovative treatment based on plasma-derived proteins, offering a new path of hope to children and adults suffering from orphan diseases. We’re turning innovation into real solutions to save lives.
Are you looking to apply your expertise in protein purification to technically stimulating projects? As a Technical Services Specialist, you will contribute to technology transfer, capacity expansion, and process validation, while playing a key role in process optimization, technical documentation, and risk analysis in a production environment.

Responsibilities

MORE SPECIFICALLY, YOU WILL BE RESPONSIBLE FOR:

  • Participating in process validation and preparing technical documentation in accordance with regulatory requirements
  • Assessing risks to product quality for both current products and those in development
  • Developing and supporting the preparation, execution, and performance reporting of pilot and engineering runs
  • Acting as a person-in-plant to oversee outsourced technical activities
  • Representing the department as a subject matter expert in protein purification and related analytics during investigations
  • Initiating and following up on change controls, deviations, investigations, and exception reports related to new or existing products and validation protocols

YOU ARE THE RIGHT PERSON FOR THIS ROLE IF YOU HAVE:

  • A Bachelor’s degree in biochemistry, biology, chemistry, or process engineering with a minimum of 7 years of experience, or a Master’s degree with at least 5 years of relevant experience
  • Relevant R&D experience in biologics or biotechnology-derived products
  • Experience in the development of technical processes for biologics or analytical assays
  • Strong knowledge of quality risk management tools (e.g., FMEA, HACCP) and regulatory guidelines (Health Canada, FDA, ICH, EU)
  • Understanding and application of analytical methods to guide protein-based process development
  • Excellent command of English (spoken and written) and spoken French
  • Ability to work independently and collaboratively within cross-functional teams, with rigor and strong organizational skills
  • Experience in project management, data analysis, basic statistical tools (e.g., Minitab), and MS Office applications
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