Job Description
Spécialiste II, Validation / Validation Specialist II
Posting Start Date:  12/11/25
Country/Region:  Canada
State/Province:  Quebec
Job Location:  Laval – INRS Building 28
Place of Employment: 
Contract Duration:  Permanent
Spécialiste II, Validation / Validation Specialist II

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.

Job description

Would you like to apply your expertise in qualification and validation project management to a revolutionary and innovative project? As a Validation Specialist, you will contribute to validation in accordance with project plans, schedules, and objectives, while playing a key role in drafting procedures and protocols.

 

More specifically, you will be responsible for:

· Manage qualification and validation projects according to established project plans, timelines, and objectives;

· Participate in the design, evaluation, and implementation of new and existing equipment and systems, as well as processes in a GMP environment;

· Write and execute validation studies for cleaning and shipping procedures;

· Write and/or revise standard operating procedures (SOPs);

· Coordinate validation activities with other departments

 

 

You are the right person for this role if you have:

· Manage qualification and validation projects • You have a bachelor's degree in engineering, chemistry, or biotechnology;

· You have at least 5 years of experience in a similar role, which has allowed you to develop exceptional expertise in all aspects of validation;

· You are comfortable in an environment where quality and traceability are at the heart of the way things are done (GMP, ISO, etc.);

· You believe that spending time on the floor on a regular basis helps improve your expertise and problem-solving skills;

 

You are able to easily convey your technical knowledge to people who are less familiar with your field of expertise;

· You are able to read, write, and express yourself in both English and French

 

 

Prometic offers you:

· A fantastic team that strives to do things in the best possible way;

· A relaxed working environment;

· A start-up culture that values autonomy, innovation and collaboration;

· A competitive salary and benefits package;

· A unique opportunity to change lives through your commitment and contribution.

 

Send us your resume right away

Prometic is an equal opportunity employer.

Job Summary

What you'll do

Qualifications and need-to-know

Knowledge of French is required for positions permanently located in Quebec so incumbents can communicate with their colleagues and suppliers in Quebec as necessary.

Other language requirement

Another language is required for this position in order to communicate with partners and colleagues, who are predominantly located outside Quebec and to understand the technical and scientific documentation used in our industry.

 

Kedrion Biopharma Canada is committed to equal employment opportunities.

 

For more information, visit our websitehttps://www.kedrion.ca/   

 

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