Role Overview
LAPORTE is hiring a Senior Engineer/Specialist, Pharmaceutical Validation. This is a full-time role in CA. Part of LAPORTE's Risk hiring. Full responsibilities, required qualifications, and the apply link are listed in the description below.
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Job Description
LAPORTE is a consulting engineering firm specializing in pharmaceutical, agrifood, industrial biotech and industrial plant processes, which has been in business for 25 years. Today, the company has 25 offices across North America and Europe, and over 480 employees with a passion for engineering.
We offer a stimulating environment where autonomy, collaboration and professional growth are at the heart of our daily work. We believe in a flexible working environment that values work-life balance while encouraging efficiency and creativity on a daily basis.
Discover an employer who takes care of its greatest asset: its employees!
LAPORTE is seeking a senior pharmaceutical validation engineer or specialist with ideally at least 5 years of experience in the validation and qualification of pharmaceutical equipment to join its Greater Vancouver team, located in Burnaby, BC. Our validation engineer will play a key role in managing validation activities, including drafting master documents, executing protocols, and ensuring compliance with Good Manufacturing Practices (GMP).
Responsibilities
- Drafting master validation documents (e.g., Validation Master Plan (VMP), risk analysis, cleaning matrix, User Requirements Specification (URS));
- Draft and execute equipment/system (IQ/OQ/PQ), process, and cleaning qualification protocols;
- Coordinate and ensure compliance with GMP during validation activities and general operations;
- Support our clients’ QA/Compliance teams in initiating change notices or reporting deviations to trigger CAPA, Change Control, deviations, or other relevant actions within the scope of validation activities;
- Manage client accounts.
Requirements
- Bachelor’s or master’s degree in science, engineering, or other relevant disciplines;
- Minimum of 5 years of experience in the pharmaceutical industry, in a manufacturing setting, or in consulting;
- Strong knowledge of Good Manufacturing Practices (GMP);
- Knowledge of pharmaceutical manufacturing processes;
- Willingness to travel (to client sites).
Benefits
What we offer
- Competitive Salary: Competitive salary commensurate with experience and industry standards;
- Health and Wellness Programs: Comprehensive group health insurance coverage from day one (medical, dental, vision, childcare);
- Retirement Plans: Employer-contributed RRSP plan at 4%;
- Flexible Work Arrangements: Hybrid work mode, with a minimum of 2 days per week in the office;
- Professional Development: A work environment that encourages empowerment and professional growth. Professional reimbursement fees (e.g., APEGA, APEGS, EGBC, etc…) covered by the company;
- Career Advancement Opportunities: Mentorship programs, training, cross-department opportunities, etc.;
- Work-Life Balance: 3 weeks of regular vacation with 1 week of paid vacation during the Christmas holidays. 1 week of Personal/Sick leave ;
- Inclusive Culture: A diverse, flexible, and non-conformist work environment that values equity, work-life balance, and promotes efficiency in daily tasks with enormous growth opportunities;
- Team-Building Activities: Lunch & Learn sessions, team retreats, outdoor activities, family get-togethers, and workshops;
- Other Benefits: Public transport and telephone reimbursement
#mid-senior-level
#engineering-services
Send us your application today. We look forward to meeting you!
The LAPORTE team
Frequently Asked Questions
How do I apply for the Senior Engineer/Specialist, Pharmaceutical Validation position at LAPORTE?
Use the Apply button above to submit your application directly to LAPORTE. Most applications take less than 5 minutes if your resume and contact details are ready, and you'll be routed to the employer's official application system to finish.
Where is the Senior Engineer/Specialist, Pharmaceutical Validation position at LAPORTE located?
This position is based in CA. LAPORTE has not indicated remote or hybrid options for this role, so candidates should plan for on-site work.
What does a Senior Engineer/Specialist, Pharmaceutical Validation at LAPORTE earn?
LAPORTE has not disclosed a salary range in this posting. Many employers share specifics later in the interview process; you can also ask during a recruiter screen if compensation transparency is important to you.
When was the Senior Engineer/Specialist, Pharmaceutical Validation role at LAPORTE posted?
This role was posted on May 14, 2026 (31 days ago). It's still listed as actively hiring; we re-confirm openings against the source system multiple times per day and remove closed roles.
How much experience does the Senior Engineer/Specialist, Pharmaceutical Validation role at LAPORTE require?
This is a senior-level position. Most senior roles call for 5+ years of directly relevant experience. LAPORTE lists their specific requirements in the description below, so review the must-have qualifications closely before applying.
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