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- Employment type
- Full-time
- Experience level
- Senior · 5+ years
- Apply by
- Nov 2, 2026
- Posting language
- English
- Working hours
- 40 hours per week
- Seniority
- Mid-Senior level
Job summary
Develop process engineering and layout documentation, conduct GMP audits and design reviews, and commission and qualify equipment, utilities, and pharmaceutical systems. Perform manufacturing, cleaning, sterilization, and computer system validation, manage projects, and contribute to the company’s commercial development.
Job details
PBE Expert Inc Careers Job offer Senior & Intermediate Process Engineers Description Of The Company & Job Opening PBE Expert Inc is a consulting company in Pharmaceuticals, Biotechnology, Cannabis, Morphine, Medical Devices, Natural Health Products (NHP), Cosmetics, Food Supplements and Food Industries that works in Canada but also internationally. Candidates Will Be Involved In The Following Tasks Process engineering, Layout: URS, BOD, DDE, PFD, P&ID. GMP compliance audit of sites & Design Review. Commissioning & Qualification of equipment, utilities and pharma / ICH systems Q9 : FAT, SAT, DQ, IQ, OQ, PQ. Manufacturing Process Validation, Cleaning & Sterilization Validation according to the new FDA2011 & ANSM2015 guides. Computer validation (CSV), according to CFR21, part 11, GAMP. Project management, GANT. The candidate will also be involved in contributing to the commercial development of PBE Expert Inc (Bonus$$$). Requirements 5 years experience in Clean Process Design. Mastery of ASME BPE, ISO-14644, ISPE, GAMP. Experience +3 years Validation, URS, GAMP, CSV, ERP. Project management & Skills in comics are assets. Autocad ability is an asset. Canadian resident or citizen. GMP Control, cGMP FDA, ANSM/EMA & Health Canada. Dynamic, proactive, organizational, communicative. Ability in MS Project is an asset. Advanced English (At least 8/10) is an asset. Excellent written and oral expression in French and English. Available for projects abroad and in Canada Outside Qc. Working conditions & Social benefits Flexible hours. PBE office located in Laval, in front of bus stops and close to the Metro and the 440. Very user-friendly working environment. In-house training offered to employees. Involvement in projects in Canada but also internationally. Very beautiful challenges to take up. Ping-pong competition during break times. Medication insurance available to employees. End of year bonus. Admission to RVER & RRSP for employees. PBE Expert Inc. professional insurance coverage Statutory holidays. Possibility of work from home negotiable in appropriate period. Career development to a position of responsibility. Apply Bureau CANADA Pour toute information commerciale, de partenariat et marketing avec PBE Expert Inc +1 (514) 616-2692 pbe@pbe-expert.com 301, 9200 Meilleur, Montréal, QC, H2N 2A9 Nous Sommes Aussi Au Tunisie +(216) 96-751-330 pbe@pbe-expert.com ENTREZ EN CONTACT Suivez nos activités Tunisie +(216) 96-751-330 pbe@pbe-expert.com ENTREZ EN CONTACT Suivez nos activités
What you’ll do
Develop process engineering and layout documentation, conduct GMP audits and design reviews, and commission and qualify equipment, utilities, and pharmaceutical systems. Perform manufacturing, cleaning, sterilization, and computer system validation, manage projects, and contribute to the company’s commercial development.
Requirements
Candidates should have at least five years of clean process design experience and more than three years of experience with validation, URS, GAMP, CSV, and ERP. Knowledge of ASME BPE, ISO 14644, ISPE, and GMP regulations is expected; Canadian residency or citizenship, strong French and English communication, and availability for travel in Canada and abroad are also specified.
Benefits
- Flexible Hours
- In-House Training
- Medication Insurance
- Year-End Bonus
- RVER and RRSP
- Professional Insurance Coverage
- Statutory Holidays
- Work-from-Home Option
- Career Development
Listed skills
- Project management · Preferred
- AutoCAD · Preferred
Other relevant skills
Identified from the job description. Confirm important requirements above.
- Process Engineering
- Clean Process Design
- Process Layout
- GMP Compliance
- Commissioning and Qualification
- Process Validation
- Cleaning Validation
- Sterilization Validation
- Computer System Validation
- Project Management
- ASME BPE
- ISO 14644
- GAMP
- AutoCAD
- MS Project
- Technical Communication
Job areas
- Engineering
- Consulting
- Healthcare
- Manufacturing