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Gestionnaire, Validation / Manager, Validation - Job Opportunity at Jubilant HollisterStier General Partnership

Montreal, Canada
Full-time
Senior
Posted: April 19, 2025
On-site
CAD 120,000 - 150,000 annually based on seniority and market conditions in Montreal pharmaceutical sector

Benefits

Competitive base salary with comprehensive medical coverage
Enhanced dental care program
Robust disability insurance protection
Strategic retirement savings plan with employer matching
Progressive wellness program focused on employee health
Professional development and growth opportunities

Key Responsibilities

Lead strategic validation masterplan development and implementation for site-wide operations
Direct comprehensive validation protocols across sterile manufacturing processes
Manage technical compliance with regulatory requirements and GMP standards
Oversee cross-functional validation teams and contractor relationships
Drive quality assurance programs and regulatory inspection preparation
Lead departmental budget management and resource allocation

Requirements

Education

Bachelor's Degree, preferably in Science/Engineering

Experience

8-10 years of related work experience in the pharmaceutical industry, preferably in sterile pharmaceutical manufacturing

Required Skills

In-depth knowledge of GMP regulations Thorough knowledge of validation principles Strong written and verbal communication skills Strong computer skills Knowledge of sterilization processes Understanding of PLC software Project management expertise Strong negotiation skills
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Sauge AI Market Intelligence

Industry Trends

Increasing focus on sterile manufacturing capabilities due to growing biopharmaceutical sector Rising demand for validation expertise in complex manufacturing environments Enhanced regulatory scrutiny driving need for sophisticated validation approaches Growing integration of automated systems requiring specialized validation knowledge

Role Significance

Typically manages team of 5-8 validation specialists with matrix responsibility across departments
Senior leadership position with direct impact on product quality and regulatory compliance

Key Projects

Sterile manufacturing process validation programs Facility and equipment qualification initiatives Regulatory compliance and inspection preparation Cross-functional quality system implementations

Success Factors

Deep technical expertise in pharmaceutical validation Strong regulatory knowledge and compliance focus Effective cross-functional leadership capabilities Strategic project management skills Advanced problem-solving abilities

Market Demand

High demand due to specialized expertise required and growing sterile manufacturing sector

Important Skills

Critical Skills

Sterile manufacturing expertise - essential for core operations Regulatory compliance knowledge - crucial for maintaining licenses Project management - key for complex validation programs Technical writing - vital for documentation requirements

Beneficial Skills

Change management skills Risk assessment capabilities Digital system validation expertise Cross-cultural communication abilities

Unique Aspects

Specialized focus on sterile manufacturing validation
Cross-border operations between Canada and US
Integration with larger international pharmaceutical network
Growth-oriented organization with expansion plans

Career Growth

Typical progression to director level within 3-5 years based on performance and organizational growth

Potential Next Roles

Director of Validation Quality Assurance Director Technical Operations Director Site Quality Head

Company Overview

Jubilant HollisterStier General Partnership

Jubilant HollisterStier is a significant player in contract manufacturing for sterile injectables and other pharmaceutical products

Growing presence in North American pharmaceutical manufacturing with strong international backing
Strategic Montreal location serving North American market with international reach
Professional environment focused on quality and compliance with opportunities for advancement
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