Jobs in Oakville

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Within 25 km of Oakville

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GMP Engineering Inc.

Technical Writer (Pharmaceutical Engineering Contractor)

Oakville, ON, Canada

$50 to $80 USD / hour · Full-time

Within 25 km of Oakville · About 5.2 km from the city centre

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Job details

Pay: $50 to $80 USD / hour
Job type: Full-time
Apply by: Apr 18, 2027
Posted: Oct 20, 2026

Original job description

We are a specialized engineering company with international exposure and subject matter expertise in the design, fabrication and qualification of sterile, high purity and potent containment process equipment and plants. We are growing our company size and capabilities through recruitment of talented professionals. We offer a true creative engineering design work environment with a wide range of interesting projects in the bio-pharmaceutical, personal care and food industry.

POSITION:

We are seeking an independent engineering contractor to develop clear, accurate, GMP-compliant controlled documentation for pharmaceutical facilities, systems, equipment, and processes in collaboration with client engineering, automation, quality, validation, and operations teams.

SUMMARY:

Working with project and site stakeholders, you will be responsible for drafting, revising, and coordinating the approval of:

Standard Operating Procedures (SOPs) for process operations and automation systems
Process narratives, operating descriptions, job aids, and work instructions
Master Environmental Monitoring Plan (MEMP) documentation
Master batch records and associated manufacturing instructions
Industrial hygiene (IH) test plans
System, equipment, and component criticality assessments
Validation Master Plans (VMPs), including cleaning VMPs
Supplier Quality Management System (SQMS) consumable lists
Production consumable lists, mappings, and related traceability documentation

SKILLS:

Strong technical writing, editing, organization, and attention to detail, with the ability to translate engineering, automation, quality, and validation information into clear user-focused documents.
Working knowledge of GMP documentation, document control, and regulated pharmaceutical operations.
Effective collaboration with subject matter experts and cross-functional reviewers; able to independently manage multiple documents, priorities, review cycles, and deadlines.

QUALIFICATIONS:

Bachelor’s degree in engineering
Experience within the pharmaceutical industry

LOCATION:

The primary work location will be our Oakville, Ontario office

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More about this job

Responsibilities

Draft, revise, and coordinate approval of GMP-compliant controlled documentation for pharmaceutical facilities, systems, equipment, and processes. Collaborate with engineering, automation, quality, validation, and operations stakeholders to manage document reviews, priorities, and deadlines.

Requirements

Requires a bachelor’s degree in engineering and experience in the pharmaceutical industry. Candidates should have strong technical writing and editing skills, working knowledge of GMP documentation and document control, and the ability to collaborate with subject matter experts while independently managing multiple documents and deadlines.

Skills

Technical Writing
Editing
GMP Documentation
Document Control
Pharmaceutical Operations
Standard Operating Procedures
Process Narratives
Operating Descriptions
Work Instructions
Master Batch Records
Environmental Monitoring Plans
Industrial Hygiene Test Plans
Criticality Assessments
Validation Master Plans
Cross-Functional Collaboration
Document Coordination

Visa sponsorship

Not detected in the job text

Keywords

GMP
Pharmaceutical Engineering
Sterile Process Equipment
High-Purity Systems
Potent Containment
Controlled Documentation
Document Control
Standard Operating Procedures
Process Narratives
Operating Descriptions
Job Aids
Work Instructions
Master Environmental Monitoring Plan
Master Batch Records
Manufacturing Instructions
Industrial Hygiene
Criticality Assessments
Validation Master Plan
Cleaning Validation
Supplier Quality Management System
Production Consumables
Traceability Documentation
Automation Systems
Quality Assurance
Validation
Pharmaceutical Manufacturing

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