Find work in Canada.

586,859 jobs across our Canadian network. How we count

Jobs in Canada

25+ jobs

Email me new jobs Save this search

Added 13 mins ago
R
Senior Manager - WM Business Risk
RBC
Toronto, ON
- Full-time
Reporting to the Director, WM Business Risk, the Senior Manager, Business Risk will lead operational risk/regulatory compliance reviews and provide expert feedback on the operational risk…
Added 13 mins ago
AI
Procurement Specialist
American Iron and Metal
Hamilton, ON
- Full-time
Evaluate supplier quotations based on pricing, quality, lead time, service, and payment terms.
Added 28 mins ago
C
Senior Specialist Procurement - Travel & HR
CN
Quebec, QC
- Full-time
Lead operational execution for asset monetization initiatives, including surplus inventory disposition, scrap metal and rail sales, and retired capital equipment sales across network regions
Added 28 mins ago
C
Rail Track Maintainer - Production (Prairie West)
CN
Invermay, SK
- Internship
Unload ballasts and distribute track material
Added 28 mins ago
EK
Intermediate Interior Designer
Earls Kitchen + Bar
Vancouver, BC
- $70,000 to $85,000 CAD / year
- Full-time
…materials, SketchUp modeling, and construction drawings. You’ll also lead FF&E coordination and on-site installations, with opportunities to travel to project sites across North America.…
Added 28 mins ago
R|
Project Manager
RI-MUHC | Research Institute of the MUHC | #rimuhc
Montreal, QC
- Contract
Clinical supervision and quality assurance: Supervise and train clinical research staff and lead scoring reviews to support inter-rater reliability, consistency, and ongoing clinical…
Added 28 mins ago
CM
Mechanical Engineering SME (Subject Matter Expert), Capital Projects
Cyclic Materials
Toronto, ON
- Full-time
…external teams accountable for quality and performance. The Lead provides final technical review and sign-off, bringing deep expertise and experience to the…
Added 28 mins ago
E
Principal Product Manager, Agent Intelligence
Equinix
Toronto, ON
- Full-time
…stays internal, customer-facing content uses only approved material, and confidential details never cross between…
Added 28 mins ago
N
Real Estate Program Manager
Nokia
Ottawa, ON · Kanata, ON
- Full-time
The Real Estate Program Manager will lead program-level coordination of Nokia’s lab consolidation and relocation initiatives. The role will bring together Business, R&D IT, Real Estate,…
Added 28 mins ago
R
Recycling Auditor
Reconomy
Brampton, ON
- $22.5 CAD / hour
- Full-time
…platform solutions, we overcome challenges in consumer goods and material take-backs worldwide and connect all stakeholders within the reverse logistics value chain. Our goal is to generate…
Added 28 mins ago
Health and Safety Manager (GRD)
Price Industries Limited
Winnipeg, MB
Lead and support workplace inspections, task risk assessments, change reviews, and other formal risk-assessment activities.
Added 28 mins ago
Administrative Legal Assistant/ILA B061-26
Legal Aid BC
Kelowna, BC
Provide administrative and legal administrative support for the Department, Managing Lawyer, Lead Lawyer, Staff Lawyer, roster lawyers lead and/or Paralegal/Advocate. Provide front line…
Added 28 mins ago
T
Manager, Compliance Governance & Operations (5664)
TD
Toronto, ON
- Full-time
The Manager will independently lead surveillance initiatives and workstreams, provide subject matter expertise, drive execution across stakeholders, and escalate material risks and issues…
Added 28 mins ago
CE
Lead Process Engineer
CANUSA EPC LLC
Calgary, AB
- Full-time
CANUSA EPC is looking for an experienced Lead Process Engineer to join our growing Calgary engineering team.
Added 28 mins ago
D
Delivery coordinator, Project management
Desjardins
Levis, QC · Montreal, QC · Complexe Desjardins Montréal
- Full-time
As a project delivery manager, you help direct material, time, IT and human resources on cross-sector projects to meet objectives on time and on budget. You analyze project feasibility and…
Added 28 mins ago
D
Delivery coordinator, Project management
Desjardins
Levis, QC · Montreal, QC · Complexe Desjardins Montréal
- Full-time
As a project delivery manager, you help direct material, time, IT and human resources on cross-sector projects to meet objectives on time and on budget. You analyze project feasibility and…
Added 28 mins ago
Director, IT Program and Project Management
HS Financial Technologies
Halifax, NS
The Director, IT Program and Project Management will lead the planning, governance, and delivery of complex, cross-functional initiatives across the Global Technology organization. The role…
Added 43 mins ago
B
Managing Director & Head, Credit and Portfolio Management
BMO
Toronto, ON · FCP
- Full-time
Provide effective challenge on material credit, underwriting and portfolio risk; escalate significant policy, governance or risk concerns.
Added 43 mins ago
Batcher
Amrize
Hemlo, ON
Lead a healthy workplace culture based on respect and performance.
Added 43 mins ago
Operations Manager Rosser, MB
Cosentino
Winnipeg, MB
…warehouse. Your daily tasks include control of shipping/receiving material, organization & inventory management, ensuring that all appropriate safety regulations are being implemented, and…
Added 44 mins ago
CC
Technician Laboratory/QC
Cabot Corporation
Saint-Jean-sur-Richelieu, QC · St. Jean
- Full-time
…“Creating for Tomorrow,” we are focused on our core strengths to lead in performance and sustainability – today and into the…
Added 44 mins ago
CI
Shipping Supervisor
Cooke Inc.
NB
- Full-time
Lead, train, and schedule shipping staff to meet productivity and performance goals
Added 59 mins ago
FM
Quality Engineer
Fresenius Medical Care
Richmond Hill, ON
- Full-time
Lead Material Review Board activities, segregation and quarantine, and disposition (use-as-is, return to supplier, scrap).
Added 59 mins ago
C
Senior Supply Chain Analyst & Planning Lead
Cryopak
Montreal, QC
- Full-time
Cryopak Industries is seeking a Senior Supply Chain Analyst & Planning Lead to support and optimize our manufacturing planning activities, including MRP, materials management, inventory…
Added 59 mins ago
M
Skills Development Advisor, APART Program
Maarut
Montreal, QC
- Contract
support the discipline Lead for the first release of the APART initiative. The

Teva Pharmaceuticals

Operations Technical Writer - 12 month contract

Whitchurch-Stouffville, ON, Canada

The typical hiring range for this position is $60,480-$75,600. · Full-time

Apply About employer

Applications open in a new tab.

Job details

Pay: The typical hiring range for this position is $60,480-$75,600.
Job type: Full-time
Apply by: Dec 4, 2026
Posting language: English
Posted: Nov 4, 2026

Original job description

We Are Teva

We’re Teva, a leading innovative biopharmaceutical company, enabled by a world-class generics business. Whether it’s innovating in the fields of neuroscience and immunology or delivering high-quality medicine worldwide, we’re dedicated to addressing patients’ needs now and in the future. Here, you will be part of a high-performing, inclusive culture that values fresh thinking and collaboration. You'll have the room to grow, the flexibility to balance life with work, and the opportunity to better health worldwide, together.

Our Team, Your Impact

We are seeking an Operations Technical Writer to support our Manufacturing team in a GMP-regulated pharmaceutical production environment. In this role, you will be responsible for creating, revising, and maintaining controlled manufacturing documentation while supporting investigations related to deviations, non-conformances, and quality events. This position is ideal for someone who enjoys technical writing, problem-solving, and collaborating across multiple departments to drive compliance and operational excellence.

How You’ll Spend Your Day

Technical Documentation

Author, revise, and maintain controlled GMP documentation, including:
- Standard Operating Procedures (SOPs)
- Work Instructions (WIs)
- Job Aids
- Equipment Manuals
- Cleaning Procedures
- Manufacturing Support Documents
- Forms and Templates
- Training Materials
Ensure documents meet site quality standards, formatting requirements, and regulatory expectations.
Translate complex technical processes into clear and user-friendly instructions for operational personnel.

Investigations & Quality Support

Lead and support investigations involving manufacturing deviations, non-conformances, procedural events, equipment issues, and quality concerns.
Gather and assess information from batch records, equipment logs, electronic systems, environmental data, and employee interviews.
Perform Root Cause Analysis (RCA) using tools such as:
- 5 Whys
- Fishbone Diagrams
- FMEA
Assess impact on product quality, compliance, patient safety, and operational performance.
Author investigation reports and support timely closure of quality events and CAPAs.

Training & Continuous Improvement

Develop and update training materials.
Partner with subject matter experts to document best practices and manufacturing standards.
Support document lifecycle management within electronic quality management systems.
Promote consistency and standardization across manufacturing documentation.

Required

Your Skills and Experience

College Diploma in Science or a related discipline.
Minimum 1 year of experience in a GMP-regulated pharmaceutical, biotechnology, medical device, or manufacturing environment.
Experience authoring and revising controlled documentation.
Strong technical writing and editing skills.
Knowledge of Good Manufacturing Practices (cGMP).
Proficiency with Microsoft Office (Word, Excel, PowerPoint, and Visio).

Preferred

Bachelor's Degree in Science, Engineering, or a related field.
4+ years of pharmaceutical manufacturing experience, preferably in oral solid dosage manufacturing.
Experience using quality systems such as TrackWise, Veeva, MasterControl, or similar platforms.
Experience conducting investigations and developing CAPAs.

Knowledge & Skills

Technical Writing Excellence
Root Cause Analysis & Investigations
Critical Thinking & Problem Solving
Attention to Detail
Document Control & Quality Systems
Knowledge of Health Canada, FDA, ICH, and PIC/S GMP requirements
Understanding of oral solid dose manufacturing processes, including dispensing, granulation, compression, coating, encapsulation, packaging, and cleaning

How We’ll Take Care Of You

At Teva Canada we provide a rewarding and collaborative work experience, with career growth and development opportunities for employees, in a safe and caring environment! The typical hiring range for this position is $60,480-$75,600. The base pay offered may vary depending on job-related knowledge, skills, experience, education, and internal equity. In addition to base salary, this role may qualify for an annual bonus based on employment type. Certain positions may also be eligible for a sales commission structure as part of the overall compensation package. Beyond base pay, Teva also offers a comprehensive suite of wellness and benefits programs tailored to role and employment type, that continue to rank among the best in our industry! Our competitive offerings are designed to provide flexibility, security, and meaningful choices, empowering employees to thrive both personally and professionally throughout their journey with us.

As part of our commitment to well-being, employees may have access to:

Teva Canada’s choices Benefit Plan including Health, Dental, Disability, Life Insurance
Employee Assistance Program & Virtual Health Programs
Retirement Savings Programs
Employee Stock Purchase Plan (ESPP)
Time for yourself or those you care about, through paid time for Vacation, Wellness days, Care/Sick days, Teva Days and Volunteer Days
Education Assistance Program
Recognition programs such as Employee Service Awards
Employee Discounts
And much more!

More exciting details on the specific total rewards offerings to be provided at the offer stage depending on the position and employment type hiring for. This position will fill a current vacancy and Teva Canada may use an artificial intelligence (AI) system to assist with the initial screening and evaluation of job applications by analyzing for relevant skills, professional experience, and education, that best match the posted job qualifications. It is important to note that all final decisions in this process are made by a member of the hiring team.

Already Working @Teva?

Make sure to apply through our internal career site on Twist - your one-stop shop for career development

Teva’s Equal Employment Opportunity Commitment

Teva Pharmaceuticals is committed to equal opportunity in employment. It is Teva's global policy that equal employment opportunity be provided without regard to age, race, creed, color, religion, sex, disability, pregnancy, medical condition, sexual orientation, gender identity or expression, ancestry, veteran status, national or ethnic origin or any other legally recognized status entitled to protection under applicable laws. We are committed to a diverse and inclusive workplace for all. If you are contacted for a job opportunity, please advise us of any accommodations needed to support you throughout the recruitment and selection process. All accommodation information provided will be treated as confidential and used only for the purpose of providing an accessible candidate experience.

Apply About employer

More about this job

Responsibilities

Create, revise, and maintain controlled GMP manufacturing documents, training materials, and related records, ensuring they meet site quality and regulatory requirements. Lead or support investigations into manufacturing and quality events, perform root cause analysis, assess impacts, and help close investigations and CAPAs.

Requirements

A college diploma in science or a related discipline and at least one year of experience in a GMP-regulated pharmaceutical, biotechnology, medical device, or manufacturing environment are required. Candidates should have controlled-documentation experience, strong technical writing skills, and cGMP knowledge; a science or engineering bachelor’s degree, four or more years of pharmaceutical manufacturing experience, and quality-system or investigation experience are preferred.

Skills

Technical Writing
Controlled Documentation
Good Manufacturing Practices
Root Cause Analysis
Investigations
Corrective and Preventive Actions
Document Control
Quality Systems
Critical Thinking
Problem Solving
Attention to Detail
Microsoft Office
Regulatory Compliance
Training Material Development
Oral Solid Dosage Manufacturing

Benefits

Health Insurance
Dental Insurance
Disability Insurance
Life Insurance
Employee Assistance Program
Virtual Health Programs
Retirement Savings Programs
Employee Stock Purchase Plan
Paid Vacation
Wellness Days
Care and Sick Days
Volunteer Days
Education Assistance
Employee Recognition Programs
Employee Discounts

Visa sponsorship

Not detected in the job text

Keywords

GMP
cGMP
Standard Operating Procedures
Work Instructions
Job Aids
Equipment Manuals
Cleaning Procedures
Manufacturing Documentation
Document Lifecycle Management
Electronic Quality Management Systems
TrackWise
Veeva
MasterControl
Microsoft Word
Microsoft Excel
Microsoft PowerPoint
Microsoft Visio
Root Cause Analysis
5 Whys
Fishbone Diagrams
FMEA
Deviations
Non-Conformances
CAPA
Batch Records
Health Canada
FDA
ICH
PIC/S
Oral Solid Dosage Manufacturing

Report this job