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Added 6 mins ago
SH
Casual Infusion Nurse - Duncan, Langford, Courtenay, BC
Sentrex Health Solutions
Duncan, BC
- Part-time
As the clinic’s lead operator, the Infusion Nurse is responsible for ensuring all requirements are met from both a quality compliance standpoint and a quality patient care perspective. This…
Added 6 mins ago
EM
Automotive Detailer - Car Washer - Calgary Airport
Enterprise Mobility
Calgary, AB
- Full-time
…the industry. As an Auto Detailer and Car Washer, you will lead our commitment to exceptional cleaning practices, exceeding standard protocols to ensure the health and safety of…
Added 6 mins ago
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Senior Associate SIEM Implementation
PwC
Calgary, AB · Vancouver, BC · Ottawa, ON · Toronto, ON · Montreal, QC
- Full-time
Lead technical deliverables for SIEM implementation and operations including Microsoft Sentinel, Google SecOps, Palo Alto XSIAM, and Devo.
Added 6 mins ago
BR
Game Day Lead (Calgary)
Brodie Rec League
Calgary, AB
- $22 to $28 CAD / hour
- Full-time
…recreational basketball by delivering an elevated, professional-quality experience rooted in culture, competition, and community. Our mission is to make every league night the best night of…
Added 6 mins ago
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Nurse Practitioner Clinical Lead, HCP Onboarding & Clinical Education
Felix
Remote, Canada
- $108,000 to $120,000 CAD / year
- Contract
- Remote
Founded in 2019, Felix is a digital healthcare company that puts the patient in control of their own health and wellbeing. We’re passionate about building technology and beautiful customer…
Added 6 mins ago
GD
AI Governance & Risk Manager
General Dynamics Missions System International
Ottawa, ON
- $120,000 to $160,000 CAD / year
- Full-time
Reporting to the Chief Digital & Information Officer (CDIO), the Manager, AI Governance & Risk will lead the establishment, execution, and continuous evolution of the enterprise AI…
Added 6 mins ago
NH
Operations Manager
NOVO Health Services
Burlington, ON
- Full-time
…industry. NOVO Health keenly focuses on safety and infection control and provides its partner hospitals with a value-driven linen management control system that measures and monitors linen…
Added 21 mins ago
Demand Planning & Inventory Control - Demand Planner I
EQI
Canada
…particularly with EQI’s Account Managers, Project Engineers, Quality Engineers, and global personnel in the Production Control and Logistics functions. This role level will manage customer…
Added 21 mins ago
A
Underwriting Manager, Middle Market Package
AXA
Toronto, ON
- Full-time
As Underwriting Manager you will lead the Middle Market underwriting team focusing on property and casualty package for mid-sized businesses across Canada. Working with brokers and clients…
Added 21 mins ago
AG
Master Scheduler
AXIUS GROUP LLC
Toronto, ON · North York, ON
- Full-time
Working with Production, Program Management, Supply Chain, Engineering, Quality, and Shipping and Receiving, the Master Scheduler develops executable schedules, monitors attainment,…
Added 21 mins ago
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(CAN) Bakery Department Manager
Walmart
Halifax, NS
- Full-time
To lead all Bakery Associates and department processes to ensure a high level of customer service while meeting production targets.
Added 21 mins ago
MT
Controls Engineer
Modern Technical Staffing Inc.
Toronto, ON
- Full-time
Overview Lead the design, standardization, and migration of control system hardware/software as we unify multiple controller platforms into a single Soft PLC architecture. This role focuses…
Added 36 mins ago
D
Delivery coordinator, Project management
Desjardins
Montreal, QC · Complexe Desjardins Montréal
- Full-time
…prioritize and coordinate work to meet objectives. You ensure the quality of deliverables and the performance and engagement of contributors. Your projects and initiatives require extensive…
Added 36 mins ago
S
Laboratory Technician - Conventional
Semex
Kemptville, ON
- Full-time
Understanding of lab production,quality control, production database maintenance and recording
Added 36 mins ago
BG
Auto Body Refinisher (Guelph)
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Guelph, ON
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Added 36 mins ago
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Senior ML/AI Engineer, Advanced Analytics & Modelling - Customer Intelligence Platforms
Canadian Tire Corporation
Toronto, ON
- Full-time
The successful candidate will lead the transition of the third party-developed engine into a fully owned CTC capability. This includes mastering the existing code, prompts, models, data…
Added 36 mins ago
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Auto Body Technician (Halifax Downtown)
Boyd Group Services
Halifax, NS
- Full-time
…in collision and glass services. As we continue to grow and lead the industry, we ensure you have the resources and the team behind you to move your career…
Added 36 mins ago
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Product Engineer (Cabico Coaticook)
Cabico
Coaticook, QC
- Full-time
Engineer our products with our plant’s and machines’ capabilities in mind, to build a quality product at the best cost and in the shortest lead time.
Added 36 mins ago
A
Plant Director
Agropur
Burnaby, BC
- Full-time
The Plant Director oversees and is accountable for the productivity/efficiency of the Burnaby plant, quality control, maintenance, shipping, engineering, employee and union relations,…
Added 36 mins ago
I
Frontend Developer - Angular
Infoya
Toronto, ON
- $70,000 to $80,000 CAD / year
- Full-time
…troubleshooting, and collaborate with architects, business analysts, quality analysts, and project managers to deliver accessible, reliable…
Added 36 mins ago
AC
Senior Manager, U.S. Corporate Tax
ACCA Careers
Winnipeg, MB
- Full-time
Maintain high quality control and apply specialized knowledge to anticipate, identify and address issues relevant to the client’s business, financial entries and reports
Added 36 mins ago
TH
Clinical Research Project Coordinator
The Hospital for Sick Children
Toronto, ON
- Full-time
The CRPC will primarily lead study activities at the SickKids site and, where SickKids is the coordinating centre, support participating sites with study start-up, regulatory documentation,…
Added 51 mins ago
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Director, Digital & Information Management
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Mississauga, ON · Toronto, ON
- Full-time
Lead the development and execution of the Digital and Information Management strategy for a large-scale nuclear new build project.
Added 51 mins ago
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Stage - Hiver - Responsable de la gestion des stocks / Internship-Winter-Material Management Lead
RTX
Longueuil, QC
- Full-time
Added 51 mins ago
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Scientist II
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- Full-time
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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

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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.

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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

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