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Added 8 mins ago
TW
Program Director & Full-Time Tenure-Track MA CPSY Faculty
Trinity Western University
Langley (District), BC · Langley, BC
- Full-time
…the National Survey of Student Engagement; holds two Canada Research Chairs; wins National Championships in U Sports; and emphasizes experiential learning to prepare graduates to make a…
Added 8 mins ago
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Clinical Research Associate (CRA) – Oncology | Canada
Scimega | Expert Oncology CRO
Canada
- Full-time
…corporate standards, and applicable regulations, the Clinical Research Associate (CRA) is the main line of communication between the study team and the site…
Added 8 mins ago
LD
Occasional Teachers - Intermediate/ Senior Technology
London District Catholic School Board
London, ON
- Full-time
Current in understanding of research, integrating technology and best instructional practices
Added 8 mins ago
LD
Occasional Teachers - Intermediate/ Senior Mathematics
London District Catholic School Board
London, ON
- Full-time
Current in understanding of research, integrating technology and best instructional practices
Added 8 mins ago
LD
Occasional Teachers - Intermediate/ Senior Business
London District Catholic School Board
London, ON
- Full-time
Current in understanding of research, integrating technology and best instructional practices
Added 8 mins ago
LD
Occasional Teachers - Intermediate/ Senior Computer Studies
London District Catholic School Board
London, ON
- Full-time
Current in understanding of research, integrating technology and best instructional practices
Added 8 mins ago
LD
Occasional Teachers - French
London District Catholic School Board
London, ON
- Temporary
Current in understanding of research, integrating technology and best instructional practices
Added 23 mins ago
C
Assistant Clinical Project Manager - Hybrid
Clario
Montreal, QC
- Full-time
…operational support to the Project Management team at NeuroRx Research. NeuroRx Research is a leader in advanced brain image analysis and project management, serving the pharmaceutical and…
Added 38 mins ago
S|
Clinical Research Associate (CRA) – Oncology | Canada
Scimega | Expert Oncology CRO
Toronto, ON
- Full-time
…corporate standards, and applicable regulations, the Clinical Research Associate (CRA) is the main line of communication between the study team and the site…
Added 1 hour ago
WF
Inventory Finance – Commercial Associate
Wells Fargo
Mississauga, ON
- Full-time
Research industry trends, customer needs and competitive developments to support product and commercial strategies.
Added 1 hour ago
Assistant/ Associate/ Full Professor - Academic Core Obstetrician and Gynecologist
University of Toronto
Toronto, ON
…full-time clinical academic appointment at the rank of Assistant, Associate or Full Professor, or as Lecturer with a commitment to achieve rank of Assistant Professor within the 3-year…
Added 1 hour ago
Quality Assurance Associate
Canadian Blood Services
Calgary, AB · Edmonton, AB · Kelowna, BC · Vancouver, BC · Saint John, NB · St. John's, NL · Dartmouth, NS · Brampton, ON · Hamilton, ON · London, ON · Ottawa, ON · Toronto, ON · Ancaster, ON
Canadian Blood Services is looking for a Temporary full-time Quality Assurance Associate (QAA) to join our dynamic Quality Assurance team.
Added 2 hours ago
SG
Junior Quantitative Advisor-QIS
Societe Generale
Montreal, QC
- Full-time
This Associate-level role is designed for a junior quantitative professional who combines strong analytical and programming skills with intellectual curiosity and a practical approach to…
Added 2 hours ago
TS
Contract and Compliance Analyst
T&T Supermarket
Richmond, BC
- $65,000 to $85,000 CAD / year
- Full-time
Reporting to the Associate Director, Contract and Compliance, the Contract and Compliance Analyst will help strengthen T&T’s contracting and compliance practices.
Added 2 hours ago
UO
Team Lead, VFMP Patient Program
University of British Columbia
Vancouver, BC · VCH | Vancouver General Hospital - Gordon and Leslie Diamond Health Care Centre (VGHHCC)
- $6,143.67 to $8,830.25 CAD / month
- Full-time
At UBC, we believe that attracting and sustaining a diverse workforce is key to the successful pursuit of excellence in research, innovation, and learning for all faculty, staff and…
Added 2 hours ago
C
Associate, Enterprise Strategy and Corporate Development
CIBC
Toronto, ON
- Full-time
…to provide a broad range of analytical, financial modelling, research, presentation preparation and project management support. You'll also be part of a Corporate Development team that…
Added 2 hours ago
Associate, Recruitment & Admissions
Simon Fraser University
Burnaby, BC
Simon Fraser University is a leading research university, advancing an inclusive and sustainable future. Our purpose – the essence of SFU – is to create and connect knowledge, learning and…
Added 2 hours ago
MG
Associate Platform Engineer
Mobility Global
London, ON
- Full-time
Participate in design decisions, including new technology research and prototyping.
Added 2 hours ago
UO
Lecturer / Assistant / Associate Professor Diagnostic Neuroradiology - St. Michael's Hospital
University of Toronto
Toronto, ON
- $200,000 CAD / year
…academic appointment at the rank of Lecturer or Assistant / Associate Professor at the University of Toronto. The anticipated start date is flexible, starting from January 1,…
Added 2 hours ago
UO
Assistant / Associate / Full Professor Breast Radiology - St. Michael's Hospital
University of Toronto
Toronto, ON
- $200,000 CAD / year
…full-time clinical academic appointment at the rank of Assistant / Associate / Full Professor. The anticipated start date is February 1,…
Added 2 hours ago
Donor Centre Associate - Blood Collection
Canadian Blood Services
Lethbridge, AB
Canadian Blood Services is looking for a Temporary full-time Donor Centre Associate - Blood Collection to join our dynamic Collections team in our AB-Lethbridge donor centre.
Added 3 hours ago
R|
Research Associate
RI-MUHC | Research Institute of the MUHC | #rimuhc
Montreal, QC
- Full-time
The MyeliNeuroGene Research Laboratory, directed by Dr. Genevieve Bernard, MD, MSc, a clinician-scientist, is looking for a motivated person to fill the position of full-time Research…
Added 3 hours ago
R|
Fellowship and Bursary Administrative Assistant
RI-MUHC | Research Institute of the MUHC | #rimuhc
Montreal, QC
- Full-time
Do you want to work for a world-renowned research institute that pushes the boundaries of biomedical science and health research? Right here in Montreal! At the Research Institute of the…
Added 3 hours ago
R|
Clinical Research Manager
RI-MUHC | Research Institute of the MUHC | #rimuhc
Montreal, QC
- Full-time
Do you want to work for a world-renowned research institute that pushes the boundaries of biomedical science and health research? Right here in Montreal! At the Research Institute of the…
Added 3 hours ago
MU
EVENTS COORDINATOR (BAND LEVEL 8)
Memorial University, Newfoundland and Labrador
St. John's, NL
- Full-time
Reporting to the Associate Director, Guest Accommodations/Conference and Event Services, the Events Coordinator will work as part of a collaborative team in the management, promotion,…

Teva Pharmaceuticals

Quality Associate II

Toronto, ON, Canada

Full-time

Apply About employer

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Job details

Job type: Full-time
Apply by: Dec 3, 2026
Experience: 3+ years of relevant experience in the pharmaceutical industry.
Posting language: English
Posted: Nov 3, 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

QA Associate

We are looking for a Quality Assurance Associate II to join our team. In this role, you will be responsible for reviewing and approving changes in SAP MDG related to GXP fields, creating and approving inspection plans in SAP and providing support as needed, reviewing and approving stability reports, conducting corporate standard gap assessments, evaluating and closing change controls, as well as auditing executed batch records. You will support new product launches and the release of imported products to the Canadian market, including assessing the impact of critical GMP-related issues. The role also involves reviewing supplier documentation related to product launches, product releases, validation activities, deviations, and change controls.

As a Quality Assurance Associate II, you will lead and support investigations related to deviations, Out-of-Specification (OOS), and Out-of-Trend (OOT) results, while ensuring compliance with regulatory and quality requirements. Additionally, you will investigate product complaints and ensure the timely review, closure, and approval of records within the Quality Management System (QMS), collaborating closely with both internal and external stakeholders to drive quality and compliance across operations.

How You’ll Spend Your Day

Review and approve changes in SAP MDG related to GxP field, create and approve inspection plans in SAP and provide support as needed.
Provide quality oversight for activities related to imported products.
Review and approve GMP documentation for products supplied by Teva affiliates and third-party manufacturers, including release documentation, deviations, validations, and change controls.
Perform product release activities for Teva affiliate and third-party products destined for the Canadian market.
Collaborate with Teva affiliates and Local-to-Local (L2L) third-party suppliers to ensure GMP compliance, adherence to Quality Agreements, and timely resolution of quality issues.
Support the compliant and timely launch of products manufactured by Teva affiliates and third-party partners through effective coordination with internal and external stakeholders.
Investigate, review, and approve product complaints, ensuring timely closure of records within the Quality Management System (QMS).
Conduct thorough investigations of quality deviations and perform impact assessments related to Critical Incident Notifications and Alerts affecting imported products.
Monitor and report quality metrics and KPIs, including deviations, CAPAs, and batch release cycle times; prepare monthly and quarterly trend reports and drive timely completion of quality actions.
Perform executed batch record reviews for products supplied from non-MRA countries
Prepare, review, and approve Annual Product Reviews (APRs) for imported and L2L manufactured or packaged products.
Support Vendor Master Data activities and ensure accuracy of quality-related information.
Review internal procedures and corporate standards, conduct gap assessments, and update SOPs to ensure ongoing compliance.
Oversee retain sample management activities, including receipt, storage, SAP updates, and destruction of expired samples in accordance with established procedures.
Support compliance initiatives, quality projects, regulatory inspections, and audit activities as required.
Lead and manage special projects involving cross-functional teams and Teva Global affiliates.
Perform other related duties as assigned.

Your Skills And Experience

Bachelor's degree in Chemistry, Biochemistry, Pharmacy, Microbiology, Life Sciences, or a related scientific discipline from a Canadian university, or an equivalent degree recognized by a Canadian university or accredited Canadian credentialing body.
3+ years of relevant experience in the pharmaceutical industry.
Experience in Quality Assurance, Quality Control, or other GMP-regulated environments.
Knowledge of USP, BP, and EP compendial methods and the ability to interpret and apply analytical testing methods.
Experience conducting analytical method evaluations and investigating Out-of-Specification (OOS) and Out-of-Trend (OOT) results.
Strong understanding of Good Manufacturing Practices (GMP), current Good Manufacturing Practices (cGMP), and Standard Operating Procedures (SOPs).
Working knowledge of quality systems including deviations, CAPAs, change controls, product complaints, and batch record review processes.
Proficiency with Oracle, LIMS, QMS, SAP MDG, Microsoft Excel, and Microsoft Word.
Thorough understanding of pharmaceutical manufacturing, packaging, laboratory, and testing operations.
Strong analytical, investigation, problem-solving, and organizational skills.
Excellent written and verbal communication skills with the ability to collaborate effectively with internal and external stakeholders.

Also Good to Have

Salary Range

How We’ll Take Care Of You

At Teva, better health starts from within, and that includes you. From day one, you’ll be supported with benefits designed to help you thrive in and out of work. This includes generous annual leave, reward plans, flexible working schedules (dependent on role), access to tailored health support, and meaningful ways to give back to the community.  When it comes to your career, you’ll be encouraged to explore, evolve, and shape your path. Twist, our one-stop shop for career development platform, gives you access to a wide range of possibilities, from learning programs and short-term projects to opportunities for internal growth. Here, you’ll be part of a culture that empowers you to reach your goals and prioritize your wellbeing every step of the way. 

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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

Review and approve GMP documentation, SAP MDG changes, inspection plans, product releases, batch records, stability reports, and annual product reviews for imported and partner-manufactured products. Lead quality investigations and complaint reviews, monitor quality metrics, maintain compliance documentation and sample management, and coordinate launches, audits, and cross-functional quality projects.

Requirements

Requires a bachelor's degree in a relevant scientific discipline and at least three years of pharmaceutical industry experience in Quality Assurance, Quality Control, or another GMP-regulated environment. Candidates should understand GMP, pharmaceutical quality systems, compendial methods, and analytical investigations, and be proficient with Oracle, LIMS, QMS, SAP MDG, Excel, and Word.

Skills

Quality Assurance
Good Manufacturing Practices
Quality Management Systems
Deviation Investigations
CAPA Management
Change Control
Product Complaints
Batch Record Review
Out-of-Specification Investigations
Out-of-Trend Investigations
SAP MDG
LIMS
Oracle
Analytical Method Evaluation
Regulatory Compliance
Stakeholder Collaboration

Benefits

Annual Leave
Reward Plans
Flexible Working Schedules
Health Support
Community Giving Opportunities
Career Development Programs
Internal Growth Opportunities

Visa sponsorship

Not detected in the job text

Keywords

Quality Assurance
Pharmaceutical Manufacturing
GMP
cGMP
SOP
Quality Management System
SAP MDG
SAP
Oracle
LIMS
Microsoft Excel
Microsoft Word
Deviations
CAPA
Change Controls
Product Complaints
Batch Record Review
Out-of-Specification
Out-of-Trend
USP
BP
EP
Analytical Methods
Product Release
Annual Product Reviews
Validation
Supplier Documentation
Quality Agreements
Vendor Master Data
Retain Sample Management

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