Quality Analyst II - 6 month contract

We Are Teva

Our Team, Your Impact

How You’ll Spend Your Day

• 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.


• Draft, revise, negotiate, and maintain Quality Agreements with manufacturing sites, contract packagers, contract laboratories, and other external partners.


• Perform executed batch record reviews for products supplied by Teva affiliates.


• 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.


• Maintain establishment licenses for imported products and coordinate renewals as required.


• 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, 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.

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 $76,680-$94,600.  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. Teva Canada may utilize AI- driven insights on skills and capabilities as part of our candidate recruitment process to align candidates with potentially suitable opportunities more effectively.  Our recruiters and hiring managers remain the principal decision makers in the recruitment process.

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