דרושים ב-Teva ב-Canada, Toronto

Financial Planning & Analysis:

Conduct monthly financial analysis, including variance analysis, performance tracking, and scenario modeling.

Prepare and present comprehensive monthly reporting packages to management, highlighting key trends, risks, and opportunities.

Strategic Change Management & Automation:

Identify and implement opportunities to streamline reporting and analysis through automation and BI best practices.

Communicate complex financial information in a clear, concise, and actionable manner to both financial and non-financial stakeholders.

Support ad hoc analysis, special projects, and continuous improvement initiatives as required.

Other Duties as Assigned:

Ensure compliance with internal policies, procedures, and external regulations.

Proactively seek opportunities for professional development and process improvement.

• Education Required: Bachelor’s degree in Finance, Accounting, Business, or related field. Advanced degree (CPA, CFA, or MBA) is an asset.
• 7+ years of progressive experience in financial planning & analysis, business finance, or related roles. Working knowledge of US GAAP and/or IFRS.
• Experience in the pharmaceutical or healthcare industry is an asset.
• Strong analytical and problem-solving skills.
• Excellent communication and presentation skills.
• Strong business acumen and partnership orientation.
• Ability to work independently as an IC and within cross-functional teams.
• Proven ability to provide consultative advice and decision support.
• Strong experience with ERP systems (especially SAP) and business intelligence tools (e.g., Power BI) is required.
• Advanced proficiency in Excel, PowerPoint, and financial modeling.
• Demonstrated experience with automation and process improvement.

The internal career site is available from your home network as well. If you have trouble accessing your EC account, please contact your local HR/IT partner.

• Support the month-end and year-end close processes, ensuring timely and accurate financial reporting in compliance with US GAAP and a SOX control environment.
• Manage general ledger activities, including journal entries, account reconciliations, and variance analysis.
• Liaise with Global Business Service teams to ensure that offshore processes are running smoothly, that work is reviewed and that issues are addressed in a timely manner.
• Coordinate with internal and external auditors during quarterly reviews and annual audits, ensuring all documentation is complete and accurate.
• Ensure compliance with Teva’s internal controls and SOX requirements, and lead remediation efforts where needed.
• Prepare and analyze weekly cash flow reports and quarterly cash flow forecasts.
• Manage liquidity and payment processes, ensuring adequate funding for business operations.
• Collaborate with FP&A and Commercial Finance teams to provide insights into cash flow trends, working capital optimization, and financial risks.
• Act as a key liaison with corporate treasury and corporate accounting teams to align policies, reporting standards, and strategic initiatives.
• Coordinate yearly transfer pricing activities with cross-functional teams while ensuring that information is complete and accurate.
• Lead initiatives to streamline accounting and treasury processes, leveraging automation and system enhancements (e.g., SAP, Vistex, etc.).
• Assist with other ad-hoc duties, reporting and projects.

• Bachelor’s degree in finance, accounting, or a related field; CPA and or MBA required
• Experience Required: Minimum 7–10 years of progressive experience in accounting and treasury functions. Experience in the pharmaceutical or healthcare industry is an asset.
• Experience in a multinational or matrixed organization.
• Strong attention to detail and accuracy in financial data handling.
• An analytical mindset with the ability to identify and resolve discrepancies.
• Effective time management and organizational skills.
• Strong communication skills to collaborate with internal teams and external partners.
• Ability to work independently and take ownership of assigned responsibilities.
• Adaptability in a fast-paced, matrixed environment.
• Solid understanding of US GAAP and general accounting principles.
• Proficiency in SAP (FI/CO modules) and Microsoft Office Suite (especially Excel).
• Familiarity with treasury operations, cash forecasting, and banking activities.
• Experience with ERP systems and financial reporting tools.
• Experience with BI and related tools/systems.
• Travel Requirements: 5-10%

The internal career site is available from your home network as well. If you have trouble accessing your EC account, please contact your local HR/IT partner.

The Microbiology Manager is responsible for overseeing all microbiological testing activities in compliance with GMP, GLP, and regulatory requirements. This role leads a team of microbiologists performing testing on commercial and stability products, environmental monitoring, water testing, and microbial identification. The Manager ensures data integrity, regulatory compliance, and continuous improvement within the microbiology laboratory while providing technical leadership and supporting investigations.

• Oversees microbiological testing of commercial and stability products, environmental monitoring, water testing, and microbial identification. using compendial and in-house methods.
• Contributes to the management of the Quality Control Laboratory by actively participating in and facilitating meetings, addressing and resolving operational and management issues that arise.
• Supervise and lead the Microbiology Lab, responsible for performance management, mentoring, and professional development.
• Provides coaching, feedback, and technical guidance to ensure consistent performance and adherence to best practices.
• Effectively communicates, exhibits the company values, maintains priorities and monitors training to ensure a high standard of performance.
• Responsible for staff in accordance with the OHSA, Teva EH&S policies and procedures (including WHMIS, PPE etc.).
• Ensures staff are trained in, and adhere to, safe operational practices and work procedures.
• Prepares weekly schedules and assigns laboratory tasks to support manufacturing and release timelines.
• Ensures accurate and timely generation, review, and approval of test data and reports.
• Ensures data integrity across all microbiological operations by enforcing proper documentation practices, system controls, and adherence to ALCOA+ principles.
• Troubleshoots complex technical issues related to microbiological methods, equipment, and test results.
• Serves as a subject matter expert (SME) and key contact during regulatory inspections for all microbiology-related areas, providing data support, explanations, and audit readiness oversight.
• Maintains compliance with GMP, GLP, and corporate quality policies.
• Reviews and approves laboratory documentation, including test results, investigations, deviations, and change controls.
• Supports timely initiation and tracking of required laboratory investigations.
• Leads and support projects focused on process optimization, method improvement, and regulatory compliance.
• Collaborates with cross-functional teams in various business units such as Quality Control, Quality Assurance, Manufacturing, and Regulatory Affairs.
• Generates trending reports and completes analysis, metric development, and continuous improvement initiatives.
• Manages laboratory resources, including media, reagents, and consumables, ensuring cost-effective operations.
• Identifies, Prevents, and proactively corrects workplace hazards and conditions. Performs incident /accident investigations, root cause analysis, and establish appropriate corrective actions as needed.
• Role modelling of EHS practices to prevent the release of materials/energy, reduce EHS impacts, and ensure adherence to EHS regulatory requirements and procedures.
• Performs other related duties as required.

• Bachelor’s degree in Microbiology or a related scientific field; advanced degree preferred
• Minimum of 8 years of relevant experience in a pharmaceutical microbiology laboratory, with relevant leadership experience
• Strong technical expertise in microbiological methods and instrumentation, including endotoxin testing systems, microbial identification platforms (e.g., Vitek, Biolog, Omnilog), autoclaves, and sterility isolators
• In-depth understanding of GMP/GLP regulations, compendial standards (USP, EP, JP), and pharmaceutical microbiology principles
• Proven ability to ensure data integrity and compliance with data governance requirements
• Excellent analytical, problem-solving, and troubleshooting skills
• Strong communication and documentation abilities, with proficiency in writing technical reports and SOPs
• Proficient in Microsoft Office (Word, Excel, PowerPoint) and laboratory information systems
• Demonstrated leadership, organizational, and time management skills with the ability to manage multiple priorities
• Experience representing the microbiology function during regulatory audits and customer inspections, ensuring readiness and robust data presentation
• Committed to fostering a positive, inclusive, and safety-conscious work environment
• Demonstrates excellent written and verbal communication skills in order to:
  • Interpret analytical data and discuss the issues/problems with the supervisor and peers if required
  • Write in a lucid format, GLP/AITs, SOP’s, analytical reports and other relevant QC documents
• Good computer skills with proficiency in Microsoft Office and Labware LIMS, SAP navigating online compendia publications,
• Analytical methods and techniques common to QC Microbiology Lab
• GMP, cGMP and other regulatory requirements

The internal career site is available from your home network as well. If you have trouble accessing your EC account, please contact your local HR/IT partner.

What You’ll Do

• Manage assigned customer portfolios to ensure timely payment of open invoices, reduce past due balances, and minimize days outstanding
• Review and recommend actions on orders placed on credit hold
• Support direct customers with credit applications, credit card setup, and resolution of invoice and statement issues
• Assist retail customers in processing deductions via credit card applications
• Review and resolve deduction balances, including:
• Timely assessment of newly deducted claims
• Obtaining missing documentation
• Identifying deduction reasons
• Routing debits to relevant departments for validation
• Submit credit memo requests for validated and approved debits
• Match open deductions against credit memos or unapplied cash, reconcile variances, and initiate collection efforts for invalid deductions
• Maintain accurate updates in the claim management system
• Communicate regularly with internal teams (commercial and intercompany partners) and external contacts (customer AP/AR departments)

• Maintain AR records to ensure aging is current, credits and collections are applied, and uncollectible amounts are accounted for
• Review and identify newly created deduction claims, gather supporting documentation, and update the claim management system
• Direct debit memos to appropriate departments for validation and follow up on resolution status
• Reconcile invalid variances and initiate timely collection efforts, escalating disputes when necessary
• Perform account maintenance to identify credit-to-debit correlations and submit for offset
• Respond promptly to inquiries from customers, internal departments, and management
• Adhere to Teva’s Safety, Health, Environmental, and Code of Conduct policies

Excellent communication skills in English

High School Diploma

3+ years of AR and deduction resolution experience

Strong attention to detail

Proficiency in Excel

SAP experience

Completed college degree or higher

Prior experience in the pharmaceutical industry

Minimum one year of accounting experience

The internal career site is available from your home network as well. If you have trouble accessing your EC account, please contact your local HR/IT partner.

The QA Associate II supports change control management, review, and approval for Commercial quality related activities. This individual is responsible for processing and managing controlled documents that are under the scope of Commercial quality. The QA Associate II performs product launches and releases of imported products (Teva Affiliates and 3rd Party) to market and impact assessment with respect to the critical GMP issues. Reviews supplier documentation related to product launches and releases, validations, deviations, change controls, etc. The QA Associate II also conducts investigations related to deviations, OOS and OOT, and supports drug establishment licensing management, as required. The QA Associate II investigates Product Complaints and ensures the timely closure and approval of the records in QMS as required, and as needed to support with on-time launches of 3rd party product in coordination with internal and external groups. In addition, the QA Associate II supports with establishing systems and processes for Commercial Quality Canada to align with IM Commercial Quality.

• Manages change control processes, reviews, and approves, for Commercial Quality related activities.
• Responsible for processing and managing controlled documents that are under the scope of Commercial Quality.
• Provides oversight of activities associated with imported products from Teva affiliates and 3rd Party and interacts with EMSO QA who manages 3rd party suppliers to ensure compliance with GMPs.
• Reviews and approves GMP documentation associated with Teva affiliates and 3rd Party supplied finished products including release documentation, deviations, validations, change records, etc.
• Supports completion of stability report updates for products imported from Teva affiliates.
• As required, supports with the drug establishment licensing management.
• Performs release of Teva affiliates and 3rd Party products to Canadian market.
• Liaises with Teva affiliates to ensure compliance with GMPs, adherence to Quality agreements and resolve quality issues.
• Ensures compliant, on-time launches of Teva affiliates and 3rd Party manufactured products in coordination with internal and external groups.
• Investigates, reviews and/or approves product complaints and ensures the timely closure of records in Harmony TrackWise.
• Performs comprehensive and detailed investigations for quality deviations (DRs) in a timely manner. Performs impact assessment for imported products towards Critical Incident Notification / Alerts.
• Performs Executed Batch Record Review for Teva affiliate products.
• Reviews internal procedures and Corporate Standards, performs gap assessments and updates SOPs accordingly.
• Supports with establishing systems and processes for Commercial Quality Canada to align with IM Commercial Quality.
• Supports other Compliance functions and projects as required.
• Supports inspections.
• Leads / manages special projects that require collaboration with cross-function teams and Teva Global Affiliates.
• Other related duties as required.

• Holds a Canadian university degree or a degree recognized as equivalent by a Canadian university or Canadian accreditation body in a science related to the work being carried out.
• Three (3) + years of relevant experience in Change Control, Documentation, Quality Control and/or Quality Assurance. Knowledge of Health Canada Regulation related to importation requirements. Experience in Word, Excel, QMS
• Preferred: Five (5) years of relevant experience in Quality Control, Quality Assurance or Operations or a proven track record within pharmaceutical industry
• Good working knowledge of SAP, QMS, Excel and Word. Must be proficient in MS word.
• Good knowledge of SOPs, GMPs and cGMPs applicable to Quality Operations and Importation.
• Thorough understanding of manufacturing, packaging and laboratory operations.
• Advance writing skills: Ability to clearly and logically explain ideas in a concise and organized manner with the use of proper grammar.
• Planning/Organizational skills: Highly organizational skills used to set and manage priorities, handle multiple tasks in a timely manner, and ability to consistently evaluated work processes and outcomes
• Problem solving: Must demonstrate ability to solve moderately complex problems and analyze and apply appropriate solutions. Identifies and solves problems by gathering and applying information from a variety of sources. Must demonstrate ability to recognize critical situations and respond appropriately. Analyzes relationships among several parts of a problem or situation. Ability to anticipate obstacles and think of next steps. Recognizes multiple casual links: several causes of events, several consequences of actions, or multiple part chain of events. (A leads to B leads to C).
• Interpersonal skills: Educates internal and external customers on facts by taking into account differences in level of understanding, needs and expectations.
• Strong analytical, time management and organizational skills.
• Excellent verbal and written communication skills.

The internal career site is available from your home network as well. If you have trouble accessing your EC account, please contact your local HR/IT partner.

The Quality Assurance Associate will provide support to operations by providing oversight to activities associated with the manufacturing and packaging of bulk and finished products by Teva affiliates and 3rd party suppliers to ensure compliance with GMPs. In addition, will review and approve supplier documentation related to product release, validation, deviation, change controls, etc. In addition, perform release of Teva Affiliates and 3rd party products to market and impact assessment with respect to the critical GMP issues. The Quality Assurance Associate will investigate product complaints and ensure the timely closure and approval of the records in Harmony Trackwise as required, and as needed support with on-time launches of Teva Affiliates and 3rd party product in coordination with internal & external groups.

• Provide oversight of activities associated with the manufacture & packaging of bulk & finished products by Teva Affiliates and 3rd party suppliers to ensure compliance with GMPs.
• Review & approve GMP documentation associated with Teva Affiliates and 3rd party supplied bulk & finished products including release documentation, deviations, validations, change controls, etc.
• Perform release of Teva Affiliates and 3rd party products to market.
• Liaise with Teva Affiliates and 3rd party suppliers to ensure compliance with GMPs, adherence to Quality agreements & to resolve quality issues.
• Ensure compliant, on-time launches of Teva Affiliates and 3rd party products in coordination with internal & external groups.
• Investigate product complaints and ensure the timely closure and approval of the records in Harmony Trackwise, as required.
• Perform comprehensive and detailed investigations for quality deviations (DR's) related to Teva Affiliates and 3rd party products in a timely manner.
• Provide metrics to Teva Global/ Track KPIs for overdue deviations, CAPAs, batch release cycle time, etc; Generate/trend monthly and quarterly reports.
• Follow up and facilitate the completion of change controls, DRs, CAPAs and CAPAERs in a timely manner.
• Request stability data from the suppliers and perform stability review for all Teva Affiliates and 3rd party products.
• Draft/revise, negotiate and execute Quality Agreements with manufacturing site, contract packagers, contract laboratories, etc.
• Perform impact assessment for Teva Affiliates and 3rd party products towards Critical Incident Notifications / Alerts.
• Perform Executed Batch Record Review for Teva Affiliates and 3rd party products.
• Review internal procedures and Corporate Standards, perform gap assessment and update SOPs accordingly.
• Perform retain sampling activities: conduct the receipt of retain samples, updating SAP / storage of retain samples and destruction of expired retain samples as per procedures.
• Support other compliance functions and projects as required.
• Lead/ Manage special projects that require collaboration with cross-functional teams and Teva Global Affiliates.

Perform other duties as required.

• Minimum of 1 (one) year relevant experience in Quality Control, Quality Assurance.
• Knowledge of USP, BP EP, compendia methods as well as ability to read and interpret house methods.
• Preferred: 3 (three) + years relevant experience in Quality Control, Quality Assurance or a proven track record within pharmaceuticals.
• Good working knowledge of SAP, LIMS, Trackwise, Excel and Word.
• Good knowledge of SOPs, GMPs and cGMPs applicable to Quality Operations and Manufacturing.
• Thorough understanding of manufacturing, packaging
• Advanced writing skills: Ability to clearly and logically explain ideas in a concise and organized manner with the use of proper grammar.
• Planning/Organizational skills: highly organizational skills used to set and manage priorities, handle multiple tasks in a timely manner, and ability to consistently evaluate work processes and outcomes.
• Problem solving skills: Must demonstrate ability to solve moderately complex problems and analyze and apply appropriate solutions. Identifies and solves problems by gathering and applying information from a variety of sources. Must demonstrate ability to recognize critical situations and respond appropriately. Analyzes relationships among several parts of a problem or situation. Ability to anticipate obstacles and think of next steps. Recognizes multiple casual links: several causes of events, several consequences of actions or multiple part chain of events (A leads to B leads to C).
• Interpersonal skills: Educates internal and external customers on facts by taking into account differences in level of understanding, needs and expectations.
• Strong analytical, time management and organizational skills.
• Excellent verbal and written communication skills.

The internal career site is available from your home network as well. If you have trouble accessing your EC account, please contact your local HR/IT partner.

• Market/industry knowledge: new product launch/listings, generic penetration/erosion, government policy and customer knowledge (i.e., listing, regulations, formulary management assumptions and knowledge that can be translated into forecast assumptions and changes)
• Ensure that high quality forecasts are developed by leveraging market, customer and product knowledge in combination with Teva production plans to develop product plans and forecasts that best represent the Teva business and manage growth and new business.
• Chair and communicate in customer collaboration meetings recovery dates, back orders and product plans.
• Manages the forecasts, supply and service levels for all strategic and private label accounts.
• Prepare relevant material/analytical support to facilitate all relevant departments with product life cycle management, capacity planning, safety stock levels, obsolete analysis or inventory shortages.
• Prepare new product forecasts using input from IQVIA data, Marketing and Sales, Project Management (PMO), external contacts.
• Preparation (in conjunction with PMO/Supply) of new product market share scenario review or product obsolescence review at monthly NPIM meetings.
• Work with Market Access, Marketing and Customer Care to ensure proper set-up of all New Product launches.
• Analyze and make changes to the reserve quantities with the objective of preventing stock outs for strategic accounts while minimizing and managing the back orders for all other accounts.
• Develop allocation plans when inventory does not cover the total demand to optimize profit and service as well as protect long term business.
• Work with supply planning in the management of ATP dates for all customers. Provide supply chain feedback on product priorities.
• Develop and publish the weekly backorder reports and Drug Shortage details.
• Management of all new customer listings to bring on new demand and protect the listings ongoing. Collaborate with supply chain and customers on inventory plans, update forecasts, the listings database and applicable reserve tables.
• All other tasks as required

• Education: Bachelor’s degree or College Diploma in Business, Supply Chain, Life Sciences, or a related field.
• Experience: Minimum 3-5 years of experience in forecasting, supply chain, or related roles.
• Knowledge of the pharmaceutical market, including new product launches, generic market dynamics, government policy, and customer requirements.
• Ability to develop accurate forecasts using market, customer, and product insights, as well as production plans.
• Leading customer collaboration meetings and communicating supply updates, recovery dates, and product plans.
• Demonstrated experience managing forecasts, supply, and service levels for strategic and private label accounts.
• Analytical skills to optimize reserve quantities, prevent stock outs, and manage back orders.
• APICS certification is an asset
• Sound knowledge of statistical forecasting techniques.
• Hands-on experience with advanced planning systems (i.e. SAP/APO Advanced MS Office skills, specifically Excel)
• Strong knowledge of IQVIA reporting / data

The internal career site is available from your home network as well. If you have trouble accessing your EC account, please contact your local HR/IT partner.