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. You'll have the room to grow, the flexibility to balance life with work, and the opportunity to better health worldwide, together.

Cleaning Validation

Specialist 12 month contract We are seeking a detail-oriented and motivated Cleaning Validation Specialist to join our team. In this role, you will support and execute cleaning validation activities to ensure compliance with cGMP requirements and global regulatory standards. You will collaborate with cross-functional teams, including Quality Assurance, Quality Control, Operations, Engineering, and MS&T;, to maintain validated cleaning processes and support continuous improvement initiatives.

Assist in the preparation, execution, and reporting of cleaning validation studies. Collect, review, and organize cleaning validation data. Evaluate cleaning validation results against established acceptance criteria.

Support periodic reviews of the cleaning validation program. Prepare and revise validation protocols, reports, risk assessments, and related documentation. Ensure validation documentation complies with GMP requirements, company procedures, and applicable regulatory standards.

Support investigations related to cleaning validation deviations, excursions, and out-of-trend results. Maintain validation records and ensure all documentation remains audit and inspection ready. Coordinate validation activities with QA, QC, Operations, Engineering, and MS&T; teams.

Schedule and manage cleaning validation activities to align with manufacturing operations. Participate in risk assessments, including FMEA, gap assessments, and other quality risk management activities. Support the identification of worst-case products, equipment trains, and sampling locations.





Contribute to continuous improvement initiatives related to cleaning procedures and validation practices. Trend validation data to identify recurring issues and opportunities for process enhancement. Ensure compliance with cGMP, Health Canada, FDA, EMA, and internal quality system requirements.

Participate in investigations, CAPAs, change controls, and regulatory inspection support activities. Bachelor's degree in Science, Engineering, Pharmacy, or a related discipline. ~1 to 3 years of relevant experience, preferably within the pharmaceutical, biotechnology, or regulated manufacturing industry. ~ Knowledge of cleaning validation principles, GMP regulations, and pharmaceutical manufacturing processes is preferred. ~ and European regulatory requirements, including GMP/GLP requirements, WHMIS, and workplace safety standards. ~ Experience with validation documentation, investigations, CAPAs, and change controls is considered an asset. ~ Proficiency with Microsoft Office Suite (Word, Excel, PowerPoint, Outlook) and quality systems such as LIMS, Veeva, TrackWise, and Knowledge Tree. ~ Strong organizational, time management, and multitasking skills with the ability to manage multiple priorities. ~ Willingness to travel occasionally to other Teva sites as required. ~ A strong commitment to quality, compliance, and continuous improvement. ~ A passion for maintaining high standards in pharmaceutical manufacturing and validation processes.

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 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.

Teva Canada's choices Benefit Plan including Health, Dental, Disability, Life Insurance Employee Assistance Program & Virtual Health Programs Retirement Savings Programs Time for yourself or those you care about, through paid time for Vacation, Wellness days, Care/Sick days, Teva Days and Volunteer Days Recognition programs such as Employee Service Awards 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. Teva Pharmaceuticals is committed to equal chance 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. 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.

📌 Cleaning Validation Coordinator - 12 month contract (Cedar Valley)
🏢 Teva
📍 Cedar Valley