Senior Validation Expert

Date: Feb 5, 2026

Location:

Haarlem, Netherlands, 2031 GA

Company: Teva Pharmaceuticals

Job Id: 66010

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.

The opportunity

A highly skilled and experienced Senior Validation Engineer with expertise in validation/re-qualifications of Equipment/System including Project work/Changes/CAPAs. In addition knowledge of steam sterilizers/autoclaves, lyophilizers, depyrogenation tunnels, smoke studies/air flow visualization studies & validation related to within the pharmaceutical industry. You will play a critical role in ensuring compliance with regulatory requirements and industry standards while optimizing operational efficiency and product quality.

How you’ll spend your day

Lead and participate in equipment qualification activities, including Installation Qualification (IQ), Operational Qualification (OQ), and Performance Qualification (PQ).
Support execution of validation protocols/plans for Validations/Re-qualifications of steam sterilizers/autoclaves, lyophilizers, depyrogenation tunnels, smoke studies/air flow visualization studies or any other manufacturing assets or utilities
In case of deviations; Document, notify & co-ordinate for corrective action, and close out.
Provide technical expertise and guidance on validation-related issues to project teams and stakeholders.
Collaborate with cross-functional teams to ensure validation activities align with production schedules, project timelines and quality expectations.
Conduct risk assessments and impact analyses related to validation activities and propose appropriate mitigation strategies.
Draft, review and assess validation data, deviations, and change controls to ensure compliance with regulatory requirements and Teva internal quality standards.
Draft, review and assess periodic review data/ report.
Ensure adherence to Good Manufacturing Practice (GMP) and Good Documentation Practice (GDP) during validation activities.
Support during internal/external inspections/Audits in addition to representing relevant topics as an SME & having solid knowledge to communicate with authorities.
Mentor and provide training to junior validation team members, sharing knowledge and best practices.

Your experience and qualifications

Bachelor's or higher degree in a relevant scientific or engineering discipline.
Minimum 4~5 years of experience in validation/CQV within the pharmaceutical industry - Sterile environment would represent an asset), Knowledge of experience in GMP including V-Model & SDLC (System Documentation Life Cycle) methodologies.
Sterile environment is a nice to have
Strong analytical, problem-solving, organizational and project management skills.
Team player with attention to detail and strong can-do mentality
Excellent written and verbal communication skills, including the ability to effectively collaborate with multidisciplinary teams

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. 

Already Working @TEVA?

If you are a current Teva employee, please apply using the internal career site available on "Employee Central". By doing so, your application will be treated with priority. You will also be able to see opportunities that are open exclusively to Teva employees. Use the following link to search and apply: Internal Career Site

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.

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.