Key Skills

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. Who We Are At Teva Haarlem, PM&O drives process excellence, technology transfers, product lifecycle management and continuous improvement initiatives. The PM&O team provides project leadership and governance across strategic and operational programs supporting site objectives. The Opportunity Lead complex cross-functional MS&T projects including technology transfers, product transfers, process improvements, remediation programs and strategic site initiatives. Key Responsibilities Lead end-to-end project execution from initiation to closure. Develop project plans, timelines, budgets and risk management strategies. Coordinate cross-functional teams and stakeholders. Drive governance, reporting, and project performance tracking. Support technology transfer, validation and process optimization activities. Ensure compliance with GMP and regulatory requirements. Manage risks, issues and escalation processes. Promote operational excellence and continuous improvement. Qualifications & Experience Bachelor’s or Master’s degree in Pharmacy, Engineering, Life Sciences or related field. Minimum 5 years of experience in pharmaceutical manufacturing, MS&T or project management. Proven experience leading complex projects in a GMP environment. Strong stakeholder management and communication skills. Fluent in English. Preferred Qualifications PMP, PRINCE2 or Lean Six Sigma certification. Experience with technology transfers, product transfers, validation and product lifecycle management. Experience in global matrix organizations. Competencies Strategic thinking, leadership, problem solving, strong execution focus, collaboration, data-driven decision making and adaptability. 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? 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.

Core Responsibilities

Lead complex MS&T projects from initiation through closure, including technology and product transfers, process improvements, remediation, and strategic site initiatives. Coordinate cross-functional teams, manage plans, budgets, risks, governance, and reporting, and support compliant validation and process optimization.

Requirements

A bachelor’s or master’s degree in Pharmacy, Engineering, Life Sciences, or a related field is required, along with at least five years of experience in pharmaceutical manufacturing, MS&T, or project management. Candidates should have experience leading complex projects in a GMP environment, strong communication and stakeholder management skills, and fluency in English; project management or Lean Six Sigma certification is preferred.

Benefits

• Annual Leave
• Reward Plans
• Flexible Working Schedules
• Health Support
• Career Development Opportunities