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.
How You’ll Spend Your Day
-
Managing and coordinating sterile drug manufacturing processes (aseptic manufacturing, sterilization, filling)
-
Ensuring manufacturing processes comply with GMP, regulatory requirements, and internal procedures
-
Leading and developing the team by setting clear goals, monitoring performance, providing support and professional development, and fostering collaboration and a proactive work culture
-
Production planning in line with business objectives, capacity, and delivery deadlines
-
Initiating and leading manufacturing process improvement projects, including identifying optimization opportunities, applying Lean/Six Sigma methodologies, monitoring effectiveness and results, and driving continuous improvement
-
Overseeing occupational health and safety, environmental protection, and fire safety by continuously monitoring standards, training employees, and initiating corrective actions to ensure a safe and compliant working environment
-
Participating in internal and external inspections and audits
-
Managing deviations, CAPA activities, and risk assessments
-
Monitoring key performance indicators (KPIs) and reporting to senior management
-
Introducing new technologies and optimizing existing manufacturing processes
Your Skills and Experience
-
University degree (Master’s level, 300 ECTS) in a relevant field – Pharmacy, Biotechnology, Chemical Engineering, or related technical sciences
-
Several years of professional experience and a high level of expertise in the pharmaceutical industry, particularly in manufacturing, maintenance, quality assurance, and validation; experience in sterile drug manufacturing is an advantage
-
Proven experience in managerial roles and working in multidisciplinary teams
-
Project management experience with demonstrated measurable results
-
In-depth knowledge of GMP regulations and work in controlled (cleanroom) environments
-
Strong organizational and leadership skills
-
Decision-making and problem-solving abilities
-
Proficient (active) knowledge of English
Also Good to Have
-
Experience in managing projects and implementing new production lines
-
Knowledge of Lean principles and continuous process improvement
-
Excellent communication and interpersonal skills
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.