Teva Product Pipeline Manager - Associate Director 

United Kingdom, England, Wakefield 

622771614

We would like to invite applications for the role of.

• You will manage Teva’s pipeline of generics and biosimilars, from initial concept through to commercialization.
• Lead the coordination of product development across cross-functional teams, ensuring a seamless transition from early-stage research to late-stage development and commercialization.
• Define and drive the strategic direction for generics and biosimilars products in alignment with Teva’s overall product portfolio and business objectives.
• Conduct market and competitive analyses to inform the selection and prioritization of new generics and biosimilars opportunities.
• Collaborate with internal teams (e.g., regulatory, manufacturing, commercial, medical affairs, quality & Launch Excellence) to ensure smooth and timely development and launch of generics and biosimilars.
• Engage with external stakeholders such as (NHSE , MVA , wholesalers ,BBA , BGMA )
• Continuously monitor the market dynamics for generics and biosimilars, including regulatory trends, pricing strategies, and competitor activities.
• Stay abreast of industry innovations, scientific advancements, and regulatory shifts that may impact the development and positioning of generics and biosimilars.
• Regularly update senior management on the progress of the generics and biosimilars pipeline, highlighting key developments, challenges, and opportunities.
  

• Experienced in managing the product lifecycle of generics and biosimilars, including the preparation of regulatory submissions, clinical trials, and commercial strategy.
• A strong project manager, with the ability to manage multiple products simultaneously and ensure timely delivery.
• An excellent communicator, with the ability to present complex information to senior leadership and external stakeholders.
  

• A degree in Life Sciences, Pharmacy, or a related field (preferred).
• A minimum of 5-7 years of experience in pharmaceutical product development, with at least 3-5 years in managing generics and/or biosimilars development.
• Strong understanding of the regulatory and commercial landscape for generics and biosimilars, including knowledge of FDA, EMA, and other global regulatory requirements.
• Proven track record in managing cross-functional teams in the development of generics and/or biosimilars.
• Strong problem-solving abilities and analytical skills to identify and address challenges in product development and commercialization.
  

• Enjoying time with your families (25 days of annual leave, Pension scheme, company car or car allowance)
• Looking after your health (Life & Critical Illness Insurance, Private health insurance for your and your family, Sports and Health Programme – including health days and nutritional counselling, On-site Canteen)
• Recognizing your value (Recognition programs to reward our employees with our company bonus scheme)
• Boosting your potential (Virtual Learning Centre)
• Well-being and D&I focused company.
  

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