Neuchâtel NPI Program Lead

Posted 4 Days Ago
Be an Early Applicant
Neuchâtel, CHE
Hybrid
159K-219K Annually
Expert/Leader
Healthtech • Software • Analytics • Biotech • Pharmaceutical • Manufacturing
Takeda exists to create better health for people, brighter future for the world.
The Role
Leads Neuchâtel’s portfolio of pharmaceutical new product introduction programs from feasibility through commercial launch. Coordinates manufacturing, quality, engineering, supply chain, regulatory, finance, and external partners; manages integrated plans, budgets, resources, risks, governance, validation, technology transfers, and inspection readiness. The role also guides portfolio priorities, improves program delivery practices, and coaches project managers and functional leads.
Summary Generated by Built In

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Job Description

About the Role

Join us as our NPI Program Lead. You will lead the Neuchâtel site’s portfolio of new product introduction programs, helping bring new drug substances and drug products through transfer, implementation, and launch. You will connect teams across manufacturing, quality, engineering, supply chain, regulatory affairs, and other functions, as well as external partners, to support safe, compliant, and timely program delivery within approved budgets.

How You Will Contribute

Reporting to the Site Engineering Head, you will play a key role in aligning site priorities with broader network priorities, guiding decisions across complex programs, and supporting successful commercialization and product lifecycle execution. Your work will help the site coordinate its resources, manage risks, and deliver outcomes that support both business objectives and cross-functional teams. Your responsibilities are to:

  • Lead new product introduction programs from feasibility through commercial implementation, including technical transfers, validation campaigns, and launches.
  • Build and manage integrated program plans by setting milestones, governance, critical paths, scope, schedules, budgets, and resource plans.
  • Coordinate cross-functional teams across manufacturing, quality, engineering, supply chain, regulatory affairs, finance, and other functions to resolve issues and make decisions.
  • Guide portfolio priorities and resources by assessing capacity, supporting business cases, and reporting program performance.
  • Manage program risks and changes by developing mitigation plans, escalating critical issues, and supporting inspection readiness and compliance.
  • Improve program delivery practices by standardizing methods, strengthening governance and reporting, and sharing lessons learned.
  • Coach project managers and functional leads to build program management capabilities across the organization.

Qualifications

  • Bachelor’s degree in engineering, life sciences, pharmaceutical sciences, or a related discipline.
  • At least 10 years of experience in pharmaceutical or biotechnology manufacturing environments.
  • Significant experience leading large, cross-functional programs.
  • Experience in drug substance or drug product manufacturing operations.
  • Experience managing technology transfers, capital projects, or new product introductions.
  • Advanced knowledge of good manufacturing practice requirements.
  • Ability to manage program and portfolio priorities, risks, resources, and change.
  • Strong stakeholder management, influence, leadership, and executive communication skills.
  • Full proficiency in French and English.

LocationsCHE - Neuchatel

Base Salary Range:

CHF159,300.00 - CHF219,010.00

The estimated salary range reflects an anticipated range for this position. The actual base salary offered may depend on a variety of factors, including the qualifications of the individual applicant for the position, years of relevant experience, specific and unique skills, level of education attained, certifications or other professional licenses held, and the location in which the applicant lives and/or from which they will be performing the job.


For information about our benefits, please click here.

Worker TypeEmployee

Worker Sub-TypeRegular

Time TypeFull time

Skills Required

  • Bachelor’s degree in engineering, life sciences, pharmaceutical sciences, or a related discipline
  • At least 10 years of experience in pharmaceutical or biotechnology manufacturing environments
  • Significant experience leading large, cross-functional programs
  • Experience in drug substance or drug product manufacturing operations
  • Experience managing technology transfers, capital projects, or new product introductions
  • Advanced knowledge of Good Manufacturing Practice requirements
  • Ability to manage program and portfolio priorities, risks, resources, and change
  • Strong stakeholder management, influence, leadership, and executive communication skills
  • Full proficiency in French and English

Takeda Compensation & Benefits Highlights

The following summarizes recurring compensation and benefits themes identified from responses generated by popular LLMs to common candidate questions about Takeda and has not been reviewed or approved by Takeda.

  • Retirement Support — Employer-funded retirement is described as notably strong, combining a dollar-for-dollar 401(k) match with an additional company contribution that scales with age and service. Access to an employee stock purchase plan further supports long-term wealth building.
  • Parental & Family Support — Paid bonding leave for all parents, substantial adoption/surrogacy reimbursement, and robust caregiver resources (backup care and Maven family-forming support) are emphasized as core strengths. These offerings create a comprehensive safety net for a range of family situations.
  • Healthcare Strength — Multiple medical plan options (nationwide PPO/HSA and regional HMOs), employer HSA funding, and integrated mental-health and well-being programs signal depth in coverage. Preventive care is covered in-network, and plan choices by state expand access.

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The Company
HQ: Cambridge, MA
50,000 Employees
Year Founded: 1781

What We Do

For over 240 years, Takeda’s propensity to evolve has driven the next generation of innovation, and as a future-focused organization, we’re continuing to drive forward with endurance in our steadfast pursuit to achieve the best outcomes for our patients in a rapidly changing world.  We have been preparing for this period of value creation by investing in data, digital and technology, and we’re proud of our employees and their commitment to turning groundbreaking ideas into life-changing impacts.   Since our founding in Japan, integrity and putting patients first have been at the heart of our identity, and we will emerge ready for our future as one of the most trusted and science-driven digital biopharmaceutical companies. Join a team where your innovation impacts lives.   Together, we’ll realize improved outcomes by improving data quality, enhancing launch execution and improving the patient journey. You’ll play a critical role in accelerating data collection and increasing accuracy across all parts of the business. Patients across the globe will benefit from access to treatments afforded by greater opportunities and efficiency in our research and development.  

Why Work With Us

We connect to our history and Japanese heritage through everything we do to bring our purpose, values, vision, and imperatives to life. We are committed to bringing better health and a brighter future to patients. Being a part of Takeda means having the opportunity to be a part of something bigger than yourself.

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