CMC Lead, Launch Product, Small Molecules

Posted Yesterday
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2 Locations
Hybrid
117K-161K 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 global CMC strategy, development, manufacturing, and lifecycle management for a launched small-molecule pharmaceutical product. Coordinates Pharmaceutical Sciences, Global Supply & Quality, MSAT, manufacturing sites, and product teams to make CMC decisions, resolve complex issues, manage technology excellence initiatives, and support commercialization. Accountable for prioritization, scientific content, lifecycle activities, resource utilization, cross-functional alignment, and handoff of late-stage products to commercial teams.
Summary Generated by Built In

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Job Description

Title: CMC Lead, Launch Product, Small Molecules Location: Bengaluru, India (Primary)Location: Zurich, Switzerland (Secondary)About the role:

As a CMC Lead, Launch Product, Small Molecules, you will provide strategic and operational leadership for the CMC execution and lifecycle management of a key launched product within Takeda’s small molecule portfolio. You will serve as the CMC Leader and primary interface between Pharmaceutical Sciences, Global Supply & Quality (GSQ), and manufacturing technology organizations, ensuring scientific excellence, robust lifecycle stewardship, and optimal resource utilization across competing priorities. You will build, develop, motivate and lead a global team of experts responsible for CMC content of a key launched product within the Takeda’s small molecule portfolio, You will also provide strong direction in prioritization of life cycle management and technology excellence activities to optimize resource utilization given competing requirements for key development small molecule program.

How will you contribute:
  • Lead the cross functional GSQ CMC team to support effective product development activities with Pharmaceutical Sciences Organization.

  • Lead the GSQ CMC team to develop a robust life cycle management for Takeda’s key small molecule assets.

  • Represent CMC matters within Takeda’s Global Product Teams.

  • Provide strong leadership for initiatives which are complex or span across multiple products.

  • Accountable for the scientific/CMC contents related to a SM asset, take into consideration of business impact to the GSQ organization.

  • Ability to lead the Small Molecules CMC team to effectively resolve issues relating to CMC matter, also at times with the Pharmaceutical Sciences organization, when needed.

  • Ability to work across all GSQ functions, including internal and external manufacturing sites, and Pharmaceutical Sciences to define directions relating for robustness technology excellence and innovation including digital solutions and data analytics.

  • Accountable for key CMC decisions and provide recommendations to have a direct impact on program’s outcome.

  • Has a deep and broad understanding of small molecule product development, manufacturing, the regulatory environment, life cycle management, trends in innovation, and financial acumen.

  • Ability to influence broadly within GSQ organization and Takeda Product Teams to drive decisions, alignment, and conflict resolution for complex cross-functional CMC and technology excellence issues.

  • Work closely with the PMs to drive to the success of the CMC team.

  • Full accountability for complex decisions regarding the development of the SM asset.

  • Accountable for the decision relating to Life Cycle Management activities, and able to effectively manage SMEs from all functional areas to execute the decisions made.

  • Works alongside Pharmaceutical Sciences organization and influence and be accountable for decisions made having impact to the commercialization of the key asset.

  • Works across MSAT small molecule organization (including API and DP) to align CMC Development and LCM activities within the various GSQ functional organizations

  • Works across MSAT global functions as needed for business metrics and align on LCM procedures.

  • Works across MSAT small molecule (API and DP), Pharmaceutical Sciences, and Site Manufacturing Sciences groups to align on vision and priorities for LCM activities. 

  • Works with the MSAT CMC LCM group on coordination of hand-off of late stage products to the commercial team.

What you bring to Takeda:
  • A bachelor degree in engineering or life sciences.

  • Minimum 10 to 15 years experience in pharmaceutical development and manufacturing.

  • Experience operating globally in a matrixed organization highly preferred.

  • Experience defining the strategy and roadmap for complex, cross-functional initiatives.

  • Strategic enterprise thinking, finding innovative ways to serve patients build reputation and trust.

  • Creating the environment that inspires and enables people.

  • Focusing on the few priorities and provide superior results.

  • Elevating capabilities for now and the future.

  • Capable of analyzing and solving complex problems through innovative thought and experience, as well as, project management tools.

  • Scope includes innovation in manufacturing equipment, manufacturing processes, and use of digital technology to provide data-driven approaches.

LocationsIRL - Dublin - Baggot StreetIND - Bengaluru

Base Salary Range:

€116,800.00 - €160,600.00

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 or life sciences
  • 10 to 15 years of experience in pharmaceutical development and manufacturing
  • Experience operating globally in a matrixed organization
  • Experience defining strategy and roadmaps for complex, cross-functional initiatives
  • Strategic enterprise thinking and innovative problem-solving
  • Ability to create an environment that inspires and enables people
  • Ability to prioritize key objectives and deliver superior results
  • Ability to elevate organizational capabilities for current and future needs
  • Ability to analyze and solve complex problems using innovative thinking, experience, and project management tools
  • Knowledge of manufacturing equipment, manufacturing processes, and digital technology for data-driven approaches

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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