Manager Vaccines MS&T Drug Products (f/m/d)

apartmentTakeda placeSingen (Hohentwiel) calendar_month 

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Job Description

Are you looking for a patient-oriented, innovation-driven company that inspires you and promotes your career? Then take your future in your hands and become part of Takeda as a

Manager Vaccines MS&T Drug Products (f/m/d)

Takeda Vaccines Business Unit is seeking a highly motivated individual for the role of Manager Vaccines MS&T Drug Products. In this role you will provide technical expertise and leadership for the Tetravalent Dengue Vaccine formulation and fill-finish as well as Diluent manufacturing activities.
Supporting our external and internal manufacturing to remain operational, continuously improve, and innovate you will assume broad responsibility for tech transfers, process qualification and validation and commercial manufacturing at drug product manufacturing sites.

Process package transfer, at scale studies, PPQ, process monitoring, and continuous process improvements are key focus areas for the role. High level of exposure and interaction to other functional areas supporting late-stage development, product life cycle management and commercial operations in a matrix organization is part of the role assignment.

Your main responsibilities:

  • Maintain scientific and technical support of commercial manufacturing to support productivity, quality, and compliance goals and improvements
  • Ensure robust manufacturing and analytics, process monitoring, and knowledge management are in place to support product goals for safety, compliance, productivity, and supply
  • Supporting further development troubleshoot management of quality systems (such as change controls, deviations, etc.) in collaboration with internal and external partners
  • Working with Development, Manufacturing, Engineering, Business Excellence, etc., Teams to plan and manage process improvements, scale-up, technical transfers and life-cycle management
  • Developing and implementing manufacturing solutions to enhance quality, costs and robustness of vaccine drug product and diluent manufacturing processes
  • Providing scientific and technical support of commercial manufacturing at partners to support corporate goals for supply strategies, productivity, quality, and compliance
  • Ongoing technical support for change control, deviation investigations and CAPA management as required during development and commercial manufacturing
  • Partnering with internal and external stakeholders communicate, escalate and resolve program issues both within Takeda and with external manufacturing partners
  • Partnering with engineering to provide process inputs for process fit assessments and to define process requirements for new manufacturing facilities
  • Working cross-functionally, develop robust proposals for scale-up and technology transfer of vaccine products, and for life-cycle management changes
  • Representing Vaccines MS&T Drug Products in cross-functional teams for engineering, qualification and validation of new and existing vaccine and diluent manufacturing facilities, processes, technology transfers
  • Building partnerships in the areas of engineering and process equipment to drive awareness of new technologies for best-in-class manufacturing operations

Your profile:

  • Bachelor or Master with solid experience in start-up, tech transfer, and/or sustaining cGMP for drug product processes in manufacturing or biopharmaceuticals
  • Experience working with live viruses vaccines preferred
  • Scientific and technical knowledge regarding formulation, filling, freeze-drying and visual inspection unit operations in biopharmaceutical manufacturing, including single-use technologies
  • A self-starter and team player who can balance the needs of an entrepreneurial environment with the requirements of structured product development
  • Proven ability to work with efficiency across multiple project teams and business functions in a matrix environment
  • Able to lead and manage technical teams, serve as a partner and influence others
  • Demonstrated cross-functional team experience
  • Willingness to travel
  • Work proficiency in Englisch is mandatory, German and other languages knowledge is a plus

In this position you will report to the Head of Drug Product Operations.

Your benefits:

  • Attractive and competitive salary
  • Open-minded and modern working environment
  • Hybrid working model
  • 30 vacation days
  • Company pension plan
  • Further education and training
  • Commuting allowance
  • Attractive Relocation Package including brokerage fees
  • Subsidized canteen
  • Subsidized sports programs
  • Disability insurance
  • Long-term account with various possible uses
  • Employee discounts
  • Employee Stock Purchase Plan
  • Company accident insurance
  • Performance-related bonus
  • Trusted working hours
  • Employee Referral Program
  • Deferred compensation as desired
  • Global Wellbeing Program
  • Interactive online courses for employees' children
  • Employee Recognition Program

About Us:

Takeda is a global, values-based, R&D-driven biopharmaceutical leader headquartered in Japan, committed to discover and deliver life-transforming treatments, guided by our commitment to patients, our people, and the planet.

In Singen, around 1,300 employees specialize in the production of liquid, semi-solid and freeze-dried medicines. Singen is the only production site in the global Takeda network for the manufacture of our new dengue fever vaccine. Takeda Singen is a regionally significant employer and has been awarded the independent Top Employer certificate several years in a row.

The site is characterized by its high level of diversity (e.g., more than 55 nationalities and over 40% of leaders are women), its long company history and its excellent development opportunities. The town of Singen (Hohentwiel) is located on the beautiful Lake Constance in Baden-Württemberg with a view of the Alps and close proximity to France, Liechtenstein, Austria, and Switzerland.

How we will support you:

Takeda is proud of its commitment to create a diverse workforce and to provide equal employment opportunities to all employees and applicants for employment without regard to ethnicity, color, religion, sex, sexual orientation, gender identity, gender expression, parental status, national origin, age, disability, citizenship status, genetic information or characteristics, marital status, or any other characteristic protected by law.

If you are living with disabilities, chronic illness, or neurodiversity, please feel free to let us know so that we can provide you with appropriate support during the application process.

Locations

Singen, Germany

Worker Type

Employee

Worker Sub-Type

Regular

Time Type

Full time

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