T

Thermo Fisher Scientific

Makes lab instruments, reagents and supplies

Director of R&D - Autoimmunity

Biology & BiotechConfirmed live in the last 24 hours
Full-timeFreiburg im Breisgau, GermanyNo salary listed

About the Job

Requirements

  • An advanced degree in Immunology, Biochemistry, Molecular Biology, Biomedical Engineering, or a related field is required.
  • At least 10 years of professional experience in in vitro diagnostic assay development is required.
  • Extensive experience leading and coaching people leaders and individual contributors, building high-performing R&D teams, and developing organizational capabilities for the future is required.
  • Demonstrated ability to establish clear priorities across a complex R&D portfolio, make prioritization and trade-off decisions with teams and stakeholders, and allocate resources in line with strategic and business priorities is required.
  • Demonstrated success delivering innovative products from concept through commercialization using stage-gate product development processes, and managing complex projects, budgets, and resources in a dynamic environment with competing priorities is required.
  • Strong scientific expertise relevant to autoimmune disease areas is required.
  • Strong understanding of quality systems and regulatory requirements, including FDA, ISO, and GMP, is required.
  • Demonstrated success leading organizational change, evolving ways of working, strengthening accountability and collaboration, and shaping culture and mindset to improve organizational effectiveness is required.
  • Effective communication and presentation skills, including the ability to create clarity, alignment, and engagement through change, are required.
  • Ability to influence and collaborate across functions and navigate a complex matrix organization is required.
  • A strategic mindset paired with business acumen and customer orientation is required.
  • Proficiency in English is required.

Responsibilities

  • Define and execute the Autoimmunity R&D strategy and roadmap in alignment with portfolio and innovation priorities.
  • Prioritize programs and allocate resources across innovation, lifecycle management, and regulatory commitments.
  • Contribute to lifecycle planning for line extensions, upgrades, cost optimization, and portfolio rationalization.
  • Lead end-to-end assay development, including feasibility, design, risk analysis, verification, and validation.
  • Drive research on biomarkers and disease-relevant targets for potential diagnostic applications, and translate selected opportunities into the closed, fully automated in vitro diagnostic platform.
  • Ensure compliance with IVDR, FDA 21 CFR 820, ISO 13485, and applicable regulations.
  • Oversee design history files, technical documentation, risk management activities, and regulatory submissions in collaboration with Regulatory Affairs.
  • Ensure audit readiness and effective corrective and preventive action execution.
  • Provide technical oversight of post-market surveillance and performance monitoring.
  • Lead investigations into complaints, trends, and field issues, ensuring timely root cause analysis and corrective actions.
  • Address assay variability, stability, raw material changes, and manufacturing deviations.
  • Support supplier changes, material obsolescence management, and supply continuity.
  • Build and develop high-performing R&D teams.
  • Foster a culture of scientific rigor, accountability, and continuous improvement.
  • Develop succession pipelines and technical career paths.
  • Operate effectively within a global, matrixed organization.
  • Partner with Product Innovation, Marketing, Quality and Regulatory, and Medical Affairs to translate clinical, customer, and portfolio needs into product requirements.
  • Collaborate with Clinical Affairs on validation strategies and studies.
  • Develop and maintain scientific collaborations with key opinion leaders, clinical networks, academic institutions, and external partners.
  • Provide R&D governance of external research collaborations, including coordinating appropriate nondisclosure agreements, confidential disclosure agreements, and material transfer agreements with relevant functions.
  • Represent R&D in governance forums and executive reviews.

Desired Qualifications

  • German proficiency is highly preferred.

About the Company

Thermo Fisher Scientific

Makes lab instruments, reagents and supplies

Thermo Fisher Scientific makes and sells the instruments, chemicals, consumables and lab services that drug companies, hospitals, universities and industrial labs use for research, testing and production. Its products cover work from gene sequencing and protein analysis to diagnostic tests and lab freezers, and its distribution arm ships supplies to labs worldwide. Drug developers also hire it to run clinical trials and to manufacture medicines under contract. It earns money from consumables that labs buy again and again, along with instrument sales, service contracts and outsourcing fees. The company traces its roots to Thermo Electron, founded in 1956, which merged with Fisher Scientific in 2006, and it is based in Waltham, Massachusetts.

Company size
10,001+
Company stage
IPO
Headquarters
Waltham, MA
Founded
1956

Recently Posted Jobs

Explore more opportunities at Thermo Fisher Scientific

See more jobs