Senior Scientist - Particulates Analytics for Biotherapeutics

Johnson & Johnson Co.; Schaffhausen; On-site; CHF 110,000 - 160,000; Full time

Benefits offered by this job

Multinational team

Competitive salary

Career opportunities

Job summary

Johnson & Johnson in Schaffhausen, Switzerland, seeks a scientist to advance the CoE for particle counting in biotherapeutics within GMP environments. You will coordinate early and late phase programs, validate methods, and transfer to manufacturing and QC labs, drafting regulatory submissions and supporting marketed products.

You will contribute to the center of excellence, supervise SME activities, and collaborate across R&D and supply chain to ensure compliant, robust analytical approaches

Qualifications

• MS with 5+ years of life science or pharma development experience, or PhD with 2+ years.
• Strong analytics, project coordination and presentation skills.
• Experience with regulatory submissions and GMP environments is advantageous.
• Excellent English communication; German desirable.

Responsibilities

• Lead project coordination and method validation of particulate assays for biotherapeutics.
• Expand particle analytics portfolio for cell and gene therapy products.
• Coordinate validations and technology transfers per guidelines and health authority expectations.
• Collaborate with partners and represent SME in project meetings.
• Draft scientifically sound documents and compile data for regulatory submissions.
• Ensure end-to-end understanding of business processes and drive efficiency.
• Explore new technologies and perform scientific scouting.
• Work in a diverse, team-oriented environment with colleagues worldwide.

Skills

Analytical reasoning

Biochemistry

CMC

Project coordination

Regulatory writing

Communication skills

GMP knowledge

English proficiency

German desired

Education

M.S. in Life Sciences

PhD in Life Sciences

Tools

Analytical instruments

Job description

Johnson & Johnson in Schaffhausen, Switzerland, seeks a scientist to advance the CoE for particle counting in biotherapeutics within GMP environments. You will coordinate early and late phase programs, validate methods, and transfer to manufacturing and QC labs, drafting regulatory submissions and supporting marketed products.

You will contribute to the center of excellence, supervise SME activities, and collaborate across R&D and supply chain to ensure compliant, robust analytical approaches