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MSAT Bio DP TO Pr. Scientist

Job in 8200, Schaffhausen, Kanton Schaffhausen, Switzerland
Listing for: Johnson & Johnson
Full Time position
Listed on 2026-03-01
Job specializations:
  • Engineering
    Process Engineer, Quality Engineering, Manufacturing Engineer, Biomedical Engineer
Salary/Wage Range or Industry Benchmark: 30000 - 80000 CHF Yearly CHF 30000.00 80000.00 YEAR
Job Description & How to Apply Below

At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and Med Tech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity.

Job

Function

Supply Chain Engineering

Job Sub Function

Process Engineering

Job Category

Scientific/Technology

All Job Posting Locations

Schaffhausen, Switzerland

Job Description

MSAT Bio DP VO Principal Engineer

As a Principal Scientist/ Principal Engineer in Global MSAT your primary role is as Technical Owner (TO), with specific responsibility for significant program/brand.

The TO is the voice of MSAT in the Value Chain Team and responsible for the technical aspect of the Lifecycle Management structure and strategy of DP during their commercial lifespan.

Principal Responsibilities
  • Onsite presence at CMO in Visp, Switzerland - minimum 3 days a week
  • Represents MSAT and the technical team in the Value Chain Team (VCT) and provides the required manufacturing technical support
  • Participates in the VCT to develop the long-term supply strategy including scenario development and E2E impact analysis
  • Supports the VCT to identify improvement/innovation opportunities, to build project business cases and to prioritize projects (product related)
  • Owns the coordination of all product-related technical activities
  • Monitors technical process and product performance
  • Identifies and implements opportunities for active decrease in manufacturing COG’s
  • Implements or follows-up on execution of technical projects
  • Deploys the platform standardization policy as appropriate
  • Supports failure investigations (escalation of quality or compliance events)
  • Reviews technical product & process risk profile and criticality analysis
  • Implementing and supporting new platforms innovations or changes in life cycle management products
  • Provides this expertise as well to External Manufacturing related to the Biotherapeutics Platform
Leadership Responsibilities / Individual Contribution
  • The successful candidate will be an integer person with a high level of self-awareness and adaptability.
  • Proven leadership in providing integration of activities and information across multifunctional groups and matrix teams
  • Ability to foster team productivity and cohesiveness and to work collaboratively to execute, deliver and get results through the various matrix teams
  • Ability to influence peers, superiors, and partners
  • Understands the technical aspect of the lifecycle strategy of products
  • Applies the science-based risk approach and regulatory intelligence
  • Understands culture differences
Qualifications

Master’s degree in Science or Engineering (Biomedical, Biochemical, Chemical Technology, Biotechnology, Pharmacy, (biological) Engineering; Life Science Technology) or equivalent. Advanced degree PhD/PDEng or equivalent preferred.

Experience And Skills Required
  • 10+ years of relevant experience and BS degree or equivalent OR 6+ years with advanced degree MS/MBA/Ph.D. or equivalent. Experience of process validation. Preferably in the field of large molecule Drug Product.
  • Manufacturing experience within a GMP regulated environment
  • Excellent interpersonal and communication skills
  • Languages:

    Fluent in written and spoken English
Preferred
  • Experience in Life Cycle Management, DP development and project management.
Specific Systems

Document mgmt. systems such as Tru Vault, etc. SAP, MS Office applications, Track Wise, Planisware, MS-project, Minitab or similar statistical software

Based in Switzerland close to major JNJ site with up to 10 % travel- project dependent

Skills
  • Agile Decision Making
  • Business Savvy
  • Coaching
  • Corrective and Preventive Action (CAPA)
  • Crisis Management
  • Critical Thinking
  • Disruptive Innovations
  • Emerging Technologies
  • Industrial Hygiene
  • Lean Supply Chain Management
  • Organizing
  • Process Control
  • Process Engineering
  • Product Costing
  • Program Management
  • Project Schedule
  • Science
  • Technology
  • Engineering
  • Math (STEM) Application
  • Technical Research
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