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Job Function:
Supply Chain EngineeringJob Sub Function:
Process EngineeringJob Category:
Scientific/TechnologyAll Job Posting Locations:
Schaffhausen SwitzerlandJob Description:
MSAT Bio DP VO Principal Engineer
Position Summary:
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 COGs
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
Masters 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:
Requirements: 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 TruVault etc. SAP MS Office applications TrackWise Planisware MS-project Minitab or similar statistical software
Based in Switzerland close to major JNJ site with up to 10 % travel- project dependent
.
Required Skills:
Preferred 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 and Math (STEM) Application Technical ResearchRequired Experience:
IC
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