Global Clinical Production Enablement Lead

Roche

. Collaborate with the planning organization as the initial point of contact for product requirements .

Posted 9/29/2026full-timeKaiseraugst • SwitzerlandSeniorWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in supply chain management, project management, and production efficiency methodologies, ensuring timely and compliant clinical trial supply and order management. Proficient in ERP systems and capable of driving decisions in cross-functional environments while maintaining high attention to detail.

Highest-signal resume keywords

Supply Chain ManagementProject ManagementGMP Environment ExperienceERP System ExperienceProduction Efficiency Methodologies

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Supply Chain PrinciplesProject ManagementGMP KnowledgeERP Systems (SAP, OMP, APO)Lean ManufacturingSix SigmaImpact AssessmentOrder ManagementKit Design FeasibilityMaterial Readiness

Soft Skills

Problem-Solving SkillsAttention to DetailWritten CommunicationVerbal CommunicationTeamwork

Certifications & Qualifications

Master's DegreeAPICS CertificationSCOR Certification

Industry Keywords

Clinical Trial SupplyProduction EnablementCross-Functional CollaborationCultural AwarenessNegotiation Skills

Tech Stack

Tools & technologies

ERP

About the role

Key responsibilities & impact

Collaborate with the planning organization as the initial point of contact for product requirements
Support new molecule introduction and molecule oversight
Initiate work center activities within the Production Enablement organization
Determine standard and non-standard configurations and ensure kit design feasibility with stakeholders
Ensure material readiness for study timelines and successful order preparation
Drive on-time, in-full production
Perform impact assessments for new projects, including capacity, new technology, and shipping requirements
Drive decisions and resolve issues affecting end-to-end order lead time from source to delivery
Incorporate study, product, and process knowledge from supply setup through depot receipt
Make decisions regarding kit designs, booklet selection, system setup, and material availability
Ensure timely global clinical trial supply, order management, finished goods release, and delivery to Roche depots in accordance with local standards and regulatory requirements

Requirements

What you’ll need

Academic degree or equivalent diploma, preferably in Business, Life Sciences, or Engineering
5+ years of work experience in a GMP environment or equivalent supply chain functions
Hands-on ERP system experience, such as SAP, OMP, or APO
Full use and application of basic Supply Chain, Business Process, and cGMP theories, principles, and techniques
Knowledge and application of production efficiency methodologies, such as 5S, Lean Manufacturing, or Six Sigma
Proven experience managing projects from initiation to delivery
Experience working in cross-functional and cross-cultural environments
Experience demonstrating matrix leadership
Strong problem-solving skills and high attention to detail
Excellent English skills required
Basic German skills beneficial
Strong written and verbal communication skills
Cultural awareness, active listening, social competence, teamwork, negotiation skills, and customer-focused relationship building
Master's degree, APICS, and/or SCOR certification is a plus

Benefits

Comp & perks

Equal Opportunity Employer
Opportunity to contribute to life-changing healthcare solutions
Globally distributed, cross-cultural work environment
Professional growth and development opportunities