Recipe Data Steward Lead — Roche
- Location
- Basel
- Contract
- full-time
- Posted
- 6 days ago
Role overview
At Roche you can show up as yourself, embraced for the unique qualities you bring.
Our culture encourages personal expression, open dialogue, and genuine connections, where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally.
This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come.
- At Roche you can show up as yourself, embraced for the unique qualities you bring.
- Our culture encourages personal expression, open dialogue, and genuine connections, where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally.
- Key Responsibilities:
- Drive System Configuration: Collaborate with Subject Matter Experts (SMEs) to perform impact analyses, feasibility studies, and templates/system configuration mock-ups.
- & Experience:
- Education: Bachelor’s degree in Engineering, Biological Sciences, or a related field (with 5+ years of experience); or a Master’s degree (with 3+ years); or a PhD (with 0-2 years).
Main responsibilities
- Key Responsibilities:
- Drive System Configuration: Collaborate with Subject Matter Experts (SMEs) to perform impact analyses, feasibility studies, and templates/system configuration mock-ups.
- Implement Configuration Changes: Own the end-to-end implementation of newly approved system elements, structures, and process steps.
- Manage Data Ontology: Maintain and implement standard nomenclature, data classifications, and conventions across our global recipe systems.
- Support and Train Communities: Act as the central focal point for our global recipe builder community, developing prototypes and leading on-the-job training.
- Ensure Operational Excellence: Partner across departments to resolve technical challenges, maintain a continuous state of inspection readiness, and assure Quality/Good Manufacturing Practices (GMP) compliance. Who You Are
- You are a structured, analytical thinker who thrives on organizing complex data and collaborating across global networks.
- You enjoy translating user needs into system designs and have a passion for detail and continuous improvement.
Key requirements
- & Experience:
- Education: Bachelor’s degree in Engineering, Biological Sciences, or a related field (with 5+ years of experience); or a Master’s degree (with 3+ years); or a PhD (with 0-2 years).
- Industry Expertise: Strong background in biologics manufacturing operations, process development, or process tech transfers.
- Systems & Data Experience: Proven experience with process specification tools, enterprise recipe management systems, data ontologies, or database solution configuration.
- Technical Knowledge: Solid understanding of global biopharma regulatory environments and Good Manufacturing Practices (GMP). Collaborative Skills: Except
What the company offers
- We will build a strong cross-functional and inclusive community, put the power of data into the hands of our people, further develop the Lean and Digital skills across PT, and scale up our Digital and Advanced Analytics solutions, for the benefit of our colleagues and patients.
Application process
- Lead Global Standardization: Act as the expert for business harmonization, ensuring global recipe builders apply consistent standards for molecules, buffers, and media solutions.
- In this dynamic dual-hatted role, you will make a substantial impact on the overall user experience of our global Process Knowledge Management (PKM) application.
- As part of the Basecamp 2.0 Operational Support Network Team (OSNT), you will lead our business standardization efforts while directly driving templates and system configuration changes.
Company and context
- To do so, we have formed a new organization called PT Digital and Operational Excellence (PTE) with the aspiration to build industry-leading digital and lean operations across functions and our entire manufacturing footprint.
- PTE is the new organization that will catalyze the global development and execution of PT’s Digital and Operational Excellence strategy to enable PT to realize our performance promises.
- We aim to activate data citizenship and digital mindset, revolutionize our FAIR data ecosystem and systems landscape, re-design excellent processes, and generate transformative insights.
- We collaborate closely with global functions to deliver impactful value to our patients. The Opportunity
Additional details
- Join Roche, where every voice matters.
- We collaborate closely with global functions to deliver impactful value to our patients.
- Ensure Operational Excellence: Partner across departments to resolve technical challenges, maintain a continuous state of inspection readiness, and assure Quality/Good Manufacturing Practices (GMP) compliance. Qualifications & Experience:
- Technical Knowledge: Solid understanding of global biopharma regulatory environments and Good Manufacturing Practices (GMP). Collaborative Skills: Except
Notes and original content
- The Position
- The Opportunity
- Ensure Operational Excellence: Partner across departments to resolve technical challenges, maintain a continuous state of inspection readiness, and assure Quality/Good Manufacturing Practices (GMP) compliance.
- Who You Are
- Qualifications & Experience:
- Technical Knowledge: Solid understanding of global biopharma regulatory environments and Good Manufacturing Practices (GMP).
- Collaborative Skills: Except
Questions about this listing
What salary does Roche offer for this role?
Roche lists CHF 85'500 - 129'500 gross per year for this position in Basel. This is the salary published in the original listing (or, when the employer omits a figure, a realistic estimate for the role and sector) — the calculator on this site converts it to your actual net take-home once cross-border tax and social contributions are applied.
Is this a full-time role, and what type of contract does Roche offer?
This listing is a full-time position. The contract type shown here comes directly from the employer's original posting; always confirm exact hours, notice period and probation length with Roche during the application process, since these details can vary by role even within the same contract category.
Do I need a cross-border work permit for a role in Basel?
EU/EFTA residents living in the border zone of the country adjoining Canton Basel can apply for a G permit; the Swiss employer files it with that canton's migration office after the contract is signed. Border-zone rules and processing times vary by neighbouring country and canton, so confirm the specifics with Basel's cantonal migration office or with HR during the application.
How do I apply for this position at Roche?
Use the "Apply now" button on this page — it links directly to Roche's original listing at roche.wd3.myworkdayjobs.com, so your application goes straight to the employer's own applicant-tracking system. Frontaliere Ticino does not collect or forward applications itself.
