Facility Excellence (Compliance) Lead Packaging — Roche
- Location
- Kaiseraugst
- Contract
- Full-time
- Posted
- 17 days ago
Full description
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. Join Roche, where every voice matters.
Please use the position title in the “object” ...
Your future team is strategically positioned within Manufacturing Supports and belongs to the Manufacturing Unit Assembly & Packaging. Cross-functional collaboration takes place here to ensure smooth operations and the high quality standards in production.
As Facility Excellence Lead, you are responsible for coordinating overarching and building-specific compliance activities. Your main goal is to ensure uninterrupted and stable production through continuous improvements while strictly adhering to GMP compliance. In addition, you provide professional and personnel leadership for your team and create an environment that promotes self-organization, personal responsibility, and peak performance.
The opportunity
In this position, you will take on responsible tasks and make a significant contribution to the success of our production:
- People management of the team, including recruitment, feedback discussions, and targeted development of employees through active application of the VACC model (Visionary, Architect, Coach, Catalyst).
- Responsibility for overarching, building-specific compliance activities to ensure seamless GMP compliance, as well as implementation of the hygiene and zoning concept.
- Coordination, approval and training of SOPs as well as ensuring ownership for deviations, CAPAs, changes and multi-site assessments.
- Review and operational release of qualification and validation plans/reports as well as active support and implementation of quality risk management activities (QRM).
- Preparation, support and follow-up of official inspections, audits and customer visits on site.
- Example of lean thinking and application of LPS methods to continuously improve quality, efficiency and cost structure.
- Promoting an open, collaborative work environment with a strong culture of trust and a transparent speak-up and error culture.
Who you are
To succeed in this role, you will have the following qualifications and attributes:
- A completed pharmaceutical, scientific or technical degree (or comparable training) coupled with at least 2 years of relevant professional experience in the pharmaceutical environment with appropriate compliance and cGMP knowledge.
- Practical experience in dealing with CAPAs, changes and process descriptions/optimisation (SOP) as well as preparation and support of internal and external inspections
- In-depth knowledge of quality systems and current cGMP regulations with the firm conviction: "Robustness and compliance before speed".
- Strong leadership skills as Visionary, Architect, Coach and Catalyst with a strong local presence to inspire the team.
- A solution-oriented, positive and self-reflective personality with strong communication skills to promote an open error culture.
- Very good knowledge of German and English, both written and spoken.
Ready to take the next step? We look forward to hearing from you. Apply now to discover this exciting opportunity!
Who we are
A healthier future drives us to innovate. Together, more than 100,000 employees across the globe are dedicated to advance science, ensuring everyone has access to healthcare today and for generations to come. Our efforts result in more than 26 million people treated with our medicines and over 30 billion tests conducted using our Diagnostics products. We empower each other to explore new possibilities, foster creativity, and keep our ambitions high, so we can deliver life-changing healthcare solutions that make a global impact.
Let's build a healthier future, together.
Roche is an Equal Opportunity Employer.
Requirements
Strong leadership skills as Visionary, Architect, Coach and Catalyst with a strong local presence to inspire the team.
Very good knowledge of German and English, both written and spoken.
Questions about this listing
What salary does Roche offer for this role?
The original listing does not state a salary. Our estimate for this role and sector in Kaiseraugst is CHF 85'500 - 129'500 gross per year — an estimate, not a figure communicated by Roche. The calculator on this site converts a gross salary into 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 Aargau?
EU/EFTA citizens living in an EU/EFTA state can apply for a G permit and can work anywhere in Switzerland: border zones no longer apply to them, and they must return home at least once a week. The Swiss employer files the request with Canton Aargau's migration office after the contract is signed. Processing times vary by canton, so confirm the specifics with Aargau'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.
