Process Manager Production (m/f/d) — Siegfried
- Location
- Zofingen
- Contract
- full-time
- Posted
- 29 days ago
Role overview
Expect to grow", personally and professionally: At Siegfried, we offer exciting challenges and ample opportunities to showcase your talents.
As a trusted and respected partner to the pharmaceutical industry, we uphold the highest standards in safety, quality and sustainability, while fostering a culture that empowers you to thrive.
Join a rapidly expanding global company, where diverse perspectives and experiences come together in a collaborative environment.
- Expect to grow", personally and professionally: At Siegfried, we offer exciting challenges and ample opportunities to showcase your talents.
- As a trusted and respected partner to the pharmaceutical industry, we uphold the highest standards in safety, quality and sustainability, while fostering a culture that empowers you to thrive.
- Main Responsibilities:
- Implement, support, and optimize existing and new production processes with regard to cycle time, yield, and costs while complying with cGMP guidelines.
Main responsibilities
- Main Responsibilities:
- Implement, support, and optimize existing and new production processes with regard to cycle time, yield, and costs while complying with cGMP guidelines.
- Assess new processes and technologies for feasibility and suitability in chemical manufacturing facilities.
- Support, monitor, and evaluate product campaigns, including defining improvement and process optimization measures.
- Own process and procedure documentation, material balances, and SAP manufacturing recipes.
- Act as process lead / process owner in investment projects.
- Share responsibility for planning, implementing, and ensuring compliance with regulatory requirements relating to cGMP, SHE, authorities, etc. for your products. Requirements:
- Completed university degree (University of Applied Sciences, ETH, or university) in Chemistry, with a focus on Chemical Engineering, Industrial Chemistry, or Organic Chemistry.
- Professional experience in chemical or pharmaceutical production or in a pilot plant; experience in a cGMP environment is an advantage.
- 3+ years of experience in a similar function.
Company and context
- As a fully integrated CDMO, Siegfried is one of the few organizations today that can carry out the development and manufacturing of APIs and finished dosage forms under one roof.
- This unique combination of know-how and experience makes us the most trusted partner in the pharmaceutical industry.
- Siegfried is a leading CDMO (Contract Development & Manufacturing Organization) headquartered in Zofingen, Switzerland.
- The company operates manufacturing sites in Evionnaz (Valais), Zofingen (Aargau), and Schlieren (Zurich).
Additional details
- Here, you'll find a workplace that values both collective success and your individual contributions—offering long-term opportunities to grow and make an impact.
- Share responsibility for planning, implementing, and ensuring compliance with regulatory requirements relating to cGMP, SHE, authorities, etc. for your products.
- Business-fluent German and English, both written and spoken.
- Staff restaurant / cafeteria: Meals at preferential rates You can park at a discounted rate
Notes and original content
- Your Profile:
- Requirements:
- Your Benefits:
- Staff restaurant / cafeteria: Meals at preferential rates
- You can park at a discounted rate
Questions about this listing
What salary does Siegfried offer for this role?
Siegfried lists CHF 85'500 - 129'500 gross per year for this position in Zofingen. 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 Siegfried 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 Siegfried 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 residents living in the border zone of the country adjoining Canton Aargau 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 Aargau's cantonal migration office or with HR during the application.
How do I apply for this position at Siegfried?
Use the "Apply now" button on this page — it links directly to Siegfried's original listing at siegfried.wd103.myworkdayjobs.com, so your application goes straight to the employer's own applicant-tracking system. Frontaliere Ticino does not collect or forward applications itself.
