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Analytical Project Manager

Job in Zofingen, Aarau / Aargau, Aargau, Switzerland
Listing for: Siegfried
Full Time position
Listed on 2026-11-02
Job specializations:
  • Pharmaceutical
    Regulatory Compliance Specialist, Pharmaceutical Science/ Research
Salary/Wage Range or Industry Benchmark: 120000 - 180000 CHF Yearly CHF 120000.00 180000.00 YEAR
Job Description & How to Apply Below
Location: Zofingen

Analytical Project Manager This website stores cookies on your computer. These cookies are used to collect information about how you interact with our website. We use this information in order to improve and customize your browsing experience and for analytics about our visitors both on this website. To find out more, see our Privacy Policy.### Analytical Project Manager Apply:
Hybrid:
Zofingen:
Full time:
Posted 5 Days Ago:
R26 _774
** Expect to grow **, persönlich und beruflich:
Bei Siegfried erwarten Sie spannende Herausforderungen und zahlreiche Möglichkeiten, Ihre Talente unter Beweis zu stellen. Als ein vertrauenswürdiger und angesehener Partner der pharmazeutischen Industrie halten wir höchste Standards in den Bereichen Sicherheit, Qualität und Nachhaltigkeit ein – und fördern gleichzeitig eine Kultur, die Sie dazu befähigt, erfolgreich zu sein. Werden Sie Teil eines schnell wachsenden, globalen Unternehmens, in dem vielfältige Perspektiven und Erfahrungen in einem kooperativen Umfeld zusammenkommen.

Hier finden Sie einen Arbeitsplatz, der sowohl kollektiven Erfolg als auch Ihre individuellen Beiträge wertschätzt – und Ihnen langfristige Möglichkeiten bietet, sich weiterzuentwickeln und etwas zu bewirken.
** Your Role:
** Over the past years, Siegfried AG has strengthened its position as a leading global partner in the pharmaceutical industry. To support our continued growth, we are expanding our capabilities at our site in Zofingen, Switzerland.
The Zofingen site manufactures complex active ingredients for human and veterinary medicine, as well as additives for food and beverages.
More than 90 colleagues in our laboratories develop innovative processes and ensure compliance with the highest quality standards. Through their expertise, they contribute to reliable, efficient and customer-oriented production. We offer a dynamic working environment with varied responsibilities and challenging assignments.
*
* Your Profile:

**** Your Role
*** Coordinate all analytical activities within assigned projects, including method development, transfer, validation and troubleshooting, from initial evaluation through commercial production
* Provide scientific leadership and analytical expertise for assigned Small Molecules projects and technologies
* Represent Siegfried in project-related customer meetings, both on-site and virtually
* Serve as the key interface between Analytics, Chemical Development, Production, Quality Assurance and other specialist functions
* Support the transfer of analytical knowledge and methods from Analytical Development to Quality Control
* Prepare, maintain and review analytical documentation including specifications, method descriptions, validation and transfer reports, development and campaign reports
* Represent analytical topics during customer audits and authority inspections
* Track and monitor  analytical project costs against the project budget
* Ensure compliance with current Good Manufacturing Practice (cGMP) requirements and safety standards within the area of responsibility
* Contribute to consistently high standards of quality and safety  
** Your Profile
**** Technical Expertise
*** A Master’s or PhD degree in Chemistry, Pharmacy or a comparable academic qualification provides the right foundation for this role
* 2–3 years of professional experience in pharmaceutical analytics
* Strong knowledge of chromatographic analytical techniques (e.g. High-Performance Liquid Chromatography (HPLC), Gas Chromatography (GC)) for Small Molecules is essential
* Knowledge of spectroscopic and wet chemistry analytical techniques for Small Molecules is an advantage
* Experience working in a Good Manufacturing Practice (GMP)-regulated environment is an advantage  
** Personal Strengths
***…
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