Senior Lab Technician Analytics

Your role

• Verantwortung für den analytischen Entwicklungsteil von Kundenprojekten im Bereich Drug Substance – von der frühen Entwicklungsphase bis zur Prozessreife
• Entwickeln, Optimieren und Troubleshooting von chromatographischen Methoden (HPLC, UPLC, GC, GC-Headspace)
• Implementieren, validieren und transferieren von chromatographischen Analysemethoden
• Analysieren der pharmazeutischen Wirksubstanzen und Zwischenprodukte, teilweise cGMP-konform
• Unterstützung beim Unterhalt und Betreuung unseres modernen Geräteparks

• Berufserfahrung in einer ähnlichen Funktion, gute HPLC / GC Kenntnisse und Interesse an chromatographischen Trenntechniken
• Ausbildung als Chemielaborant / in EFZ oder vergleichbare Ausbildung mit Schwerpunkt Analytik
• Erfahrung mit Tools wie Empower / Chromeleon, LIMS, MS-Office, etc.
• GMP ist von Vorteil

• Teamarbeit ist ihnen wichtig, um Prozesse gemeinsam weiterentwickeln zu können.
• Sie sind proaktiv und übernehmen gerne Verantwortung
• Sie besitzen eine exakte Arbeitsweise, um qualitativ hochstehende Resultate zu liefern
• Selbstständiges Arbeiten und Organisation von Projektarbeiten macht ihnen Spaß
• Gute Englischkenntnisse sind wichtig. Idealerweise sprechen Sie auch Deutsch. Falls nicht, sind Sie bereit es zu lernen

• Flexible working hours make it possible to combine family, free time and career
• Parking is available at a reduced rate
• Health insurance :
  Discounts up to 10% on additional insurances with our partners for you and your partner / family
• Share purchase plan is generous with us and can be designed individually
• Family allowance : all employees entitled to child and / or education allowances receive an additional monthly family allowance
• Child allowance :
  Siegfried AG increases the child allowance by 10% compared to the cantonal statutory rate
• Individual further training opportunities by arrangement
• Reka money :
  Siegfried AG grants employees a 20% discount
• Pension fund :
  Our company pension fund is attractive and contributions can be arranged individually
• Staff restaurant / cafeteria : meals at preferential conditions
• Central location :
  Close to the train station with very good public transport connections
• Free credit card (Corner Card) for our employees
• Language courses in German for interested employees

In the Midst of People’s Lives – Across the Globe The Siegfried Group is one of the world’s leading Custom Development and Manufacturing Organizations (CDMOs) developing and producing active pharmaceutical ingredients (API), intermediates and finished dosage forms. As our core competence, we successfully integrate chemical and pharmaceutical capabilities into a single business model. The Siegfried name stands for highest quality, efficiency, flexibility and safety.

Present in Europe, Asia and North America, we serve a broad global customer base from major international pharmaceutical companies down to small biologic‑pharmaceutical organizations. For them we develop and produce product innovations on a large scale to finished products. We integrate our offer seamlessly into the customers’ value chain. Our comprehensive services range from early‑stage Research & Development services such as synthesis, scale‑up, formulation development, stability studies and method development all the way through to manufacturing services, ranging from preclinical R&D material for clinical trial purposes to commercial production.

We are able to produce about 200 of the approximately 1500 registered drug substances used in medicine. Moreover, we produce 20 percent of global demand for caffeine. Consequently, nearly 1 billion individuals come into contact with Siegfried products.

Zofingen is the hub of the Siegfried Group. The production facility at our Zofingen headquarters supplies our customers around the globe with exemplary Swiss quality. The Siegfried company is a popular employer in the Zofingen region, where we meet our social responsibility by training apprentices.

• Development and commercial manufacture of active pharmaceutical ingredients (APIs) and corresponding intermediates
• Fully compliant with cGMP and SHE (Safety, Health and Environmental) standards

• Manufacture of high potency active ingredients in development and production
• Micronization in development and production

• Contract manufacturing of new active ingredients