Your role
1. Assistenz der Leitung von Umweltschutzlabor und Kläranlage. Stellvertretung für den Leiter UWS-Labor/Kläranlage
2. Koordinierende Aufgaben für die Organisation im Laborbereich (UWS Labor). Zusammenarbeit mit der Sachbearbeitung Abfall/Abwasserentsorgung
3. Überwachung der Kläranlage im Hinblick auf Einhaltung der Grenzwerte. Betreuung und Optimierung der Online Analytik
4. Kontakt zu Behörden (RP Detmold) und zu Entsorgungsanlagen (externe Kläranlagen)
5. Bearbeitung von Projekten zur Optimierung der Kläranlage
6. Verfahrenstechnische Ausarbeitung zu alternativen Reinigungsverfahren, Durchführung von Versuchen in der Laborkläranlage, Umsetzung im Großmaßstab auf der Kläranlage bzw. in Abwasservorbehandlungsanlagen
7. Begleitung der Untersuchung von Einzelabwasserströmen zur geeigneten Behandlung, Durchführung von Arbeitsplatzkonzentrations-sowie internen Emissionsmessungen
8. Mitarbeit bei der Erstellung des Abwasserkatasters
Your profile
9. Ingenieurabschluss; z.B. als Chemie-, Umwelttechnologie- oder Verfahrensingenieur
10. Umfangreiche Fachkenntnisse aus dem Bereich Abwasserreinigung
11. Weitgehende Fachkenntnisse aus dem Bereich organische Chemie und Verfahrenstechnik
12. Vertiefende Kenntnisse zur Untersuchung von Abwässern/Klärschlämmen wünschenswert
13. Gute Englischkenntnisse
14. Ausgeprägte Fähigkeit zum selbstständigen Arbeiten
15. Kommunikations- und Teamfähigkeit
Working at Siegfried
Siegfried's work environment is dynamic and international. With a highly professional and motivated team, the company operates in a future-oriented business field. Siegfried possesses a unique culture that leverages cultural differences to create a competitive advantage. Siegfried places highest priority on providing a flexible, diverse and discrimination-free working environment in which employees can develop personally and professionally, advance innovation and deliver superior performance. We strive to provide a work environment where employees can take on challenging jobs and associated responsibilities that best serve their personal and technical development and can benefit from the success of our company. The company regulations in respect of compensation and career development opportunities apply to all Siegfried sites. Additional conditions of employment are governed by location-specific circumstances, legislation and customs.
Who we are
In the Midst of People’s Lives – Across the GlobeThe 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.
What we do in Minden
For the last 80 years, Siegfried PharmaChemikalien Minden GmbH has been producing active pharmaceutical ingredients (APIs) and the corresponding intermediates at its Minden facility, to meet worldwide demand from the pharmaceutical industry. We also produce ingredients for the cosmetics and food industries.
Main activities
16. Development and commercial manufacture of active pharmaceutical ingredients (APIs) and corresponding intermediates
17. Fully compliant with cGMP and SHE (Safety, Health and Environmental) standards
Special features
18. Handling of high potency substances in development and production
19. Comprehensive handling of solids in production
20. Production capacity: 1450 m³
21. Reactors: 0.2–30 m³
22. Handling of highly toxic substances in encapsulated plants
23. Successful transfers of new products into commercial production
24. Biotechnology implementations
Strategic importance
25. Contract manufacturing of new active ingredients