Country China
City Nantong
Functional Area Operations
Job Group Production
Employment Type Permanent Contract
Working time Full-time
At its locations around the world, Siegfried offers employees exciting career opportunities in international settings. We cultivate multidisciplinary cooperation and encourage our staff to actively shape and influence their careers. This approach, coupled with our dynamic working environment, make Siegfried an attractive employer.
Your role
Operate process equipment to produce effective pharmaceutical intermediates and final products in accordance with standard operating procedures, batch records, safety and other requirements
Able to operate production equipment and systems on the post with the support of other colleagues
Able to clean and reset the equipment
Truthfully and properly make records according to GMP
Actively participate in and maintain good workshop maintenance and cleanliness
Provide process and safety improvement suggestions, and report safety hazards in time
Timely analyze, handle and report deviations and anomalies in the production process
Timely identify and solve problems that occur or may occur in all production steps
Improve personal work ability through continuous learning
Your profile
Secondary school or high school degree or above , major in chemical industry is preferred.
English skill is preferred
Capable of shift work
2+ years of experience working in a chemical or pharmacy plant
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 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.
What we do in Nantong
Nantong is our cGMP manufacturing site in China supplying all Western countries and China.
Main activities
- Pilot and commercial manufacturing of drug substances (APIs) and related intermediates and raw materials
- All fully cGMP and SHE compliant
Features
- 300 m³ cGMP manufacturing capacity: 1 – 10 m³ reactors
- Powerful rectification and solvent recovery
- Short path distillation
- 5 non-GMP pilot suites (0.1 – 2 m³)
- Technology in pilot and commercial: – 100 to 250 °C
- Hydrogenation up to 40 bar
- Chlorination, bromination, alcylation
Strategic importance
- Manufacturing of APIs at the end of their life cycles
- Manufacturing of intermediates and raw materials of both innovative and generic APIs
- Competitive cost structure and Swiss level of compliance and quality