General Information

Country China

City Nantong

Functional Area Research & Development

Job Group Quality Control

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

Perform sampling of materials, including raw materials, package materials and final products.
Responsible for the routine management of sampling room in warehouse and sampling tools.
Participate certain lab management work, e.g.: reference standard, highly toxic reagents, sampling, retain sample; 
Carry out sample testing according to the SOPs,including raw material, IPC,Intermediate, API.
Compile analytical reports or CoAs; 
Participate in QC personals training; 
Participate in new projects transfer, e.g.: raw material selection, and method verification and transfer; 
Draft specifications and analytical procedures; 
Participate in the investigation of OOS, OOT and deviation;
Participate in drafting, maintenance and follow up relevant QC procedures; 
Cooperate with supervision to complete work of authority/ clients audits.
Responsible for managing group members and work arrangements, ensuring that materials are released within the due date.

Your profile

Pharmaceutical or Chemical or Instrument analysis or similar background is preferred (college or above).
More than 5 years’ experience in Quality control related job.
Have solid experience in instrumental analysis, e.g. Chromatograph analysis, or Spectrometry analysis or Particle Size analysis or potentiometric titration, or Wet chemistry analysis, or Microbial analysis experience.
Have Drug GMP relevant knowledge and practical implementation experience, e.g. cGMP, EU-GMP, State GMP.
Have knowledge on Pharmacopeias, e.g. USP, EP, CP.
Good oral and written English skill.

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