Senior Instrument Engineer

3 months ago

Nantong, China Siegfried Full time
Your role

Responsible to guide the instrument and automation maintenance and continuing improvement for instrument part of equipment in whole factory. Archive related technical documents. 

Responsible for instrument and automation equipment maintenance, maintenance plan and implementation, responsible for acceptance and archive for monthly, weekly, daily upkeep and annual overhaul.

Responsible for technical support of instrument equipment and DCS/BMS system of the plant and responsible for professional knowledge training to instrument maintenance. 

Responsible for the plant instruments calibration.

Cooperating with Lead Engineer of Instrument. 

Assist company to complete GMP verification related work.

Your profile

At least 5 years working experiences for guide the instrument and automation maintenance and continuing improvement for instrument part of equipment.Has working experience in pharmaceutical factory is preferred Good to know how to work at safety area & explosion-proof area & cleaning room, familiar to electrical issue like power panel, instrument and PLC, etc.Good knowledge of automation, instrument, and operation skill to DCS control system.Be good at: practical experience in field maintenance, safety attitude, team work, committed to result. Bachelor degree or above

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

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