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Engineer, Process (pharmaceutical)

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Onsite

Engineer, Process (pharmaceutical)

益科德(上海)有限公司

Engineer, Process (pharmaceutical)

Skills

Compliance

2 months ago

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Important information


Contract type:

Permanent

Location:

Shanghai, China

Work mode:

Onsite

Published on:

7 August 2026

What they need


该职位来源于猎聘 As the process engineer, this role is responsible for

  • Participate in engineering project teams to design aseptic and biotech processing facilities with specific emphasis in one or more of the following: upstream/downstream insulin processing, included media preparation, buffer preparation, Inoculum, seed expansion, fermentation producing, centrifugal separation, Harvest, purification process, CIP/SIP.
  • Perform feasibility study, conceptual, basic, detailed designs and work package preparation for insulin projects.
  • Drafting, Preparation of layout, BFD, PFD, PID, etc.
  • Drafting annual production capacity and batch calculation
  • Drafting production scheduling
  • Drafting mass balance calculations
  • Perform hydraulic, heat load, production planning, utilities calculation etc.
  • Responsible for equipment package. Work with clients, vendor and other third parties to prepare datasheets, and specification.
  • Multi-discipline, highly interactive team to establish process design basis, develop process options and optimizations of selected design, and calculate and organize data for process flow sheets
  • Assesses compliance with applicable safety and environmental issues
  • Support field construction efforts, including reviewing submittals, responding to questions from clients and contractors, and performing field walks.
  • Support bio-pharma life science project in various phase such as support qualification work, C&Q (Commissioning and Qualification)
  • Familiar with each of insulin process operation GMP requirement (operation background and cleanness grade).
  • Perform technical and business presentations with clients and employees
  • Capability of preparing URS/Specification and process layout, personal/material/equipment /waste flows
  • Support validation team to prepare DQ/IQ/OQ protocols.
  • Contributes to departmental efforts by accomplishing related tasks as needed.
  • Accept project arrangements and business travel Professional experience & education
  • Bachelor’s Degree : Chemical Engineering / Chemistry / Bio-medical Engineering
  • Minimum 3 year experience in engineering company in pharmaceutical industry
  • Experience using drawing tool such as CAD, Revit, Plant 3D, PDMS.
  • Experience in develop layout, PFD, PID, specification, datasheet
  • Experience in some basic engineering calculation, such as heat load calculation, hydraulic calculation, etc.
  • Candidate with additional site experience and Qualification experience will have added advantage

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