WuXi AppTec

  • Manufacturing Engineer

    Job Locations CN
    Job ID
    2018-4003
  • Overview

    Company introduction:

     

    Wuxi Biologics is a world-class CMO with the most comprehensive capability and technology platform serving clients globally in the biopharmaceutical and health care industries from discovery to commercialization.  The company is publically listed in Hong Kong, with a market capital of $13 billion.  Our dream is to ensure “every drug can be made and every disease can be treated” to become a reality for both Wuxi Biologics and our clients/strategic partners.  The company has sites/offices in China, US, EU, Asia and Israel.  The company currently has 3,000 employees, and are providing services to over 200+ clients globally, including 13 of the top 20 biopharmaceutical companies.

    Responsibilities

    Job Description:

     

    • The scope of the position will assist the Manufacturing Groups [Upstream Processing (USP) or Downstream Processing (DSP)] to carry out cell culture fermentation activities and/or purification activities. Specific activities will include, but not limited to, developing batch records, writing protocols, preparing final reports, drafting SOPs, analyzing data, initiating deviations, performing facility fit, working with clients to address their needs and managing client relationships.
    • The facility fit activities will include evaluating the project from equipment availability, size, quantity and time, or any of the combination to ensure the success of transferring a project into our cGMP manufacturing facility.
    • The candidate will learn biologics manufacturing processes from media preparation, buffer preparation, inoculation, seed transfer/expansion, GMP production, harvest, loading products onto columns (Protein A, Cation Exchange, Anion Exchange), viral inactivation, viral removal, concentration, UF/DF and Bulk fill of drug substance into bottles/bags.
    • The candidate will occasionally lead the investigation of deviations.
    • The candidate will interact with supporting groups (PEV, Engineering, QC, QA, AIS, EHS, etc.) to ensure the manufacturing operations running smoothly and seamlessly.
    • The candidate will work with the cross functional team to address and resolve issues and report any incompliant & technical issues to department heads and senior management.
    • This person should have some experience in pharmaceutical industry.
    • Candidates with experience in downstream processing (DSP), Upstream processing (USP), QC, QA , Process Development (PD), equipment & process validation or Manufacturing Science and Technology (MSAT) experience will be considered first.
    • The candidate must know how to use Microsoft Excel, MS Project and Powerpoint.
    • The candidate will work on any other tasks to be assigned by the company.

     

    Qualifications

    Qualifications:

     

    Education: BS, or MS or PhD in Chemical Engineering, Biochemical Engineering, Biomedical Engineering, Bioscience, or Biotechnology.

     

    Experience required: 0 - 3 years in biopharmaceutical manufacturing, QC, QA, MST, Engineering or PEV. 

     

    Other: The candidate must have the following attributes: Can do attitude, good organizational skill, attention to details, follow instruction and work well with people.

     

     

    Equal Opportunity Employer Minorities/Women/Veterans/Disabled

     

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