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Jobs in Singapore   »   Jobs in Singapore   »   Quality Assurance / Control Job   »   QC Manager, Customer Projects
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QC Manager, Customer Projects

Lonza Biologics Tuas Pte. Ltd.

Lonza Biologics Tuas Pte. Ltd. company logo

Today, Lonza is a global leader in life sciences operating across three continents. While we work in science, there’s no magic formula to how we do it. Our greatest scientific solution is talented people working together, devising ideas that help businesses to help people. In exchange, we let our people own their careers. Their ideas, big and small, genuinely improve the world. And that’s the kind of work we want to be part of.

Did you know that we are the 1st biologics contract manufacturer in Singapore? We offer you exposure to upcoming biotech and established pharmaceutical companies and to the manufacturing technology needed to produce mammalian treatments and cell therapies of tomorrow. Our global manufacturing network is recognized for its reliable, high-quality services, regulatory track record, global footprint, innovative technology platforms and extensive experience – we, in Singapore are proud to be part of this global network.

The Manager, Customer Projects, QC will be responsible for coordinating with external customers and working inter-departmentally to enhance communications at all levels and ensure that work activities, compliance and documentation issues are resolved in a timely manner.

Key responsibilities:

  • Superior ability to troubleshoot all applicable equipment / methods (subject matter expertise). Strong ability to manage multiple priorities.
  • Strong ability to manage multiple priorities.
  • Source of expertise for rest of staff.
  • Work with tech transfer teams to prepare new processes; act as responsible lab designee.
  • Own & Lead Special projects, often complex in nature; including direct responsibility for leading various teams to successful completion of various projects.
  • Validation / Tech or Process Transfer Work: Lead execution, troubleshooting, coordination, client interaction.
  • Can identify lab problems, troubleshoot, identify and complete or coordinate corrective action.
  • Work inter-departmentally to enhance communications at all levels and ensure that work activities, compliance and documentation issues are resolved.
  • Lead and approve report (Example: Method Qualification / Validation, / Investigations).
  • Ensuring that the project is completed within the approved budget
  • Includes the overall project coordination of resource planning, cost estimating, cost budgeting, and cost control as part of the SOW (Scope of Work) assessment.
  • Act as interface with clients, QC, and line management for integrated project budget/resources.
  • Ensure that the various elements of the project are properly coordinated including overall coordination of project plan development, project plan execution and change control.
  • Manage the process of cross-functional integration of operational activities for the project team.
  • Provide expert planning and operational support to the project.
  • Contribute to the creation of the development plan/production plan and other project information.
  • Any other tasks as and when assigned by Manager.


Key requirements:

  • Degree/Diploma in a relevant Chemistry, Science field or Equivalent.
  • Relevant work experience preferably with Lab experience in a biotech or medically related field.
  • Relevant experience and accomplishment to dictate final position for which the candidate may qualify.
  • Advantage if candidate is able to lead the shift team to meet the in-process demand samples turnaround time.
  • Good understanding of HPLC and Empower software.
  • Understanding and execution of spectroscopy, and other assigned methods which may include chromatography methods (HPLC), ELISA, PCR, CE, SDS-PAGE, IEF, icIEF, TOC, Protein concentration (A280 or SoloVPE), osmolality, potency methods, appearance and other physiochemical methods.
  • Provide support in HPLC equipment maintenance and qualification.
  • Well versed in cGMP regulations.
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