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Senior Manufacturing Specialist I

Job description

Job Description



  • Ensure operational efficiency and compliance by managing technical documentation, addressing non-conformances, and implementing corrective actions.
  • Streamline processes and drive continuous improvement across manufacturing operations.
  • Effective change management, thereby fostering process enhancements and ensuring compliance with regulatory standards.

Operations and Technical

  • Conduct technical writing and collaborate with Operations and cross-functional team to investigate non-conformance issues.
  • Develop and implement corrective and preventive measures together with the Operations team and cross-functional team.
  • Manage change processes to enhance operations. Develop and conduct training modules for Operations and new employee onboarding.
  • Analyze key performance indicators and execute strategies to optimize workflows.
  • Author and revise GMP-related documents.
  • Collaborate on the creation, revision, and enhancement of electronic batch records.
  • Lead or participate in projects aimed at enhancing operations or new product introduction.
  • Utilize quality management systems and operations-related software, such as Trackwise, LIMS, SAP, POMSnet, Delta-V or others.
  • Prepare and support regulatory inspections and internal audit.
  • Engage in projects aimed at continuous operational improvement.
  • Engage in regular GEMBA walkdowns.
  • Organize regular meetings with cross-functional teams to discuss and update daily operational matters.

Safety

  • Ensures a safe work environment by adhering to regulatory and global/local Environmental, Health, and Safety (EHS) policies.

Quality

  • Ensure investigations are conducted and completed promptly and to a high standard.
  • Ensure that process improvements are relevant and beneficial to the manufacturing operations.
  • Verify the accuracy of impact assessments and ensure corrective and preventive actions are relevant.
  • Serve as point of contact for change management documentation and investigations during audits and inspections.

Schedule

  • Strive to complete investigations in a timely manner to minimize any potential impact on batch release timelines or shipment schedules.
  • Ensure that process improvement changes are executed on schedule as planned for the production run.

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Company information

Company
AbbVie
Location
Singapore
Singapore
Posted
8 months ago

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