Shift Manufacturing Engineer

4 days ago


Singapur, Singapore Antaes Consulting SA Full time
  • Contribute to Life Science projects for Antaes Asia clients
  • Oversee the execution of manufacturing batches according to defined instructions, ensuring strict compliance with SOPs, training, and real-time monitoring of critical process steps for seamless operations.
  • Collaborate on the development, review, and optimization of batch and cleaning recipes within DCS systems such as DeltaV and POMS, including manual and ad-hoc documentation.
  • Lead or contribute to digitalization and continuous improvement initiatives aimed at enhancing process efficiency, reducing complexity, and supporting strategic site goals.
  • Support troubleshooting efforts during process deviations or equipment issues by coordinating timely corrective actions with cross-functional teams.
  • Provide training and guidance to chemical operators on operational best practices, equipment changes, OSW, and risk assessments.
  • Participate in the commissioning, qualification, and validation phases of capital projects to ensure smooth integration into routine operations.
  • Maintain compliance with environmental, health, and safety policies by participating in safety risk assessments and process hazard analysis as the operations representative.
  • Ensure documentation accuracy by proactively resolving batch record discrepancies, contributing to investigations, and supporting timely CAPA implementation.
  • Monitor shift deliverables, anticipate operational challenges, and ensure production timelines are met, highlighting potential delays to supervisors when necessary.
  • Uphold plant readiness standards at all times, ensuring the facility remains audit-ready and operationally sound
  • Contribute to the promotion of Antaes services on top of assistance provided to clients

Job Description:

  • Contribute to Life Science projects for Antaes Asia clients
  • Oversee the execution of manufacturing batches according to defined instructions, ensuring strict compliance with SOPs, training, and real-time monitoring of critical process steps for seamless operations.
  • Collaborate on the development, review, and optimization of batch and cleaning recipes within DCS systems such as DeltaV and POMS, including manual and ad-hoc documentation.
  • Lead or contribute to digitalization and continuous improvement initiatives aimed at enhancing process efficiency, reducing complexity, and supporting strategic site goals.
  • Support troubleshooting efforts during process deviations or equipment issues by coordinating timely corrective actions with cross-functional teams.
  • Provide training and guidance to chemical operators on operational best practices, equipment changes, OSW, and risk assessments.
  • Participate in the commissioning, qualification, and validation phases of capital projects to ensure smooth integration into routine operations.
  • Maintain compliance with environmental, health, and safety policies by participating in safety risk assessments and process hazard analysis as the operations representative.
  • Ensure documentation accuracy by proactively resolving batch record discrepancies, contributing to investigations, and supporting timely CAPA implementation.
  • Monitor shift deliverables, anticipate operational challenges, and ensure production timelines are met, highlighting potential delays to supervisors when necessary.
  • Uphold plant readiness standards at all times, ensuring the facility remains audit-ready and operationally sound
  • Contribute to the promotion of Antaes services on top of assistance provided to clients
This is some text inside of a div block.

Job Requirements:

  • Degree in Life Science, Chemical Engineering, Science or equivalent
  • At least 2 years of experience in working in a GMP manufacturing environment is preferred
  • Able to work comfortably in 12-hour rotating shift (Day/Night)
  • Strong process knowledge and interest to guide and mentor
  • High adaptability and ability to lead and work with cross functional team
  • Strong communication and writing skills
  • Excellent communication skills, both written and verbal
CDI

To join our Life Sciences team in Vaud, we are looking for aCompliance Specialist – Quality Control.

The project :

  • Help the Quality Control (QC) team with daily compliance-related tasks.
  • Investigate and manage issues like deviations and non-conformities.
  • Review lab data to ensure it meets quality standards.
  • Handle documentation for deviations, investigations, CAPAs, and change controls.
  • Improve data integrity processes and report progress.
  • Write, review, and update procedures and quality documents.
  • Stay informed on new regulatory updates that affect QC.
  • Prepare for audits and communicate with auditors and regulatory agencies.
  • Suggest and implement process improvements.
  • Support training and make sure the team follows compliance training.
  • Work closely with QA and other departments to solve compliance issues.
  • Provide training on GxP regulations and best practices.
  • Stay current with industry standards and regulations.
CDI

CDI

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  • Saint Kitts and Nevis +1
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Shift Manufacturing Engineer

CDI

This is some text inside of a div block.

Job Description:

  • Contribute to Life Science projects for Antaes Asia clients
  • Oversee the execution of manufacturing batches according to defined instructions, ensuring strict compliance with SOPs, training, and real-time monitoring of critical process steps for seamless operations.
  • Collaborate on the development, review, and optimization of batch and cleaning recipes within DCS systems such as DeltaV and POMS, including manual and ad-hoc documentation.
  • Lead or contribute to digitalization and continuous improvement initiatives aimed at enhancing process efficiency, reducing complexity, and supporting strategic site goals.
  • Support troubleshooting efforts during process deviations or equipment issues by coordinating timely corrective actions with cross-functional teams.
  • Provide training and guidance to chemical operators on operational best practices, equipment changes, OSW, and risk assessments.
  • Participate in the commissioning, qualification, and validation phases of capital projects to ensure smooth integration into routine operations.
  • Maintain compliance with environmental, health, and safety policies by participating in safety risk assessments and process hazard analysis as the operations representative.
  • Ensure documentation accuracy by proactively resolving batch record discrepancies, contributing to investigations, and supporting timely CAPA implementation.
  • Monitor shift deliverables, anticipate operational challenges, and ensure production timelines are met, highlighting potential delays to supervisors when necessary.
  • Uphold plant readiness standards at all times, ensuring the facility remains audit-ready and operationally sound
  • Contribute to the promotion of Antaes services on top of assistance provided to clients
This is some text inside of a div block.

Job Requirements:

  • Degree in Life Science, Chemical Engineering, Science or equivalent
  • At least 2 years of experience in working in a GMP manufacturing environment is preferred
  • Able to work comfortably in 12-hour rotating shift (Day/Night)
  • Strong process knowledge and interest to guide and mentor
  • High adaptability and ability to lead and work with cross functional team
  • Strong communication and writing skills
  • Excellent communication skills, both written and verbal
Our positions are open to people who have been recognized as disabled workers. T&S Group promotes diversity and equality in the workplace. All qualified M/F candidates are considered for employment on an equal basis. #J-18808-Ljbffr

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