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Shift Manufacturing Engineer

ANTAES ASIA PTE. LTD.

Singapore

On-site

SGD 60,000 - 80,000

Full time

2 days ago
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Job summary

A leading company in Life Sciences seeks a qualified individual to oversee and contribute to various projects in a manufacturing environment. This role involves ensuring compliance with SOPs, mentoring team members, and actively participating in process optimization initiatives. Candidates should have a relevant degree and experience in GMP settings, ready to thrive in a fast-paced, collaborative atmosphere.

Qualifications

  • At least 2 years experience in a GMP manufacturing environment preferred.
  • Able to work 12-hour rotating shifts.
  • Strong communication and writing skills.

Responsibilities

  • Oversee execution of manufacturing batches, ensuring compliance with SOPs.
  • Lead digitalization initiatives and support troubleshooting efforts.
  • Provide training to chemical operators on best practices.

Skills

Process knowledge
Adaptability
Communication

Education

Degree in Life Science or Chemical Engineering

Job description

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

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
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