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Thermo Fisher Scientific
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Director, Manufacturing Engineering .

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  • Posted 14 days ago
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20-25 Years

Biotechnology

Job Description

  • Lead GMP Plant Site Engineering and Expansion Projects, including recruiting, training, and developing the team.
  • Direct operations, maintenance, Commissioning, Qualification and Validation (CQV), spare parts management, planned shutdown and calibrations, ensuring uninterrupted supply of process equipment, clean utilities and black utilities, facilities.
  • Develop and lead the engineering budget, prioritising resources to meet compliance and business objectives.
  • Collaborate with Thermo Fisher SMEs to implement corporate guidelines and share good practices across sites.
  • Guide staff in handling equipment files, technical materials, fixed assets, contracts, energy, and engineering per GMP standards.
  • Establish and lead all aspects of calibration systems for measuring instruments and ensure compliance with GMP requirements.
  • Coordinate internal and external audits, inspections, and quality system implementation.
  • Handle and report equipment accidents, participate in investigations, and recommend corrective actions.
  • Lead the maintenance team's activities, including inspections, verification, and corrective actions.
  • Lead hiring, onboarding, development, mentoring, and succession planning for engineering staff.
  • Ensure the GMP project aligns with the design basis through collaboration with the EPCM firm, enabling seamless commissioning, qualification, and validation (CQV).
  • Coordinate environmental, quality, and safety (EHS) compliance during construction and facility engineering to prevent production safety incidents.
  • Address safety hazards, equipment selection, configuration, and energy efficiency in design reviews.
  • Maintain effective communication with the construction team to monitor progress and lead plant facilities during and post-construction.

Key Requirements/Qualifications

Education:

  • Bachelor's/ Master's degree or equivalent experience in Engineering or a related field required.

Experience:

  • 20 years of Good Manufacturing Practice (GMP) experience in the pharmaceutical industry. Strong understanding of cGMPs and Engineering compliance requirement for Singapore HSA, EMA and US FDA, customer audits. Master certain technical knowledge in HAVC, Utility and Process Equipment, Water systems, Electrical and Automation etc.

Proficiencies:

  • Expertise is internal, corporate, customer and regulatory auditing.
  • Advanced presentation skills for senior executive/board-level audiences.
  • Outstanding skill in establishing positive relationships with teams from different functions, collaborators, and SMEs.
  • Excellence in driving functional, technical, and operational performance.
  • Proficient in solving complex problems, proactive and assertive approach.
  • Agile and resilient in fast-paced settings
  • Effective conflict resolution skills.

Date Posted: 27/05/2025

Job ID: 115373405

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About Company

Thermo Fisher Scientific is a leading global biotechnology company that provides innovative solutions for scientific research, healthcare, and diagnostics. Headquartered in Waltham, Massachusetts, the company offers a wide range of products and services, including laboratory equipment, analytical instruments, reagents, and software. Thermo Fisher supports customers in accelerating life sciences research, solving complex analytical challenges, and improving patient diagnostics and therapies.

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Last Updated: 28-09-2025 03:05:07 PM
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