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Engineering Manager

CLEARLAB SG PTE. LTD.

Singapore

On-site

SGD 80,000 - 110,000

Full time

2 days ago
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Job summary

A leading medical device manufacturer in Singapore is seeking an experienced engineer to lead initiatives focusing on equipment performance and automation design. The ideal candidate should possess a degree in engineering and have over 10 years of experience in high-volume manufacturing, including strong leadership skills and in-depth knowledge of safety regulations. Expertise in SolidWorks and PLC systems is essential. This is an opportunity to drive projects that ensure continuous improvement and compliance with industry standards.

Qualifications

  • Minimum of 10 years of experience in a high-volume manufacturing environment.
  • At least 5 years leading complex, technology-driven projects.
  • Hands-on experience in automation machine design.

Responsibilities

  • Ensure Overall Equipment Effectiveness (OEE) meets performance levels.
  • Drive improvement initiatives to achieve cost savings.
  • Oversee facilities maintenance activities to ensure operations.

Skills

Leadership
FDA
Workplace Safety
ISO
Capital Equipment
PLC
CNC
Machining
Engineering Design
PLC Programming
Concept Development
Manufacturing
Commissioning
Software Development
People Management

Education

Bachelor’s degree or higher in Engineering

Tools

SolidWorks
PLC Programming platforms
Job description
Roles & Responsibilities
  • Ensure Overall Equipment Effectiveness (OEE) meets targeted performance level.
  • Drive the Engineering team in executing improvement initiatives to achieve cost savings and productivity targets.
  • Review equipment designs and processes to ensure compliance with safety standards.
  • Oversee and manage facilities maintenance activities and troubleshoot equipment issues to ensure uninterrupted operations.
  • Identify and recommend cost‑saving initiatives to reduce operational expenses.
  • Provide leadership and direction to Technical, Moulding, Equipment, Process Engineers, as well as Workplace Safety functions.
  • Lead and take ownership of in‑house and automation machines, including software development, covering concept development, design, budgeting, testing, commissioning, upgrades, and continuous improvement.
  • Monitor and ensure environmental validation activities comply with ISO standards, FDA regulations, and other applicable regulatory requirements.
Requirements
  • Bachelor’s degree or higher in a relevant Engineering discipline.
  • Minimum of 10 years of experience in a high‑volume manufacturing environment.
  • At least 5 years of proven experience leading and delivering complex, technology‑driven projects.
  • Hands‑on experience in automation machine design and PLC programming, with practical knowledge of machining processes including CNC, conventional milling, lathe, and grinding.
  • Strong understanding of risk and hazard assessment methodologies for chemical and / or medical device manufacturing environments.
  • Knowledge of legal and safety regulations related to the installation of heavy capital equipment and permit‑to‑work requirements in a medical device manufacturing setting.
  • Experience in conceptual, basic, and detailed engineering design, as well as project management.
  • Demonstrated leadership capability with strong collaborative and people‑management skills.
  • Excellent verbal and written communication skills.
  • Ability to perform effectively in a fast‑paced and dynamic work environment.
  • Proficient in SolidWorks for mechanical design.
  • Basic knowledge of PLC and HMI programming platforms including Allen‑Bradley, Mitsubishi, Keyence, Omron, and similar systems desired.

Tell employers what skills you have

  • Leadership
  • FDA
  • Workplace Safety
  • ISO
  • Capital Equipment
  • PLC
  • CNC
  • Machining
  • Engineering Design
  • PLC Programming
  • Concept Development
  • Manufacturing
  • Commissioning
  • Software Development
  • People Management
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