Associate Process Engineer

Merit Medical Systems; Singapore; On-site; SGD 50,000 - 70,000; Full time

Job summary

Merit Medical Systems in Singapore is looking for an Associate Process Engineer to lead the process engineering team and ensure optimal machine uptime for production. You will be responsible for managing automation projects and leading engineering efforts aimed at improving yield, output, and quality.

The ideal candidate should have a minimum diploma in mechanical or electrical engineering with 3 to 5 years of experience in a manufacturing environment, preferably in the medical device or pharmaceutical industries. Strong familiarity with assembly processes and project management skills are essential.

Qualifications

• Minimum Diploma in mechanical/electrical with 3 to 5 years' experience in manufacturing process environment.
• Familiarization with assembly process, automation, tooling & fixtures designs.
• Working knowledge on cGMP manufacturing setting.

Responsibilities

• Lead Process engineering team for production objectives.
• Manage equipment maintenance and upgrades.
• Ensure compliance with quality policies and safety regulations.

Skills

Project management

Validation experience

Assembly process knowledge

Automation

Education

Diploma in mechanical/electrical

Job description

## Associate Process EngineerApplylocations: Singapore, Singaporetime type: Full timeposted on: Posted Todaytime left to apply: End Date: 16 September 2026 (30+ days left to apply)job requisition id: JR115598**Work Shift:**NIGHT**Work Schedule:****Why Merit?**At Merit Medical, our mission is to create innovative medical devices that improve lives. Our goal is to hire and develop people who want to build something special through hard work, team effort, and commitment. Together, we are making a difference in the lives of patients around the world.**JOB FUNCTIONS*** Lead Process engineering team to ensure seamless support to the value stream in meeting their respective objectives.* To lead the engineering initiatives to ensure optimal machine up-time is available for production.* Lead automation projects including equipment upgrade and assembly process productivity initiatives.* Lead and manage engineering efforts that are needed to improve yield, output and quality. Ensure the PM and calibration activities are done as per the schedule* Provide engineering expertise in achieving equipment reliability and process capability to achieve desired OEE metrics.* Manage optimal deployment of engineering resources and efficient use of the budget.* Lead the validation activities and projects by providing necessary engineering support and resources.* Plan and execute equipment maintenance/ upgrade by embarking on structured equipment risk assessment and prioritization.* Work with cross functional teams (Tech team) to achieve equipment effectiveness through total productive maintenance program and process capability through process enhancement and validation.* Work with team to execute continuous improvement projects to minimize operational disruption and achieve productivity savings.* Accountable for capital expenditure initiation and spending control* Ensure compliance with quality policies, procedures, and practices through appropriate communication, training, and education.* Maintain a safe and healthy work environment by complying with all related safety regulations and environmental policies in the Company.**INTERACTION****Internal parties** - Required to communicate effectively with all levels of associates.**External parties** - Required to communicate with other Merit Plants, Corporate/Regional/Businesses, suppliers, subcontractors and government agencies as and when required.**JOB SPECIFICATIONS****Education**Minimum Diploma in mechanical/electrical with 3 to 5 years' experience in manufacturing process environment. Preferably from Medical device/Pharmaceutical industries.**Relevant Experience*** Familiarization with assembly process, automation, tooling & fixtures designs are desired.* Experience in project management; as well as validation are preferred.* Working knowledge on cGMP manufacturing setting**Others*** Technical specialization in assembly/ automation process preferred.* Knowledge of U.S FDA regulations, the Medical Devices Regulation (2017/745), ISO 13485 Quality System Standard, ISO 14971 Risk Management are added advantage.To see more on our culture, go to www.merit.com/careers.