Associate Process Engineer

• Lead Process engineering team to ensure seamless support to the value stream

• To lead the engineering initiatives to ensure optimal machine up-time is available

• Lead automation projects including equipment upgrade and assembly process

• 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

• Provide engineering expertise in achieving equipment reliability and process

• Manage optimal deployment of engineering resources and efficient use of the

• Lead the validation activities and projects by providing necessary engineering

• 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

• Work with team to execute continuous improvement projects to minimize

• Accountable for capital expenditure initiation and spending control
• Ensure compliance with quality policies, procedures, and practices through

• 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,

• Experience in project management; as well as validation

• Working knowledge on cGMP manufacturing setting

Others:

• Technical specialization in assembly/ automation

• Knowledge of U.S FDA regulations, the Medical Devices

Regulation (2017/745), ISO 13485 Quality System

Standard, ISO 14971 Risk Management are added

advantage.