Production Staff - Medical Device Manufacturing Industry

Key Responsibilities

• Operate production machinery and equipment in accordance with approved Standard Operating Procedures (SOP).

• Perform product assembly processes based on technical drawings and work instructions.

• Ensure all production activities comply with Good Manufacturing Practice (GMP) and applicable quality standards.

• Conduct in-process inspections to ensure products meet defined specifications.

• Complete and maintain accurate production records and batch documentation.

• Maintain cleanliness, orderliness, and hygiene standards within the production and cleanroom areas.

• Report any deviations, non-conformities, or equipment malfunctions to the Production Supervisor.

• Support continuous improvement initiatives to enhance productivity, efficiency, and product quality.

• Adhere to workplace safety regulations and company policies at all times.

Qualifications

• Minimum Bachelor’s Degree (S1) in Chemical Engineering, Pharmacy, Biomedical Engineering, or related disciplines.

• Fresh graduates are encouraged to apply.

• Basic understanding of manufacturing processes and quality systems.

• Familiarity with Good Manufacturing Practice (GMP); knowledge of ISO 13485 is an advantage.

• Good documentation skills with strong attention to detail.

• Proficient in basic computer applications (Microsoft Office).

• Able to work effectively both independently and as part of a team.

• Willing to work in shifts if required.

• Fit and able to work in a controlled/cleanroom environment.

• Non-smoker (mandatory requirement).