Job Description
**Job Description Summary**
**Job Description**
+ Support the team in automation, system control, MES and equipment engineering functions.
+ Participate and support projects identified in the plant priority matrix and support strategic initiatives.
+ Prepare test procedures, work instruction and validation protocol.
+ Prepare engineering reports, presentations, Standard Operating Procedures (SOPs), and documentation following medical device regulatory standards.
+ Support day‑to‑day tasks to ensure smooth manufacturing operations in a cleanroom or controlled environment.
+ Execute process validation.
+ Perform any other tasks as assigned
**Job Requirements:**
+ Currently pursuing a Bachelor’s degree in Mechanical/Electrical / Electronics /Industrial & Systems Engineering related fields
+ Strong interest in Medtech manufacturing and process engineering.
+ Good analytical, problem‑solving, and communication skills.
+ Comfortable working in a regulated and clean room environment – training will be provided.
+ Able to commit to at least 3–6 months of internship.
+ Proficient in MS Office; familiarity with CAD, statistical tools, or programming (Python/MATLAB) is a plus but not required.
Required Skills
Optional Skills
.
**Primary Work Location**
SGP Tuas - Tuas Plant
**Additional Locations**
**Work Shift**
Becton, Dickinson and Company is an Equal Opportunity/Affirmative Action Employer. We do not unlawfully discriminate on the basis of race, color, religion, age, sex, creed, national origin, ancestry, citizenship status, marital or domestic or civil union status, familial status, affectional or sexual orientation, gender identity or expression, genetics, disability, military eligibility or veteran status, or any other protected status.
**Job Description**
+ Support the team in automation, system control, MES and equipment engineering functions.
+ Participate and support projects identified in the plant priority matrix and support strategic initiatives.
+ Prepare test procedures, work instruction and validation protocol.
+ Prepare engineering reports, presentations, Standard Operating Procedures (SOPs), and documentation following medical device regulatory standards.
+ Support day‑to‑day tasks to ensure smooth manufacturing operations in a cleanroom or controlled environment.
+ Execute process validation.
+ Perform any other tasks as assigned
**Job Requirements:**
+ Currently pursuing a Bachelor’s degree in Mechanical/Electrical / Electronics /Industrial & Systems Engineering related fields
+ Strong interest in Medtech manufacturing and process engineering.
+ Good analytical, problem‑solving, and communication skills.
+ Comfortable working in a regulated and clean room environment – training will be provided.
+ Able to commit to at least 3–6 months of internship.
+ Proficient in MS Office; familiarity with CAD, statistical tools, or programming (Python/MATLAB) is a plus but not required.
Required Skills
Optional Skills
.
**Primary Work Location**
SGP Tuas - Tuas Plant
**Additional Locations**
**Work Shift**
Becton, Dickinson and Company is an Equal Opportunity/Affirmative Action Employer. We do not unlawfully discriminate on the basis of race, color, religion, age, sex, creed, national origin, ancestry, citizenship status, marital or domestic or civil union status, familial status, affectional or sexual orientation, gender identity or expression, genetics, disability, military eligibility or veteran status, or any other protected status.
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