Title: Production Technician, Ops, Jurong

Requisition ID: 73398

Date: Feb 24, 2026

Location:

Jurong, SG, SG

Department: Operations

Description:

At West, we’re a dedicated team that is connected by a purpose to improve patient lives that has been at the center of our Company for more than a century. Our story began when Herman O. West solved the problem of supplying penicillin in mass quantities to the US Government during World War 2. Through our work to deliver thousands of life-saving and life-enhancing injectable medicines to millions of patients daily, West’s indelible mark on the healthcare industry has just begun. A name started our story. How will yours help write our future?

There’s no better place to join an inclusive community of professionals with opportunities for lifelong learning, growth and development. Supported by benefit programs, we empower the physical, mental, emotional and financial health of our team members and their families.

We believe in giving back to help those in need in the communities where we live and work. And are equally committed to creating a healthier environment and planet through our sustainability efforts.

Job Summary

In this role, you will perform production process to deliver daily target and conduct training to enhance team's competency.

Essential Duties and Responsibilities

Must be certified in all 3 levels of products with full to deliver quality products
Execute production activities according to SOPs (Standard Operating Procedures), safety and quality requirements
Escalate safety hazards and potential safety risks via "See-Do-Say" submissions
Perform quality check and escalate any abnormality findings to Production Lead, Sr. Production Lead, Production Supervisor
Carry out material system transactions accurately
Carry out training activities and work closely with Training Lead in certifying team members
Perform 1st level trouble shooting, follow and execute OCAP (Out of Control Action Plan) procedures effectively
Suggest, participate and support Kaizen projects or any continuous improvement activities in the line
Escalate and provide feedback whenever there is an abnormality occurrence in the line

Education

Technical Certificate with 2 to 3 years of work experience

Work Experience

2 to 3 years prior work experience in Pharmaceutical or Medical Device Industries, or in another GMP setting preferred

Preferred Knowledge, Skills and Abilities

Knowledge of Good Manufacturing Practises (cGMP) requirements would be an advantage
Proficiency in Microsoft Office and job related computer applications
Support and contribute to Lean Sigma programs and activities towards delivery of the set target
Must be able to read and interpret documents such as safety rules, operating and maintenance instructions, procedure manuals and process specification, and ensure that all associated paperwork is completed accurately.
Must be willing to work in a controlled cleanroom environment, which involves the wearing of a gown, cap and relevant personal protective equipment.
Able to be aware of all relevant SOPs as per Company policy as they are related to the position covered by this Job Description
Self-motivated
Effective time management and multi-tasking skills
Excellent attention to detail
Trouble shooting skills
Goal/ results orientated
Good verbal reasoning, numerate ability
Proven ability to work in a team environment

Physical Requirements

Medium-Exerting up to 50lb/22kg of force occasionally and/or up to 20lbs/9kg of force frequently, and/or up to 10lbs/4kgs of force constantly to move objects.

West is an equal opportunity employer and we value diversity at our company. We do not discriminate on the basis of race, religion, color, national origin, gender, sex, gender identity, sexual orientation, age, marital status, veteran status, or disability status. If you have a special need that requires accommodation in order to apply to West, please send an email to Apply.Accommodation@westpharma.com. Where permitted by law, an offer of employment with West Pharmaceutical Services, or any of its subsidiary or affiliate companies, is contingent upon the satisfactory completion of background screening.