Manufacturing Associate I: Hands-On Operations & Quality

Biopharma Careers; Singapore; On-site; SGD 70,000 - 110,000; Full time

Job summary

Amgen Singapore Manufacturing is seeking an Associate Manufacturing I to support daily production activities and maintain compliance with SOPs and GMP requirements. The role involves execution of routine processes, documentation, and collaboration with cross-functional teams on process improvements.

The candidate should have a science or engineering background with related experience and be able to work across shifts in a regulated manufacturing environment.

Qualifications

• Bachelor’s Degree in Science or Engineering or related field plus relevant experience.
• Experience with laboratory and process equipment and basic troubleshooting.
• Regulatory knowledge and ability to adhere to SOPs and safety guidelines.
• Familiarity with GMP and Good Documentation Practices (GDP).

Responsibilities

• Support daily production requirements across the facility.
• Follow SOPs and Job Plans for operations, maintenance and analytics.
• Perform and monitor critical processes and validate routines.
• Prepare Batch Records, SOPs and technical reports.
• Possess basic troubleshooting and thorough documentation review skills.
• May participate on cross-functional teams and support continuous improvements.

Skills

Emerson DeltaV

OSI PI

LIMS

TrackWise

Regulatory knowledge

GMP knowledge

Technical writing

MS Office

Analytical testing

Problem solving

Quality systems

Education

Bachelor’s Degree in Science or Engineering

Associate’s Degree in Science or Engineering

High School Diploma in Science or Engineering / GED with 6 years related experience

1 year of experience in regulated environment

Tools

CBT

Job description

Amgen Singapore Manufacturing is seeking an Associate Manufacturing I to support daily production activities and maintain compliance with SOPs and GMP requirements. The role involves execution of routine processes, documentation, and collaboration with cross-functional teams on process improvements.

The candidate should have a science or engineering background with related experience and be able to work across shifts in a regulated manufacturing environment.