Associate Manufacturing I

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

Career Category

Manufacturing

Job Description

Associate Manufacturing I

Amgen Singapore Manufacturing

What you will do

• Support daily production requirements throughout the facility
• Operations, maintenance and analytical testing will be performed according to Standard Operating Procedures (SOPs) and Job Plans, as required
• Perform and monitor critical processes, execute routine validation protocols, and prepare documents such as Batch Records, SOPs and technical reports
• Perform basic troubleshooting and assist in the review of documentation for assigned functions
• May participate on cross-functional teams
• Responsible for owning NC/CAPAs
• May identify, recommend and implement improvements related to routine functions
• Ability to apply ergonomics principles to the work environment and maintain focus during repetitious tasks over the course of a shift
• Some tasks performed consist of occasional strenuous, repetitive movements involving the following bending, hand/wrist twisting and reaching out for height on a daily basis, as well as standing for the long hours on the production floor in accordance to shift duration
• Ability to perform manual lifting, carrying, pushing and/or pulling items with an average weight of
• All listed tasks and responsibilities are deemed as essential functions to this position; however, business conditions may require reasonable accommodation for additional tasks and responsibilities.

What we expect of you

Qualifications

• Bachelor’s Degree in Science or Engineering and 2 years of directly related experience OR
• Associate’s Degree in Science or Engineering and 4 years of directly related experience OR
• High School Diploma in Science or Engineering / GED and 6 years of directly related experience
• 1 year of experience in regulated environment
• Experience and basic troubleshooting skills with laboratory and process equipment
• Experience with Emerson DeltaV, OSI PI, LIMS, TrackWise
• Ability to understand, apply and evaluate basic chemistry, biology and physical principles
• Regulatory knowledge
• Ability to adhere to regulatory requirements, written procedures and safety guidelines
• Ability to evaluate documentation/data according to company and regulatory guidelines
• Ability to interact with inspectors (internal and external)
• Ability to interpret and apply Good Manufacturing Practice (GMP) knowledge
• Basic statistical mathematical skills
• Ability to organize work, handle multiple priorities and meet deadlines
• Technical writing capabilities
• Proficient presentation and facilitation skills
• Detail oriented as well as flexible and adaptable to changing priorities and requirements
• Ability to perform computer operations, such as ability to navigate in MS Office and complete Computer Based Training (CBT)
• Mechanical ability/expertise
• Understanding of analytical methods
• Ability and willingness to work any shift in support of operations that may include 24/7

Your selection for this role will be subject to fulfilling the medical requirements of this job scope. If so, you will be informed of the medical check(s) that you may need to undergo. All medical related expenses incurred from this medical check shall be borne by the company.

What you can expect of us

• Vast opportunities to learn and move up and across our global organization
• Diverse and inclusive community of belonging, where teammates are empowered to bring ideas to the table and act
• Generous Total Rewards Plan comprising health, finance and wealth, work/life balance, and career benefits

As we work to develop treatments that take care of others, so we work to care for our teammates’ professional and personal growth and well-being.

Apply a career that defies imagination

careers.amgen.com

Equal Opportunity Statement

Amgen is an Equal Opportunity employer and will consider you without regard to your race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, or disability status.

We will ensure that individuals with disabilities are provided a reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request an accommodation.