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Associate Manufacturing I

Amgen

Associate Manufacturing I

full-timePosted: Jul 29, 2026Updated: Aug 28, 2026Singapore Manufacturing - Tuas

Job Description

Career CategoryManufacturingJob DescriptionAssociate Manufacturing I Amgen Singapore ManufacturingHOW MIGHT YOU DEFY IMAGINATION?Amgen is one of the world’s leading independent biotechnology companies. For over 4 decades, Amgen has pioneered biotechnology breakthroughs, to bring state-of-the-art medicines from laboratory to the patient. Amgen has not only discovered and developed innovative human therapeutics, but has invested in cutting edge manufacturing capability and support services to deliver these exciting therapies to medical teams around the world. Japan and Asia Pacific (JAPAC) is the fastest growing region in Amgen. Now we are hiring an Associate Manufacturing I in Amgen Singapore Manufacturing. LiveWhat you will doAfter training is completed, this position will be required to work on a rotational overnight shift. Amgen’s state-of-the-art biotechnology manufacturing and process development capabilities help us realize the potential of our pipeline for patients around the world. The new Amgen facility is capable of manufacturing both clinical and commercial products.Support daily production requirements throughout the facilityOperations, maintenance and analytical testing will be performed according to Standard Operating Procedures (SOPs) and Job Plans, as requiredPerform and monitor critical processes, execute routine validation protocols, and prepare documents such as Batch Records, SOPs and technical reportsPerform basic troubleshooting and assist in the review of documentation for assigned functionsMay participate on cross-functional teamsResponsible for owning NC/CAPAsMay identify, recommend and implement improvements related to routine functionsAbility to apply ergonomics principles to the work environment and maintain focus during repetitious tasks over the course of a shiftSome 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 durationAbility to perform manual lifting, carrying, pushing and/or pulling items with an average weight of <12kg on production floor with or without the assistant of mechanical aidAll listed tasks and responsibilities are deemed as essential functions to this position; however, business conditions may require reasonable accommodation for additional tasks and responsibilities. WinWhat we expect of youQualificationsBachelor’s Degree in Science or Engineering and 2 years of directly related experience ORAssociate’s Degree in Science or Engineering and 4 years of directly related experience ORHigh School Diploma in Science or Engineering / GED and 6 years of directly related experience1 year of experience in regulated environmentExperience and basic troubleshooting skills with laboratory and process equipmentExperience with Emerson DeltaV, OSI PI, LIMS, TrackWiseAbility to understand, apply and evaluate basic chemistry, biology and physical principlesRegulatory knowledgeAbility to adhere to regulatory requirements, written procedures and safety guidelinesAbility to evaluate documentation/data according to company and regulatory guidelinesAbility to interact with inspectors (internal and external)Ability to interpret and apply Good Manufacturing Practice (GMP) knowledgeBasic statistical mathematical skillsAbility to organize work, handle multiple priorities and meet deadlinesTechnical writing capabilitiesProficient presentation and facilitation skillsDetail oriented as well as flexible and adaptable to changing priorities and requirementsAbility to perform computer operations, such as ability to navigate in MS Office and complete Computer Based Training (CBT)Mechanical ability/expertiseUnderstanding of analytical methodsAbility 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. ThriveWhat you can expect of usAs 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.Vast opportunities to learn and move up and across our global organizationDiverse and inclusive community of belonging, where teammates are empowered to bring ideas to the table and actGenerous Total Rewards Plan comprising health, finance and wealth, work/life balance, and career benefits Apply a career that defies imaginationIn our quest to serve patients above all else, Amgen is the first to imagine, and the last to doubt. Join us.careers.amgen.com Equal Opportunity StatementAmgen 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. .

Locations

  • Singapore Manufacturing - Tuas

Skills Required

  • regulated environmentintermediate
  • Emerson DeltaVintermediate

Required Qualifications

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

Responsibilities

  • After training is completed, this position will be required to work on a rotational overnight shift. Amgen’s state-of-the-art biotechnology manufacturing and process development capabilities help us realize the potential of our pipeline for patients around the world. The new Amgen facility is capable of manufacturing both clinical and commercial products.
  • 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 <12kg on production floor with or without the assistant of mechanical aid
  • 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.

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