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Amgen Associate Mfg I in Singapore, Singapore

GCF Grade Level: 3 Site: Amgen Singapore Manufacturing (ASM)

Role Description:

Amgen’s Manufacturing department is looking for talented and dedicated individuals for a full time position.

The position will be with Amgen’s Singapore facility focused on synthetic API manufacturing.

Amgen’s state-of-the-art manufacturing and process development capabilities help us realize the potential of our pipeline for patients around the world. This Amgen facility is capable of manufacturing commercial drug substance, vital to our supply chain.

The Associate Manufacturing will be responsible for manufacturing synthetic API’s and executing manufacturing duties. Under general supervision, they will 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. The Associate Manufacturing will perform and monitor critical processes, execute routine validation protocols, and prepare documents such as Batch Records, SOPs and technical reports. They will perform basic troubleshooting and assist in the review of documentation for assigned functions. The Associate Manufacturing may participate on cross-functional teams, have the responsibility of owning NC/CAPAs and change controls, and may identify, recommend and implement improvements related to routine functions. Further, the Associate Manufacturing will ensure that operations are conducted in a safe and compliant manner.

Education / Licenses

  • Bachelor’s degree OR

  • Associate’s degree and 4 years of directly related experience OR

  • High school diploma / GED and 6 years of directly related experience

Competencies and skills:

Fluency in written and spoken English

Experience and basic troubleshooting skills with process equipment

Ability to understand, apply and evaluate basic chemistry, biology and physical principles

  • Ability to adhere to written procedures and safety guidelines

  • Ability to interpret and apply Good ManufacturingPractice (GMP) knowledge

  • Ability to organize work,handle multiple priorities and meet deadlines

  • Demonstrated written and oral communication skills

  • Technical writing capabilities

  • Problem solving skills

  • Proficient presentation and facilitation skills

  • Mechanical ability/expertise

  • Understanding of analytical methods

  • Ability and willingness to work any shift in support of operations that may include 24/7 in a team environment.