Singapore Job Openings
Amgen
Specialist QA I
Singapore
November 5, 2024
Specialist Quality Assurance
Amgen Singapore Manufacturing
HOW 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 Specialist Quality Assurance in Amgen Singapore Manufacturing.
Responsible for providing oversight and leadership for quality systems execution and operations support, the Specialist Quality Assurance will support Facilities & Engineering (F&E), Quality Control (QC), Supply Chain, Digital Technology & Innovation (DTI), Process Development (PD) or Validation (all non-direct manufacturing areas) for the Biologics and Synthetic Manufacturing plants.
Main Responsibilities:
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.
In our quest to serve patients above all else, Amgen is the first to imagine, and the last to doubt. Join us.
careers.amgen.com
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.
Amgen Singapore Manufacturing
HOW 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 Specialist Quality Assurance in Amgen Singapore Manufacturing.
Live
What you will doResponsible for providing oversight and leadership for quality systems execution and operations support, the Specialist Quality Assurance will support Facilities & Engineering (F&E), Quality Control (QC), Supply Chain, Digital Technology & Innovation (DTI), Process Development (PD) or Validation (all non-direct manufacturing areas) for the Biologics and Synthetic Manufacturing plants.
Main Responsibilities:
- Provide quality oversight to plant operations, ensuring appropriate application and execution of GMP compliance requirements and Amgen Quality Management System in plant operations through phases of commissioning, process qualification, regulatory approval and market supply
- Support routine GMP documentation review activities (e.g. SOPs, logbooks, work orders, validation documents, periodic reviews) and ensure key performance indicator met targeted metrics
- Co-lead and support the deployment of Amgen quality systems, including management review, validation, deviation, change control and CAPA and ensure that the systems are managed in compliance with c GMP expectations
- Review and approve deviations, investigations, unexpected result investigations, change controls, and other quality records (with focus on highly complex records). Participate in and lead complex root cause investigations for deviations
- Lead Quality Assurance support in New Product Introduction (NPI) team
- Coach site Quality Assurance professionals on resolution of complex problems
- Participate in regulatory inspections, and interact directly with regulatory inspectors
- Supporting other Quality Assurance initiatives/activities such as continuous improvement projects, supplier quality, stability program and product quality review.
Qualifications
- Doctorate degree in Science OR
- Master’s degree and 4 years of directly related experience OR
- Bachelor’s degree and 6 years of directly related experience OR
- Diploma and 8 years of directly related experience
- Preferred 8 years related work experience (manufacturing, process development, or quality assurance) in the pharmaceutical / biologics industry with progressively increasing responsibility and demonstrated experience in project management, quality assurance, and quality systems.
- Direct experience with bulk manufacturing of biopharmaceuticals/API preferred.
- Demonstrated proficiency of written and verbal communication skills (including technical writing and presentations) with ability to communicate and collaborate effectively with technical and senior management staff.
- Experience with regulatory audits and inspections
- Problem solving skills with the ability to apply logic and assess data to reach decisions and solutions related to compliance and product quality.
Thrive
What 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 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
Apply now
for a career that defies imagination
In 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 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.
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