Specialist Mfg I

Amgen; Singapore; On-site; SGD 90,000 - 120,000; Full time

Job summary

Amgen Singapore seeks a Manufacturing Specialist to drive New Product Introduction and equipment introductions, coordinating across Manufacturing, QA, Supply Chain and Engineering. You will manage complex cross‑functional projects, develop schedules, and ensure documentation readiness for new products.

With strong leadership and communication, you will help drive productivity, digital tool adoption, and regulatory readiness while aligning with site budgets and strategic goals.

Qualifications

• Must have advanced degree or equivalent GMP experience.
• Demonstrated ability to lead and collaborate with cross‑functional teams.
• Strong communication, analytical thinking, and project management skills.
• Knowledge of facility and manufacturing processes and related systems.

Responsibilities

• Lead New Product Introduction (NPI) readiness with cross‑functional teams.
• Manage site projects and drive productivity/continuous improvements.
• Develop schedules for NPI/operational readiness and budget adherence.
• Ensure readiness of manufacturing documents/systems (SOP, batch records, BOM).
• Act as SME and support regulatory inspections for NPI related activities.
• Lead New Equipment/Technology Introduction projects and digital tooling.

Skills

Leadership

Communication

Analytical thinking

Project management

Change management

Education

Doctorate Degree

Master’s degree in Engineering/Science and 2 years experience

Bachelor’s degree in Engineering/Science and 4 years experience

Diploma in Engineering/Science and 8 years experience

Tools

MS Project

MS Excel

SAP

PI-Vision

Smartsheet

Spotfire

Job description

Career Category

Manufacturing

Job Description

Join Amgen's Mission to Serve Patients

At Amgen, our shared mission to serve patients living with serious illnesses drives everything we do. Every team member plays an important role in helping advance science and deliver medicines that make a meaningful difference for patients around the world.

Amgen fights the world's toughest diseases by harnessing the best of biology and technology. We draw on our scientific expertise to push beyond what is known today and help people live longer, fuller lives.

If you are energized by collaboration, continuous learning, and meaningful work, we invite you to join our team and help make an impact.

Specialist Manufacturing I

What you will do

Amgen has built a next generation biologics facility in Singapore as part of its global expansion strategy. We are seeking to appoint a well-qualified and experienced individual to assume the role of Manufacturing Specialist. With minimal direction or supervision, the Manufacturing Specialist will be the primary contact representing manufacturing as part of New Product/Technology Introduction. This role will also offer the opportunity to manage manufacturing related projects, drive productivity/continuous improvement initiatives, manage the site project prioritization process, as well as engaging management to develop, manage and ensure adherence to department financial budgets.

Responsibilities

New Product Introduction (NPI)

• Lead manufacturing to support site/facility fit assessments for new product


• Represent ASM in Digital Tech Transfer (DTT) initiatives


• Identify and drive improvements in NPI workflow


• Serve as NPI lead and responsible for cross‑functional NPI readiness (Manufacturing/Supply chain/Engineering/Automation//EHS/Validation) during New Product Introduction


• Develop and manage schedule for NPI/operational readiness. Ensure adherence to committed schedule/budget


• Responsible for readiness of manufacturing documents/systems to support new product introduction, including but not limited to SOP, SUD, batch records, BOM


• Manage and serve as Subject Matter Expert (SME) during regulatory inspections for NPI related change controls, deviations/investigations, corrective/preventative actions

New Equipment/Technology Introduction

• Project lead for site projects impacting manufacturing (including change control ownership)


• Lead cross‑function and complex projects using project management skills


• Develop project deliverables, schedules and ensure adherence by cross‑functional team


• Actively engage networks, other Amgen sites and technology providers to identify potential advancement in technologies


• Support development of business cases/feasibility assessments for new equipment/technology introduction


• Provide user inputs during development of URS, commissioning, qualification protocols


• Develop and lead wet tests when required during new process equipment or product introduction

Productivity/Continuous Improvements

• Responsible for manufacturing productivity targets and track timely completion of initiatives to achieve productivity savings


• Support continuous improvement/productivity initiatives when needed (including change control ownership for improvement projects)


• Support manufacturing for EIO/OIA awards submissions


• Identify and/or implement transformational changes to current business processes/systems, specifically related to rapid NPI and high run rate production (run rate assessment)


• Work with cross functional teams to value stream, identify bottlenecks and eliminate waste

Digitalization

• Drive digital transformation initiatives within manufacturing by developing and implementing digital tools, dashboards, and workflow solutions that enhance project visibility, standardize processes, and improve cross‑functional collaboration and execution efficiency


• Seek technological, automation or digitalization advancement to improve business workflows

Finance

• Responsible for manufacturing budget development, management, and review


• Support manufacturing management on requests related to finance


• Support purchase requisition transactions in SAP

What we expect of you

• Doctorate Degree


• Master’s degree in Engineering/Science and 2 years of experience in pharmaceutical company or GMP environment OR


• Bachelor’s degree in Engineering/Science and 4 years of experience in pharmaceutical company or GMP environment OR


• Diploma in Engineering/Science, and 8 years of experience in pharmaceutical company OR GMP environment


• Demonstrated ability to lead/work well with teams, open to changes and new ideas


• Strong communication skills - ability to lead meetings and communicate effectively


• Strong analytical and critical thinking capability – ability to respond to changes, gather required data, evaluate options, and communicate analysis recommendations to facilitate decision making


• Attention to details, strong organizational/project management skills and error‑proofing habits


• Knowledge of facility and manufacturing processes


• Knowledge of tools and systems (MS Project, MS Excel, SAP, PI‑Vision, Smartsheet, Spotfire)


• Ability to create and standardize business/work processes


• Ability to coach, train and develop manufacturing associates

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

As we work to develop medicines for patients, we also invest in our people. Through competitive benefits, development opportunities, and a collaborative culture, we'll support your growth both professionally and personally.

About

As an organization dedicated to improving the quality of life for people around the world, Amgen fosters an inclusive environment of diverse, ethical, committed and highly accomplished people who respect each other and live the Amgen values as we continue advancing science to serve patients. Together, we compete in the fight against serious disease.

Amgen is an Equal Opportunity Employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability status, or any other basis protected by applicable law.

We will ensure that individuals with disabilities are provided 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 accommodation.