Amgen Singapore Manufacturing Pte. Ltd Posted October 16, 2026

Engineer I – Process Engineering (Biologics)

Singapore Manufacturing, Singapore Full time
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Amgen Singapore Manufacturing Pte. Ltd is the source of truth for this posting and owns the application process. We surface normalized context and market comparison you won't find on the original listing.

About this opportunity

Career Category

Engineering

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.

Engineer I – Process Engineering (Biologics Process Equipment)

What you will do

Reporting to the Senior Engineer/ Team Lead/ Manager, this Process Engineer position is primarily responsible for providing operation and New Product Introduction (NPI) support for ASM1 Process Equipment. This role will serve as a system owner for an assigned portfolio of process-support equipment in ASM for the Process Engineering team in the Facilities & Engineering department, which collaborates with Engineering Support and Maintenance team, to deliver uninterrupted plant operations. This function operates in conjunction with the manufacturing team to ensure the appropriate and timely completion of cGMP maintenance activities with minimum disruption to manufacturing. The scope covers both upstream and downstream process areas, including cell culture and harvest filtration, as well as viral inactivation, purification and drug substance bulk fill.

This role will assume the system owner role, taking ownership of various process equipment that are used for manufacturing process or supporting manufacturing process. It will be the technical resource or equipment subject matter expert (SME) for assigned systems to ensure that the equipment operates, function and performs as intended and is maintained in a validated state. Scope of work includes managing, planning and implementation of changes, driving deviation investigations, resolving equipment related process interruptions and development of equipment maintenance program.

This role requires highly cross functional interactions with key site functions to ensure success in production and release performance. Individual must be able to effectively communicate and collaborate closely with the team members and various SME to ensure equipment are operational to sustain daily operations, resolve operation challenges and implement effective measures to address the challenges to ensure without compromising on safety and compliance. It offers a broad exposure to all key aspects of GMP manufacturing as well as tactical and strategic teamwork within the extended worldwide engineering network.

In addition, it will also provide advance technical support to ensure the readiness of the equipment/ facility for successful introduction of new products in ASM. The role will be a liaison between corporate engineering and site operations in the design and implementation of new equipment and/or equipment modifications.

Main Responsibilities :

Daily Operations

Own the day-to-day engineering support, equipment performance, validated state, maintenance plans and lifecycle actions for an assigned portfolio of ASM1 Process Equipment.

Present equipment qualification and equipment related investigations and quality management system records in all site regulatory inspections

Subject matter expert for process equipment performance and operation to ensure safety, compliance and sustained operation

Effectively communicate and collaborate with cross function stakeholders to address operational challenges and concerns to ensure sustained operation and minimal interruptions to operations activities.

Lead equipment investigations of moderate complexity, identify root causes, assess technical options, recommend corrective and preventive actions, and drive approved actions to closure. Effectively communicate to the customers on the subsequent plans, short term, and long-term mitigating actions.

Collaborate closely with cross functional SME to implement effective corrective, preventive action and improvements to eliminate or mitigate future recurrence.

Ensure operation continuity through asset lifecycle management planning, assess and identify impact to safety, compliance, operational schedule and cost.

Perform periodic review and maintain process equipment in validated state.

Perform assessment for equipment during new product introduction, change controls and other qualifications activities to ensure equipment are in its validated state.

Accountable for deviation/change control associated to process equipment performance. Act as technical owner for assigned deviations and change controls, ensuring accurate technical assessment, timely execution and closure. Final approval remains with designated Engineering and Quality approvers.

Own defined equipment-readiness deliverables for NPI and site projects, including qualification support, punch-list closure, maintenance and spare-parts readiness, and system turnover

Provide technical guidance to Manufacturing, Maintenance, Quality and project teams for assigned equipment and coordinate implementation of agreed technical solutions.

Continuous improvements, Innovation and operational sustainability

Participate in related AMGEN network forums to determine innovative opportunities to improve reliability, efficiency, agility and differentiation.

Continuously improve business intelligence capabilities utilizing big data analysis tools to extract, analyze and trend performance data for predictive monitoring and troubleshooting.

Actively seek opportunities for continuous improvement to improve efficiencies and differentiation through flexible use of advance technologies and best industry practices.

Benchmark equipment performance (e.g., reliability, productivity) and determine improvement plans.

Build system and capabilities to drive improvements to equipment reliability and maintenance optimization

Periodically review and/or improve equipment safety, maintenance strategy, spare parts, and other continuous improvement opportunities to enhance reliability.

Design & Project Engineering:

Support the functional lead in providing ASM1 Process Equipment readiness support for NPI, GLAM and Site Projects for Process-Support Equipment Where appropriate, provide engineering advice to commissioning and qualification activities including FAT, SAT, automation checkouts, IQ, OQ, PQ, and asset/preventive maintenance/spare parts creation for new process equipment.

Participate in the system walk-down, ensure the closure of punch items and support the takeover of the system from the project team.

Develop technical solutions to technical problems of moderate complexity requiring analysis and engineering judgment.

Organization Leadership

Work in teams by educating customers on lesson learns, collaborate with customers managers to identify knowledge or trainings gaps.

Deliver strong result in the right way by consciously being a role model that ensure results are deliver without compromising on core AMGEN values.

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

Basic Qualifications

 

Master’s degree in Engineering OR

Bachelor’s degree in Engineering and 2 years of directly related experience OR

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

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

Preferred Qualifications

Able to work independently under general direction and independently manages familiar assignments, escalating novel or high-impact issues.

Experience in managing various stakeholders expectations related to process equipment in biopharmaceutical.

Good communications skills, both oral and written, including presentation skills.

Good interpersonal and facilitation skills necessary to forge consensus among competing client interests while ensuring objectives are met.

Strong analytical skills and knowledge of industry trends to identify potential improvement opportunities. Ability to combine technical problem-solving skills with business acumen to determine best business solution.

Problem solving skills require the application of scientific and engineering theory and calculations and creative skills in the development of hypotheses and approach.

Working knowledge of biopharmaceutical processes such as chromatography, buffer / media tanks, viral filtration, tangential flow filtration, inoculation, bioreactors, harvest, single use technologies and critical utilities is preferred.

Experience in validation processes such as generation/execution of Installation/Operation/Performance qualification documentation is preferred

Knowledge in Automation systems and processes such as RD’s, Delta-V,  BMS, ladder logic and PLC is preferred.

Demonstrated project management skills (schedule/cost development, facilitation, collaboration, basic project management, completion and follow-up) and application of concepts will be an advantage.

Flexibility to work off-hours.

Knowledge of Total Productive Maintenance, Reliability Centered Maintenance concepts is an added advantage.

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.

Apply now and help transform the lives of patients while transforming your career.

careers.amgen.com

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.

 

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Job details

Seniority
Not listed
Function
Manufacturing & CMC
Therapeutic area
Not listed
Location
Singapore Manufacturing, Singapore
Employment type
Full time

How this role compares

Computed from every other active Manufacturing & CMC role in our database, not just this employer's listings.

We currently track 3634 comparable Manufacturing & CMC roles across 172 biopharma companies.

3634Comparable roles tracked
3364Currently active
172Companies hiring similar roles
62Countries represented

Salary context

887 of 3634 peers report a salary range (USD, annualized)

Peers share this role's job function. This posting doesn't list a seniority level, so peers aren't narrowed by seniority either -- the range below may span more levels than usual.

This roleSubject Not listed on this posting
Highest disclosed · Head of Analytical Development · ModernaTX, Inc. $272,200/yr – $490,100/yr
Peer group range $0 – $381,150 (median $123,600)

Where these roles are based

Top locations among the 3634 comparable roles

United States1680
Germany244
India165
France148
Ireland125
China118

+ 56 more countries

Seniority mix

1607 of 3634 peers have a known seniority level

Senior416
Manager366
Intern/Fellow/Postdoc243
Associate157
Principal132
Director116
Associate Director115
Senior Director53
Executive/VP9

Therapeutic area mix

26 of 3634 peers have a known therapeutic area; the rest are genuinely unlabeled, not hidden

Vaccines & Infectious Disease17
Oncology3
Rare Disease3
Respiratory1
Dermatology & Aesthetics1
Immunology1

Similar opportunities

The closest matches from our peer group, ranked by how similar they are, not how well you'd qualify for them -- treat this as market context, not a guaranteed shortlist; a weak match is labeled as one below.

40%similar
Tuas, Singapore Senior
Same function Same country
40%similar
Glaxo Wellcome Manufacturing Pte Ltd Tuas, Singapore
Same function Same country
40%similar
Glaxo Wellcome Manufacturing Pte Ltd Tuas, Singapore
Same function Same country
40%similar
Glaxo Wellcome Manufacturing Pte Ltd Jurong, Singapore
Same function Same country
40%similar
Glaxo Wellcome Manufacturing Pte Ltd Jurong, Singapore
Same function Same country
40%similar
Glaxo Wellcome Manufacturing Pte Ltd Jurong, Singapore
Same function Same country

Notify me about similar jobs

Get an email when we spot other openings like this one – same job function, comparable seniority, roles you'd actually want to see.

Or follow a whole field: get every new Manufacturing & CMC job in Singapore, and choose locations and companies.

How we calculate "similar"

No black box, no LLM guesswork: a deterministic score built from four normalized attributes. Here's this role's own peer group at different match levels, so you can see the mechanism, not just the result.

Every comparison starts from the same 100-point budget: 25 for working in the same function, 40 for the same therapeutic area, 20 for the same or adjacent seniority, 15 for the same country. A dimension we can't confirm on both sides contributes nothing, never a guess, never a free pass.

40%
Senior/Biotechnologist (contracted till 30 Nov 2027)
· Tuas, Singapore · Senior
Function Therapeutic area Seniority Country
40%
Operations Technician (Pilot Plant) Trainee (Attach and Train Programme)
Glaxo Wellcome Manufacturing Pte Ltd · Jurong, Singapore · Seniority not listed
Function Therapeutic area Seniority Country
40%
Head of Engineering & Projects (Modulus)
Sanofi-Aventis Singapore Pte Ltd · City of Singapore, Singapore · Seniority not listed
Function Therapeutic area Seniority Country
40%
Associate Engineer
Sanofi-Aventis Singapore Pte Ltd · City of Singapore, Singapore · Associate
Function Therapeutic area Seniority Country
Unmatched or unknown dimensions score exactly the same: 0 points, never a partial guess. A role we know almost nothing about beyond its function bottoms out at 25%; it never inflates to 100% just because there's little to compare against. Seniority uses a defined ladder (Associate → Manager → Associate Director → Senior → Principal → Director → Senior Director → Executive/VP) so "Director" and "Senior Director" count as adjacent, but "Director" and "Executive/VP" do not.