Explore industrial engineering jobs, focusing on optimizing complex systems and processes. These roles demand analytical skills and a knack for problem-solving, aiming to boost efficiency and productivity across various sectors. What Jobs are available for Industrial Engineering in Singapore?
Showing 93 Industrial Engineering jobs in Singapore
Industrial Engineering Manager
$120000 - $240000 Y
ASM Front-End Manufacturing Singapore Pte. Ltd.
Posted today
Job Viewed
Job Description
Step into a career with ASM, where cutting edge technology meets collaborative culture.
For over 55 years ASM has been ahead of what's next, at the forefront of innovation and what's technologically possible. With more than 4,500 ASMers representing 70 nationalities, our people and our advanced semiconductor devices are playing a crucial role in trends such as 5G, cloud computing, AI, and autonomous driving. But we're more than just a tech company. We value diversity, inclusion and sustainability as we strive to make a positive impact on the world. Our development programs help support your growth, shaping your future and pushing the boundaries of innovation to unleash potential.
Job's mission
This role is central to driving lean transformation and operational excellence at ASM's Singapore manufacturing site. As Industrial Engineering Manager, you'll lead initiatives that improve productivity, reduce costs, and embed a culture of continuous improvement. Your work will directly support ASM's mission to deliver cutting-edge semiconductor solutions through efficient and scalable operations.
What you will be working on
- Collaborate with Manufacturing Managers and team members to drive a strategy of continuous improvement, challenging the status quo
- Provide Lean development and training through Kaizen participation and visual controls.
- Optimize value streams by eliminating waste and improving flow across manufacturing.
- Design and own the Kaizen roadmap in partnership with Manufacturing Managers.
- Facilitate office and factory walkthroughs to identify improvement opportunities and escalate actions.
- Lead continuous improvement programs focused on labor hour reduction and cycle time improvements.
- Actively participate in Kaizen events as both team member and leader.
- Implement sustainable, results-oriented improvements—not just coach them.
- Collaborate with supervisors and cell leads to improve single-piece flow.
- Ensure Standard Work and transactional processes are created and followed.
- Use performance and KPI boards to track team progress and escalate support needs.
- Apply strong analytical skills and scientific problem-solving methods.
- Demonstrate deep understanding of assembly and production methods.
- Apply knowledge of Kanban and material replenishment systems.
- Manage Tool Room operations for Manufacturing.
- Collaborate across global teams and functions.
What we are looking for
- Bachelor's degree in Engineering, Science, or related discipline.
- Minimum 5 years' experience in Manufacturing, Process, Industrial Engineering, or Production Management.
- Proven track record in project management and implementation.
- Strong analytical and problem-solving skills.
- Excellent communication, leadership, and motivational abilities.
- Practitioner of Lean Manufacturing concepts.
What sets you apart
- Master Black Belt certification (ASQ or equivalent).
- Experience leading cross-functional and cross-regional teams.
- Familiarity with Kanban and other material replenishment systems.
- Strong understanding of assembly and production methods.
Apply today to be part of what's next.
ASM's career page: Industrial Engineering Manager | ASM
We make the tech that enables the chips in devices which improve lives around the world. We do this with an eye to the future, pushing the boundaries of what's possible through cutting-edge innovation, and driving the next wave of technological breakthroughs that shape how we live, work, and connect.
To learn more about ASM, find us at and on LinkedIn, Facebook, Instagram, X and YouTube.
ASM is an equal opportunity employer and considers qualified applicants for employment without regard to race, color, religion, age, nationality, social or ethnic origin, sexual orientation, gender, gender identify or expression, marital status, pregnancy, political affiliation, disability, genetic information, veteran status, or any other characteristic protected by law.
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0
Logistics Industrial Engineer
Singapore, Singapore
Applied Materials
Posted 10 days ago
Job Viewed
Job Description
**Who We Are**
Applied Materials is a global leader in materials engineering solutions used to produce virtually every new chip and advanced display in the world. We design, build and service cutting-edge equipment that helps our customers manufacture display and semiconductor chips - the brains of devices we use every day. As the foundation of the global electronics industry, Applied enables the exciting technologies that literally connect our world - like AI and IoT. If you want to push the boundaries of materials science and engineering to create next generation technology, join us to deliver material innovation that changes the world.
**What We Offer**
Location:
Bangalore,IND, Chennai,IND, Coimbatore,IND, Delhi,IND, Home / Mobile,India, Mumbai,IND, Pune,IND, Singapore,SGP
You'll benefit from a supportive work culture that encourages you to learn, develop, and grow your career as you take on challenges and drive innovative solutions for our customers. We empower our team to push the boundaries of what is possible-while learning every day in a supportive leading global company. Visit our Careers website to learn more.
At Applied Materials, we care about the health and wellbeing of our employees. We're committed to providing programs and support that encourage personal and professional growth and care for you at work, at home, or wherever you may go. Learn more about our benefits ( .
**Key Responsibilities**
Performs Methods Engineering analysis including process design, time and motion study, and recommends manufacturing line improvements.
Participates and or Leads in I.E. projects and programs within areas of responsibility. Assists in the implementation of these projects into business with quality tools, supporting processes and ongoing measures for success. Provides cost analysis and return on investment calculations associated with project selection.
Conducts/Leads ergonomics / human factors evaluations, recommends and implements improvements to work area designs.
Develops/leads and implements manufacturing facility design of plant layout, material handling systems, material staging and warehousing as desired.
Supports new products introductions by providing PLC/ePLC deliverables which include manufacturing line design and set up, material flow design, new tooling development and deployment of specialized tooling and fixtures.
Serves as a role model and sets the example, whose behavior is emulated by other engineering team members. (Safe behavior, follow proper protocols and procedures, including core values).
Calculates and maintains capacity data for materials processing, people, space, and equipment associated with production. Provides guidance to manufacturing and logistics related to effective and efficient use of assets and production processes.
Establishes standards and procedures for assigned areas of responsibility.
**Other Requirements:** This position may require standing for extended periods of time, walking, working in tight spaces, bending, squatting, twisting, kneeling, reaching, lifting, the ability to distinguish between colors, the ability to work in an environment with noise that may be difficult for some individuals with sensitivity to noise, and the use of hand and power tools.
Additionally, because this position also may involve working in a clean room, the use of appropriate Personal Protective Equipment such as coveralls, hoods, booties, safety glasses, gloves, respirators, chemical aprons, and face shields may be required.
**Functional Knowledge**
+ Demonstrates expanded conceptual knowledge in own discipline and broadens capabilities
**Business Expertise**
+ Understands key business drivers; uses this understanding to accomplish own work
**Leadership**
+ No supervisory responsibilities but provides informal guidance to new team members
**Problem Solving**
+ Solves problems in straightforward situations; analyzes possible solutions using technical experience and judgment and precedents
**Impact**
+ Impacts quality of own work and the work of others on the team; works within guidelines and policies
**Interpersonal Skills**
+ Explains complex information to others in straightforward situations
**Additional Information**
**Time Type:**
Full time
**Employee Type:**
Assignee / Regular
**Travel:**
Yes, 25% of the Time
**Relocation Eligible:**
No
Applied Materials is an Equal Opportunity Employer. Qualified applicants will receive consideration for employment without regard to race, color, national origin, citizenship, ancestry, religion, creed, sex, sexual orientation, gender identity, age, disability, veteran or military status, or any other basis prohibited by law.
Applied Materials is a global leader in materials engineering solutions used to produce virtually every new chip and advanced display in the world. We design, build and service cutting-edge equipment that helps our customers manufacture display and semiconductor chips - the brains of devices we use every day. As the foundation of the global electronics industry, Applied enables the exciting technologies that literally connect our world - like AI and IoT. If you want to push the boundaries of materials science and engineering to create next generation technology, join us to deliver material innovation that changes the world.
**What We Offer**
Location:
Bangalore,IND, Chennai,IND, Coimbatore,IND, Delhi,IND, Home / Mobile,India, Mumbai,IND, Pune,IND, Singapore,SGP
You'll benefit from a supportive work culture that encourages you to learn, develop, and grow your career as you take on challenges and drive innovative solutions for our customers. We empower our team to push the boundaries of what is possible-while learning every day in a supportive leading global company. Visit our Careers website to learn more.
At Applied Materials, we care about the health and wellbeing of our employees. We're committed to providing programs and support that encourage personal and professional growth and care for you at work, at home, or wherever you may go. Learn more about our benefits ( .
**Key Responsibilities**
Performs Methods Engineering analysis including process design, time and motion study, and recommends manufacturing line improvements.
Participates and or Leads in I.E. projects and programs within areas of responsibility. Assists in the implementation of these projects into business with quality tools, supporting processes and ongoing measures for success. Provides cost analysis and return on investment calculations associated with project selection.
Conducts/Leads ergonomics / human factors evaluations, recommends and implements improvements to work area designs.
Develops/leads and implements manufacturing facility design of plant layout, material handling systems, material staging and warehousing as desired.
Supports new products introductions by providing PLC/ePLC deliverables which include manufacturing line design and set up, material flow design, new tooling development and deployment of specialized tooling and fixtures.
Serves as a role model and sets the example, whose behavior is emulated by other engineering team members. (Safe behavior, follow proper protocols and procedures, including core values).
Calculates and maintains capacity data for materials processing, people, space, and equipment associated with production. Provides guidance to manufacturing and logistics related to effective and efficient use of assets and production processes.
Establishes standards and procedures for assigned areas of responsibility.
**Other Requirements:** This position may require standing for extended periods of time, walking, working in tight spaces, bending, squatting, twisting, kneeling, reaching, lifting, the ability to distinguish between colors, the ability to work in an environment with noise that may be difficult for some individuals with sensitivity to noise, and the use of hand and power tools.
Additionally, because this position also may involve working in a clean room, the use of appropriate Personal Protective Equipment such as coveralls, hoods, booties, safety glasses, gloves, respirators, chemical aprons, and face shields may be required.
**Functional Knowledge**
+ Demonstrates expanded conceptual knowledge in own discipline and broadens capabilities
**Business Expertise**
+ Understands key business drivers; uses this understanding to accomplish own work
**Leadership**
+ No supervisory responsibilities but provides informal guidance to new team members
**Problem Solving**
+ Solves problems in straightforward situations; analyzes possible solutions using technical experience and judgment and precedents
**Impact**
+ Impacts quality of own work and the work of others on the team; works within guidelines and policies
**Interpersonal Skills**
+ Explains complex information to others in straightforward situations
**Additional Information**
**Time Type:**
Full time
**Employee Type:**
Assignee / Regular
**Travel:**
Yes, 25% of the Time
**Relocation Eligible:**
No
Applied Materials is an Equal Opportunity Employer. Qualified applicants will receive consideration for employment without regard to race, color, national origin, citizenship, ancestry, religion, creed, sex, sexual orientation, gender identity, age, disability, veteran or military status, or any other basis prohibited by law.
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1
Manager/ Engineer(Process Quality Assurance)
$90000 - $120000 Y
STATS ChipPAC Pte. Ltd.
Posted today
Job Viewed
Job Description
- Define and implement Quality Assurance strategies for process stability, risk mitigation, and regulatory/customer compliance.
- Conduct process audits and internal layered audits, ensuring timely follow-up, verification, and closure of findings.
- Establish and enhance in-process control gates to strengthen risk mitigation.
- Train Quality A operators and engineers on customer-specific requirements, SOPs, and quality standards.
- Perform process, product, equipment, and recipe buy-off to ensure readiness and compliance before release.
- Conduct ESD audits and ensure compliance with ESD S20.20 requirements.
- Review and approve Statistical Bin Limits (SBL), Statistical Yield Limits (SYL), Out-of-Control (OOC), and Out-of-Spec (OOS) events.
- Chair weekly Quality Deep Dive meetings with Operations to review performance, risks, and improvement actions.
- Drive defect reduction programs, Quality Control Circles (QCC), and Continuous Improvement Projects (CIP).
- Lead and validate 8D, FMEA, and RCA activities, ensuring robust CAPA implementation.
- Perform in-line quality audits, SPC monitoring, and process verifications to sustain control.
- Prepare, maintain, and ensure compliance of process quality documentation (Control Plans, FMEA, PPAP, APQP, and MSA deliverables).
- Instill and promote a Zero Defects mindset and culture across operations.
- Identify and implement Poka-Yoke solutions and automation in quality checks.
- Ensure strict adherence to Quality Management System procedures, control plans, and work instructions on the production floor.
- Ensure successful recertification and compliance to ISO 9001, IATF 16949, ISO 27001, ISO Common Criteria), and ESD S20.20.
- Support customer audits, corporate automotive program requirements, and facilitate internal audits.
- Track, monitor, and achieve departmental KPIs, reporting progress to management.
- Lead or participate in process improvement initiatives, cross-functional task forces, and CIP reviews.
- Develop, maintain, and continuously improve operational specifications.
- Review, interpret, and implement customer requirements into internal processes.
- Develop and maintain QA databases, digital workflows, and control systems for efficiency and traceability.
Requirements:
- Degree in Engineering, Electrical, Electronic disciplines or its equivalent with 3 years relevant experience.
- Preferably 3 years' semiconductor working experience in Quality Control Assurance field or related experience in Semiconductor Manufacturing, wafer industries or Automotive industries.
- Good auditing experience in semiconductor industry preferred.
- Certified Auditor for ISO9001 / IATF16949 / ISO 27001 / ESD S20:20, VDA6.3 / VDA6.5 will be an added advantage.
- Understanding of 5 Core Tool (APQP,PPAP,FMEA,SPC,MSA) will be an added advantage.
- Good interpersonal, communication and presentation skill.
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2
Principal Industrial Engineer(Industry 4.0)
$120000 - $200000 Y
Collins Aerospace
Posted today
Job Viewed
Job Description
Job Description
We are seeking an experienced and highly skilled Principal Industrial Engineer to lead and drive implementations of Industry 4.0 solutions across Collins Aerospace manufacturing sites. As a senior member of the team, you will take on a leadership role in the implementation of advanced manufacturing technologies, IoT systems, and automation solutions that drive efficiency, quality, and innovation in industrial operations. This position demands deep technical expertise, a strategic mindset, and will serve as a mentor to junior engineers while ensuring the successful delivery of complex projects. In addition, you will be a key contributor to our continuous improvement and innovation efforts, helping to shape the future of our industrial operations.
Roles and Responsibilities
(Essential roles, responsibilities and activities a candidate can expect to assume in this position)
- Lead the design and integration of Industry 4.0 technologies into new and existing systems, ensuring seamless integration and performance.
- Lead the design and optimization of complex automation projects, ensuring high levels of efficiency and scalability.
- Lead large scale industrial engineering projects aimed at improving manufacturing/ operational processes, increasing efficiency and productivity.
- Conduct comprehensive evaluations of manufacturing/ operational sites to identify inefficiencies, performance gaps, and areas for process optimization and improvement.
- Drives discussions with leadership teams to align engineering initiatives with business objectives and operational goals.
- Lead and champions best practices in the development of detailed process documentation and standardization.
- Evaluate and recommend new technologies, tools, and systems to enhance manufacturing and operational capabilities by staying ahead of industry trends and implementing innovative solutions that drive continuous system improvement and performance.
- Ensures compliance with industry standards and best practices in system design, deployment and maintenance.
- Provide technical guidance and mentorship to junior engineers and cross functional teams.
Qualification and Education Requirements ):
Bachelor's or Master's degree in Industrial/ Mechanical Engineering or related field
Minimum years of experience in role:
At least 10-12 years
Preferred Skills (if any):
- Minimum 10–12 years of experience in industrial engineering, with experience leading large projects from proof of concept through full scale implementation.
- Comprehensive knowledge of manufacturing and automation systems, with specialized expertise in control systems (PLC/SCADA) technologies for efficient process monitoring and control
- Proven ability to design and implement advanced automation solutions, including but not limited to robotics, AOI applications, and integration with predictive maintenance systems.
- Strong organizational and project management skills with the ability to manage multiple priorities.
- Expertise in system optimization, troubleshooting, and design of experiment (DoE) methodologies.
- Basic understanding of network architecture and cybersecurity in industrial environments.
- Exceptional problem-solving, critical thinking, and communication skills, with the ability to convey technical concepts to non-technical stakeholders.
- Proven leadership skills, with experience mentoring junior engineers or leading a technical team.
- Expertise in Lean Manufacturing, Six Sigma and continuous improvement framework will be a plus.
- Knowledge in MES, ERP integration will be a plus.
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3
Process Engineering
Singapore, Singapore
$120000 - $180000 Y
DE NORA WATER TECHNOLOGIES, LLC (SINGAPORE BRANCH)
Posted today
Job Viewed
Job Description
Role Summary
The Process Engineering & Integration Manager is responsible for leading process engineering initiatives and driving integration projects across the region, related to water and wastewater applications. This role ensures that engineering processes, tools, and practices are standardized, optimized, and aligned across locations and functions. The manager will serve as a key facilitator in integrating new processes, technologies, and acquired businesses into the organization while ensuring compliance, efficiency, strategic growth and operational excellence.
Key Responsibilities
- Process Engineering
- Lead process design, standardization, and optimization across engineering and operations.
- Review existing process engineering capabilities with the objective of developing and maintaining best practices, tools, templates, procedures, and process documentation to ensure consistency and efficiency.
- Lead the collaboration amongst various engineering disciplines in mechanical, electrical, automation/controls to improve existing processes and support new processes application initiatives.
- Monitor & optimize process performance using KPIs and implement continuous improvement methodologies.
- Layout options for a future global Process Engineering team that may include the management and use of offshore engineering, and/or set up between multiple Engineering offices for technical process solutions.
- Provide guidance on complex process engineering challenges and ensure resolution to minimize downtime at site.
- Integration Management
- Manage engineering-related integration activities for transformation initiatives and M&A projects.
- Align engineering processes, tools, and systems across locations, ensuring seamless integration into divisional standards.
- Act as a key liaison between technical teams during integration projects.
- Identify engineering gaps and support the harmonization of practices (e.g., mathematical templates, data structures, regulatory, etc).
- Collaboration & Leadership
- Work closely with engineering managers, project managers, and regional leaders to drive alignment and adoption of processes.
- Provide technical guidance and coaching to engineering teams on process excellence and integration.
- Report progress, risks, skill gaps and results of integration and process improvement projects to divisional leadership.
Required Skills & Competencies
- Technical & Process Expertise
- Strong background in process engineering using different water and wastewater technologies.
- Proficiency in process solutions design, optimization, and continuous improvement tools.
- Familiarity with building or integrating technical engineering teams in complex or M&A environments.
- Project & Change Management
- Proven ability to manage cross-functional projects with multiple stakeholders.
- Strong organizational and time management skills to balance multiple tasks or integration initiatives.
- Experience with change management and stakeholder communication.
- Analytical & Problem-Solving
- Strong analytical skills to identify inefficiencies or engineering skills gaps and propose data-driven improvements that will drive the achievement of the organization's objectives.
- Ability to develop and track KPIs to measure success of process solutions and integration activities.
- Soft Skills
- Excellent communication skills to work across technical and non-technical stakeholders.
- Collaborative mindset with the ability to influence without direct authority.
- Adaptability and resilience in fast-paced, evolving environments.
Education & Experience
- Bachelor's degree in engineering (Mechanical, Chemical, Industrial, or related field).
- Master's degree in chemistry or industrial environmental engineering.
- 8–10 years of experience in water treatment process engineering & solutions, and collaboration with other business functions (operations, sales, supply chain, etc.)
- Proven ability and experience in developing engineering mathematical templates used to calculate and optimize water or wastewater treatment process flows.
- Hands-on involvement in building engineering teams and solution capabilities or integration projects (systems, processes, or M&A-related) is a must.
- Minimum 4 years' experience in managing engineering teams that can provide industrial and municipal water and wastewater treatment solutions.
- Fluency in English and other languages are a plus.
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4
Sales Engineer (Industrial Automation, Factory Automation, Class 3 w Car) DP72
$80000 - $120000 Y
TRUST RECRUIT PTE. LTD.
Posted today
Job Viewed
Job Description
Responsibilities
- Drive sales and account management, focusing on commercial negotiation and business growth, while providing technical support as needed.
- Manage and grow existing accounts.
- Generate new business opportunities and leads.
- Support technical discussions with Technical Support Team and clients when required.
- Meet assigned sales targets and contribute to team revenue goals.
- Collaborate with internal teams to ensure customer satisfaction and timely delivery.
Requirements
- Higher Nitec / Diploma / Degree in Engineering, Automation, Mechatronics, or related technical fields
- Min 1 year of sales experience.
- Strong communication, negotiation, and presentation skills.
- Self-motivated, target-driven, and commercially savvy
How to Apply:
Interested applicants, kindly click on "APPLY NOW"
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5
QC Support Expert
Singapore, Singapore
Sanofi EU
Posted today
Job Viewed
Job Description
Job title : QC Support Expert
Hiring Manager: Quality Control Manager
Location: Aventis Pharma Manufacturing, Jurong, Singapore
Transform Lives Through Excellence in Quality Control
At Sanofi, we deliver 4.3 billion healthcare solutions to people every year, transforming the practice of medicine through breakthrough science that improves people's lives. Our Manufacturing & Supply teams ensure this impact through flawless planning and meticulous attention to detail. With your expertise in Quality Control, you'll help us protect more people from infectious diseases and bring hope to patients and their families worldwide.
Your Impact
As our Quality Control Support Expert, you'll be the cornerstone of laboratory excellence, ensuring compliance, efficiency, and continuous improvement in our quality control operations. Your expertise will directly contribute to patient safety and product quality through:
Key Responsibilities:
Equipment & Systems Management
- Ensure comprehensive lifecycle management of QC laboratory equipment
- Lead qualification and maintenance operations for QC equipment
- Establish metrics and monitor qualification activities to identify trends
- Ensure all QC equipment are properly qualified and maintained
- Serve as SME for Labware LIMS and collaborate with global functions
Technical Leadership & Method Management
- Lead compendial compliance assessment and adherence for the QC laboratory
- Support annual method reviews within the product review framework
- Lead periodic analytical method control trend reviews and recommend improvements
- Support the invalid assay trending program in the QC laboratory
- Participate in Change Control Request facilitation for QC test methods
Digital & Data Management
- Implement and maintain QC digital solutions (core and local models)
- Ensure proper documentation, review, and approval of qualification deliverables
- Record all required data and calculations in compliance with cGMP and Data Integrity requirements
- Provide technical system administrator support for QC GXP computerized systems
Quality & Compliance
- Maintain site validation master plan and procedures related to ALCM and CPV
- Investigate and resolve quality control events promptly
- Provide support during regulatory inspections and audits
- Represent the site in Communities of Practice (CoPs) led by global teams
- Deputize as QC Manager when required
Safety & Continuous Improvement
- Ensure compliance with HSE policies and site procedures
- Embrace Zero Incident Mindset and adhere to Life Saving Rules
- Lead initiatives for continuous improvement in QC support processes
- Practice and communicate laboratory safety standards
What You Bring
- Strong chemistry background with technical expertise in laboratory equipment qualification and analytical method validation
- Experience with LIMS and laboratory computerized systems
- Knowledge of cGMP, data integrity requirements, and regulatory standards
- Excellent problem-solving skills and attention to detail
- Strong communication and collaboration abilities
- Commitment to quality, safety, and continuous improvement
Why Join Us?
Join our team and be part of a mission that matters. At Sanofi, you'll have the opportunity to grow professionally while making a meaningful difference in patients' lives. Your expertise in quality control will directly contribute to our ability to deliver safe, effective healthcare solutions globally.
Ready to get started? Apply now and help us chase the miracles of science to improve people's lives.
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6
Calibration Engineer
Singapore, Singapore
Medtronic
Posted 10 days ago
Job Viewed
Job Description
At Medtronic you can begin a life-long career of exploration and innovation, while helping champion healthcare access and equity for all. You'll lead with purpose, breaking down barriers to innovation in a more connected, compassionate world.
**A Day in the Life**
As a **Calibration Engineer II** at **Medtronic** , you will be responsible for executing and improving calibration processes to ensure accuracy, compliance, and efficiency across our manufacturing and laboratory environments. You will apply your metrology knowledge to support production, and facilities teams by ensuring that all Inspection, Measuring, and Test Equipment (IMTE) are calibrated, traceable, and compliant with internal standards and global regulations.
**Responsibilities may include the following and other duties may be assigned.**
+ Oversee the calibration process of a wide variety of equipment (mechanical, electrical, dimensional, temperature, pressure, etc.).
+ Review, analyze, and approve calibration certificates and reports from internal and external calibration providers.
+ Investigate and document Out of Tolerance (OOT) conditions, perform root cause analysis, and impact assessments.
+ Ensure all calibration activities comply with ISO 17025, FDA, ISO 13485, and Medtronic quality standards.
+ Manage and maintain the calibration database (e.g., IndySoft).
+ Develop and update calibration procedures, work instructions, and equipment specifications.
+ Initiate and execute change control activities related to calibration processes, procedures, intervals, and equipment specifications within a regulated industry.
+ Support internal and external audits related to calibration and metrology.
+ Collaborate with cross-functional teams (Production, Quality, Engineering, etc.) to support equipment qualification and validation.
+ Provide technical guidance and training to technicians and junior engineers as needed.
+ Lead or participate in continuous improvement initiatives, including Six Sigma, 5S, and Lean methodologies.
**Required Knowledge and Experience:**
+ Bachelor's Degree in Engineering (e.g., Mechanical, Electrical, Electronics, or related field).
+ Minimum 2 years of experience in calibration/metrology, preferably in a regulated industry - medical, pharmaceutical, aerospace
+ Strong knowledge of metrology principles and calibration standards.
+ Experience with calibration software/CMMS.
+ Familiarity with applicable standards: ISO 17025, ANSI/NCSL Z540.3, ISO 13485, FDA CFR Part 820.
+ Strong analytical, documentation, and problem-solving skills.
+ Effective verbal and written communication skills.
+ May be required to work in cleanroom environments and around production equipment.
+ May require flexible hours to support calibration events or shutdowns.
**Physical Job Requirements**
The above statements are intended to describe the general nature and level of work being performed by employees assigned to this position, but they are not an exhaustive list of all the required responsibilities and skills of this position.
**Benefits & Compensation**
**Medtronic offers a competitive Salary and flexible Benefits Package**
A commitment to our employees lives at the core of our values. We recognize their contributions. They share in the success they help to create. We offer a wide range of benefits, resources, and competitive compensation plans designed to support you at every career and life stage.
**About Medtronic**
We lead global healthcare technology and boldly attack the most challenging health problems facing humanity by searching out and finding solutions.
Our Mission - to alleviate pain, restore health, and extend life - unites a global team of 95,000+ passionate people.
We are engineers at heart- putting ambitious ideas to work to generate real solutions for real people. From the R&D lab, to the factory floor, to the conference room, every one of us experiments, creates, builds, improves and solves. We have the talent, diverse perspectives, and guts to engineer the extraordinary.
Learn more about our business, mission, and our commitment to diversity here ( lead global healthcare technology and boldly attack the most challenging health problems facing humanity by searching out and finding solutions.
Our Mission - to alleviate pain, restore health, and extend life - unites a global team of 95,000+ passionate people.
We are engineers at heart- putting ambitious ideas to work to generate real solutions for real people. From the R&D lab, to the factory floor, to the conference room, every one of us experiments, creates, builds, improves and solves. We have the talent, diverse perspectives, and guts to engineer the extraordinary.
**We change lives** . Each team member, each day, helps to improve and redefine how the world treats the most pressing health conditions, from heart disease to diabetes. Our industry leadership comes from the passion and ingenuity of our people. That's who we are. Working alongside one another, we use science, medicine, and a profound understanding of the human body to build extraordinary technologies that can transform lives.
**We build extraordinary solutions as one team** . With one Medtronic Mindset defining how we work. Speed and decisiveness run through our DNA. Diverse perspectives inspire our bold answers to any challenge that comes our way. And we deliver results the right way, breakthrough after patient breakthrough.
**This life-changing career is yours to engineer** . By bringing your ambitious ideas, unique perspective and contributions, you will.
+ **Build** a better future, amplifying your impact on the causes that matter to you and the world
+ **Grow** a career reflective of your passion and abilities
+ **Connect** to a dynamic and inclusive culture that welcomes the challenge of life-long learning
These commitments set our team apart from the rest:
**Experiences that put people first** . Respect for people is the hallmark of our humanity. It fuels our team to positively impact even a single life. And it means we put our people first at Medtronic as well, creating a culture of belonging and always pushing to get you the career-building resources you need.
**Life-transforming technologies** . No matter your role, you contribute to technologies that transform lives. What we build empowers patients to live life on their terms.
**Better outcomes for our world** . Here, it's about more than the bottom line. Our Mission to improve human welfare drives us. We advance healthcare, society, and equity with every design, inside and outside our walls.
**Insight-driven care** . Fresh viewpoints. Cutting-edge AI, data, and automation. You're shaping the future of healthcare technology and defining the next generation of breakthroughs in care
It is the policy of Medtronic to provide equal employment opportunity (EEO) to all persons regardless of age, color, national origin, citizenship status, physical or mental disability, race, religion, creed, gender, sex, sexual orientation, gender identity and/or expression, genetic information, marital status, status with regard to public assistance, veteran status, or any other characteristic protected by federal, state or local law. In addition, Medtronic will provide reasonable accommodations for qualified individuals with disabilities.
For sales reps and other patient facing field employees, going into a healthcare setting is considered an essential function of the job and we expect our employees to comply with all credentialing requirements at the hospitals or clinics they support.
This employer participates in the federal E-Verify program to confirm the identity and employment authorization of all newly hired employees. For further information about the E-Verify program, please click here ( .
For updates on job applications, please go to the candidate login page and sign in to check your application status.
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To request removal of your personal information from our systems please email
**A Day in the Life**
As a **Calibration Engineer II** at **Medtronic** , you will be responsible for executing and improving calibration processes to ensure accuracy, compliance, and efficiency across our manufacturing and laboratory environments. You will apply your metrology knowledge to support production, and facilities teams by ensuring that all Inspection, Measuring, and Test Equipment (IMTE) are calibrated, traceable, and compliant with internal standards and global regulations.
**Responsibilities may include the following and other duties may be assigned.**
+ Oversee the calibration process of a wide variety of equipment (mechanical, electrical, dimensional, temperature, pressure, etc.).
+ Review, analyze, and approve calibration certificates and reports from internal and external calibration providers.
+ Investigate and document Out of Tolerance (OOT) conditions, perform root cause analysis, and impact assessments.
+ Ensure all calibration activities comply with ISO 17025, FDA, ISO 13485, and Medtronic quality standards.
+ Manage and maintain the calibration database (e.g., IndySoft).
+ Develop and update calibration procedures, work instructions, and equipment specifications.
+ Initiate and execute change control activities related to calibration processes, procedures, intervals, and equipment specifications within a regulated industry.
+ Support internal and external audits related to calibration and metrology.
+ Collaborate with cross-functional teams (Production, Quality, Engineering, etc.) to support equipment qualification and validation.
+ Provide technical guidance and training to technicians and junior engineers as needed.
+ Lead or participate in continuous improvement initiatives, including Six Sigma, 5S, and Lean methodologies.
**Required Knowledge and Experience:**
+ Bachelor's Degree in Engineering (e.g., Mechanical, Electrical, Electronics, or related field).
+ Minimum 2 years of experience in calibration/metrology, preferably in a regulated industry - medical, pharmaceutical, aerospace
+ Strong knowledge of metrology principles and calibration standards.
+ Experience with calibration software/CMMS.
+ Familiarity with applicable standards: ISO 17025, ANSI/NCSL Z540.3, ISO 13485, FDA CFR Part 820.
+ Strong analytical, documentation, and problem-solving skills.
+ Effective verbal and written communication skills.
+ May be required to work in cleanroom environments and around production equipment.
+ May require flexible hours to support calibration events or shutdowns.
**Physical Job Requirements**
The above statements are intended to describe the general nature and level of work being performed by employees assigned to this position, but they are not an exhaustive list of all the required responsibilities and skills of this position.
**Benefits & Compensation**
**Medtronic offers a competitive Salary and flexible Benefits Package**
A commitment to our employees lives at the core of our values. We recognize their contributions. They share in the success they help to create. We offer a wide range of benefits, resources, and competitive compensation plans designed to support you at every career and life stage.
**About Medtronic**
We lead global healthcare technology and boldly attack the most challenging health problems facing humanity by searching out and finding solutions.
Our Mission - to alleviate pain, restore health, and extend life - unites a global team of 95,000+ passionate people.
We are engineers at heart- putting ambitious ideas to work to generate real solutions for real people. From the R&D lab, to the factory floor, to the conference room, every one of us experiments, creates, builds, improves and solves. We have the talent, diverse perspectives, and guts to engineer the extraordinary.
Learn more about our business, mission, and our commitment to diversity here ( lead global healthcare technology and boldly attack the most challenging health problems facing humanity by searching out and finding solutions.
Our Mission - to alleviate pain, restore health, and extend life - unites a global team of 95,000+ passionate people.
We are engineers at heart- putting ambitious ideas to work to generate real solutions for real people. From the R&D lab, to the factory floor, to the conference room, every one of us experiments, creates, builds, improves and solves. We have the talent, diverse perspectives, and guts to engineer the extraordinary.
**We change lives** . Each team member, each day, helps to improve and redefine how the world treats the most pressing health conditions, from heart disease to diabetes. Our industry leadership comes from the passion and ingenuity of our people. That's who we are. Working alongside one another, we use science, medicine, and a profound understanding of the human body to build extraordinary technologies that can transform lives.
**We build extraordinary solutions as one team** . With one Medtronic Mindset defining how we work. Speed and decisiveness run through our DNA. Diverse perspectives inspire our bold answers to any challenge that comes our way. And we deliver results the right way, breakthrough after patient breakthrough.
**This life-changing career is yours to engineer** . By bringing your ambitious ideas, unique perspective and contributions, you will.
+ **Build** a better future, amplifying your impact on the causes that matter to you and the world
+ **Grow** a career reflective of your passion and abilities
+ **Connect** to a dynamic and inclusive culture that welcomes the challenge of life-long learning
These commitments set our team apart from the rest:
**Experiences that put people first** . Respect for people is the hallmark of our humanity. It fuels our team to positively impact even a single life. And it means we put our people first at Medtronic as well, creating a culture of belonging and always pushing to get you the career-building resources you need.
**Life-transforming technologies** . No matter your role, you contribute to technologies that transform lives. What we build empowers patients to live life on their terms.
**Better outcomes for our world** . Here, it's about more than the bottom line. Our Mission to improve human welfare drives us. We advance healthcare, society, and equity with every design, inside and outside our walls.
**Insight-driven care** . Fresh viewpoints. Cutting-edge AI, data, and automation. You're shaping the future of healthcare technology and defining the next generation of breakthroughs in care
It is the policy of Medtronic to provide equal employment opportunity (EEO) to all persons regardless of age, color, national origin, citizenship status, physical or mental disability, race, religion, creed, gender, sex, sexual orientation, gender identity and/or expression, genetic information, marital status, status with regard to public assistance, veteran status, or any other characteristic protected by federal, state or local law. In addition, Medtronic will provide reasonable accommodations for qualified individuals with disabilities.
For sales reps and other patient facing field employees, going into a healthcare setting is considered an essential function of the job and we expect our employees to comply with all credentialing requirements at the hospitals or clinics they support.
This employer participates in the federal E-Verify program to confirm the identity and employment authorization of all newly hired employees. For further information about the E-Verify program, please click here ( .
For updates on job applications, please go to the candidate login page and sign in to check your application status.
If you need assistance completing your application please email
To request removal of your personal information from our systems please email
Is this job a match or a miss?
This advertiser has chosen not to accept applicants from your region.
7
Automation Engineer (PLC)
Singapore, Singapore
Cognizant
Posted 10 days ago
Job Viewed
Job Description
Cognizant is seeking a skilled Siemens PLC engineer with 4-6 years of relevant experience to support our upcoming PLC projects. The ideal candidate will have a strong background in designing, coding, and testing Siemens PLC systems using the TIA portal, with specific experience in the pharmaceutical industry. While expertise in Building Management Systems (BMS) is preferred, we are also open to candidates with experience in Process Control Systems (PCS).
**Responsibilities**
+ **Design, Code, and Test Siemens PLC Systems** : Utilize the TIA portal to design, code, and test Siemens PLC systems, ensuring they meet project specifications and industry standards.
+ **Pharmaceutical Industry Experience** : Apply your knowledge of the pharmaceutical industry to develop and implement PLC solutions that comply with regulatory requirements and enhance operational efficiency.
+ **Desigo CC System** : Work with the Desigo CC system to integrate and manage building automation and control systems.
+ **BMS/PCS Expertise** : Leverage your expertise in Building Management Systems (BMS) or Process Control Systems (PCS) to support various projects and ensure seamless integration with other systems.
+ **Hardware Design and Engineering** : Design and engineer hardware components for PLC systems, ensuring they are robust, reliable, and meet project requirements.
+ **Site Support and Troubleshooting** : Provide on-site support and troubleshooting for PLC systems, addressing any issues that arise during installation, commissioning, and operation.
+ **Interface with Other Systems** : Ensure PLC systems interface effectively with other systems, including SCADA, HMI, and other automation and control systems.
+ **Project Execution** : Manage and execute PLC projects from inception to completion, ensuring they are delivered on time, within budget, and to the required quality standards.
**Requirements**
+ **Experience** : 4-6 years of relevant experience in Siemens PLC engineering, with a focus on the pharmaceutical industry.
+ **Technical Skills** : Proficiency in using the TIA portal for PLC design, coding, and testing. Experience with the Desigo CC system and BMS/PCS is highly desirable.
+ **Problem-Solving** : Strong troubleshooting skills and the ability to provide effective on-site support.
+ **Communication** : Excellent communication skills, with the ability to interface effectively with clients, project teams, and other stakeholders.
+ **Project Management** : Proven experience in managing and executing PLC projects, with a track record of delivering successful outcomes.
+ **Certifications** : Relevant certifications in Siemens PLC systems, BMS, or PCS.
+ **Industry Knowledge** : In-depth knowledge of regulatory requirements and best practices in the pharmaceutical industry.
**About Cognizant**
Cognizant (Nasdaq: CTSH) engineers modern businesses. We help our clients modernize technology, reimagine processes and transform experiences so they can stay ahead in our fast-changing world. Together, we're improving everyday life. See how at or @cognizant.
#LI-CTSAPAC
#LI-TL1
Cognizant is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to sex, gender identity, sexual orientation, race, color, religion, national origin, disability, protected Veteran status, age, or any other characteristic protected by law.
**Responsibilities**
+ **Design, Code, and Test Siemens PLC Systems** : Utilize the TIA portal to design, code, and test Siemens PLC systems, ensuring they meet project specifications and industry standards.
+ **Pharmaceutical Industry Experience** : Apply your knowledge of the pharmaceutical industry to develop and implement PLC solutions that comply with regulatory requirements and enhance operational efficiency.
+ **Desigo CC System** : Work with the Desigo CC system to integrate and manage building automation and control systems.
+ **BMS/PCS Expertise** : Leverage your expertise in Building Management Systems (BMS) or Process Control Systems (PCS) to support various projects and ensure seamless integration with other systems.
+ **Hardware Design and Engineering** : Design and engineer hardware components for PLC systems, ensuring they are robust, reliable, and meet project requirements.
+ **Site Support and Troubleshooting** : Provide on-site support and troubleshooting for PLC systems, addressing any issues that arise during installation, commissioning, and operation.
+ **Interface with Other Systems** : Ensure PLC systems interface effectively with other systems, including SCADA, HMI, and other automation and control systems.
+ **Project Execution** : Manage and execute PLC projects from inception to completion, ensuring they are delivered on time, within budget, and to the required quality standards.
**Requirements**
+ **Experience** : 4-6 years of relevant experience in Siemens PLC engineering, with a focus on the pharmaceutical industry.
+ **Technical Skills** : Proficiency in using the TIA portal for PLC design, coding, and testing. Experience with the Desigo CC system and BMS/PCS is highly desirable.
+ **Problem-Solving** : Strong troubleshooting skills and the ability to provide effective on-site support.
+ **Communication** : Excellent communication skills, with the ability to interface effectively with clients, project teams, and other stakeholders.
+ **Project Management** : Proven experience in managing and executing PLC projects, with a track record of delivering successful outcomes.
+ **Certifications** : Relevant certifications in Siemens PLC systems, BMS, or PCS.
+ **Industry Knowledge** : In-depth knowledge of regulatory requirements and best practices in the pharmaceutical industry.
**About Cognizant**
Cognizant (Nasdaq: CTSH) engineers modern businesses. We help our clients modernize technology, reimagine processes and transform experiences so they can stay ahead in our fast-changing world. Together, we're improving everyday life. See how at or @cognizant.
#LI-CTSAPAC
#LI-TL1
Cognizant is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to sex, gender identity, sexual orientation, race, color, religion, national origin, disability, protected Veteran status, age, or any other characteristic protected by law.
Is this job a match or a miss?
This advertiser has chosen not to accept applicants from your region.
8
Process Development Senior Engineer
Singapore, Singapore
Amgen
Posted 10 days ago
Job Viewed
Job Description
**Process Development Senior Engineer**
**Amgen Singapore Manufacturing , Singapore**
**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 a **Process Development Senior Engineer** in **Amgen Singapore Manufacturing** .
**Process Development Senior Engineer**
**Live**
**What you will do**
Let's do this. Let's change the world. In this vital role you, the PD Senior Engineer will provide scientific and technical leadership within the Process Development group at Amgen's Next Generation Biologics Manufacturing Facility in Singapore. This is one of the most advanced biotech manufacturing facilities in the world: employing the latest technologies for single use processing, connected processing, and real-time process analytical technologies.
Main Responsibilities:
+ Assume a Subject Matter Expert role within ASM Process Development for cell culture and commercial process support.
+ Experienced in Technology Transfer of new process and technology to commercial site.
+ Must have strong knowledge of cell culture and product recovery.
+ Must have good understanding of process characterization and process scale up to resolve technical issues observed during transfer / manufacturing at large scale.
+ Able to lead small team and lead projects focused on non-routine activities including facility start up, process qualification through to regulatory filing, process performance monitoring, floor support, and troubleshooting of unit operations.
+ Integrate trends, data and information into plans, deliverables and recommendations
+ Manage key projects to deliver site goals while meeting quality, schedule, and cost objectives.
+ Lead productivity projects, process optimization, complex investigation, and product life cycle management.
+ Collaborate with cross-functional teams and network drug substance teams to resolve process challenges by applying advanced technical principles and concepts for troubleshooting.
All listed tasks and responsibilities are deemed as essential functions to this position; however, business conditions may require reasonable accommodations for additional tasks and responsibilities.
**Win**
**What we expect of you**
**Qualifications**
+ Doctorate degree OR
+ Master's degree and 2 years of directly related experience OR
+ Bachelor's degree and 4 years of directly related experience OR
+ Diploma and 8 years of directly related experience
+ Relevant work experience in the commercial manufacturing environment within the biotechnology or pharmaceutical industries
+ Experience with regulated environments (i.e. cGMP) required
+ In depth cell culture process knowledge, including disposables technologies and harvest technologies
+ Experienced in providing floor support, troubleshooting unit operations, and resolving and documenting investigations to support cGMP production
+ Comprehensive understanding of commissioning, qualification and verification protocol execution requirements
+ Comprehensive experience in process characterization and process monitoring programs
+ Strong communication skills (technical writing and verbal communication/presentation)
+ Problem solving skills requiring the application of strong scientific and engineering theory and calculations and creative skills in the development of hypotheses and approach
+ Familiarity with documentation in a highly regulated environment
+ Interacts effectively with variety of communication and working styles
+ Ability to independently determine when additional resources are required to solve problems
+ Demonstrated skills in the following areas:
+ Basic project management
+ Commissioning and Qualification
+ Scheduling
+ Collaboration
+ Completion and follow-up
+ Ability to provide solutions to a large variety of technical problems
**Thrive**
**What you can expect of us**
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.
+ 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
**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.**
**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.
**Amgen Singapore Manufacturing , Singapore**
**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 a **Process Development Senior Engineer** in **Amgen Singapore Manufacturing** .
**Process Development Senior Engineer**
**Live**
**What you will do**
Let's do this. Let's change the world. In this vital role you, the PD Senior Engineer will provide scientific and technical leadership within the Process Development group at Amgen's Next Generation Biologics Manufacturing Facility in Singapore. This is one of the most advanced biotech manufacturing facilities in the world: employing the latest technologies for single use processing, connected processing, and real-time process analytical technologies.
Main Responsibilities:
+ Assume a Subject Matter Expert role within ASM Process Development for cell culture and commercial process support.
+ Experienced in Technology Transfer of new process and technology to commercial site.
+ Must have strong knowledge of cell culture and product recovery.
+ Must have good understanding of process characterization and process scale up to resolve technical issues observed during transfer / manufacturing at large scale.
+ Able to lead small team and lead projects focused on non-routine activities including facility start up, process qualification through to regulatory filing, process performance monitoring, floor support, and troubleshooting of unit operations.
+ Integrate trends, data and information into plans, deliverables and recommendations
+ Manage key projects to deliver site goals while meeting quality, schedule, and cost objectives.
+ Lead productivity projects, process optimization, complex investigation, and product life cycle management.
+ Collaborate with cross-functional teams and network drug substance teams to resolve process challenges by applying advanced technical principles and concepts for troubleshooting.
All listed tasks and responsibilities are deemed as essential functions to this position; however, business conditions may require reasonable accommodations for additional tasks and responsibilities.
**Win**
**What we expect of you**
**Qualifications**
+ Doctorate degree OR
+ Master's degree and 2 years of directly related experience OR
+ Bachelor's degree and 4 years of directly related experience OR
+ Diploma and 8 years of directly related experience
+ Relevant work experience in the commercial manufacturing environment within the biotechnology or pharmaceutical industries
+ Experience with regulated environments (i.e. cGMP) required
+ In depth cell culture process knowledge, including disposables technologies and harvest technologies
+ Experienced in providing floor support, troubleshooting unit operations, and resolving and documenting investigations to support cGMP production
+ Comprehensive understanding of commissioning, qualification and verification protocol execution requirements
+ Comprehensive experience in process characterization and process monitoring programs
+ Strong communication skills (technical writing and verbal communication/presentation)
+ Problem solving skills requiring the application of strong scientific and engineering theory and calculations and creative skills in the development of hypotheses and approach
+ Familiarity with documentation in a highly regulated environment
+ Interacts effectively with variety of communication and working styles
+ Ability to independently determine when additional resources are required to solve problems
+ Demonstrated skills in the following areas:
+ Basic project management
+ Commissioning and Qualification
+ Scheduling
+ Collaboration
+ Completion and follow-up
+ Ability to provide solutions to a large variety of technical problems
**Thrive**
**What you can expect of us**
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.
+ 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
**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.**
**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.
Is this job a match or a miss?
This advertiser has chosen not to accept applicants from your region.
9