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ABOUT US


Company name: Edwards Lifesciences (Singapore) Pte Ltd.

Edwards Lifesciences is the global leader in patient-focused medical innovations for structural heart disease, as well as critical care and surgical monitoring. Driven by a passion to help patients, the company collaborates with the world’s leading clinicians and researchers to address unmet healthcare needs, working to improve patient outcomes and enhance lives.

We manufacture our products in several locations including the United States, Puerto Rico, the Dominican Republic, Costa Rica, Switzerland and Singapore.

We partner with physicians to innovate products designed to help patients live longer, healthier and more productive lives. We focus on medical technologies that address large and growing patient populations in which there are significant unmet clinical needs.

Driven by our patient-focused innovation strategy, our 11,000 employees live the values of our company’s Credo, which closes with the tagline of “Helping patients is our life’s work, and life is now.”


Career Opportunities



Career With Us


Permanent Position: Associate/Analyst, Planner
No. of Openings: 1
Pre-requisites: Bachelor’s Degree in Engineering/ Business or equivalent, min 2 years’ experience in the manufacturing environment with supply chain experience
Key Responsibilities:
To minimize production time and costs, efficiently organize the use of resources and maximize efficiency in the workplace
Perform daily scheduling and execute demand changes
Require to achieving on-time delivery, meet inventory target and inventory turn, reduction on aged non-moving inventory, month-end shipment attainment


Permanent Position: Coordinator, Documentation
No. of Openings: 1
Pre-requisites:
Minimum 2 - 3 years of working experience, preferably in a similar capacity
Good communication and interpersonal skills
Proficient in Microsoft Office
Must be able to work independently as well as in a team environment
Key Responsibilities:
Scan, verify and upload documents into Product Data Management system, including WO (Work Orders), Protocol/Report etc
Review and archive Quality Records such as Qualification package, Preventive Maintenance forms, Training records, etc
Verify changed document for completeness and accuracy, and ensure change category and appropriate approval are chosen in the change control request system
Ensure timely update to the Site Master Signature Log
Perform Annual Lab Notebook Review
Review, follow and perform job functions in compliance with established work instructions and adherence with SOPs, including recording traceable information on device history records


Permanent Position: Manager, Manufacturing
No. of Openings: 1
Pre-requisites:
Bachelor’s Degree in Mechanical, Industrial or Electrical Engineering
At least 8 years of working experience, preferably in medical device industry with at least 5 years in supervisory position
Key Responsibilities:
Direct and coordinate all production activities which include: the implementation and administration of the department’s policies and procedures
Develop and maintain production performance metrics that support the key business drivers and be responsible for each metric’s performance
Prepare short and long term plans in order to meet production schedule requirements and ensure department operations is in compliant to GMP and SOP


Permanent Position: Microbiologist
No. of Openings: 2
Pre-requisites:
Bachelor of Science (Microbiology or related discipline)
Minimum 3 years of direct pharmaceutical or medical device experience
Key Responsibilities:
Perform routine microbial/chemistry testing services using established procedures/protocols
Evaluate and assist in the feasibility, development and implement of critical systems and sterilization equipment. Lead and collaborate with other functional teams in new processes/equipment qualifications
Conduct root cause analysis for product/sample failures and Out-of-Specifications (OOS). Recommend and ensure implementation of corrective and preventive actions


Permanent Position: Senior / Engineer, Manufacturing Engineering (Software)
No. of Openings: 1
Pre-requisites:
Degree in Electrical, Electronics or Computer Engineering or related disciplines
Minimum 4 years’ relevant experience with strong technical background in software engineering
Key Responsibilities:
Lead software engineering activities for global and internal capital projects including new equipment, capacity expansion and new technology implementation
Provide leadership and technical support for technology transfers to Singapore
Initiate software validation plan, perform software risk management, etc and conduct root cause analysis on process and equipment software related issues


Permanent Position: Senior/Engineer, Manufacturing Engineering (Operations)
No. of Openings: 2
Pre-requisites:
Bachelor's Degree in Mechanical, Industrial, Biomedical, Chemical, Electrical or Manufacturing Engineering
More than 5-8 years of experience in the medical device or relevant industry, with background in process/manufacturing engineering or product / process development or equipment design
Demonstrates proven track record of Technical, Product & Process Expertise, with strong analytical and problem solving abilities
Well versed in Project Management & necessary complimentary management tools
Proficient in the use of MS Office (Word, Excel, Powerpoint), AutoCad/ProE, PLC Programming
Certified/Experience in Lean Manufacturing & Six-Sigma Tools & Principles
Organized and demonstrates good Communication, Interpersonal & Presentation Skills
Ability to work Independent and as part of a team
Key Responsibilities:
Provide day to day engineering support to manufacturing operations to achieve key business objectives involving Quality, Productivity, Order Fulfillment, MBC, NCR
Lead/Manage/Participate in Continuous Improvement initiatives, involving Lean Manufacturing & Six Sigma projects to improve Quality, Productivity and Business Process Flow
Lead/Manage/Participate in cross functional initiatives involving Product/Process/Equipment Development, Enhancements, Qualification, Transfers, Validations and Special Projects
Review/Establish/Maintain/Train on SOPs, to be in compliance to cGMP, Environmental Health & Safety regulations, relating to Maintenance, Reliability & Reproducibility of Product/Process/Equipment in support of manufacturing operations
Review/Establish/Update/Maintain new and existing Product Part Numbers, Drawings, Bill of Materials (BOM), and Work Order Routings
Lead/Participate/Support in all internal & external audits by relevant Regulatory Bodies
Lead/Manage/Participate in root cause analysis on major manufacturing concerns. Provide recommendations & Execute implementation of agreed action plans
Lead/Manage/Participate in cross functional/interplant initiatives relating to NEW Process/Equipment Development, Transfers & Qualification Strategies, Master Validation Policies/Planning


Permanent Position: Senior/Engineer, Operations, Manufacturing Engineering (Automation)
No. of Openings: 1
Pre-requisites:
Bachelor’s degree in Mechanical engineering is required
More than 8 years of experience in factory automation, with more than 3 years in equipment design for medical device industry
Strong technical background in process engineering and third party system integrations
Proficient with mechanical design techniques using AutoCAD, ProE or SolidWorks 3D modeling software
Experience in project management, SPC, Lean and Six Sigma Principles
Knowledge of Programmable Logic Control (PLC) and able to read P&ID diagram
Strong analytical and problem solving skills
Must have prior experience designing a variety of jigs and fixtures, tooling and aids for manufacturing support
Must be organized, have good communication, interpersonal and presentation skills
Proactive, initiative and assertive
Ability to lead and manage multiple projects in a timely manner
Well verse in Microsoft office and applications (e.g. Words, Excel, Powerpoint, etc)
Key Responsibilities:
Lead engineering activities for global and internal capital projects including new plants, plant expansions and new technology implementations
Provide leadership and technical support for technology transfers to Singapore, including project planning and engineering review of equipment
Design, procure, develop, commissioning and qualify new equipment
Work closely with cross functional teams to provide innovative engineering solutions for continue process improvements
Lead and support conceptual engineering, project cost estimations, vendor selections, detailed process designs and conduct equipment feasibility study
Conduct root cause analysis on process and equipment related issues. Recommends and ensure implementation of corrective and preventive actions


Permanent Position: Supervisor, Manufacturing
No. of Openings: 5
Pre-requisites:
Diploma or Bachelor’s Degree in Engineering/Science with 4 to 6 years previous working experience in similar capacity
Supervisory experience in managing a large team (more than 70)
Good interpersonal communication skills
Proactive, good initiative and team player
Proficient in MS Office & application (Excel, Words, Powerpoint, etc)
Must be able to perform shift work (Mon - Fri; 1st Shift: 6.30am - 3.15pm; 2nd Shift: 3.30pm - 12am) and support weekend duties when required
Key Responsibilities:
Lead and manage manufacturing team and resources in performing daily tasks in order to maintain smooth production operations and on-time delivery to customers (internal/external)
Responsible for People Management - Performance, Development, Training, Engagement, Attendance, EHS, Discipline
Responsible for Quality Management – Meet Yields Targets, Compliance to Quality System Requirements
Involve in Cost Improvement and Management through Lean & Six Sigma Projects.


Permanent Position: Supervisor, Quality
No. of Openings: 1
Pre-requisites:
Diploma or Bachelor’s Degree in Engineering/Science
Good understanding of Quality Assurance and Quality Control principles
Experience working in multi-cultural teams with cultural sensitivity
Excellent communication and interpersonal relationship skills; possessing strong collaboration skills in partnering with cross functional stakeholders in order to achieve objectives
Strong analytical and problem skills are required.
Must be able to perform shift work (Mon - Fri, 2nd Shift: 3.30pm - 12am) and support weekend duties when required
Experience working in a medical device industry, preferred
Key Responsibilities:
Supervise employees and quality activities pertaining to the production of products and/or manufacturing processes in - and with quality/technical knowledge of - 1 or more production areas, depending on the complexity of the areas, in addition to conducting performance reviews, including resolving performance issues
Oversee the scheduling of work orders and team performance metrics
Ensure appropriate staffing for all positions
Accountable to ensure staff is appropriately trained to perform assigned work
Accountable for productivity and quality metrics of staff, and provide regular progress reports and quality metrics to management and cross-functional stakeholders
Partner with engineering on investigations and/or corrective actions, perform non-conformance investigations for review with engineering, assures documentation content is valid, may participate in improvement projects


Permanent Position: Technician, Facilities (2nd Shift)
No. of Openings: 1
Pre-requisites:
Minimum Nitec in Mechanical/Electrical Engineering, Building Services, Facilities Management
At least 3 year of relevant experience in facilities/building maintenance in pharmaceutical or critical facilities
Proficient in MS Office
Possess good analytical, troubleshooting and problem solving skills
Self-motivated and has the ability to work independently
Candidates will more years of experience may be considered for a senior technician role
Key Responsibilities:
Manage facilities maintenance in clean rooms and offices
Attend to in-house customers' enquiries via email and phone
Liaise with contractors to handle facilities works
Perform routine preventive maintenance to ensure facility equipment run smoothly and building systems operate efficiently
Support senior technician for any facility system breakdown


Permanent Position: Technician, Lab
No. of Openings: 1
Pre-requisites: Diploma in a Science discipline (Microbiology/Chemistry) or a relevant ITE certificate with at least 2 years of direct pharmaceutical or medical device experience
Key Responsibilities:
Perform routine microbial/chemistry testing services using established procedures/protocols
Support testing in validation/ revalidation activities for critical systems and sterilization equipment
Support root cause analysis for product/sample failures and Out-of-Specifications (OOS)

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