Assoc Assembler Day Shift

About the Role

The team at Edwards Lifesciences is dedicated to creating innovative solutions that transform patients' lives. As an Associate Assembler, you will be an integral part of this process, applying your skills and expertise to help bring new products to market. With a strong focus on continuous improvement, you will have the opportunity to develop your skills and advance your career in a dynamic and supportive environment.

In this role, you will be working on a day shift, Monday to Thursday, from 5:45am-4pm. You will be required to work with minimal supervision, following detailed manufacturing instructions and adhering to regulatory and company guidelines.

What You Will Do

• Assemble medical devices with precision and accuracy, using a range of tools and equipment
• Follow work order instructions and drawings, using computers to navigate and enter parts status data
• Perform inventory reconciliation at the start of each day and when transitioning to new work orders
• Review and follow established work instructions and SOPs, recording traceable information on device history records
• Enter data into manufacturing data systems, as required
• Perform line clearance, cleaning and sanitizing work stations at the start of each shift and when transitioning to new work orders
• Ensure all required components and tools are ready for the build
• Conduct self-assessments of your work, including visual inspections under magnification
• Provide constructive feedback to colleagues, based on sequential work reviews
• Escalate work issues and changes in equipment performance to your supervisor for assessment and correction
• Work effectively in a team environment, collaborating with colleagues and supervisors to achieve common goals

What We Are Looking For

• Leaving Certificate or equivalent
• Good communication skills, with the ability to read, comprehend, and speak English
• Elementary-level understanding of numerical functions
• Ability to adhere to Edwards Environmental Health and Safety and Quality guidelines
• Proven ability to complete, retain, and incorporate training coursework in the performance of new and advanced work procedures
• Ability to work with minimal supervision, following detailed manufacturing instructions
• Ability to work in a team environment, primarily with colleagues and supervisors
• Flexibility to work overtime, as required

Nice to Have

• Previous experience in a manufacturing environment, preferably in the medical device industry
• Familiarity with regulatory and company guidelines, related to medical device manufacturing
• Basic computer skills, with the ability to use software applications and enter data accurately

Benefits and Perks

• Competitive salary and benefits package
• Opportunity to work with a leading medical device manufacturer
• Collaborative and dynamic work environment
• Professional development and training opportunities
• Flexible working hours and overtime opportunities
• Access to cutting-edge technology and equipment
• Comprehensive health and safety program
• Recognition and reward programs

• Develop your attention to detail and precision skills, as these are critical for success in this role
• Familiarize yourself with regulatory and company guidelines, related to medical device manufacturing
• Highlight your ability to work with minimal supervision and follow detailed instructions
• Emphasize your teamwork and communication skills, as these are essential for success in this environment
• Be prepared to provide examples of your experience with quality control and assurance processes
• Research the company culture and values, to demonstrate your understanding of the organization's mission and goals
• Showcase your problem-solving skills and ability to think critically, as these are highly valued in this role