Manufacturing Product Builder

About Haemonetics

Haemonetics is dedicated to attracting motivated individuals seeking a fulfilling and stimulating career within a diverse and dynamic workplace. Our commitment focuses on the production of innovative medical devices adhering strictly to international quality and regulatory standards.

Job Overview

The role involves active participation in the manufacturing of medical devices, requiring adherence to rigorous quality standards such as ISO 13485, FDA regulations (21 CFR Part 820), Medical Device Directives (93/42/EEC and 2007/47/EC), and the Vivasure Medical Quality Management System. The Manufacturing Product Builder will operate within the Manufacturing Team and assist other company functions as needed.

Primary Responsibilities

• Assemble sub-components and final devices, including packaging processes for clinical tests and market distribution.
• Perform visual and dimensional inspections on parts and assemblies according to established procedures.
• Manage materials issuance to the production line and prepare equipment and fixtures for operations.
• Support material control activities such as incoming inspections, part tracking, and issuance.
• Engage in training sessions to gain proficiency in manufacturing and inspection tasks promptly.
• Assist with in-process device testing, documenting all relevant data thoroughly.
• Identify improvement opportunities to enhance product quality and throughput, actively participating in implementation.
• Provide guidance and training to fellow team members regarding assembly, inspection, and testing practices when necessary.
• Adhere strictly to all released work instructions and procedural requirements.
• Accurately complete all quality documentation aligning with Good Documentation Practice (GDP) standards.
• Maintain reliability by consistently meeting attendance, schedule compliance, production, and quality benchmarks.

Qualifications and Experience

• Minimum educational requirement is Leaving Certificate or its equivalent; possession of a third-level academic qualification is beneficial.
• At least 4 years of experience in medical device manufacturing, with a minimum of 2 years working in a cleanroom environment or equivalent experience.
• Experience with GDP and GMP standards is advantageous.

Skills and Competencies

• Strong communication skills and a team-oriented attitude.
• Capability to undertake diverse manual tasks that require fine motor abilities and dexterity.
• Proactive approach with a high degree of initiative and meticulous attention to detail.
• Ability to work effectively with minimal supervision.
• Familiarity with computer applications including Microsoft Excel and Word is desirable.

Compensation and Benefits

The offered base salary ranges from €32,300 to €43,700 annually, adjusted based on factors such as location, education, skills, and relevant experience. Employees may also receive incentives including discretionary annual bonuses and potential participation in long-term incentive plans, governed by the company’s policies. A comprehensive benefits package is included.

Further compensation details are available upon request as per local regulations by contacting Human Resources directly.