QA Supervisor at Teleflex Medical - Spain

Kamunting, Perak, Malaysia -

Full Time

Start Date

Immediate

Expiry Date

27 Jan, 26

Salary

0.0

Posted On

29 Oct, 25

Experience

2 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Team Leadership, Operational Oversight, Quality Assurance, Continuous Improvement, Compliance, Documentation, Collaboration, Problem-Solving, Organizational Skills, Communication Skills, Data Analysis, Regulatory Knowledge, ISO 13485, GMP Standards, SAP Proficiency, Performance Evaluation

Industry

Medical Equipment Manufacturing

Description

Expected Travel: None Requisition ID: 12891 About Teleflex Incorporated As a global provider of medical technologies, Teleflex is driven by our purpose to improve the health and quality of people’s lives. Through our vision to become the most trusted partner in healthcare, we offer a diverse portfolio with solutions in the therapy areas of anesthesia, emergency medicine, interventional cardiology and radiology, surgical, vascular access, and urology. We believe that the potential of great people, purpose-driven innovation, and world-class products can shape the future direction of healthcare. Teleflex is the home of Arrow™, Barrigel™, Deknatel™, LMA™, Pilling™, QuikClot™, Rüsch™, UroLift™ and Weck™ – trusted brands united by a common sense of purpose. At Teleflex, we are empowering the future of healthcare. For more information, please visit teleflex.com. Global Operations - Global Operations is a complex and diverse organization within the company which is responsible for product fulfilment to all our customers from end to end. We pride ourselves on being totally Customer Centric in our unrelenting focus on Improving Quality, Service and Value as perceived by our customers. Our employees are dedicated to the Global Operations Enterprise Excellence journey. Join a dynamic, growing team that offers healthcare providers an array of medical technology solutions that make a difference in patients’ lives.Position Summary The Supervisor will oversee daily quality related tasks at manufacturing floor. This role involves ensuring compliance with industry regulations, written procedures and work instruction, finding out noncompliance at shop floor and in cross functional team activities and to highlight/resolve them following appropriate procedures. This role required to manage quality inspectors at shop floor who are testing product quality with respect to written specification. This role is responsible to ensure high quality products are being manufactured by ensuring all in-process quality related checks performed at specified intervals. This role also required to review and ensuring completeness of all manufacturing batch records prior to release of finished products in market. The Supervisor will collaborate with other departments to drive continuous improvement.Principal Responsibilities 1. Team Leadership: - Supervise and mentor a team of quality inspectors at shop floor. - Conduct regular performance evaluations and provide constructive feedback. - Foster a collaborative and positive work environment.2. Operational Oversight: - Monitor daily quality operations at shop floor to ensure efficiency and compliance with SOPs/Work Instructions - Coordinate work schedules, assign tasks, and manage workflow to meet targets. - Troubleshoot and resolve quality related issues promptly.- Having good data analysis skills and able to manage/ prioritize tasks3. Quality Assurance: - Ensure all activities comply with industry standards and regulatory requirements (e.g., FDA, ISO 13485). - Implement and maintain quality control processes to uphold product standards. - Conduct regular audits and inspections.4. Continuous Improvement: - Identify opportunities for process improvement and implement best practices. - Participate in cross-functional teams to develop and implement improvement projects. - Monitor and report on key performance indicators (KPIs).5. Compliance and Documentation: - Ensure accurate and timely documentation of processes, procedures, and incidents. - Maintain up-to-date knowledge of regulatory requirements and industry trends.6. Collaboration: - Work closely with others to align on organizational goals. - Facilitate effective communication within the team and across the organization. - Represent the department in meetings and project discussions wherever requiredEducation / Experience Requirements Bachelor’s degree in engineering, Life Sciences, or a related field.- Minimum of 2-3 years of experience in the medical device or related industries- Strong knowledge of USFDA regulations, ISO 13485, and GMP standards.- Proven ability to lead and develop a high-performing team- Good problem-solving, organizational, and communication skills.- Proficiency in relevant software and tools (MS Office), SAP shall be additional benefitSpecialized Skills / Other Requirements Note: As with all positions, due to the dynamic nature of Teleflex Medical business, key responsibilities may evolve and change over time. Teleflex is an equal opportunities employer. At Teleflex, we follow a comprehensive hiring process. We do not accept unsolicited resumes from agency recruiters or 3rd party firms. We do not make unsolicited job offers. We do not ask for money or require equipment purchase up-front. Teleflex, the Teleflex logo, Arrow™, Barrigel™, Deknatel™, LMA™, Pilling™, QuikClot™, Rüsch™, UroLift™ and Weck™ are trademarks or registered trademarks of Teleflex Incorporated or its affiliates, in the U.S. and/or other countries. © 2025 Teleflex Incorporated. All rights reserved.

Responsibilities

The Supervisor will oversee daily quality-related tasks on the manufacturing floor, ensuring compliance with industry regulations and resolving noncompliance issues. This role also involves managing quality inspectors and ensuring high-quality products are manufactured through in-process quality checks.