Qms Specialist

Find what drives you on a team with a more than a 70-year history of discovery, determination, and innovation. As a global leader in high-tech filtration, separation, and purification, Pall Corporation thrives on helping our customers protect people. Our products serve a wide range of markets, so if your interests lie along the spectrum of Life Sciences to Industrial, you will find a rewarding role here. For the exponentially curious, Pall is a place you can thrive and amplify your impact on the world.

Pall is proud to work alongside a community of nine fellow Danaher Life Sciences companies. Together, we’re pioneering the future of science and medicine, developing products that enable researchers in the fight to save lives.

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The QMS Specialist is responsible for the administration, maintenance and optimization of the quality management system for the new manufacturing facility in Singapore to meet the requirements of ISO 9001:2015. Coordination of document control activities, internal audit programs, CAPA management, Management Review and Smartsolve training and support. This person will have a key role in the implementation of the QMS for the new site working with both the local team and the Global Quality and Regulatory function.

This position is part of the Quality Department and will be reporting to our Quality Manager and based in Benoi, Singapore - Onsite.

In this role, you will have the opportunity to:
- Provide guidance and support to cross-functional teams to establish a robust quality system for our business processes through the development, deployment, maintenance, and continuous improvement of our QMS policies, work instructions and records, in accordance with ISO9001: 2015- Administration and participation in the site's internal audit program to drive improvement in our business processes, through audit scheduling, reporting and follow-up actions, CAPA management, trend analysis and feedback to site and Quality leadership and process owners.- Ensure customer and regulatory requirements are integrated into our site QMS activities and provide regulatory compliance documentation for site activities and products.- Reporting, analysis & improvement of Quality Key Performance Indicators as defined for Site QMS through the use of Danaher Business System (DBS) and participation in cross-functional kaizen events- Provide in-region support for QMS-related activities, e.g. management review, Smartsolve helpdesk admin and audit program

The essential requirements of the job include:- Minimum 3 years of relevant working experience in a high-volume manufacturing environment, or quality-regulated industry- Comprehensive knowledge of ISO9001:2015 to coordinate and lead activities with multiple functions on site- Ability to perform a variety of duties and efficiently organize activities to meet business priorities, demonstrated a sense of urgency and flexibility to achieve results- Building strong working relationships across diverse functions, backgrounds, and locations. Flexibility to accommodate different time zones as needed to support our global activities

It would be an advantage if you possess previous experience in:
- Certified Lead/Internal auditor for ISO9001:2015- Knowledge of MicroE manufacturing or relevant industry- Proficiency in Japanese as the role will require liaising with our counterparts in Japan

When you join us, you’ll also be joining Danaher’s global organization, where 80,000 people wake up every day determined to help our customers win. As an associate, you’ll try new things, work hard, and advance your skills with guidance from dedicated leaders, all with the support of powerful

Danaher Business System

tools and the stability of a tested organization.

At Danaher, we value diversity and the existence of similarities and differences, both visible and not, found in our workforce, workplace and throughout the markets we serve. Our associates, customers and shareholders contribute unique and different perspectives as a result of these diverse attributes.

If you’ve ever wondered what’s within you, there’s no better time to find out.