QMS Manager

Location: Netherlands

SIRE Life Sciences® is the market leader in life science recruitment. We believe the recruitment market needs to gear up in technology and continues innovation. We like technology, in a life science market driven on science, we couldn’t stay behind; we drive Recruitment Science. Investing a majority of our turnover in technology enables us to use unique Resource Technologies. By using highly advanced algorithms, we enable our team of Resource & Data Strategists© to maintain the most advanced, detailed and complete Life Sciences network in Europe. This big data enables us to work Reverse Recruitment©: we first analyze the market in-depth before we go out to the market. Because we analyze the whole market, we can compare facts and data. This enables us to do Facts & Big Data Recruitment©, making sure we, or better yet, you find the right career!

THE COMPANY

Our client is a professional Medical Devices organization, based in Netherlands.

A leading health technology company focused on improving people's lives through education, engagement, and empowerment they make it possible to help those affected by the disease live a fulfilling life. Innovation, a systematic approach and a path to value is how they distinguish themselves. An organisation with an international character and a lot of opportunities to develop yourself and grow.

ROLE DESCRIPTION

The Quality Manager is responsible for overall development, implementation, and maintenance of the organization’s Quality Management System (QMS). You work is based on the following three principles: simplify, clarify and control. You provide hands-on ownership to the site documentation system, master document lists and database/s, but also support to internal customers/site departments in the application, maintenance and improvement of
quality systems and department-specific processes.

RESPONSIBILITIES

As a QMS manager you will be managing the QMS transition of the PQMS/PEPF and manage its deployment in the Markets, but also locally managing plans for all QMS parts in scope while maintaining compliance and effectiveness throughout the duration of the transition to the PQMS. You ensure the addition and management of any local QMS documents are in line with the evolution of the PEPF and the PQMS. Furthermore
- Following processes and operational policies in selecting methods and techniques for obtaining solutions
- Manage document management activities for involved processes
- You act as an advisor to subordinates to meet schedules and/or solve problems

REQUIREMENTS

• Experience with working in a disciplined regulated industry and in applying automated technology.
• Seasoned knowledge of ISO 9001 and ISO 13485 (preferable including ISO 9001:2015 and ISO 13485:2016)
• Strong analytic skills
• Demonstrated ability to understand and develop processes.
• Excellent organizational and Project management skills with an attention to detail and follow-through
• Professional English written and verbal communication skills
• Ability to influence others to achieving goals
• Ability to work under a minimum of supervision
• Hands-on mentality

OTHER

• Minimum of five years of similar work experience.
• Has a complete knowledge of company products and services

Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Patricia Oses Equiza.