SIRE Life Sciences®

Quality Officer

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 Utrecht Netherlands.

They are an international provider in Medical Device products that develop unique state of the art devices with the goal to improve life and surgical activities.

ROLE DESCRIPTION

Due to increasing growth and expansion of the team the company is looking for Quality specialists in the field of Medical Devices. You will support the production of the Medical Devices by ensuring compliancy to all requirements and standards that apply to the company and the products currently made or will be made. You will be part of a team of Quality specialists and will be reporting to the Quality supervisor.

RESPONSIBILITIES

Your main responsibility will be safeguarding the quality and compliancy concerning all regulations and standards. You will conduct with the team tests during the production process and after, assess and analyses inspections concerning quality and make sure that products satisfy all standards. Other responsibilities will be:
• Assist in research when deviation of quality is assessed
• Support the estimations of processes and write procedures and instructions
• Participate in validation projects
• Safeguarding the compliancy of all activities done in the company to SOP’s, relevant GMP and safety/health regulations

REQUIREMENTS

• 2+ years of relevant experience, clean room is a plus
• Experience with Quality Systems
• Experience with ISO 13485 is a big plus
• Strong communicative skills

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

Prosimy o aplikowanie poprzez przycisk znajdujący się po prawej stronie ogłoszenia.
SIRE Life Sciences®

Czy chcesz otrzymywać oferty pracy na podobne stanowiska?

Utwórz powiadomienie e-mail
Zapisz mnie

Zapisani kandydaci otrzymują informacje jako pierwsi.

Podziel się ze znajomymi