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Quality Assurance Team Lead

SIRE Life Sciences®

Netherlands, zagranica

SIRE Life Sciences®

Quality Assurance Team Lead

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 Gelderland Netherlands.

They are a fast growing and dynamic company cent. Their focus lies on manufacturing sterile medicinal products that have unique niche qualities to help the lives of millions in the future.

ROLE DESCRIPTION

The company is looking for an experienced Quality Assurance specialist who can take care of their Quality Management System and improve where necessary concerning all intern and external regulations. You are independent and area able to increase Quality consciousness within the company. Your position will be a visible role in the company with a hands-on mentality and will be actively communicating to other teams and external organizations. The project is expected to take 8 months.

RESPONSIBILITIES

You will be responsible of a team off five quality specialists and will coordinate daily tasks accordingly to the strategy of the company. With this you other responsibilities will be:
• Independently maintain the QMS according to a variety of authorities and governments (FDA, Notified Bodies, etc.)
• Estimate current Quality Aspects and processes regarding the Medical Devices in produce
• Participate, Initiate and perform intern and extern projects regarding improvement of the quality, QMS and cGMP-compliance
• Participate in audits

REQUIREMENTS

• A Bachelor degree
• At least 5 years’ experience within the Quality Assurance with at least 2 year experience within Medical Devices
• Additional courses and/or experience with QMS, GMP and intern and external audits
• Experience within a production environment
• Excellent communicative skills as a lead and external contact

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®

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