Cleaning Validation Consultant

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 Rhône France.

Medical Device company with a broad portfolio of medical devices. The manufacturing plant in the Lyon area, produces sterile devices.

ROLE DESCRIPTION

As a Cleaning Validation Consultant, the main purpose of this assignment is the validation of cleaning processes.

You will be author of cleaning validation protocols and reports. This will include the supervision of these practices.

The Cleaning Validation Consultant will perform risk assessments for sterile and non-sterile device cleaning processes.

RESPONSIBILITIES

- Validation of Cleaning processes
- Develop and write cleaning validation protocols and reports
- Perform risk assessments

REQUIREMENTS

- Technical or Scientific degree
- At least 5 years of experience in Cleaning Validation within a Medical Device environment
- Fluent in French and English

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.