SIRE® is the market leader in Life Sciences recruitment. We believe the recruitment market needs to gear up in technology and continuous innovation. We like technology, in a Life Sciences 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!Our client is a professional Pharmaceutical organisation, based in Waals-Brabant Belgium.

The Company

They believe that everyone deserves a chance at a healthy life, without illness and full of possibilities. They focus every day on delivering transformative innovations that bring us more intelligent and personalized care.

Role Description

Follow correct working laboratories equipment, systems and utilities by performing daily checks, calibration and qualification.
In collaboration with internal customers, organize the installation of laboratory equipment’s and perform qualification and validation using reports and protocols. If necessary, create the necessary documents.

Responsibilities

- Responsible to follow/maintain/validate the testing machines (like particules counters, electronic microscopes, tensile tester);
- Participate to the selection, acquisition and implementation on site of new lab equipments;
- Schedule and manage the periodic calibrations and qualifications in collaboration with internal customer and equipment providers of the assigned equipment;
- Responsible for the develompent and completion of the documents and protocols related validation/qualification of the equipments;
- In collaboration with Quality Assurance and experts, is responsible to implement new guidances, norms, in the assigned procedures and if necessary, create new procedures;
- Uses the procedures and equipment management tools, archives the documents related to calibration and validation;
- In case of equipment failure, may participate in technical investigation;
- Is able to give technical guidance/training to colleagues.

Requirements

- Basic Knowledge about GMP/GDP;
- Well organized, is able to manage several equipment’s in the same time;
- Team player;
- Communicates easily;
- Take personal accountability for assigned equipment’s/project;
- Analytical mindset;
- Able to summarize and easily explain complex situation;
- Proactive in her/his reporting.

Other information

Education: min. 3 years after high school / with background in electromechanical, chemistry. Biochemistry;
Experience: at least 12 months.

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