Quality Control Engineer

Location: Belgium

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, Biotechnology, Clinical Research and Healthcare organisation, based in Antwerpen Belgium.

The Company

Our colleagues all over the world work together to have a positive health impact for everyone, everywhere. As we continue to develop health care products and activities, we are constantly looking for new talents.

At this moment we are looking for highly qualified candidates for the function: Quality Control Engineer

Role Description

The department is responsible for the release of products, PQS, GMP, etc.).

This function is responsible for executing and documenting all versions of the product to the laboratory of the product assessment procedure for continuous improvement of products and processes. This position is the primary contact for the chemical and microbiological laboratory in case of quality deviations.

This function reports to the QA Lead within the quality team responsible for the Laboratory (Chemical and Microbiological).

Responsibilities

Evaluate incidents in the Laboratory (Chemical and Microbiological) and prepare for the QA Manager / QA lead.
Evaluate and approve Laboratory research reports (LIR) related to Out-of-Specification results, questionable results and recommendations for QA Manager / QA lead.
Evaluate laboratory examinations, corrective and preventive actions and verify the progress to be made.
Coordinating cross-functional research in complex cases and working closely with the Laboratory (Chemical and Microbiological) and various departments.
Ensure that products are manufactured and packaged in Puurs and that the external companies in Puurs comply with the company and legal requirements.
Ensure that products are purchased and used at the Puurs plant to meet the legal requirements of the company.
Operate and maintain the Quality Assurance systems.
Approval of qualification documents relating to the Laboratory (Chemical and Microbiological).
Approve master documents and SOPs.
Prepare the quality assessment.
Support for continuous improvements of products and processes door:
Research into quality deviation (events / QARs)
Trending of LIR, events and QARs
Participation in operations, product and system teams and practical for the evaluation of the fixed operations
Wear in the timely delivery of products.

Requirements

University degree in a scientific discipline, preferably in pharmacy
Preferably experience in the laboratory.
Experience with quality research is an advantage.
Analytical skills
Good communication skills, both oral and written, in English and English
Excellent documentation skills (technical report writing in Dutch / English)
Good time management and pre-skills
Human interactions (diplomacy, persuasion, assertiveness, ...)

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