QC 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 and Healthcare organisation, based in Antwerpen Belgium.

The Company

The company makes medicines and vaccines that help people when they are ill and contribute to the prevention of diseases. We are working on new, innovative treatments that are the lives of patients going their human disease. Sells some of the world's best-known and most prescribed drugs and vaccines. Participates in powerful partnerships with other parties active in health care. Contributing globally to healthcare, many thousands of colleagues - in more than 175 countries.

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 product review procedures 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) from Qa Manager / QA lead.
Evaluate laboratory tests, 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 closed in Puurs and that external companies in Puurs meet the legal requirements of the company.
Ensure that products are purchased and used in the Puurs factory 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 business documents and SOPs.
Prepare the quality assessment.
Support for continuous improvements of products and processes door:
Research into quality deviations (events / QARs)
Trending of LIR, events and QARs
Participation in operations, product and system teams and practical experience
Wear in the timely delivery of products.
qualifications

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, also as written, in English and English
Excellent documentation skills (technical report writing in Dutch / English)
Good time management and pre-skills
Human interactions (diplomacy, conviction, assertiveness, ...)
The company is an employer with fair opportunities in good regulation.

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.