Compliance Lead / Pharma / Permanent / Brussels region
Location: BelgiumSIRE® 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 Brussels Hoofdstedelijk Gewest Belgium.
- Batch records reviewing and associated documents after production
- Project leader for the new QA projects
- Actively contribute to continuous improvement initiatives
- Point of contact in case of audits and be involved in internal audits
- You will give QA trainings to colleagues (GMP training, Quality issues training, new SOP/Policies,…)
- Work with relevant departments to ensure timely closure of quality actions
- Back-up of the Head of Quality
• Professional experience required: Min.8 years in a QA position
Specific skills required:
• Perfect knowledge of GMP in a regulated environment
• Excellent interpersonal skills
• Strong problems solving skills, issue resolution and root cause analysis
• Language: French, English
Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Martijn van Nieuwenhovensss.
The Company
The are a pharmaceutical (manufacturing) company for ingredients & products. They support leading pharmaceutical & biotechnology companies to achieve product success for their patients’ healthier lives.Role Description
You will be part of the QA Department and ensure that the products are in accordance with the GMP regulation. Under the direction of the Head of Quality, you will be in charge to improve continuously the Quality system regarding the GMP requirements and in case of quality issues and problem solving techniques you will assure the successful outcomes of company and external Health Authority.Responsibilities
- You will provide QA support for deviations, change controls, CAPA, ...- Batch records reviewing and associated documents after production
- Project leader for the new QA projects
- Actively contribute to continuous improvement initiatives
- Point of contact in case of audits and be involved in internal audits
- You will give QA trainings to colleagues (GMP training, Quality issues training, new SOP/Policies,…)
- Work with relevant departments to ensure timely closure of quality actions
- Back-up of the Head of Quality
Requirements
Minimum qualifications: Master degree Sciences• Professional experience required: Min.8 years in a QA position
Specific skills required:
• Perfect knowledge of GMP in a regulated environment
• Excellent interpersonal skills
• Strong problems solving skills, issue resolution and root cause analysis
• Language: French, English
Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Martijn van Nieuwenhovensss.
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