Quality Compliance Officer/ Auditor
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 Oost-Vlaanderen Belgium.
- You support adequate CAPA management
- You ensure adequate management of quality contracts
- You support implementation of new GMP legislation and guidelines in the GMS (for the domain(s) assigned to you)
- You have multiple contacts with internal stakeholders (production, QC, Supply chain, R&D, ...) and external stakeholders (representatives of customers or authorities)
- You make sure that continuous improvement is embedded in your own performance and that of the company. You understand and apply OE concepts and tools.
- You have knowledge of GMP legislation and guidelines
- You have gained several years of relevant professional experience in an industrial environment
- You have excellent communication skills, both in Dutch and English (spoken and written)
- You possess IT-skills (eg MS Outlook, Word, Excel, Powerpoint). Preferable you also have knowledge of Sharepoint
- You have good organization and scheduling skills.
- You know how to deal with pressure and deadlines
- Proven experience with Operational Excellence (Lean/Six sigma) is an asset
The Company
The Client is a leader in the pharmaceutical industry, a global manufacturer of high-quality pharmaceuticals and specialty chemicals.Role Description
In this role you will be responsible for quality related man for qualitative and efficient management of customer audits and/or authority inspections (including scheduling, preparation, hosting and follow-up)Responsibilities
- Responsible for qualitative and efficient management of customer audits and/or authority inspections (including scheduling, preparation, hosting and follow-up)- You support adequate CAPA management
- You ensure adequate management of quality contracts
- You support implementation of new GMP legislation and guidelines in the GMS (for the domain(s) assigned to you)
- You have multiple contacts with internal stakeholders (production, QC, Supply chain, R&D, ...) and external stakeholders (representatives of customers or authorities)
- You make sure that continuous improvement is embedded in your own performance and that of the company. You understand and apply OE concepts and tools.
Requirements
- You possess a Master or Engineering degree in Chemistry / Sciences- You have knowledge of GMP legislation and guidelines
- You have gained several years of relevant professional experience in an industrial environment
- You have excellent communication skills, both in Dutch and English (spoken and written)
- You possess IT-skills (eg MS Outlook, Word, Excel, Powerpoint). Preferable you also have knowledge of Sharepoint
- You have good organization and scheduling skills.
- You know how to deal with pressure and deadlines
- Proven experience with Operational Excellence (Lean/Six sigma) is an asset
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