URGENT - Temporary - QA Coordinator 3 days a week!
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 organisation, based in Antwerpen Belgium.
Ensures the maintenance of the certifications of the quality management system
Represents quality during audits of authorities
Coordinate and ensure internal audits for GxP activities at the various sites.
Accompany auditors during external audits
Provide support to the operational teams for the analysis of nonconformities according to the methods defined thus the correct follow-up of the corrective / preventive actions.
Provide support for the qualitative assessment of subcontractors
Quality performance analysis
A master in a relevant education (pharmacy, life sciences)
Excellent communication skills
At least 3-5 years of experience in a similar role
Excellent knowledge of Quality Management Systems
Heb je interesse en wil je meer weten over deze functie, reageer dan door op solliciteer te klikken en contact op te nemen met Seppe Verhoeven
The Company
The company is an international market leader with a very strong focus on the life sciences industry. Some of the products they produce are used to battle diabetes, hart conditions and much more.Role Description
In this role you will be responsible for the development and standardization of the quality management system and you will also be responsible for the communication between sub contractors and you will also be responsible for educating your fellow colleagues in GMP guidelines.Responsibilities
Ensures that pharmaceutical sites are "inspection readiness" at all timesEnsures the maintenance of the certifications of the quality management system
Represents quality during audits of authorities
Coordinate and ensure internal audits for GxP activities at the various sites.
Accompany auditors during external audits
Provide support to the operational teams for the analysis of nonconformities according to the methods defined thus the correct follow-up of the corrective / preventive actions.
Provide support for the qualitative assessment of subcontractors
Quality performance analysis
Requirements
Fluent in both written and EnglishA master in a relevant education (pharmacy, life sciences)
Excellent communication skills
At least 3-5 years of experience in a similar role
Excellent knowledge of Quality Management Systems
Heb je interesse en wil je meer weten over deze functie, reageer dan door op solliciteer te klikken en contact op te nemen met Seppe Verhoeven
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