(Junior) Quality Manager
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 Oost-Vlaanderen Belgium.
- Daily contacts/follow-up of suppliers (subcontractors): Compiling all documentation, necessary for production and QC of final products, approval of master batch records, deviation handling, follow-up process validation
- Release of Final Products to the customer
- Follow-up of stability studies
- Customer Complaint Handling (Investigation, Report, Follow-up)
- Initiate and follow-up CAPA reports
- Minimum 2 years of experience in a similar role in a Pharmaceutical Company
- You have a Master’s degree (Pharma, Sciences, Bio..)
- Experience in a Production Environment is a plus
- You are fluent in Dutch and English
- You have a mature personality. You are assertive and like challenges. You are passionate and have strong organizational and analytical skills.
Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Seppe Verhoeven.
The Company
.Role Description
You will be working in a rapidly expanding company where innovation is key to make the next step. You are a person who has excellent communication skills, you have a minimum of two years experience in a similar role, you have knowledge of ISO 13485 and you are used to being the point of contact of customersResponsibilities
- Support the Design Transfer of new products to Operations- Daily contacts/follow-up of suppliers (subcontractors): Compiling all documentation, necessary for production and QC of final products, approval of master batch records, deviation handling, follow-up process validation
- Release of Final Products to the customer
- Follow-up of stability studies
- Customer Complaint Handling (Investigation, Report, Follow-up)
- Initiate and follow-up CAPA reports
Requirements
- Knowledge of GMP and/or ISO13485 standard- Minimum 2 years of experience in a similar role in a Pharmaceutical Company
- You have a Master’s degree (Pharma, Sciences, Bio..)
- Experience in a Production Environment is a plus
- You are fluent in Dutch and English
- You have a mature personality. You are assertive and like challenges. You are passionate and have strong organizational and analytical skills.
Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Seppe Verhoeven.
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