Associate QA | 1-3+ years experience | Breda | Shifts included
Location: NetherlandsSIRE® 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 Noord-Brabant Netherlands.
- Perform batch record review of batches assembled, packaged and labeled at ABR and contract manufacturers.
- Establish effective working relationships with Production, Warehouse, Maintenance and Engineering, QA Management and the Qualified Person
- Act as a first point of contact in case of production queries (quality related) during packaging and labeling operations.
- Review and approve batch production record data entries before production activities take place
- Perform finished product checks during (commercial) production runs
- Typically 3 years of related Quality Assurance or manufacturing experience in the pharmaceutical or medical device industry with experience in batch record review and investigations.
- Good Manufacturing Practice (GMP), Good Distribution Practice (GDP) and/ or Good Clinical Practice (GCP) knowledge with the ability to interpret and apply in mainly routine cases.
- Fluency in English language
- Open to work in shifts (!)
Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Jeroen Zanting.
The Company
Big pharmaceutical company located in Noord-Brabant is looking for a Sr. Associate QA.Role Description
- Provide QA guidance and support in the production area at ABR.- Perform batch record review of batches assembled, packaged and labeled at ABR and contract manufacturers.
- Establish effective working relationships with Production, Warehouse, Maintenance and Engineering, QA Management and the Qualified Person
Responsibilities
- Provide daily guidance and support to Production staff in regards to compliance with Standard Operating Procedures and Work Instructions.- Act as a first point of contact in case of production queries (quality related) during packaging and labeling operations.
- Review and approve batch production record data entries before production activities take place
- Perform finished product checks during (commercial) production runs
Requirements
- Bachelor degree or higher (or MBO with extensive years of relevant experience)- Typically 3 years of related Quality Assurance or manufacturing experience in the pharmaceutical or medical device industry with experience in batch record review and investigations.
- Good Manufacturing Practice (GMP), Good Distribution Practice (GDP) and/ or Good Clinical Practice (GCP) knowledge with the ability to interpret and apply in mainly routine cases.
- Fluency in English language
- Open to work in shifts (!)
Other information
Interested? Do not hesitate and reply to this vacancy or send me a message on j,zanting@sire-search.com !Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Jeroen Zanting.
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