Quality officer ( At least 1 year contract)
Location: NetherlandsSIRE Life Sciences® is the market leader in life science recruitment. We believe the recruitment market needs to gear up in technology and continues innovation. We like technology, in a life science 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!
THE COMPANY
Our client is a professional Pharmaceutical organization, based in Noord-Brabant Netherlands.
Do you want to work at a company who really serves their patients? A company who encourage our team members to have fulfilling and meaningful careers through challenging assignments, career development, and valuable opportunities? Then this company will suit you perfectly.
ROLE DESCRIPTION
You will act as a first point of contact in case of production queries (quality related) during packaging and labeling operations. Work together with production and maintenance team to resolve the quality related problems. You will be able to show your analytical, work independent, hands-on and result driven, team player and strong communication skills.
Note: This job is 5 working days (mon-fri), in 3 shift operation
RESPONSIBILITIES
You will be responsible for the review and approve batch record exception reports. Maintain to improve on quality and to limit number of errors. Next to that you will be responsible for the following:
- Perform finished product checks during (commercial) production runs
- Complete batch release preparation prior to Qualified person disposition
- The knowledge and skills necessary to perform the duties of this position are typically acquired through the following combination of education, experience and knowledge or the equivalent.
Note: You don't need to have this work experience already. Their is an 1,5 - 3 months training!
REQUIREMENTS
- MBO or college degree or BSc degree
- Typically 2 or 3 years of related Quality Assurance or manufacturing experience in the pharmaceutical or medical device industry with experience in an production site.
- GMP, GDP and/ or GCP knowledge with the ability to interpret and apply in mainly routine cases.
- Manufacturing and/or Quality analytical processes and operations.
- Excellent in English
- Quality mindset
- TrackWise, SAP, (pre) Werum PAS-X (electronic batch Records) is a pre
Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Valentijn de Krom.
