QC SpecialistPratteln, SwitzerlandConsulting Validation & Compliance
The organisation of sample management plays a central role within the customer. Analysis samples are taken during the manufacture of pharmaceutical and chemical products at various stages of production. The analysis samples must be recorded, distributed to the internal and external QC laboratories, stored and disposed of at the end of their shelf life. There are numerous interfaces to the research and QC laboratories, warehouses, production, planning and external contract laboratories. The daily interaction with local and global, internal and external partners makes the job varied and exciting. Good communication, solution-oriented and systematic work, as well as organisational talent are the key to success in this multi-faceted, responsible role.
WHAT WILL YOU DO?
- Organisation and implementation of sample collection and sample distribution of commercial finished pharmaceutical products, raw materials and active ingredients, packaging materials and medical devices.
- Coordination and realisation of sample shipments to external test laboratories, as well as transfer and control of analysis results from external test laboratories in eLIMS.
- Carrying out and documenting temperature analyses of sample and product shipments.
- Carrying out visual comparative tests of primary packaged sterile products during the release of internally manufactured products or as part of the incoming inspection of externally manufactured bulk goods.
- Creation and maintenance of SOPs and work instructions in the area of responsibility.
- Collaboration in the creation and processing of non-conformances and change requests in Trackwise, as well as assistance in the definition of corrective and preventive actions (CAPA).
- Collaboration in local and global projects.
WHO ARE YOU?
- Professional experience in a GMP-regulated environment, preferably in the field of quality control, is an advantage
- Very good organisational and communication skills, customer-oriented way of working and “can do” mentality
- Very good knowledge in the use of Microsoft Office programmes
- Experience in the control of analysis data and GMP documents, as well as experience in working with SAP, eLIMS and Trackwise are an advantage
- Very good knowledge of German and English (written and spoken)
READY TO APPLY?
Completely convinced after reading this job posting? Let’s get together! Start your application here or get in touch with our recruiter. We would love to schedule a first meeting with you!
Apply now
WHAT TO EXPECT WHEN YOU APPLY?
Application
Your journey begins with your application, which we’ll attentively review and respond to with valuable feedback.
Video call
Once you meet the position’s basic qualifications, our recruiter will connect with you to schedule a video call.
Face-to-face interview
Delve deeper into the role and responsibilities during a face-to-face interview with the hiring manager, who will share insights into your prospective position.
Technical interview
Engage with potential team members, showcasing your skills and assessing if the role is the ideal match for you.
Job offer
Congratulations, we believe you’re the perfect fit for the job!
Contract
Signed & sealed! We’re thrilled to welcome you aboard our team.
Where we are
Zwijndrecht (HQ)Baarbeek 12070 ZwijndrechtBelgium+32 3 641 17 70Show VAT information
- Agidens International NVBE0468070629
- Agidens Life Sciences NVBE0411592279
- Agidens Process Automation NVBE0465624744
GorinchemStephensonweg 64207 HB GorinchemNetherlands+31 183 64 33 44Show VAT information
- Agidens Process Automation BVNL005469272B01
- Agidens Life Sciences BVNL850983411B01
BaselHohenrainstrasse 104133 PrattelnSwitzerland+41 61 713 00 80Show VAT information
- Agidens AGCHE109416838
BrasschaatRuiterijschool 12930 BrasschaatBelgium+32 3 641 17 70
AmsterdamSuikersilo-West 301165 MP HalfwegNetherlands+31 183 64 33 44