QC Specialist
- Employment type
- Temporary
- Location
- Schaffhausen
- Company
- Randstad Inhouse Services, Hochstrasse 201, 8200 Schaffhausen
- First posted
Caring for the world … starts with the individual. This guiding principle inspires and unites the people at Johnson & Johnson. The culture of caring is at the heart of our corporate philosophy, which is anchored in the Credo.
Johnson & Johnson is an international manufacturing company and produces pharmaceutical and medical technology products as well as active pharmaceutical ingredients (APIs) for global markets at its production site in Schaffhausen. Thanks to its innovative products, processes, and technologies, Johnson & Johnson is one of the leading pharmaceutical companies in Switzerland today, and the site in Schaffhausen is simultaneously a strategic introduction and growth location.
QC Specialist
Main activities include:
Qualification of laboratory equipment in compliance with current GMP and regulatory requirements
Preparing and executing Change Control Records related to the lifecycle management of laboratory equipment
Creation & review of detailed, comprehensive, and well-structured qualification documents (e.g., Impact & Risk Assessments, IOPQ protocols, and decommissioning documents)
Drafting procedures (WIs, SOPs) related to the lifecycle management of laboratory equipment
Identification and documentation of relevant pharmacopoeia requirements for analytical devices and ensuring compliance with applicable regulatory specifications
Performing troubleshooting to diagnose and resolve problems
Supporting the investigation of deviations caused by non-conforming equipment and implementing corrective actions (CAPA)
Collaboration with suppliers and manufacturers for problem-solving (e.g., technical support for manufacturer qualifications, maintenance and calibration, troubleshooting, and investigations)
Who we are looking for:
Completed studies (Master, PhD) in a scientific subject or Bachelor's degree with relevant professional experience
Experience in a GMP environment is an advantage
Strong analytical understanding and experience with various analytical techniques
Fluent in English/German, both written and spoken
Team player and reliable personality with a precise way of working
Ideally experience with pharmacopoeias
This position is initially limited to 12 months, but offers you an excellent option for extension. If you are looking for the perfect entry into the pharma industry, this position opens the doors to one of the largest and most successful healthcare companies in the world. With us, you will start your career in a globally leading, innovative environment, benefit from excellent development opportunities, and work in a great, dynamic team. Take the opportunity to gain valuable practical experience in the Quality area and actively help shape the future of healthcare. jpid602ed9fjm jit0729jm jiy26jm
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Posted 3 days ago