Badge Record Review Specialist (m/w/d) 100%

Welcome to beeworx – your partner for your next career step! For almost 20 years, we have been supporting you in achieving your professional goals. With our fast response time and our sound expertise, we help you find the right position that matches your skills and ambitions. Whether you are looking for new challenges or simply want to develop further – with us, you get the necessary support to increase your labor market fitness and find the ideal job. Let's reshape your career together! For our customer in Sisseln, we are looking for an immediate: Badge Record Review Specialist (m/w/d) 100% You benefit from: • Free parking spaces directly at the company location • Structured and comprehensive onboarding for a successful start • Appreciative corporate culture with open communication and collegial team spirit • Exciting activity in a leading company in the pharmaceutical industry • Opportunity to further develop your GMP knowledge and your experience in quality management • Modern working environment with clear processes and high quality orientation • Long-term perspective in a dynamic and innovative working environment What awaits you: • Execution of the Batch Record Review (batch documentation review) for the areas of granulation, tableting, film coating, and packaging, as well as for GMP batches in the development area • Review of the batch documentation according to GMP guidelines and initiation of necessary corrective and deviation measures • Independent organization and prioritization of documentation reviews for timely batch release • Creation of Batch Manufacturing Reports (BMR) and maintenance of the relevant documentation • Collection and evaluation of key figures in the area of batch documentation • Ensuring compliance with GMP, safety, and environmental guidelines within your own area of responsibility • Reporting of deviations as well as potential safety and environmental risks • Close cooperation with production, quality assurance, and other specialist departments What distinguishes you: • Completed training in a GMP environment (e.g., pharmaceutical technologist, chemical laboratory technician, or comparable qualification) or several years of professional experience in the pharmaceutical industry • Several years of experience in a GMP environment as well as in handling batch documentation is an advantage • Experience in training coordination or in the onboarding of employees is a plus • Very good German skills as well as good English skills in spoken and written form. Good MS Office skills and confident handling of documentation systems • Strong communication skills and enjoyment of working in a team • Ability to convey knowledge understandably and in a target-group-oriented manner • Structured, careful, and independent way of working • Organizational talent as well as the ability to set priorities flexibly and efficiently • High resilience, quality awareness, and solution-oriented thinking • Teamwork ability, reliability, and commitment You have the talent, we offer the platform! Apply now with your current documents via e-mail (edith.weiss@beeworx.ch) and discover how you can reach new professional heights with beeworx.