Badge Record Review Specialist 100%

Badge Record Review Specialist (m/f/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 profound 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 client in Sisseln, we are looking for an immediate:
Badge Record Review Specialist (m/f/d) 100%
You benefit from:
•Free parking spaces directly at the company location
Structured and comprehensive induction 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:
Carrying out 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
Reviewing the batch documentation according to GMP guidelines and initiating 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 the 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 the GMP environment as well as in handling batch documentation is an advantage
Experience in training coordination or in the induction 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 in an understandable and audience-appropriate 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 skills, reliability and commitment
You have the talent, we provide the platform!
Apply now with your current documents via e-mail and discover how you can reach new professional heights with beeworx. jpida4e401fjm jit0832jm jiy26jm