Biologist (m/f/d)
Enter the world of innovative automation solutions in the field of diagnostics, which makes a decisive contribution to improving patient care. Our renowned client, located in the vibrant economic area of Mannheim, stands for groundbreaking technologies and a progressive working environment. Your expertise as a specialist in batch documentation is required to further develop cutting-edge technologies and optimize processes in a dynamic team.
About Randstad Professional
Randstad is one of the world's leading personnel service providers with the goal of becoming more specialized and fairer than any other company in the world of work. Through the corporate strategy "partner for talent" we find, promote and connect specialized talent with companies - worldwide, locally and always at high speed. We create powerful, diverse and agile teams and support each individual in achieving a successful career with equal opportunities.
Randstad Professional (formerly GULP) is one of Randstad's four specializations and focuses on placing specialists and managers in the future industries of IT, engineering, life science and office.
Your tasks
Review of batch documents
Checking the completed HABs for GMP-compliant documentation including timely correction in electronic batch review systems
Strict compliance with OLT (Order Lead Time) including tracking and requesting the required HAB accompanying documents
Collaboration in the processing of measures from GMP requirements
Support with GMP audits
Support with actions for inspections or QRBs/DRs (e.g. HAB research in the archive)
Revision and creation of documentation-relevant SOPs and implementation of related training
Electronic recording and evaluation of batch data
Participation in process optimization to improve good documentation practice and continuous error reduction
Preparation and printing of batch documentation
Your profile
Successfully completed scientific degree or completed training as a pharmaceutical technician/chemist (m/f/d) or comparable training
Solid professional experience in parenteral production desirable
Good knowledge of GMP regulations and GMP-compliant documentation as well as knowledge of hygiene in the pharmaceutical environment
Solid IT system knowledge (MES, SAP, Excel, Word)
Very good knowledge of German and good knowledge of English
- Attractive salary and long-term job security through membership of the group
- Up to 30 days of vacation per year
- Subsidy for company pension scheme after the end of the probationary period
- Extensive social benefits, including Christmas and vacation bonuses
EU working permit is mandatory
