Chemical laboratory technician

Vor 4 Tagen


Biberach, Deutschland GULP – experts united Vollzeit

We are currently looking for a Senior Sample Coordinator (m/f/d) for a business partner in Biberach .

A secure and fair income and good social benefits are just as important to you as a responsible job and a long-term perspective with a research-based pharmaceutical company ? Then join us - your satisfaction is our goal Apply directly online now We value equal opportunities and welcome applications from people with disabilities, whose inclusion is particularly important to us.

Here's what we offer

Attractive salary and long-term job security through group affiliation Up to 30 days vacation per year Contribution to company pension scheme after end of probationary period Extensive social benefits, including Christmas and vacation bonuses Reimbursement of travel expenses As a rule, a permanent employment contract Good chances of being taken on by our business partners Tailored further training opportunities and free language courses A wide range of employee benefits

Your tasks

The Senior Sample Coordinator carries out sample management activities independently. This field of activity includes, among other things

Creation and maintenance of sampling plans Process transfer manager for the area Organization and implementation of sample shipments GMP-compliant documentation in reports or electronic systems Independent coordination, processing and follow-up according to project or production planning schedules Presentation of data to internal specialist teams Creating relevant graphs/tables with simple statistical parameters and electronic sample management, working with databases

Your profile

Completed training as a chemical or biological laboratory technician, pharmaceutical technician, pharmaceutical commercial employee, industrial clerk or comparable training, e.g. in the field of logistics or knowledge and skills acquired elsewhere Knowledge of GMP-compliant documentation, regulations and national and international GMP regulations Ideally at least 4 years of professional experience in a GMP laboratory or production environment in the biopharmaceutical industry Confident handling of MS Office (Word, Excel, PowerPoint) Good written and spoken English skills Independent and autonomous way of working Good communication and teamwork skills, high interface competence

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