BiologistBiologist (m / f / d)

GULP – experts united; Mannheim; Vor Ort; EUR 50.000 - 70.000; Vollzeit

Zusammenfassung

Join a leading company in innovative automation solutions, contributing to diagnostics and patient care in Mannheim. As a specialist in batch documentation, you will ensure quality compliance and optimize processes in a dynamic team. This role offers attractive benefits, professional development, and a progressive working environment.

Leistungen

Attractive salary

Up to 30 days vacation per year

Contribution to pension scheme

Extensive social benefits

Christmas and vacation bonuses

Qualifikationen

• Scientific studies or training as pharmacist/chemist (m/f/d) required.
• Experience in manufacturing parenterals is desirable.
• Knowledge of GMP regulations and hygiene in pharmaceuticals.

Aufgaben

• Review batch documents and ensure GMP compliance.
• Support audits and inspections related to quality.
• Collaborate on documentation-relevant SOPs and training.

Kenntnisse

GMP regulations

Documentation

Process optimization

IT systems knowledge

German language

English language

Ausbildung

Completed scientific studies or pharmacist/chemist training

Tools

MES

SAP

Excel

Word

Jobbeschreibung

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 pioneering 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.

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
• Review of batch documents
• Checking the completed HABs for GMP-compliant documentation including prompt correction in electronic batch review systems
• Strict adherence to the OLT (Order Lead Time) incl. 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 searches in the archive)
• Revision and creation of documentation-relevant SOPs and implementation of related training courses
• 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 studies or completed training as a pharmacist / chemist (m / f / d) or comparable training
• Sound professional experience in the manufacture of parenterals desirable
• Good knowledge of GMP regulations and GMP-compliant documentation as well as knowledge of hygiene in the pharmaceutical environment
• Sound knowledge of IT systems (MES, SAP, Excel, Word)
• Very good knowledge of German and good knowledge of English