Specialist, GMP Quality Control (PCR) | Technischer Assistent (m/w/d)

Job Summary

This role involves joining a leading biopharmaceutical company in Frankfurt, contributing to the development of high-quality medicines derived from human blood plasma. The Specialist will be responsible for executing virological analyses of human plasma using Polymerase Chain Reaction (PCR) techniques within a routine laboratory setting. Key day-to-day tasks include meticulous data presentation, evaluation, and documentation, strictly adhering to GMP guidelines and standardized operating procedures. A core function involves the optimization and validation of existing PCR methods and the creation or updating of Standard Operating Procedures (SOPs). Candidates must possess a completed scientific education (such as BTA, CTA, MTA, or Bachelor) and demonstrate profound experience with Real-Time PCR, ideally gained within a routine GxP laboratory environment. Success in this role requires a highly structured, responsible, and precise working style, coupled with strong German language proficiency and basic English skills.