Biology Laboratory Technician QC Pharma (m/f/d) – qPCR & ELISA (Trainer - Pharmaceutical Representatives)

BS – Your partner for qualified specialists As an owner-managed personnel service provider, we recruit experienced specialists for leading companies in the pharmaceutical industry. We are currently looking for a Biology Laboratory Technician QC Pharma (m/f/d) with a focus on qPCR and immunoassays for our client in Frankfurt am Main – in a GMP-regulated environment with direct responsibility for the release analytics of innovative biologics.

Biology Laboratory Technician QC Pharma (m/f/d) – qPCR & ELISA

Your tasks – Analytics at the highest quality level:

• You will perform analytical tests for biologics (active pharmaceutical ingredients and finished medicinal products) in accordance with GMP requirements, focusing on identity testing (Dot Blot, ELISA) and qPCR analytics
• You will test samples within the framework of releases and stability tests in a timely manner, thereby ensuring quality for local and international partners
• Additionally, you will manage equipment as an equipment officer and independently carry out calibration and qualification measures
• You will actively participate in analytical transfers and support the implementation of new methods
• You will create regulatory, pharmaceutical-technical documentation in a timely manner with the support of the laboratory management

Your profile – GMP expertise meets analytical skill:

• Completed training as a Biology Laboratory Technician (m/f/d), alternatively also as a Chemistry Laboratory Technician (m/f/d) or Pharmaceutical Laboratory Technician (m/f/d)
• You must bring mandatory GMP experience in pharmaceutical analytics
• Knowledge of blotting and ELISA techniques as well as in the testing of medicinal products is desirable
• Good written and spoken English skills are required
• Your strengths: sense of responsibility, team orientation, and communication skills towards colleagues, supervisors, and external partners – ideally combined with SAP experience

Our offer – Precision in a professional environment

• Flextime for flexible working hours within the laboratory operations
• Work with state-of-the-art analytical technologies (qPCR, ELISA, Dot Blot) in a GMP-regulated QC laboratory
• Versatile range of tasks from routine analytics to equipment qualifications and method transfers
• Classification according to E 09 with attractive conditions of temporary employment
• Professional induction and further development in an international pharmaceutical environment

We are happy to answer any questions, please quote the reference number below.

Supplementary information: Requirements for the applicant: Advanced knowledge: ELISA (Enzyme-linked immunosorbent assay) Expert knowledge: Quality testing, Quality assurance, GMP (Good Manufacturing Practice)