Analytical Engineer (GMP)
You will be involved in the setup, validation and execution of QC methods for the analysis and release of ATMP products, to be used in clinical trials.
You will also participate in environmental monitoring sampling, raw material control, deviation investigations and review of documentation. Experience in cell culture, flow cytometry, potency assays, ddPCR, qPCR, mycoplasma, sterility and endotoxin tests would be a significant asset; particularly in the context of ATMP analysis.
Knowledge of aseptic work techniques is desirable. Prior experience working in a GMP environment is preferred for the role.
You must be capable of working as part of a team and as the company and team is very international and the business language is English, excellent English communication skills is required.
The role is suited to motivated persons with a drive to learn and grow in a complex and varied environment.
What we are looking for:- Experience working according to GMP.
- Quality control experience in the cell therapy or ATMP space.
- Experienced in writing deviation investigations, CC and CAPA’s.
- Good grasp of the underlying biology related to cell engineering.
- Experience in microbiology.
- Fluent written and spoken English.
We offer:
An international workplace, with plenty of variety in the job, interaction with all other Anocca employees and the opportunity to work at the exciting intersection of biotechnology and medicine.
Please note that we contact candidates that we would like to invite for an interview within 3 weeks after the advertisement has closed. Unsuccessful candidates will not be contacted. Compensation Monthly salary Tier 1 occupational pension plan Wellness grant Flexible work hours
We ensure unbiased recruitment by hiding your personal information such as name, email, etc. and photos from the recruiter during the screening process.