Description of the job:
They are looking for an Analytical Development Technician for a key position in their Quality Control department, with previous experience working in a molecular biology or bioassay laboratory (ELISA, qPCR and/or Immunoassays), and experience in scientific writing, keeping up to date with professional knowledge and best practices. You will maintain close collaboration with the QC department to provide support, mentoring and technology transfer of analytical techniques developed in-house. You will work closely with the USP / DSP team assisting them in the implementation of appropriate analytical techniques and managing the transfer of samples to the QC team for analysis.
Candidate profile:
- University and Master studies related to Molecular Biology, Biotechnology, Biomedicine, Pharmacy, etc.
- You have previous experience working in molecular biology or bioassay laboratory (ELISA, qPCR and/or Immunoassays).
- Experienced in scientific writing, you keep up to date with professional knowledge, experience and best practices. You possess excellent data management skills with Excel and are fluent in other Microsoft Office tools.
- You have a knowledge of English equivalent to B2 level (First Certificate of English).
- You have a high capacity to manage and work effectively within a team, with leadership.
- You demonstrate excellent organizational, interpersonal and problem solving skills.
- You have a high capacity for continuous learning, always with a vision of continuous process improvement.
- You are comfortable and resilient in a changing environment and able to adjust workload based on changing priorities.
- You are able to work quickly and accurately with a strong focus on detail, in a rigorous manner.
- You are always high quality oriented (excellence and self-demanding) and demonstrate autonomy.
- You are able to work under pressure of results and deadlines, with proactivity and responsibility.
- You like to work with a positive attitude towards change.
- You possess good oral and written communication skills.
If you are interested, please send your CV to personas@vivebiotech.com
VIVEbiotech is a Contract Development and Manufacturing Organization (CDMO) with over 20 biotech companies worldwide that have placed their trust in them. They develop and manufacture lentiviral vectors as a European leader working under both EMA and FDA standards. The lentiviral vectors produced by VIVEbiotech are used to treat a range of disorders, including haematological and solid cancers, and rare diseases. They are looking for you to be part of their Team!