GMP DSP Scietist

Basic Purpose of the Position*:
1. Primary responsibility is operational work on downstream process forthe Biolab an******** Oas******** including buffer preparat********protein pur******** an******** ******** an******** both in non-GMPan********. Implement the disposable technology for the downstreamprocess.
2. Coordination an******** of resources an******** to ensure timelymaterial supply. Ensuring cGMP readiness of facility an******** (e.g.performing of calibration an******** of equipment). Performingdocumentation of process transfers from internal an******** clients.
3. Responsible for processing of economic an******** purificationprocesses for therapeutic proteins an******** antibodies by applyingstate of the art technologies to ensure manufacturing of bulk drugsubstance an******** drug product. Being part of process transfer teamsto secure material supply for projects to support Tox an********studies.

Accountabilities*:
1. Perform purification process******** optimization an********-up tomeet all quality an******** demands.
2. Carry out preclinical an******** manufacturing of Drug Substanceand/or Drug Product.
3. Handle operational work packages within the team includingchange-over, scale-up, purification an********-process controls.
4. Exchange actively with colleagues in order to ensure best-practicesharing an******** use of resources in accordance with the supervisor.
5. Specialist for purification top******** filtration chromatographyan********.
6. Power user of AKTA (GE Healthcare) an******** (Sartorius) systems aswell as other relevant equipment use******** BI. Perform troubleshootings an******** solving when needed.
7. Ensuring goo********, material an******** handover with internalan******** partners
8. Work within a team of technical an******** personnel in a complex labin a disciplinary an******** manner.

Qualifications*:
1. Bachelor/Master, major in B******** B******** B******** Biotechnologyor Bio Engineering.
2. Experience in purification an******** processing with goo********awareness.
3. Basic knowledge an******** understanding of cGMP an******** accordingto cGMP.
4. Goo******** an******** experience in organizing a lab.
5. Practical experience with purification an******** technologies (e.g.chromatography, f******** spectrometry).
6. Basic knowledge of the actually use******** an******** in BICh******** such as AKTA/Unicorn an********.
7. Analytical an******** th******** clear argumentation an******** toreduce complex issues to the main points
8. Self confidence
9. Social competence, customer orientation an******** player

Other requirements*:
1. We are seeking to recruit a person who offers direct relevantoperational experience in process development an******** experiencewithin a biopharmaceutical company.
2. This individual will work hands-on in a cGMP laboratory an********perform cGMP ******** shift work will occur on periodic basis