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Bioanalytical Scientist (f/m) - mass spectrometry, protein chemistry

GlycoThera is a biotech company founded in 2001 and based in Hannover (Germany).  As a cGMP-certified company, we support a number of worldwide acting biopharmaceutical drugmakers in the development and the market authorization application of glycoprotein therapeutics (e.g. biosimilars). In cooperation with our (international) sponsors, we support the development of recombinant therapeutic proteins from bench-scale to large-scale production processes up to the release testing of the market products. GlycoThera is authorized to perform quality testing of medicinal products for human use for upstream and downstream processes, drug substance and drug product release, process validation studies and stability studies.
We would like to recruit at your earliest convenience a
Bioanalytical Scientist (f/m) with at least 3 years experience in the pharmaceutical / biotech industry
Excellent knowledge in the area of mass spectrometry, protein chemistry and HPLC-analytics of biopharmaceuticals is mandatory.

Job profile:
  • Timely planning and execution of analytical work packages (R&D, QC, stability/comparability testing)
  • Data evaluation and documentation according to internal procedures and GMP requirements
  • Development and validation of mass spectrometric analytical procedures according to GMP regulations
  • Support of planning, supervision and execution of device qualification and software validation in the MS laboratory according to GMP
  • Strong interaction with IT and Quality Assurance

  • Academic degree (M.Sc., PhD or equivalent) in medical or life sciences
  • Three years professional expertise in mass spectrometric analytics in a GMP regulated environment, including device qualification and method validation
  • Knowledge in additional standard biopharmaceutical / protein analysis methods (e.g. SEC, IEX, HPLC, CE)
  • Experience in analytical method development and validation
  • Know-how in primary structural analysis of polypeptides
  • Basic knowledge in current GMP regulations (EU-GMP, CFR, AMWHV)
  • Experience in project management and reporting would be beneficial
  • Excellent written and spoken English

Following a period of vocational adjustment, the applicant should be prepared to take a group leader position in conjunction with QA support.
We provide a multisided, challenging job position within a dedicated team. Based on your experience and knowledge, you will have the chance to actively influence and organize your field of activity. Moreover, you’ll have the opportunity to refine your expertise by contributing to cross-project questions in various areas of activities. Your participation in advanced internal and external training courses will be conducted and supported.

How to apply:
Please send your informative application (inclusive curriculum vitae, certificates, references, desired salary and date of commencement) solely via e-mail with max. 3 pdf-files attached to the following mailing address:
E-mail:         info@glycothera.de

GlycoThera GmbH
Feodor-Lynen-Straße 35
30625 Hannover
Tel:     ++49(0)511 978 1990 0 (Sekretariat)
Fax:    ++49(0)511 978 1990 28
Kontakt für Bewerbungen
E-mail:         info@glycothera.de
Bitte beziehen Sie sich bei Ihrer Bewerbung auf jobvector und geben Sie die folgende Referenznummer an: 20151126-01

Über GlycoThera GmbH

Entwicklung von rekombinanten Glycoprotein-Therapeutika aus tierischen Zellen, GMP-Analytik von rekombinanten Proteinen, Entwicklung von Diagnostika und Forschungsreagenzien

Mehr über die GlycoThera GmbH

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