Role Overview
For our site in Hannover (Germany) we are looking for a highly motivated Bioanalytical Scientist (f/m/d) with a strong background in mass spectrometry. The position will require strong leadership and mentoring abilities, accountability, and capacity to communicate effectively in a cross-functional team.
Key Responsibilities and Work assignments
* Independently develop and execute of mass spectrometric analyses for solving of scientific questions in the context of the biopharmaceutical development activities, e.g. characterizing with respect to Critical Quality Attributes (CQA) during e.g. Comparability Studies or Forced Degradation Studies
* Evaluation of mass spectrometric data e.g. form Multi-Attribute Methods (MAM) using corresponding data processing software such as BioPharma Compass, Byonic or Bylogic.
* Participation in device qualification, software validation and analytical method validation in the MS laboratory according to GMP regulations
* Preparation of scientific documents, such as protocols, test methods, text reports, and operating procedures
* Stays current with state-of-the-art mass spectrometry technologies and assesses the potential for applying these technologies toward our characterization platform
Your profile
Required experience:
* MSc degree in chemistry, biochemistry or related field and at least 5 years of practical experience mass spectrometry in a biopharmaceutical environment or academia
* Expertise in design and execution of mass spectrometric analytics, preferably in a GMP regulated environment including device qualification, method development and validation
* Hands on experience with analyzing proteins, peptide mapping, and assessing for impurities by LC-MS/MS
* Additional knowledge in protein analytical methods like SEC, IEX, HPLC, CE is beneficial
* As a global acting company we presume excellent communication skills, including written and oral English and German
* Passion for learning, developing and implementing new technologies to advance biopharmaceuticals discovery.
Why us?
We provide a multisided, challenging job position within a dedicated team and with extensive development opportunities. You’ll have the opportunity to refine your expertise by contributing to cross-project questions in various areas of activities. According to the requirements of the GMP environment, you will be trained in all GMP subjects which apply to the MS laboratory. Your participation in external training courses will also be supported.
Please send your full application (inclusive curriculum vitae, desired salary and date of commencement) as a pdf including earliest start date and salary expectations
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About us
GlycoThera Pharmaceutical Services is a leading global service provider for contract development and analytics for biotherapeutics at all stages of product life cycle. With our expertise in the development of biologics (recombinant proteins such as monoclonal antibodies, cytokines and hormones), manufacturing sciences, analytics, quality control and regulatory strategy we support a broad range of clients globally, from emerging biotech startups to leading global pharmaceutical companies.