HPLC Scientist, Analytical Development

pracovná oblasť

Odborníci v oblasti výpočtovej techniky, strojárstva a vedy
   Výpočtová technika
        Dizajnéri a analytici počítačových systémov

NÁPLŇ PRÁCE:

Join a dynamic and international company where everyone is responsible for delivering right on time as one team! The Department In Analytical Development (AD) we seek a skilled new colleague to work with us. AD is a part of the development area in CMC with a large interface to Quality Control. The department consists of 8 technicians, 4 scientists and 1 manager and has 4 main work areas: • Support for upstream- and downstream process development activities through analyzing samples with different HPLC and characterization methods. • Securing that an adequate set of analytical methods is implemented in relation to each customer project. This is secured by evaluating CMC generic analytical methods on samples from the individual projects, by transfer of methods from the customers as well as development of new methods. • Transfer of developed methods to QC. • Participation in troubleshooting of methods. The work environment in our department is very informal. There is constant collaboration across the entire organization, and all employees have a very professional and flexible attitude towards their work. Responsibilities and tasks As a Scientist in the AD Team, you will typically be responsible for a specific development projects implementation of analytical methods, and participate in multi-disciplinary project teams including upstream, downstream, analytical, and process transfer scientists working in close collaboration. The job includes the following tasks: • Planning and coordination of method implementation/development activities and experiments • Scientific development of analytic methods • Review analytical results • Verbal and written reporting to clients • Extended stability studies • Compatibility studies • CQA • Trouble shooting of chemical methods, especially HPLC, iCEF and CE-SDS Experience and competencies The candidate we are looking for has: • A relevant education, i.e. Master’s or PhD degree within e.g. biochemistry, protein chemistry, chemical engineering or equivalent with minimum 3-5 years’ experience • Ability to plan, execute and report analytical method implementation, transfer or development. • Flexibility and a desire to take on new tasks and responsibilities • Experience with development of analytical methods • Working and analytical experience with HPLC, iCEF and CE-SDS analysis • Broad technical experience in protein analytics testing • Strong interpersonal and communication skills both internally and with external customers • Capability to handle several projects simultaneously • Excellent communication, presentation and interpersonal skills • Good finisher CMC offers CMC offers a dynamic working place with good opportunities of working with a varied array of tasks and challenges. You will get insight into and experience with the way the various departments throughout a Contract Manufacturing Organization interact in order to achieve success. Exciting and challenging assignments will constantly come your way, and you will to a large extent be able to plan your daily work yourself. CMC offers an informal working environment, where humor is part of the daily work life. We respect each other and our individual differences. CMC’s employees have a flexible attitude and we help each other to reach deadlines together as one team. For further information please contact Helle Grann Wendelboe, Manager of the Analytical Development Team, phone +45 22 94 30 90. We will process the applications as they arrive. Therefore please submit your application and CV as soon as possible and no later than September 15th, 2015. About CMC Biologics A/S CMC Biologics (CMC) is a global Contract Manufacturing Organization (CMO) with three biomanufacturing facilities in Europe and the USA. The company provides a comprehensive range of commercial and clinical cGMP biologics manufacturing services, from DNA to active pharmaceutical ingredient (API). The company’s team and approach are tailored to each of its client’s needs, whether turnkey manufacturing or sophisticated, stand-alone analytical, formulation and stability services. CMC Biologics also offers non-exclusive license to CHEF1™, a proprietary CHO cell line development platform. CHEF1 delivers stable, high-titer, production-quality cell lines in optimized time frames. It is the foundation of CMC Biologics’ innovative approach to cell line and process development. Visit http://www.cmcbiologics.com to learn why CMC Biologics is a World Leader in process development and contract manufacturing.

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source: https://www.ec.europa.eu/eures

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