QA – IT Specialist for Validation of Computerized Systems
Join a dynamic and international company where everyone is responsible for delivering right on time as one team!
Do you want to be part of a team of 9 highly dedicated specialists that are responsible for validation and qualification activities for facility and computerized systems? Do you want to play a key role in bringing numerous pharmaceutical productions safely and efficiently to market?
Then join CMC Biologics in a new QA position and become part of an international and modern organization that delivers biopharmaceutical development and manufacturing right and on time.
Deliver quality assurance of biopharmaceutical products and API
You will be responsible for our administrative Computerized Systems, which includes periodic assessments of system validation states and coordination and support of validation work. You will participate in our critical IT projects as Quality responsible, where you will work closely together with System Owners and IT and provide assistance in all validation related work. Furthermore you will review and approve documentation such as VPL, URS, CRs, Deviations and CAPAs.
Develop your GMP skills and build relations with highly skilled people from the industry
You will cooperate closely with the other teams in QA and departments in the organization in order to ensure that all quality related activities are carried out effectively and in compliance with cGMP. Through internal and external audits, you are exposed to a lot of different ways of working with GMP and pharmaceutical manufacturing, and you can expect to build great expertise within these areas by interacting with our many different international customers.
Specialist with pharmaceutical validation experience for computerized systems
You have experiences with interpretation of global cGMP rules for computerized systems used in
API manufacturing. Our Quality System is compliant to ICH Q7 and relevant parts of FDA 21 CFR part 11, 210, 211, 600 and 610. You have a relevant IT background, academic or technical, and ideally you have knowledge in the following areas:
• Validation of computerized systems in cGMP Manufacturing areas.
• Validation of computerized systems in cGMP QC Laboratory areas.
• Facilitated computerized systems in pharmaceutical areas.
• Regulatory inspections e.g. EMA, FDA and customer audits (internal and external audits).
Join an international and agile organization
At CMC, you will get great opportunities to work with a varied array of tasks and challenges. You will get experience with our various departments as well as exciting and challenging assignments. Furthermore, you will to a large extend be able to plan your daily work yourself. CMC offers an informal working environment, where high energy and enthusiasm 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 regarding the position, please do not hesitate to contact HR business partner Jeppe Højrup, telephone +45 2294 2942 or Director Quality, Lise Marie Christensen, telephone +45 2294 3058.
To apply, please use the link below. The applications will be processed continuously, so please apply as soon as possible and no later than November 13th. 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 <a href='javascript:openLinkWindow("http://www.cmcbiologics.com")' "="" data-cke-saved-href='javascript:openLinkWindow("http://www.cmcbiologics.com")'>www.cmcbiologics.com to learn why CMC Biologics is a World Leader in process development and contract manufacturing.
