Title - Laboratory Engineer-temporary position

Job Number	1852002
Business	GE Healthcare
Business Segment	Healthcare Global Supply Chain
About Us	GE Healthcare Life Sciences provides products and services used as tools for biopharmaceutical manufacturing, drug discovery and the latest in cellular technologies, thereby enabling our customers around the world to be more productive, effective and creative. Our motivation is to create better health for more people: through our five decades of supporting the biopharmaceutical industry and its research partners to become more productive, we are helping to reduce costs, increase access and improve quality in the healthcare system. We use our expertise and know-how in imaginative ways to work with our customers to provide what’s needed today and create products and solutions to enable the medical treatments of tomorrow. We are the home of many famous brands, including Whatman, Amersham, Biacore, MicroCal, WAVE, Applied Precision and more.
Career Level	Experienced
Function	Manufacturing
Function Segment	Shop Operations
Location(s) Where Opening Is Available	Sweden
City	Uppsala
Postal Code	75184
Relocation Expenses	No
Role Summary/Purpose	Laboratory Engineer (development engineer) to the section QC Affinity, which is one of six sections for Quality Control (QC) in manufacturing Uppsala (CPU). QC Affinity consists of 11 persons. Main function is to perform Quality control of products according to established methods. A laboratory engineer is responsible for maintaining and improving existing QC analyze methods, problem solving, perform deviation investigations and act as QC responsible in New Product Introduction (NPI) projects.
Essential Responsibilities	Act as an expert on analyse techniques used in the section and solve problems of "trouble shooting character". Investigate quality problems. Individually or in co-operation with others, whether at own initiative or in compliance with supervisor's instructions, update, improve, develop and validate analyse methods in accordance with Change Control. Method portfolio owner in QC for Titration. Act as QC responsible in New Product Introduction (NPI) projects. Overall responsibility for the sections stability studies, for example interim reporting and approving of new stability study plans. Evaluate and approve analyse results. Evaluate and approve deviation investigations. Ensure that instruments are qualified and calibrated, controlled and maintained in a correct way. Perform Quality Control analyses when needed.
Qualifications/Requirements	Good interpersonal skills, goal oriented team player Theoretical and practical experience in several analyse techniques such as Liquid Chromatography (ÄKTA), titration, UV, flowability analyses, Microskopic Evaluation and Visual Examination. MSc or BSc within biotech/engineering or similar
Desired Characteristics	Theoretical and practical experience in Titration techniques Experience in project related work and in the NPI project plan Experience in Macro programming in Excel Interest in computers and instruments For information contact section manager Thomas Ekström: +46 (0)70-6520626 Preffered candidate identified