Project Documentation Specialist
GE Healthcare Bio-Sciences AB / Kemiingenjörsjobb / Uppsala
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hela Sverige Role Summary/Purpose:
Customized Bioprocess solution (CBS) is an organization within Life Sciences delivering customized bioprocess hardware. We have a matrix organisation where each customer order becomes a project with resources from project management, system design, detailed design, manufacturing transfer, sourcing and verification. Internally we are working together with R&D, After Sales, Supply Chain and Product Marketing to utilize the full strength of the Life Sciences organization.
Role Summary/Purpose
We are looking for a new colleague to join the CBS Project Documentation team. The primary responsibility of our Project Documentation Specialist is to plan and execute generation of product specific documentation, agreed with customer according to established processes.
The project documentation specialist position will report to the CBS Portfolio manager, team consisting today of 3 documentation specialists.
Quality Specific Goals:
Aware of and comply with the GEHC Quality Manual, Quality Management System, Quality Management Policy, Quality Goals, and applicable laws and regulations as they apply to this job type/position
Complete all planned Quality & Compliance training within the defined deadlines
Identify and report any quality or compliance concerns and take immediate corrective action as required
Support compliance/closure of Regulatory and Quality requirements before completing Design Outputs/Program Deliverables
Participate in continuous improvement activities by identifying and appropriately escalating process and product quality gaps, providing solutions when possible
Qualifications/Requirements
To be successful in this role we believe you have a genuine documentation interest, technical understanding and problem solving skills combined with a strong drive and customer focus.
You are comfortable working at a high pace and to deliver quality on short notice. You have experience from working in a project driven organization and thrive in an environment that offers daily challenges.
Formal requirements are:
B.SC degree with relevant technical engineering, software or application - significant - experience from biopharma industry or gained corresponding knowledge / understanding from working in this area
Experience from working with external customer contacts
English and Swedish as working language
Excellent interpersonal and communication skills
EU work permit
Desired Characteristics
M.Sc degree engineering or biopharma application
Knowledge / experience from regulated industry and how that impact documentation (GMP, GxP?)
Knowledge from GEHC Bioprocess products or other suppliers products to the biopharma industry
Understanding of and capability to manage cultural differencies
Negotiations skills
Personal traits we value in this role are:
Structured and Analytical
Great team working and leadership skills
Result oriented and good prioritizing skill
If you have any questions regarding the role, please contact Roger Nordberg 0706-955095 or
roger.nordberg@ge.comVaraktighet, arbetstid
Tillsvidare
Heltid
Publiceringsdatum2016-02-05ErsättningFast månads- vecko- eller timlön
Så ansöker duSista dag att ansöka är 2016-02-29
Klicka på denna länk för att göra din ansökanAnge följande referens när du ansöker: 2481923
FöretagGE Healthcare Bio-Sciences AB
AdressGE Healthcare Bio-Sciences AB
Björkgatan 30
75184 Uppsala
KontorsadressBjörkgatan 30
Uppsala
Övriga kontaktuppgifterTelefonnummer: 018-6120000
Jobbnummer 2655973
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