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This position is responsibly for the overall direction, coordination, implementation, execution, control and completion of specific facilities/maintenance/calibration projects at the client site.
Validation Engineer - Biotech6-8 month contract intitially - $70-$100 per hour DOEThe Validation Engineer reports directly to the Manager of Validation. You will be responsible for performing validation in a GMP biotech manufacturing facility managing large size validation projects and supervising technicians/engineers as necessary.
The Principal Validation Engineer will report directly into the Manager of Validation. This position allows for direct management of indivduals and is a major contributor to a department of quality and validation engineers.
Client located in the East Bay has an immediate need for a Principal SAS Programmer. The Principal SAS Programmer provides technical leadership in SAS and other programming support with respect to design, conduct and analysis of clinical trials.
Our client is a leading research-focused healthcare group, in the diagnostics space. With continual organizational growth and strong pipeline, their regulatory affairs team is looking to bring in a new regulatory affairs principal specialist or manager.
Contracted Weekly Hours : 38.5 Rosemount Care Home is a 60 bed home offering general nursing care including, short term, intermediate, respite and palliative care. Our team of RGNs are extremely well trained to cater for all our residents needs.
Rate: $50/hr.Location: Dublin CaProposed Duration: 6 monthsKey note: Person has to have used WPF or Winforms in a professional environment.Sr. Software Engineer is responsible for the development of medical device software, including project planning, requirements analysis, design, implementation, and testing of software.
This person will participate in the day-to-day management of CRO Data Management activities (i.e., development Data Management Plan (DMP), develop and annotate CRF's, develop database specifications, design or oversee the development of edit check specifications and programs, adherence to timelines and data expectations, etc.
POSITION SUMMARY: To provide SAS programming support for the Clinical Research Programming Department. ESSENTIAL FUNCTIONS:1. Develop and document programs to create analysis datasets summarizing key clinical trial data. 2. Develop and document programs and to produce tables, listings and other reports and analyses summarizing clinical trial results.
Mechanical / Electrical Engineer, Colwyn Bay. Our client is the leading manufacturer and supplier of parts to the UK and European automotive industry.
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