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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.
Real Staffing Group is looking for a Principal Engineer for Balloon Catheter Development to join a respected medical device company in the Newark CA area.Company: The medical device company is highly respected in the industry.
Leading Pharmaceutical fortune 200 company with over 25,000 employees globally is seeking to expand its team in the Bay Area. While the company is international, this team has more of a small company feel, looking for the right cultural fit for this Sr.
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.
I am currently urgently recruiting for a mechanical design engineer for a medical device client of mine located in Dublin, CA. This is a large, reputable medical device client that is looking for an experienced, hands-on design engineer to work within their team.
Our client is a growing pharmaceutical company focused on neurology,dedicated to developing products for unmet needs in the treatment of Central Nervous System disorders.
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.
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.
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.
East Bay client in need of a process validation engineer with commercial scale chromatography experience.9 month initial contract with possibility of extension.
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