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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.
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.
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.
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.
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.
East Bay client in need of a process validation engineer with commercial scale chromatography experience.9 month initial contract with possibility of extension.
The Senior Process Validation Engineer will be responsible defining, implementing, and maintaining a robust process validation program. The process validation program includes, but is not limited to, biological growth processes, aseptic processing, cleaning, and sterilization processes.
A board certified oncologist/hematologist with industry experience who will report to the Chief Medical Officer and work collaboratively with the Clinical Study Team contributing to the strategic planning and execution of Clinical Development Plans for all compounds in clinical development.
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.
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.
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