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.
East Bay client in need of a process validation engineer with commercial scale chromatography experience.9 month initial contract with possibility of extension.
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.
Company: Medical Device Manufacturer Job Position: Contract to HireJob Location: Fremont, CA Job Summary: The software engineer designs, implements, and integrates softwareResponsibilities: •Works with software engineering team to develop automated equipment software.
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.
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.
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 position is responsibly for the overall direction, coordination, implementation, execution, control and completion of specific facilities/maintenance/calibration projects at the client site.
Initiate and lead clinical study teams as clinical director. Responsible for the successful operations of all study teams to achieve the study objectives at the highest standards and on time and budget.
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