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172462 Jobs Found for Validation Engineering Group Inc
Position Summary The Sr. Accountant will perform a variety of general accounting tasks in the Accounting Department and work collectively with team members in order to meet and exceed service expectations. Essential Functions Analyze financial information detailing assets, liabilities, and capital Compile and analyze financial information to prep...
KNZA, INC is a growing and aggressive company that is looking to add to our current team. Our group of five locally owned radio stations is now taking applications for a General Manager. This is a newly created full-time position for a visionary leader that is experienced and passionate about broadcasting, thrives in a fast-paced environment, and h...
MYAS PROGRAM DIRECTOR · Full-time position · Primary duties of the position will be within the MYAS basketball program, but will also include working with new programs and growth areas such as football, Greater Minnesota Basketball and Baseball, and others as needed. The MYAS Program Director serves the youth basketball community in Minnesota and ...
Location: Boston Massachusetts United States Job Type: regular full-timeDivision: Precision for MedicineBusiness Unit: Manufacturing SolutionsRequisition Number: 4102 Why Precision for Medicine? Welcome to the forefront of innovation in cutting edge patient treatments! We are thrilled to present an incredible opportunity to join our high performin...
Job Description General Summary: The Validation Senior Manager position will be part of the Vertex Cell and Genetic Therapy Manufacturing Operations and Technical Operations group. The role will oversee Validation personnel and support managing day-to-day Validation operations at VCGT facilities for the T1D program at the greater Boston location....
Senior Validation Engineer Salary Range : $120,000-$140,000 per year Qualifications Education or Equivalent Experience: Engineering Bachelor's Degree or equivalent Experience: 8-10 years Quality Engineering Experience Validation Process knowledge Medical Device Regulations and standards (ISO 13485, ISO 14791, 21 CFR 820, and 2017/745 (EU/MDR) Demon...
Why Precision for Medicine? Welcome to the forefront of innovation in cutting edge patient treatments! We are thrilled to present an incredible opportunity to join our high performing organization. As a leader within the life science industry, we are constantly pushing the boundaries of what is possible and redefining the standards of excellence. ...
Position Description: The CQV Engineer develops the documentation to support Commissioning, Qualifications, and Validation. These people are responsible for protocol writing and execution, field verification, and development of summary reports at the client site. Other responsibilities include planning / coordinating work and directing small teams...
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Why Precision for Medicine? Welcome to the forefront of innovation in cutting edge patient treatments! We are thrilled to present an incredible opportunity to join our high performing organization. As a leader within the life science industry, we are constantly pushing the boundaries of what is possible and redefining the standards of excellence. ...