The Quality Control Specialist has primary responsibility for the final testing of finished product and in coming raw materials using a variety of analytical techniques, confirming that specifications are met. The Quality Control Specialist has the authority to approve or reject products as necessary. Assists in the development, implementation, and maintenance of Quality

At Entegris we are committed to providing equal opportunity to all employees and applicants. Our policy is to recruit, hire, train, and reward employees for their individual abilities, achievements and experience without regard to race, color, religion, sexual orientation, age, national origin, disability, marital or military status. Riegelwood, NC Full time Posted 30+ Da

Assists clinical physicist in the development and implementation of new technology and processes Follows instructions of a medical physicist on gathering of specific commissioning data and measurements for a particular technology Follows instructions of a medical physicist on evaluation and verification of specific functions for a particular technology Performs validation

Provide field based scientific exchange and communication of FDA approved and pipeline products In support of FDA approved products, work within the Medical Science Liaison team's objectives Identify, establish, and maintain scientific relationships with opinion leaders regarding disease state and product specific information Facilitate scientific development of pipeline

Posting Details Position Information Position/Classification Title Electronics Specialist Working Title Fire Safety Specialist Competency Level Advanced Position Number 102096 Salary Grade Equivalent FLSA Non Exempt Appointment Type Permanent Full Time FTE 1 = 40 hours/week, 12 months If time limited, duration date Department Hiring Range $37,849 $64,480 EEO 1 Category Te

We are seeking a qualified and experienced Wetland Scientist to join our dynamic team. The ideal candidate will play a key role in conducting wetland and stream delineations, managing Section 404/401 Clean Water Act permitting processes, regulatory agency interaction, and conducting protected species assessments. This position offers an exciting opportunity to contribute

Performs a variety of activities involved in evaluating the extent to which clinical research processes and documentation are aligned with applicable regulations and study specific requirements. These evaluation activities are the foundation of DCRI's audit program. Additionally, this position involves other general quality management activities. NOTE This position may ha

Site Name UK London Brentford, UK Hertfordshire Stevenage, USA Massachusetts Waltham, USA North Carolina Durham, USA Pennsylvania Upper Providence Posted Date Apr 30 2024 We're excited to be moving to our vibrant new home on New Oxford Street in central London from the end of June 2024. At GSK HQ, we're building an energising space where we can connect, collaborate and ge

/Assignments Conducts high level and technically complex repairs, calibrations, qualifications, and PM's with accurate and timely GxP documentation, following PCI or client specific policies and procedures, and in a safe manner. Provides guidance, direction and effective solutions to clients and PCI technical resources. Proactively takes steps to ensure PCI and client owne

The CPL is a permanent member of the cross functional R&D global Core Team (CT) who plays a key role in defining the target disease profile (TDP), target product profile (TPP), and the development and life cycle strategies of a given project. The CPL leads the Clinical Development Plan (CDP) Team (which consists of functional leaders from within GCD e.g. Clin Pharm, Clin

Participates in the execution of experiments and generation data for design of Experiments (DoE) and statistical testing. Documents assigned projects and hours in Sun's GPM as instructed by leader Performs laboratory maintenance and housekeeping on a frequent basis. Maintains laboratory records. Performs basic mathematical calculations to adjust formulas Summarizes data a

Cell Culture Analyst Job Locations US NC Research Triangle Park ID 2024 2550 Category Research Type Full Time Overview The EPA National Student Services Contract has an immediate opening for a full time Cell Culture Analyst at EPA position with the Office of Research and Development at the EPA facility in Research Triangle Park, NC. The Office of Research and Development

Responsible for providing hazardous and non hazardous services at our client facility to meet our client's environmental needs in accordance with State and Federal environmental, health, and safety regulations. This position will work in a supervised and/or independent capacity to successfully and safely complete scheduled projects for customers. Responsibilities may incl

Work with engineers to build Prototypes and RF Application boards. Work with other technicians, engineers, and managers to identify and resolve issues related to design, manufacturing, testing, and quality control. Run Tests and diagnostics on components and systems, maintain test data and be able to discuss tests results with engineers and management. Inspect equipment c

n/a Minimum Experience/Education MS in Soil Science or closely related field Department Required Skills Experience with soil science analysis including particle size analysis and infiltration rate measurements Preferred Years Experience, Skills, Training, Education Advanced training related to sediment and erosion control research practice development Knowledge of NC guid