This is a working supervisor position. The supervisor will have a bench assignment when needed, helping to fill in schedule gaps and will maintain personal competency in areas of expertise. The supervisor will be responsible for oversight of technical personnel working evening/night shifts including assigning/directing work, addressing complaints and resolving problems. T

Receives specimens and orders appropriate tests as prescribed; processes samples for laboratory testing using various computer applications. Checks for specimen integrity and proper specimen identification. Prints and distributes reports, answers telephone calls from customers including inpatient nurses/physicians and outpatient clients. Processes specimens for multiple R

The Quality Control Inspector will be responsible for performing quality inspections and package testing on in process materials and finished products. The QC inspector will also be responsible for ensuring all policies and procedures comply with applicable FDA, state, OSHA, AATB, and ISO regulations and standards. Hours 6 30 am 3 00 pm Essential Functions Performs inspec

Site Name USA Pennsylvania Upper Providence Posted Date Apr 10 2024 Are you looking for an in vivo science role that allows you to grow professionally and contribute to the development of best in class medicines? If so, this role could be an exciting opportunity to explore. As a Study Conduct Associate Scientist, you will support preclinical discovery and development rese

Utilize lab best practices to prepare sample parts for evaluation. Identify and use the appropriate equipment to obtain required measurements Document results in standard report formats and record observations made during testing Effectively communicate results to Engineers, Metrologist and Lab Manager Maintain and calibrate a variety of dimensional inspection equipment F

Utilize lab best practices to prepare sample parts for evaluation. Identify and use the appropriate equipment to obtain required measurements Document results in standard report formats and record observations made during testing Effectively communicate results to Engineers, Metrologist and Lab Manager Maintain and calibrate a variety of dimensional inspection equipment F

The temporary research fellow will assist with preparing a manuscript examining the Everyday Discrimination Scale, its applications in relation to health and health related behaviors, and ongoing practices regarding the operationalization of the measure. Working alongside Dr. Lawrence, the temporary fellow will assist with summarizing studies identified through a systemat

The temporary research assistant will assist with preparing a manuscript examining the Everyday Discrimination Scale, its applications in relation to health and health related behaviors, and ongoing practices regarding the operationalization of the measure. Working alongside Dr. Lawrence, the temporary assistant will assist with summarizing studies identified through a sy

This position involves all aspects of receipt, storage, and delivery of specimens for testing, plus various support activities in the department. Education and Experience Requirements High School Diploma MS Office Typing/data entry skills preferred Major Duties & Responsibilities Receive and Sorts packages sent to NMS Scans FEDEX barcodes and uploads to Excel, reconciles

Receives, unpacks, completes chain of custody and related documentation, accessions into LIMS, returns samples, monitors department reports and performs support activities in the department. Education and Experience Requirements High School Diploma MS Office and typing/data entry skills with a high level of accuracy Job Duties It is the responsibility of the Specimen Proc

SHIFT Day (United States of America) Seeking Breakthrough Makers Children's Hospital of Philadelphia (CHOP) offers countless ways to change lives. Our diverse community of more than 20,000 Breakthrough Makers will inspire you to pursue passions, develop expertise, and drive innovation. At CHOP, your experience is valued; your voice is heard; and your contributions make a

Development of protocols for clinical studies. Contribute to the development of program strategy for assigned compounds/programs including participation in the preparation of clinical development plans Drafting and review of clinical scientific documents such as IND, IND amendments, Investigator Brochures, Clinical Study Reports, Annual Reports and other Health Authority

Develop, validate and optimize bioanalytical methods by using analytical techniques. Process, analyze and interpret bioanalytical data. Responsible for finding solutions to problems related to the application of bioanalytical methods. Assist in improving laboratory activity processes (method development, validation and sample analysis). Write and review bioanalytical meth

Performs site qualification, site initiation, interim monitoring, site management and close out visits (performed on site or remotely) ensuring regulatory, ICH GCP and/or Good Pharmacoepidemiology Practice (GPP) and protocol compliance. Uses judgment and experience to evaluate overall performance of site and site staff and to provide recommendations regarding site specifi

Site Name UK London Brentford, USA Pennsylvania Upper Providence Posted Date May 14 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 get ahead of disease together. Designed especially for us, it'll be one of the healt