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Pfizer
- Rocky Mount, NC
As a Validation Engineer you will be responsible for validating/qualifying the systems used to develop and/or manufacture products within a large manufacturing facility located in North Carolina, USA. You will ensure systems are running according to necessary specifications and operate within regulations to ensure data integrity and the production of quality products. Responsibilities The Validat
Posted Today
Processes incoming samples; inspects sample to insure they are in good c ondition and meet method compliance; sign appropriate chain of custody documents to receive samples; assigns laboratory numbers to all samples Routes paperwork to appropriate personnel Prepares samples for shipment to internal/external clients Performs other miscellaneous duties as assigned Stores samples; places samples in a
Posted 1 day ago
Health is everything. At CVS Health, colleagues are committed to increasing access, lowering costs and improving quality of care. Millions of times a day, we help people on their path to better health from advising on prescriptions to helping manage chronic and specialty conditions. As a Staff Pharmacist, you have a critical role at the forefront of delivering our purpose, modeling our values, and
Posted 23 days ago
IPS is hiring! We are looking for a talented Validation Engineer to join our industry leading Commissioning, Qualification and Validation (C/Q/V) team at our Morrisville, NC office. The Senior Validation Engineer performs cGMP Compliance based services (commissioning, qualification, validation, consulting, etc.) as developed and defined in project agreements with IPS' clients. They follow IPS and
Posted Today
Sales Representative, BPS Field Based Southeast US Sartorius As one of the world's leading laboratory and pharmaceutical equipment providers, Sartorius is actively shaping dynamic, innovative and high growth markets. Founded in 1870, the company earned sales revenue of more than 1.3 billion euros in 2016 according to its preliminary figures. More than 6,900 people work at the Group's approximately
Posted Today
In depth experience with bio analytical techniques such as HPLC/UPLC and Plate based assays (ELISA, etc) Hands on experience with therapeutic protein characterization (CE SDS/cIEF) using Beckman/Protein Simple instrument Experience with SDS PAGE, Western Blot, qPCR and other techniques applicable to monitor quality attributes of proteins is a plus. Produce high quality documentation suitable for p
Posted 2 days ago
Job Description Develop, manage, update and communicate project status, progress, timelines, changes in schedule, scope changes, technical and/or quality issues to all relevant personnel in the company and with the client. Serve as primary liaison to client. Facilitate sub teams and global project team (internal and client) and ensure documented communication of meetings agendas and outputs, acti
Posted 2 days ago
Patheon Inc.
- Durham, NC / High Point, NC
Brief Summary Reporting to Principal Pharmacokineticist, this position will focus on supporting our, specialty pharma development efforts. The position will work closely with Product Development scientists in High Point and other Banner Locations, in the selection of new products for development and also in the design and execution of clinical studies. This position will select CROs for conducting
Posted 2 days ago
Covance
- Philadelphia, PA / Nashville, TN / Dallas, TX / 4 more...
Posting Title Clinical Project Manager ECD Oncology US Homebased Requisition ID 68219BR Job Category Clinical Research Locations United States Nashville, TN United States Dallas, TX United States Orlando, FL United States Philadelphia, PA United States Los Angeles, CA United States Denver, CO United States Research Triangle Park, NC Shift 1 Job Posting As the drug development business of Laborato
Posted 4 days ago
Job Description Assist with and support execution of routine procedures within the biopharmaceutical development labs. execute activities according to cGMP regulations and company SOPs. Provide STAT assay coverage including 2nd shift and weekends as required by the manufacturing schedule. Assays include 280 and RP titer. Execute other analytical assays as required by the batch records. Assays may
Posted 7 days ago
Covance
- Conshohocken, PA / Princeton, NJ / Seattle, WA / 4 more...
include Participates in defining how the project will be performed and the deliverables that will be presented. Prepare Proposals Reviews and revises draft proposals that respond to client requirements following standard formats used for previous engagements. Supervise Data Collection and Analysis Identifies sources and obtains information from knowledgeable individuals, reference texts, on line d
Posted 10 days ago
Shake flask study set up using design provided by a scientist. Bioreactor preparation, autoclaving, media hold, inoculation. Media, feed, buffer preparation and filtering. Harvest of mammalian and microbial bioreactors. 3L and 15L bioreactor sampling, data entry, and some data analysis; 200L bioreactor set up, sampling, data entry, and some data analysis. Excel data entry and plotting. Bioreactor
Posted 8 days ago
Covance
- Indianapolis, IN / Madison, WI / Philadelphia, PA / 8 more...
Posting Title Senior Contract Associate Remote Opportunity! Requisition ID 66213BR Job Category Other Locations United States Atlanta, GA United States Indianapolis, IN United States Madison, WI United States Nashville, TN United States New York, NY United States Philadelphia, PA United States Princeton, NJ United States Raleigh Durham, NC United States Seattle, WA United States Washington, DC Sh
Posted 10 days ago
Covance
- Princeton, NJ / San Diego, CA / Research Triangle Park, NC
Posting Title Senior Clinical Project Manager Gastrointestinal ( GI ) Trials Requisition ID 68222BR Job Category Clinical Research Locations United States Princeton, NJ United States San Diego, CA United States Research Triangle Park, NC Shift 1 Job Posting Covance is seeking a Senior Project Manager with expertise in Gastrointestinal ( GI ) trials to join our Late Phase Project Management team.
Posted 4 days ago
Job Summary The Manufacturing Assistant position is designed as an introduction to the environment of cGMP manufacturing. This position performs all routine/non routine cleanings, builds assemblies, buffer/media preparation and supports the manufacturing operations. This position requires a shift schedule . Aseptic and Gowning Qualifications are required for this position. Must be able to document
Posted 8 days ago
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