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96 job opportunities
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| Posted On: Nov 06, 2026
Pearl River, NY 10965
On-site
6 Months, Contract
QC Chemist supporting a GMP-regulated pharmaceutical and biopharmaceutical laboratory environment. Performs wet chemistry and instrumental testing of raw materials, drug substances, drug products, in-process, and stability samples. Documents, reviews, and manages analytical data through LIMS while ...
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| Posted On: Nov 04, 2026
Ridgefield, CT 06877
On-site
12 Months, Contract
Histotechnologist supporting oncology discovery research and spatial biology capability development. Develops high-plex tissue assays, multiplex antibody panels, spatial transcriptomics workflows, and spatial datasets. Performs histology workflows including tissue processing, sectioning, staining, ...
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| Posted On: Nov 06, 2026
Scarborough, ME 04074
On-site
3 Months, Contract
Quality Control Technician supporting infectious disease diagnostic product quality in a regulated laboratory environment. Performs in-process and final-release testing for Lateral Flow, ELISA, and Molecular products. Reviews batch records, calibrates and maintains laboratory equipment, and ...
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| Posted On: Nov 06, 2026
Worcester, MA 01604
On-site
6 Months, Contract
QC Data Reviewer supporting quality assurance and quality control data review within a GMP laboratory environment. Reviews laboratory test data, assays, raw materials, environmental monitoring, in-process, final bulk, stability, and validation records. Maintains compliant laboratory records, ...
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| Posted On: Nov 06, 2026
Plymouth, MN 55442
On-site
11 Months, Contract
R&D Technician role supporting medical-device testing in a laboratory environment. Performs mechanical, electrical, conditioning, dimensional, and visual testing of electrophysiology catheters and dilators. Documents test results using good documentation practices and communicates findings to ...
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| Posted On: Nov 05, 2026
Frederick, MD 21704
On-site
6 Months, Contract
QA Documentation Associate supporting controlled documentation processes in a regulated pharmaceutical environment. Creates logbooks, files controlled documents, and maintains documentation archives. Scans, verifies, archives, and retrieves records while ensuring file accuracy. Performs timely ...
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| Posted On: Nov 05, 2026
Frederick, MD 21704
On-site
6 Months, Contract
QA Documentation Associate supporting pharmaceutical quality documentation and records processes. Creates logbooks and controlled documents while maintaining accurate, retrievable files. Scans, verifies, files, archives, and enters documentation data into systems. Requires document control, word ...
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| Posted On: Nov 04, 2026
Brea, CA 92821
On-site
12 Months, Contract
Product Development Engineer supporting medical device R&D for intravenous infusion sets and connection devices. Leads design control deliverables across product development, lifecycle management, verification, validation, and manufacturing transfer. Develops design inputs and outputs, feasibility ...
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| Posted On: Nov 03, 2026
Brea, CA 92821
On-site
12 Months, Contract
R&D Engineer supporting infusion preparation and delivery medical device products. Leads design-control deliverables for intravenous infusion sets and connection devices. Develops design inputs, test methods, protocols, feasibility studies, verification, validation, and design-transfer activities. ...
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| Posted On: Nov 03, 2026
Pleasanton, CA 94588
On-site
6 Months, Contract
Quality Control Inspector supporting medical device manufacturing operations. Performs routine visual inspection of components and finished goods. Verifies products conform to quality assurance standards. Requires one year of quality inspection experience, strong attention to detail, and English ...
Showing 1 to 10 of 96 entries