Science Writer Jobs in the United States
Kelly Science, Engineering, Technology & Telecom
Sunnyvale, CA
The Technical Writer is responsible for writing, editing, formatting, and managing the publication and translation of customer-facing documents for in vitro diagnostic Xpert tests and GeneXpert instrument systems. Working knowledge of creating and editing XML files using a DITA CCMS, Adobe FrameMaker, Adobe Acrobat, Adobe Illustrator, Adobe Photoshop, Microsoft Word, and Adobe InDesign.
Kelly Science, Engineering, Technology & Telecom
San Jose, CA
A Laboratory Systems Engineering approach is essential as these consumables are the key interface between the physics of our client’s technology and their customers’ biological assays. BS degree in Mechanical/Chemical/Materials/Biomedical Engineering or Physics/Materials/Chemistry/Biochemistry Science with 3+ years of industry experience -OR-.
Kelly Science, Engineering, Technology & Telecom
Des Plaines, IL
Your responsibilities will include: Testing and AnalysisConduct routine testing of raw materials, in-process samples, finished products, and stability samples following established methods (USP, NF, EP, JP, FCC, etc.). As a QC Technician, you’ll be at the heart of our quality operations, ensuring the integrity of our products from raw materials to finished goods.
Kelly Science, Engineering, Technology & Telecom
Minneapolis, MN
In addition to leading a high-performing team, this position emphasizes mentoring and developing team members to enhance their contributions to the organization, fostering a collaborative and innovative culture that meets the dynamic needs of clients and brands. The Research and Development (R&D) Manager is a strategic leader responsible for driving innovation and overseeing product and process development across skin care, SPF/sun care, body care, and hair care formulations.
Kelly Science, Engineering, Technology & Telecom
Princeton, NJ
Perform QC Microbiology laboratory testing, including bioburden, endotoxin, sterility, and microbial identification testing, to ensure timely generation and reporting of test results for in-process, drug substance, drug product, and stability samples in support of manufacturing operations. Strong working knowledge and hands-on experience with microbiological testing methods such as endotoxin testing, bioburden, sterility testing, microbial identification, PCR, biological indicators, and environmental monitoring.
Kelly Science, Engineering, Technology & Telecom
Allerton, IA
Manage and supervise QA laboratory activities and laboratory personnel, coordinating daily work activities and oversee instrument calibration and preventive maintenance programs as it relates to equipment used in the laboratory. The Quality Compliance Manager will be responsible for establishing, maintaining, planning, directing, and coordinating programs, procedures, and processes required for manufacturing food ingredients in compliance with local, state, and national regulatory agencies.
Kelly Science, Engineering, Technology & Telecom
Exeter, PA
Document software architecture and design using XML diagrams, flowcharts, block diagrams and other common techniques. •Intermediate working knowledge of CAN, CAN open, CAN bus, SMBus/SMB, I2C, SPI, Serial communication protocol.
Kelly Science, Engineering, Technology & Telecom
Portage, MI
Additional responsibilities of the role include: Collaborate with product SMEs to assess and determine label requirements and content: Regulatory Affairs, Product Development, Product Safety Engineering, Packaging Engineers, Clinical Sciences, Marketing, Trade Compliance, etc. The Senior Label Designer will collaborate with product SMEs to assess and gather content and is responsible for execution of label format and content compilation using specialized software.
Kelly Science, Engineering, Technology & Telecom
Ottawa, IL
Collaborates with cross-functional project teams to complete regulatory-related assignments (such as Ingredient Lists, Quantitative Formulas, CCS) for both new and existing products, and clearly communicates requirements to colleagues. This role involves supporting and selectively managing regulatory affairs matters, collaborating with supervisors and key business partners to support global regulatory programs and strategies.