Label Design Specialist

Job Title: Label Design SpecialistWe are seeking a skilled Label Design Specialist to join our team at Entegee. As a Label Design Specialist, you will be responsible for developing and testing label designs, applying GS-1 compliant barcodes, and working within a regulated medical device or pharma environment.Key Responsibilities:Design templates from...

{"title": "Packaging Art Specialist", "description": "Purpose and ResponsibilitiesThe Packaging Art Specialist is responsible for creating and editing product packaging artworks to support new product introductions and product labeling revisions. This role requires collaboration with internal Global Label Management organization representatives and...

About the RoleWe are seeking a highly skilled and creative Apparel Designer to join our team at Tillys. As a key member of our design team, you will be responsible for researching and reporting seasonal trends, assembling and delivering trend reports to our merchant team, and preparing and distributing seasonal color palettes across all classifications.Key...

About the RoleWe are seeking a highly skilled and creative Apparel Designer to join our team at Tillys. As a key member of our design team, you will be responsible for researching and reporting seasonal trends in all classifications across men's, women's, and kids' silhouettes, colors, and details.Key Responsibilities:Develop and deliver seasonal trend...

About the RoleWe are seeking a highly skilled and creative Apparel Designer to join our team at Tillys. As a key member of our design team, you will be responsible for researching and reporting on seasonal trends, assembling and delivering trend reports to our merchant team, and preparing and distributing seasonal color palettes across all classifications of...

Job SummaryThe Network Design Specialist will provide network design inputs for the creation and review of necessary documents, including VISIO and PDF files, Installation Guides and diagrams for the purpose of building a patient monitoring system.Key ResponsibilitiesWork with project management and design teams to ensure approved standards, processes are...

Regulatory Affairs Specialist IILocation: Irvine, CA (Hybrid 3 days on site)12 month AssignmentPay Rate: $45-$49/hr.We are seeking a Regulatory Affairs Specialist to support the EU's In Vitro Diagnostic Regulation (IVDR) transition activities for a medical device client. The successful candidate will be responsible for revising technical files, attending...

Job Title: Quality Systems SpecialistYoh, a Day & Zimmermann company, is seeking a Quality Systems Specialist to support the compilation and maintenance of IVDR technical files, review IVDR and other registration labeling change requests, and various quality tasks to support the QMS overall.Responsibilities:Review, approve, and process labeling and FOC...

Regulatory Affairs SpecialistThis is an exciting opportunity to contribute to the success of Cypress HCM, a leading biotech company. As a Regulatory Affairs Specialist, you will play a crucial role in supporting the transition to the In Vitro Diagnostic Regulation (IVDR) for our products.Key Responsibilities:Prioritize and monitor cases throughout the day,...

Quality System SpecialistWe are seeking a highly skilled Quality System Specialist to support our client, a leading life science and research company, in Irvine, CA. This 12-month position has the potential to extend.Key Responsibilities:Review, approve, and process labeling and FOC change requestsCompile, create, review, and update quality-related technical...

Job Title: Regulatory Affairs SpecialistSpectraforce Technologies is seeking a highly skilled Regulatory Affairs Specialist to support the development and implementation of the global regulatory strategy for SkinMedica products.Key Responsibilities:Review and prepare regulatory documents and labeling for cosmetic or OTC product registrations/updates.Research...

Job OpportunitySeeking a Quality System Specialist to support the compilation and maintenance of IVDR technical files, review IVDR and other registration labeling change requests, and perform various quality tasks to support the QMS overall.Key Responsibilities:Review, approve, and process labeling and FOC change requestsCompile, create, review, and update...

Job OverviewOur client, a global leader in life science research and healthcare, is seeking a Quality Assurance Specialist to support the compilation and maintenance of IVDR technical files. The successful candidate will review and process labeling and FOC change requests, compile and create quality-related technical file documentations, and perform various...

Job SummaryOrion Group is seeking a highly skilled Regulatory Affairs Specialist to support the development and implementation of the global regulatory strategy for company cosmetic and OTC products.The ideal candidate will have a strong understanding of personal care product industry regulatory affairs discipline throughout the product lifecycle, including...

Regulatory Affairs SpecialistJob Summary:We are seeking a highly skilled Regulatory Affairs Specialist to join our team at Roth Staffing Companies. As a Regulatory Affairs Specialist, you will be responsible for ensuring compliance with regulatory requirements for medical device products.Key Responsibilities:Represent the regulatory function on manufacturing...

Job SummaryWe are seeking a skilled Manufacturing Operations Specialist to join our team at AnDek Staffing Services. The ideal candidate will have experience in the pharmaceutical industry and possess strong manual dexterity and initiative.Key Responsibilities:Complete training modules on gowning techniques and ensure compliance with hygiene and safety...

Job Title:Electrical Engineer - Circuit Design SpecialistCreate comprehensive circuit schematics for high-speed ADC and DAC circuits, optimizing for RF performance, space constraints, and manufacturability. Utilize LTspice and LTpowerCAD to simulate high current, low voltage power supplies. Collaborate with digital design engineers, PCB designers, and...

Job OverviewCypress HCM is seeking a highly skilled Regulatory Affairs Specialist to support our In Vitro Diagnostic Regulation (IVDR) transition activities. This is an exciting opportunity to join a leading biotech company and contribute to the success of our products.Key ResponsibilitiesPrioritize and monitor cases throughout the day, providing status...

Bass Pro Shops - 71 Technology Drive West **Job Summary:** As a Fulfillment Outfitter at Bass Pro Shops, you will be responsible for performing multiple functions within the back room of the retail store. These functions include receiving merchandise, inspecting merchandise, filling orders, sorting and packing merchandise for shipment, and applying...

Job Title: Quality Systems SpecialistJob Summary:This position will support the compilation and maintenance of IVDR technical files, review IVDR and other registration labeling change requests, and various quality tasks to support the QMS overall.Responsibilities:Review, approve, and process labeling and FOC change requestsCompile, create, review, and update...