Labeling Specialist

Job DescriptionJob DescriptionJob Summary: Label Design Specialist responsible for developing and testing label designs, applying GS-1 compliant barcodes, and working within a regulated medical device or pharma environment.Requirements:Experience developing and testing label designs from templates using Codesoft and SQL databasesWorking level understanding...

Position: Sr Labeling Specialist, Req#: 9059-1Is this the role you are looking for If so read on for more details, and make sure to apply today. Location: Irvine, CA (Mostly from home, but the first couple of weeks onsite for training in the Irvine, CA office). Duration: 12+ Months Contract (with the high possibility of extension.) More on this role: What...

Position: Sr Labeling Specialist, Req#: 9059-1 Location: Irvine, CA (Mostly from home, but the first couple of weeks onsite for training in the Irvine, CA office). Duration: 12+ Months Contract (with the high possibility of extension.) More on this role: What does your group do? We design and release labels, IFUs and other labeling components supporting APM...

Position: Sr Labeling Specialist, Req#: 9059-1Location: Irvine, CA (Mostly from home, but the first couple of weeks onsite for training in the Irvine, CA office). Duration: 12+ Months Contract (with the high possibility of extension.)More on this role:What does your group do?We design and release labels, IFUs and other labeling components supporting APM...

Position: Sr Labeling Specialist, Req#: 9059-1Location: Irvine, CA (Mostly from home, but the first couple of weeks onsite for training in the Irvine, CA office). Duration: 12+ Months Contract (with the high possibility of extension.)More on this role:What does your group do?We design and release labels, IFUs and other labeling components supporting APM...

Title: Labeling Design RepresentativeLocation: Irvine, CA 92618Duration: 12 months Job Description: Role PurposeProcess pre-designed changes by using labeling software.Job FunctionsEssential Job Functions% of TimeExecute complex designed labeling changes (e.g., illustrations), using SDL and Loftware solutions. 65%Evaluate risks, provide recommendations to...

Title: Labeling Design RepresentativeLocation: Irvine, CA 92618Duration: 12 months Job Description: Role PurposeProcess pre-designed changes by using labeling software.Job FunctionsEssential Job Functions% of TimeExecute complex designed labeling changes (e.g., illustrations), using SDL and Loftware solutions. 65%Evaluate risks, provide recommendations to...

Position: Sr Labeling Specialist, Req#: 9059-1 Location: Irvine, CA (Mostly from home, but the first couple of weeks onsite for training in the Irvine, CA office). Duration: 12+ Months Contract (with the high possibility of extension.) More on this role: What does your group do? We design and release labels, IFUs and other labeling components supporting APM...

Job OverviewYoh, A Day & Zimmermann Company, is seeking a highly skilled Regulatory Affairs Specialist II to join our team. As a Regulatory Affairs Specialist II, you will be responsible for supporting the EU's In Vitro Diagnostic Regulation (IVDR) transition activities, preparing revision of technical files, updating labeling to comply with IVDR...

Regulatory Affairs Specialist II Location: Irvine, CA (Hybrid 3 days on site)12 month AssignmentPay Rate: $45-$49/hr.On behalf of our client a medical device client, we are seeking a Regulatory Affair’s specialist that will support the EU's In Vitro Diagnostic Regulation (IVDR) transition activities that will impact the company’s products currently CE...

Regulatory Affairs Specialist II Location: Irvine, CA (Hybrid 3 days on site)12 month AssignmentPay Rate: $45-$49/hr.On behalf of our client a medical device client, we are seeking a Regulatory Affair’s specialist that will support the EU's In Vitro Diagnostic Regulation (IVDR) transition activities that will impact the company’s products currently CE...

Job DescriptionJob DescriptionRegulatory Affairs Specialist II Location: Irvine, CA (Hybrid 3 days on site)12 month Assignment (Potential to extend or convert)Pay Rate: $45-$49/hr. On behalf of our client a Medical device client, we are seeking a Regulatory Affair’s specialist that will support the EU's In Vitro Diagnostic Regulation (IVDR) transition...

Regulatory Affairs Role OverviewThe Tucker Parker Smith Group (TPS Group) is seeking a seasoned Medical Device Regulatory Specialist to support the EU's In Vitro Diagnostic Regulation (IVDR) transition activities.This role will involve revising technical files, attending meetings with project managers, and updating labeling conversion tracking logs.Job...

Regulatory Affairs SpecialistJob DescriptionAt Tucker Parker Smith Group (TPS Group), we are seeking a highly skilled Regulatory Affairs Specialist to support our client's EU's In Vitro Diagnostic Regulation (IVDR) transition activities. The successful candidate will work on revising technical files, attending meetings, and supporting labeling conversion...

Job DescriptionJob DescriptionRegulatory Specialist (MDR/IVDR)Irvine, CA 92618 (*Local candidates- 3 days on site/2 days remote)$40-$45hr (Weekly pay + Benefits)1yr contract (Excellent potential for extension or permanent)Full-time- M-F 8am-5pmOur client is a global team of innovators, leaders, creators, builders, and problem solvers. They develop...

Regulatory Affairs SpecialistThe Regulatory Affairs Specialist II, will provide administrative and technical support to regulatory affairs leadership in order to facilitate compliance with U.S. and international regulatory requirements. The Regulatory Affairs Specialist provides direct Worldwide Regulatory support to lifecycle management and new product...

Regulatory Affairs SpecialistThe Regulatory Affairs Specialist II, will provide administrative and technical support to regulatory affairs leadership in order to facilitate compliance with U.S. and international regulatory requirements. The Regulatory Affairs Specialist provides direct Worldwide Regulatory support to lifecycle management and new product...

Location: Irvine, CA (Hybrid)Contract Length: 12 Months Pay Rate: $30/hr including individual healthcare coveragePosition Summary:The Regulatory Affairs Specialist supports the development and implementation of the global regulatory strategy for company cosmetic and OTC products. With supervision, the specialist reviews, plans and prepares regulatory...

Top 3-5 skills, experience or education required1. Ability to critically and effectively review detailed information to support a labelling revision including all applicable regulations.3. Detail-oriented with the ability to proofread and check documents for accuracy and consistency.Purpose Statement:The Regulatory Affairs Specialist supports the development...

Ultimate Staffing is seeking an Account Specialist to join a leading organization in the client services sector. As an Account Specialist, you will play a vital role in managing and nurturing client relationships, ensuring satisfaction, retention, and growth. This position requires excellent communication skills, a strategic mindset, and a dedication to...