Labeling Specialist/Manager - Bridge Technologies and Solutions(WMBE) : Job Details

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Job SummaryThe Regulatory Labeling Specialist/Manager is responsible for managing and overseeing the development, and review of product labels and packaging to ensure compliance with FDA requirements. This role involves working closely with cross-functional teams to support submission, review and product launches while maintaining ongoing compliance throughout the product lifecycle in alignment with Long Grove style guidelines.

Job SummaryThe Regulatory Labeling Specialist/Manager is responsible for managing and overseeing the development, and review of product labels and packaging to ensure compliance with FDA requirements. This role involves working closely with cross-functional teams to support submission, review and product launches while maintaining ongoing compliance throughout the product lifecycle in alignment with Long Grove style guidelines.DepartmentRegulatory AffairsReports ToRegulatory Affairs Manager / Director /Vice PresidentKey Responsibilities

• Labeling Compliance: Develop, review, and approve product labels and packaging materials to ensure compliance with FDA, Long Grove style guide.
• Regulatory Knowledge: Stay current with changes in regulations, guidelines, and industry best practices related to labeling and packaging. Interpret and apply regulatory requirements to ensure product labels are accurate and compliant.
• Cross-Functional Collaboration: Work closely with Regulatory Affairs, Quality Assurance, Marketing, and Product Development teams to gather information and ensure that all labels aligned with product specifications.
• Labeling Documentation: Prepare and maintain comprehensive labeling documentation, including label copies, regulatory submissions, and compliance records.
• Manage the graphic designer process between Leader Board and LGP
• Generation of side-by-side labels between the proposed label/last sequence and RLD throughout the review process

Day To Day ActivitiesKeep abreast of regulations and guidelines, generate narratives for submission graphics generation, monitor Drugs@FDA website and revise labels to align with RLD updates.Applicable Guidelines

• Complying with Labeling for Human Prescription
• Complying with 21 CFR 201.57
• Complying with Generic Drug Labeling Revisions Under Section 505(j)(10) of the Federal Food, Drug, and Cosmetic Act
• Revising ANDA Labeling Following Revision of the RLD Labeling Guidance for Industry
• Label Change Management: Manage labeling changes and updates, including coordinating with relevant departments to implement changes, conduct impact assessments, and ensure timely updates to labels and packaging.
• Project Management: Manager labeling projects from inception through implementation, ensuring that deadlines are met and that the labeling meets all regulatory and quality standards.

Qualifications

• Education: Bachelor's degree in Life Sciences, Regulatory Affairs, Chemistry, or a related field. Advanced degrees or certifications in Regulatory Affairs (e.g., RAC) are a plus.
• Experience: Minimum of 3-5 years of experience in regulatory labeling or a related field within the pharmaceutical, biotechnology, medical device, or consumer goods industry.

Seniority level

• Seniority levelEntry level

Employment type

• Employment typeContract

Job function

• Job functionOther
• IndustriesIT Services and IT Consulting

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