Regulatory Affairs Associate II

Spectraforce Technologies; Plainsboro Township (NJ); In loco; USD 55.000 - 110.000; Tempo pieno

Descrizione del lavoro

Spectralforce Technologies, Inc. is seeking a Regulatory Affairs Labeling Operations Specialist (Contractor) in Plainsboro, NJ.

The role focuses on final printed labeling for launch and lifecycle projects, ensuring compliance with FDA labeling requirements and industry best practices. The successful candidate will lead cross-functional collaboration with Regulatory Affairs, Global HQ, LPPC, and design teams to ensure on-time labeling readiness aligned with product timelines.

Competenze

• Bachelor's degree and 3+ years in pharma labeling or related environment.
• 3-5 years of experience in labeling/related processes.
• Strong knowledge of CFR labeling requirements and FDA labeling resources.
• Excellent communication and collaboration with cross-functional teams.

Mansioni

• Review labeling materials for CFR and FDA requirements.
• Identify labeling issues and coordinate resolution with stakeholders.
• Participate in cross-functional teams to support labeling projects.

Conoscenze

TVT

SPL creation

Project management

Cross-functional collaboration

Attention to detail

FDA labeling knowledge

Formazione

Bachelor's degree

Strumenti

Vault RIM (Veeva)

Esko LIFT

Adobe Acrobat

Descrizione del lavoro

Job Title

Regulatory Affairs Labeling Operations Specialist

Location

Plainsboro, NJ 08536 - Onsite preferred, remote okay

Duration

2 Years (Possibility of extension depending upon business requirements and performance)

Schedule

Mon-Fri 9am - 5pm

Top 3 Must Haves

• TVT (Text Verification Tool)
• SPL (Structured Product Labeling) Creation/Dev
• Self-Directed Project Management End-to-End

Job Description

• The client is seeking a dynamic and experienced Regulatory Affairs Labeling Operations Specialist (Contractor) to process critical tasks related to final printed pharmaceutical labeling for launch and lifecycle management projects guided by company content of labeling, FDA Patient Labeling Resources, FDA Label Negotiations and Industry trends.
• This requires labeling verification to include reviews across the product family of leaflets, carton and container labels as well as device labels.
• The ideal candidate will collaborate with cross-functional teams of Regulatory Affairs Therapeutic Area (TA) Managers, Global HQ, Labeling Projects and Planning Coordinators (LPPC), Graphic Designers, Marketing and Supply Chain.

Relationships

• Reports to labeling management in Regulatory Operations (RO), engaging with key company personnel within organization to drive successful project outcomes for assigned projects.
• Develops and maintains positive working relationships with company stakeholders, fostering effective collaboration with Regulatory Affairs (RA), Supply Chain, and HQ colleagues to ensure labeling compliance and accomplish company goals.

Key Responsibilities

• Review and provide regulatory guidance on commercial labeling materials to ensure compliance with CFR and FDA labeling requirements
• Identify labeling issues, troubleshoot, and communicate effectively with relevant stakeholders to ensure timely resolution
• Monitor, evaluate, and recommend improvements to labeling processes, quality, and system tools, in alignment with FDA regulations and industry best practices

Essential Functions

Label Development

• Assist in the Final Printed Labeling review and approval process based on final approved labeling content from FDA, collaborating with TA, LPPC, and Graphic Designers to ensure successful on-time launch of product labeling per company launch readiness timelines
• Ensures additional filing requirements are completed for approved content of labeling to include SPL Drug Listing, FDA 2253s and Puerto Rico Registrations

Labeling Tools

• Serve as an experienced user in all labeling tools with emphasis in SPL ALiCE A4L environment and highly proficient in TVT usage; other systems include Vault RIM (Veeva), Esko (LIFT Artwork Management), Adobe Acrobat, etc. As well as coordinating technical support needs with internal IT groups
• Utilizing FDA portals and tools to include ESG NexGen, FURLS, SPL Help Desk, FDALabel, Drugs@FDA and coordinating with internal groups and external agencies to resolve any issues

Regulatory Support

• Participate in cross-functional teams locally and globally, demonstrating good judgment in troubleshooting to resolve problems of moderate scope and complexity
• Competence in Lot Distribution Data Reports, CARES Act Distribution Reporting, SPL Blanket No Change Certification, FDA Establishment Registrations, FDA Annual Reports, FDA PBRER, Certificate of Pharmaceutical Products, and PRDOH Puerto Rico Registrations

Skills and Experience

• Bachelor's degree and minimum 3 years of progressively responsible experience in a pharmaceutical, biotechnology or related environment OR equivalent combination of experience and education with a concentration in labeling development and maintenance.
• 3-5 years of proven experience supporting process (brand experience is preferred over generics - but depends on candidate's experience)
• Proficiency with 21 CFR Labeling, Physician Labeling Rule (PLR), Selected Requirements of Prescribing Information (SRPI), FDA Patient Labeling Resources, Medication Guides, Instructions for Use, National Drug Codes, industry-standard labeling trends, DUNS, and FEI Registrations.
• Excellent communication, collaboration, and interpersonal skills to work effectively with cross-functional teams and key company personnel.
• Strong problem-solving abilities with a keen attention to detail and adherence to federal requirements and best practices.
• Proven ability to independently manage labeling processes, prioritize tasks, and drive successful outcomes.