Pharmaceutical Labeling Specialist
$61.16 per hourThe Fountain Group LLC
Job Description
Job Description
The Fountain Group is currently seeking a Labeling Specialist for a prominent client of ours. This position is located in below . Details for the position are as follows:
Pay: $61.16/Hour Title : Labeling SpecialistDuration : 5+ Months assignment, possibility for extension or conversion based on performance and budget.
Schedule: M-F, 8am - 5pm Possible Locations:
- Santa Monica, CA
- El Segundo, CA
- Frederick, MD
- Oceanside, CA
- Foster City, CA
- The Commercial Labeling Contractor supports the execution of labeling activities, including artwork workflows, supporting documentation, and cross-functional coordination. This role ensures timely, compliant delivery of labeling updates while maintaining inspection readiness and supporting global operations.
- 3+ years of experience in pharmaceutical/biotech labeling, regulatory operations, or supply chain
- Experience managing labeling workflows, artwork reviews, and approval processes
- Familiarity with Veeva Vault or similar systems
- Experience with Adobe Acrobat and proofreading tools (e.g., GlobalVision)
- Strong project management skills with the ability to manage multiple priorities
- High attention to detail with a strong quality and compliance mindset
- Ability to operate independently in a fast-paced, regulated environment
- Manage end-to-end labeling workflows, including form data entry, routing, reviews, and approvals (e.g., Veeva Vault)
- Coordinate label artwork development cycles, including proof review, comment consolidation, and final approvals
- Track and manage project timelines, milestones, and deliverables across multiple concurrent initiatives
- Partner with print vendors to manage artwork proofs and revisions
- Perform detailed proofreading and quality checks using tools such as Acrobat and GlobalVision
- Support change implementation, including obsolescence tracking and phase-in/phase-out coordination
- Maintain labeling documentation to ensure compliance with internal procedures and Good Documentation Practices (GDP)
- Collaborate cross-functionally with Regulatory, Quality, Supply Chain, and global stakeholders
- Proactively identify risks, manage issues, and escalate delays or concerns as needed
- Maintain trackers and provide status updates to ensure visibility to timelines and deliverables
- Experience within a highly regulated GXP environment
- Familiarity with global labeling requirements and multi-region coordination
- Nice-To-Have, but not required
- Experience with Adobe Creative Suite
- Experience with BarTender (barcode management)
- Experience working with print vendors and packaging components
If you are interested in hearing more about the position, please respond to this posting with your resume attached.
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