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Cristcot

Senior Manager/Associate Director/Director, Packaging & Labeling Operations

Cristcot

Senior Manager / Associate Director / Director of Packaging and Labeling Operations at Cristcot. Overseeing packaging and labeling activities to ensure compliance and support product supply.

Posted 6/20/2026full-timeRemote • 🇺🇸 United StatesSeniorWebsite

Tech Stack

Tools & technologies
ERP

About the role

Key responsibilities & impact
  • Provide strategic and operational oversight of packaging and labeling activities.
  • Manage internal and external stakeholders.
  • Drive continuous improvement initiatives across the product lifecycle.
  • Lead packaging and labeling operations to support clinical, commercial, and post-market activities.
  • Lead packaging validation, shipping validation, and drop test strategy and execution oversight.
  • Ensure packaging and labeling processes comply with applicable FDA, ISO, MDR, and other global regulatory requirements.
  • Own sponsor side technical oversight for primary packaging, labeling, artwork, printed packaging components, and commercial kitting of drug product and device components.
  • Develop and maintain approval, implementation, and control of packaging and labeling specifications, procedures, and documentation.
  • Partner with Quality, Regulatory Affairs, Supply Chain, Manufacturing, and Product Development teams to ensure alignment across product lifecycle activities.
  • Support product launches, design changes, market expansions, and supply continuity initiatives.
  • Provide sponsor side oversight of serialization readiness and execution at CMO.
  • Manage packaging, labeling, kitting, and serialization related vendors, including governance, issue resolution, timelines, and technical deliverables.
  • Ensure packaging and labeling activities are performed in accordance with established quality systems and applicable regulations.
  • Investigate deviations, nonconformances, CAPAs, and labeling-related quality events.
  • Assess and mitigate operational and compliance risks associated with packaging and labeling activities.
  • Lead cross-functional projects related to packaging optimization, labeling implementation, product launches, and process improvements.
  • Develop and monitor key performance indicators (KPIs) for packaging and labeling operations.
  • Establish priorities, allocate resources, and ensure timely execution of operational objectives.

Requirements

What you’ll need
  • Bachelor’s degree in Packaging Engineering, Chemical Engineering, Mechanical Engineering, Materials Science, Supply Chain, Life Sciences, or related field required.
  • Advanced degree (MS, MBA, or equivalent) preferred.
  • Senior Manager: 8+ years of experience in biotechnology, pharmaceutical, medical device, or other regulated healthcare industries with 3+ years of direct experience managing packaging and/or labeling operations.
  • Associate Director: 10+ years of experience in biotechnology, pharmaceutical, medical device, or other regulated healthcare industries with 5+ years of leadership experience in packaging, labeling, manufacturing operations, supply chain, or related functions.
  • Director: 12+ years of experience in biotechnology, pharmaceutical, medical device, or other regulated healthcare industries with 7+ years of progressive leadership experience, including responsibility for teams, budgets, and strategic initiatives.
  • Experience with external CMOs, CDMOs, packaging vendors, labeling vendors, and kitting vendors.
  • Experience working within FDA-regulated and/or ISO 13485 environments.
  • Strong knowledge of cGMP, packaging validation, shipping validation, labeling controls, artwork processes, and DSCSA governance.
  • Demonstrated experience leading cross-functional projects and managing external vendors or contract manufacturers.
  • Strong understanding of quality systems, document control, change management, and regulatory compliance.
  • Experience interacting with executive leadership, regulatory agencies, and external partners.
  • Experience supporting late stage or commercial product launch preferred.
  • Experience with combination products or medical devices preferred.
  • Experience with ERP, PLM, document management, and quality management systems.
  • Excellent project management and organizational skills.
  • Strong analytical and problem-solving capabilities.
  • Ability to work effectively in a fast-paced, growth-oriented environment.
  • Demonstrated leadership, collaboration, and stakeholder management skills.
  • Ability to travel 20-25%.

Benefits

Comp & perks
  • Health insurance
  • 401(k)
  • Paid time off
  • Flexible working arrangements
  • Professional development opportunities

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills & Tools
packaging engineeringlabeling operationspackaging validationshipping validationcGMPDSCSA governancedocument controlregulatory compliancechange managementproject management
Soft Skills
leadershipcollaborationstakeholder managementanalytical skillsproblem-solvingorganizational skillscommunication skillsstrategic oversightcontinuous improvementresource allocation
Certifications
Bachelor’s degreeMaster’s degreeMBAISO 13485 certificationFDA compliance training