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Johnson & Johnson

Makes prescription drugs and medical devices

Vision CQ Transportation Quality Associate Manager

Regulatory & Quality (Life Sciences)Confirmed live in the last 24 hours
Full-timeNo salary listed

About the Job

Requirements

  • A bachelor's degree is required.
  • A degree concentration in Life Science, Engineering, Technical Business, Quality, Regulatory Compliance, Supply Chain, Logistics, or a related discipline is preferred.
  • A minimum of five years of experience in a regulated healthcare industry, including medical devices, pharmaceuticals, and/or diagnostics, with quality, regulatory compliance, distribution, supplier quality coordination, transportation, or supply chain quality experience is required.
  • Experience supporting transportation quality operations, investigations, CAPAs, quality events, change controls, metrics reporting, trend analysis, and cross-functional project activities is required.
  • Demonstrated knowledge of applicable global regulations and experience collaborating with professionals in a matrixed environment are required.
  • Experience preparing accurate operational quality data, metrics, trends, and risk information for governance or management review, and collaborating across functions on shared investigations or issue resolution, is required.
  • Working knowledge of transportation quality management, Good Distribution Practices, quality management systems, supplier quality coordination, carrier performance, qualification activities, issue escalation, and compliant logistics operations is required.
  • Knowledge of lane and route qualification, lane mapping, temperature-controlled transportation, temperature excursion management, transportation risk assessment, and logistics-provider oversight is required.
  • Ability to partner effectively with Transportation Operations, Supply Chain, Procurement, APAC and Japan regional Commercial Quality teams, and external suppliers in a matrixed environment is required.
  • Ability to use metrics, scorecards, and trends to identify risk and drive action is required.
  • Ability to prepare clear, accurate, decision-ready Vision-specific data for governance review and collaborate with MedTech and Innovative Medicine colleagues on occasional cross-segment transportation investigations is required.
  • Fluent English and Japanese language capability is required, including the ability to communicate with Japan-based stakeholders and support review or coordination of Japan-related transportation quality documentation.
  • Travel of approximately 15–25% may be required, depending on business needs.

Responsibilities

  • Provide operational quality oversight for inter-regional transportation activities impacting APAC and Japan, partnering with regional Commercial Quality, Transportation Operations, Supply Chain, Procurement, carriers, control towers, and logistics providers.
  • Lead or support transportation-related investigations, nonconformances, CAPAs, deviations, change controls, complaints, product-impact assessments, effectiveness checks, and associated quality records through timely closure.
  • Assess and coordinate resolution of transportation incidents, temperature excursions, damage, contamination, losses, mis-deliveries, seal issues, and service failures; escalate material risks in accordance with established processes.
  • Support transportation supplier quality activities, including carrier qualification, quality agreements, supplier audits, performance reviews, corrective-action follow-up, and remediation.
  • Support transportation lane and route qualification, lane mapping, shipping-route verification, transportation risk assessments, temperature-control qualification, and network changes.
  • Provide quality support for new product introductions, transfers, business-continuity activities, and projects that change transportation routes, providers, systems, or operating processes.
  • Build, maintain, and report transportation quality metrics, dashboards, scorecards, and trend analyses; identify emerging risks, recurring issues, and improvement opportunities.
  • Maintain complete, accurate, and retrievable documentation and evidence packages to support internal audits, supplier audits, health authority inspections, and notified-body assessments.
  • Contribute to process simplification, harmonization, training, communications, and capability-building initiatives as transportation responsibilities transition into Vision CQ.
  • Prepare and validate Vision-specific transportation quality data, metrics, trend analyses, risks, and investigation insights for governance meetings and management reviews.
  • Provide Vision-specific supporting information and subject-matter input for governance requests, ensuring that Vision transportation issues, trends, and regulatory considerations are accurately represented.
  • Work with MedTech and Innovative Medicine quality colleagues on occasional cross-segment transportation investigations, contributing Vision-specific evidence, product and lane impact assessments, root-cause input, and agreed follow-up activities.
  • Provide technical quality guidance, support workflow execution, and contribute to departmental transportation quality priorities. The position has no direct supervisory responsibility.

Desired Qualifications

  • Experience supporting transportation qualification, supplier quality activities, new product introductions, network changes, remediation, and/or quality improvement activities.
  • Previous experience supporting audits or interfacing with regulatory agencies and notified bodies.
  • Quality auditing, GDP, project management, supply chain, logistics, Lean, or Six Sigma certification is desirable.

About the Company

Johnson & Johnson

Makes prescription drugs and medical devices

Johnson & Johnson develops prescription medicines and makes medical devices for hospitals, and unlike most big drugmakers, it runs both businesses under one roof. In 2015, its Darzalex became the first antibody drug approved for multiple myeloma, a blood cancer. Its medicines treat cancer, immune diseases such as psoriasis, and mental illnesses such as depression, and patented drugs bring in most of its sales. Its MedTech unit makes heart pumps, catheters that treat irregular heartbeats, surgical sutures, and Acuvue contact lenses. It was founded in 1886 to make sterile surgical dressings, is based in New Brunswick, New Jersey, and spun off its consumer brands, such as Tylenol and Band-Aid, as Kenvue in 2023.

Company size
10,001+
Company stage
IPO
Headquarters
New Brunswick, NJ
Founded
1886

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