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Johnson & Johnson

Makes prescription drugs and medical devices

Compliance Lead - Packaging & Technology

Regulatory & Quality (Life Sciences)Confirmed live in the last 24 hours
Full-timeBeerse, Belgium

About the Job

Requirements

  • A minimum of a Bachelor's degree in life sciences, engineering, pharmacy, quality, supply chain, business administration, or a related discipline, or an equivalent combination of education and relevant experience.
  • A minimum of 6 years of work experience in clinical operations or a direct supporting function within pharmaceutical operations, quality, packaging, labeling, warehousing, clinical supply, or another highly regulated environment.
  • Strong working knowledge of ICH-GxP principles, quality systems, data integrity, and regulatory expectations applicable to pharmaceutical packaging, labeling, warehouse activities, and sample flows.
  • Understanding of drug development and clinical supply processes and their interfaces with packaging, labeling, warehousing, and sample management.
  • Demonstrated experience supporting deviations, investigations, CAPAs, change controls, audits, inspections, and compliance-risk assessments.
  • Ability to work independently as a subject matter expert, influence without formal authority, manage multiple priorities, and make sound risk-based recommendations.
  • Fluent English, written and spoken.
  • Candidates must already have authorization to work in the country of employment.

Responsibilities

  • Act as the end-to-end compliance lead and subject matter expert for P&T, covering packaging processes and execution, labeling design processes and execution, local warehouse operations, and sample flows.
  • Translate applicable ICH-GxP, regulatory, quality-system, data-integrity, policy, and procedural requirements into clear, practical expectations for P&T operations.
  • Serve as the primary P&T compliance contact for internal and external audits and Health Authority inspections, coordinating readiness activities and supporting demonstration of end-to-end process integrity and compliance.
  • Coordinate inspection readiness across the assigned P&T scope, including preparation, evidence gathering, identification and escalation of key risks, response development, mitigation planning, and follow-up of commitments.
  • Liaise with QA, QS, business process owners, R&D Quality, and operational stakeholders to align compliance expectations, priorities, decisions, and actions across the end-to-end P&T organization.
  • Monitor and communicate compliance metrics, trends, and emerging risks; maintain fit-for-purpose compliance governance, routines, risk registers, and action tracking, and provide evidence-based recommendations to the Logistics and Compliance Lead.
  • Guide issue management for deviations, investigations, CAPAs, change controls, periodic reviews, and other quality-system processes, ensuring appropriate preventive and corrective actions are defined, tracked, and effectively implemented to uphold operational integrity.
  • Review and advise on procedures, work instructions, training content, specifications, and compliance controls associated with packaging, labeling, warehousing, and sample handling.
  • Support compliant introduction of new products, processes, systems, equipment, suppliers, and operating-model changes by providing timely compliance input and documenting requirements and decisions.
  • Participate as the P&T compliance representative in cross-functional operational workstreams and initiatives, providing risk-based guidance and supporting aligned implementation.
  • Support onboarding of new team members by providing role-relevant compliance orientation, training guidance, and access to applicable standards and procedures.
  • Promote a strong quality and compliance culture, employee engagement, inclusion, and adherence to Credo Behaviors by coaching stakeholders, reinforcing clear ownership, and serving as an accessible point of contact for compliance questions.
  • Build effective working relationships with P&T operations, Quality, Clinical Supply Chain, labeling functions, warehouse and sample-flow stakeholders, system owners, and relevant internal and external partners.

Desired Qualifications

  • Experience in clinical supply, pharmaceutical packaging and labeling, local warehouse activities, sample management, or related operational interfaces.
  • Experience supporting GxP audits and Health Authority inspections and interacting with Quality or regulatory stakeholders.
  • Demonstrated ability to establish compliance governance, risk-management processes, action tracking, and meaningful compliance metrics.
  • Knowledge of the J&J Quality Management Systems.
  • Proficiency with Microsoft Office and relevant quality, enterprise, packaging, labeling, warehouse, and reporting systems.
  • Experience using compliance metrics, data analytics, and visualization to identify and communicate compliance signals.
  • Dutch is preferred for effective collaboration with local operational and technical teams.
  • Willingness to travel occasionally, up to 10%, as business needs require.

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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