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Johnson & Johnson

Makes prescription drugs and medical devices

Director of Engineering - Synthetics

Engineering LeadershipPosted on Nov 10
Full-timeNijmegen, Netherlands

About the Job

Requirements

  • A bachelor's degree in Chemical, Mechanical, Biomedical, Materials, or a related Engineering discipline is required.
  • At least 10 years of engineering experience in medical device, pharmaceutical, or combination product manufacturing, including relevant people leadership experience.
  • A proven track record leading capital investment projects, including business case development, budget ownership, and delivery of new lines or facilities.
  • Demonstrated success leading complex cross-functional programs, such as new product introduction, technology transfer, or scale-up, to on-time and on-budget outcomes.
  • Experience leading technology transformation, such as automation, digitalization, or introducing new process platforms.
  • Working knowledge of current Good Manufacturing Practice (cGMP) requirements, including process validation and risk management.
  • Strategic thinking and the ability to translate vision into executable plans.
  • Financial acumen and data-driven decision-making.
  • Executive presence and clear, concise communication with senior leadership.
  • Ability to influence without authority across a global matrix organization.
  • Willingness to travel up to 30% domestically and internationally.

Responsibilities

  • Lead, coach, and develop a team of engineering managers, engineers, and technical specialists across process, equipment, automation, and facilities disciplines.
  • Set goals, priorities, and accountability, and build organizational capability through hiring, succession planning, and targeted development.
  • Foster an inclusive, purpose-driven culture that supports technical excellence, collaboration, and continuous improvement.
  • Provide leadership across sites and functions, influencing senior stakeholders to align priorities and resources.
  • Own the multi-year engineering capital plan, including capacity expansion, new manufacturing lines, equipment replacement, and facility upgrades.
  • Develop and present business cases and capital appropriation requests covering scope, cost, schedule, risk, and return on investment.
  • Lead projects from concept and design through installation, commissioning, qualification, and handover to operations.
  • Manage budgets, forecasts, and spending with Finance, and ensure projects meet committed cost, schedule, and performance targets.
  • Select and manage equipment vendors, engineering firms, contract manufacturers, and partners.
  • Lead complex cross-functional engineering programs supporting capacity expansion, new product introduction, technology transfer, scale-up, and product lifecycle management.
  • Establish program governance through integrated plans, milestones, risk registers, and stage-gate reviews.
  • Identify and mitigate technical, supply, and schedule risks, escalating issues with options and recommendations.
  • Provide data-driven updates to senior leadership on program status, resources, and key decisions.
  • Partner with site operations to sustain supply continuity, resolve technical and process issues, and deliver lifecycle, cost-improvement, and reliability projects for base business manufacturing.
  • Develop project and program management skills across the engineering organization through coaching, standard tools and templates, and hands-on program leadership opportunities.
  • Align engineering priorities with Research and Development, Quality, Regulatory, Supply Chain, and Commercial roadmaps.
  • Define and execute the engineering technology roadmap, including automation, digital manufacturing, data analytics, Industry 4.0, and artificial intelligence capabilities.
  • Evaluate, pilot, and scale process technologies to improve yield, capacity, quality, and cost.
  • Improve process robustness through Design of Experiments (DoE), Process Analytical Technology (PAT), and advanced process control.
  • Drive standardization of equipment, processes, and engineering practices across sites and external partners.
  • Provide technical leadership for medical device and drug-device or biologic-device combination product manufacturing processes.
  • Lead development, scale-up, and optimization of powder processes, including milling, blending, granulation, drying, particle-size control, powder filling, and containment.
  • Address powder-process challenges including flowability, segregation, moisture sensitivity, dust control, and operator safety.
  • Ensure process and equipment design supports sterility assurance, contamination control, and cleanroom requirements where applicable.
  • Partner with Research and Development and external partners to transfer powder and combination product technologies into commercial manufacturing.
  • Ensure engineering activities comply with applicable current Good Manufacturing Practice requirements.
  • Lead or support process validation, change control, risk management using process Failure Mode and Effects Analysis, and investigations or corrective and preventive actions with engineering root-cause analysis.
  • Support regulatory submissions and inspections with technical documentation and subject-matter expertise.
  • Uphold Environmental, Health and Safety standards, including combustible-dust and potent-compound handling where relevant.
  • Create a purpose-driven environment by aligning the company's Credo and leadership imperatives with team and enterprise strategies and goals, prioritizing patient needs and well-being.

Desired Qualifications

  • A master's degree, Master of Business Administration, or PhD is preferred.
  • Hands-on expertise in powder processing technologies, including milling, blending, granulation, spray drying, powder filling, and containment.
  • Direct experience with medical products.
  • Experience with hemostats, biosurgery, or other absorbable or biologic medical products.
  • Experience managing external manufacturing partners, suppliers, and engineering contractors in a global environment.
  • Project Management Professional, Lean Six Sigma, or equivalent certification.
  • Consulting experience.
  • Cross-functional collaboration.
  • Fact-based decision-making.
  • Lean manufacturing principles.
  • Lean supply chain management.
  • Mentorship.
  • Organizational knowledge.
  • Policy implementation.
  • Process optimization.
  • Productivity planning.
  • Project engineering.
  • Quality focus.
  • Science, technology, engineering, and mathematics application.
  • Six Sigma.
  • Supply Chain.
  • Tactical planning.
  • Technical credibility.

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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