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Johnson & Johnson

Makes prescription drugs and medical devices

Manufacturing Engineering Manager

Manufacturing EngineeringConfirmed live in the last 24 hours
Full-timeAñasco, Puerto RicoNo salary listed

About the Job

Requirements

  • A bachelor's degree in Engineering is required.
  • At least 8 years of relevant experience in manufacturing engineering, maintenance manufacturing, process development, research and development, automation, or regulated manufacturing operations is preferred.
  • People leadership or demonstrated technical/team leadership experience is required.
  • Strong communication, cross-functional collaboration, decision-making, coaching, and stakeholder management skills are required.
  • Candidates offered employment must show proof of COVID-19 vaccination or secure an approved accommodation before commencement of employment.

Responsibilities

  • Lead, coach, and develop the Manufacturing Engineering team, ensuring proper span of control, clear priorities, accountability, and effective leadership routines that support engagement, retention, and talent development.
  • Establish engineering standards, direction, and governance for manufacturing areas, ensuring effective line-side support, technical escalation, and structured problem solving across value streams.
  • Drive operational performance metrics including yield, units per person per hour (UPPH), uptime, overall equipment effectiveness (OEE), process reliability, and productivity through disciplined engineering execution, trend analysis, and risk-based prioritization.
  • Lead and execute programs and projects of moderate to high complexity, ensuring safety, regulatory compliance, company standards, operational requirements, financial discipline, and business needs are achieved.
  • Provide leadership for root cause analysis, non-conformance investigations, corrective and preventive actions, process characterization, process control improvements, and complex production or processing equipment support.
  • Ensure validation strategies and execution are robust, including factory acceptance testing (FAT), installation qualification (IQ), operational qualification (OQ), performance qualification (PQ), computer systems validation where applicable, design reviews, and readiness for regulated manufacturing implementation.
  • Build sustainable systems for resource planning, workload management, and project prioritization across day-to-day operations, strategic initiatives, and long-term process improvement work.
  • Partner cross-functionally with Operations, Quality, Maintenance, Automation, Facilities, Supply Chain, Finance, Human Resources, Talent Acquisition, and global engineering to align business needs, staffing plans, and execution deliverables.
  • Prepare and present business cases, capital appropriation requests (CARs), project estimates, schedules, forecasts, resource plans, and status updates to support timely decisions and leadership alignment.
  • Challenge the status quo and promote continuous improvement, technical excellence, standard work, and proactive risk identification across the manufacturing engineering organization.
  • Support staffing governance by ensuring roles have clear business justification, impact assessment, role expectations, equivalent pay grade alignment, and required approvals before filling positions.
  • Ensure adherence to Standard Operating Procedures, Good Manufacturing Practices, company policies, environmental, safety, occupational health, and applicable federal, state, and local regulations.

Desired Qualifications

  • An advanced degree or business/operations leadership training is preferred.
  • Experience developing engineers, managing priorities, and leading through influence is strongly preferred.
  • Experience in the medical device or pharmaceutical industry is preferred.
  • Experience in project management, financial management, resource planning, and presentation of business cases or capital appropriation requests is preferred.
  • Experience with Good Manufacturing Practice (GMP) and International Organization for Standardization (ISO) requirements, validation lifecycle, factory acceptance testing (FAT), installation qualification (IQ), operational qualification (OQ), performance qualification (PQ), process characterization, and technical investigations is preferred.
  • Experience with optical inspection systems, automated equipment, design reviews with vendors, and equipment/process optimization is preferred.

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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