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Johnson & Johnson

Makes prescription drugs and medical devices

Staff Manufacturing Engineer

Manufacturing EngineeringPosted on Nov 10
Full-timeLimerick, Ireland

About the Job

Requirements

  • A Level 8 Bachelor's degree (B.Eng. or B.Sc.) in Mechanical, Manufacturing, Production, Industrial, Automation or a related engineering discipline, or an equivalent combination of education and experience.
  • A minimum of 8 years' engineering experience in a high-volume, automated manufacturing environment, with a proven record of leading technical projects and improvements.
  • Demonstrated experience in equipment or process design, installation, qualification and validation within a regulated industry such as medical devices, pharmaceuticals or similar.
  • Deep knowledge of complex automated manufacturing equipment, including mechanical systems, pneumatics, vacuum, motion control and programmable logic controller-based controls.
  • Strong understanding of process control, statistical methods such as design of experiments, statistical process control and capability analysis, and structured root cause analysis.
  • Working knowledge of Lean Manufacturing, Six Sigma and continuous improvement tools.
  • Knowledge of equipment qualification and validation principles, Good Manufacturing Practices, change control and machine safety standards.
  • Proficiency with engineering and data analysis tools, including computer-aided design and Excel.
  • Strong analytical and scientific approach to problem solving, blending data analysis and experimentation to maximise productivity and yield.
  • Ability to influence and build consensus across functions and organisational levels, including senior stakeholders.
  • Project management, written and verbal communication skills.
  • Ability to work on own initiative, prioritise competing demands and manage multiple projects in a fast-paced environment.
  • Strong attention to detail with a commitment to safety, quality and compliance.
  • Passion for coaching and developing others, with a collaborative and continuous-learning mindset.

Responsibilities

  • Act as the senior technical authority for manufacturing equipment and processes, providing direction on complex troubleshooting, root cause analysis and long-term technical solutions.
  • Lead the design, installation, qualification, optimisation and standardisation of lens production processes, equipment, tooling and controls, ensuring solutions are scalable and, where appropriate, deployed across multiple lines and value streams.
  • Drive year-on-year improvements in equipment overall equipment effectiveness, process capability, yield and output through structured problem solving, data analysis and Lean and Six Sigma methodologies.
  • Develop and maintain technical roadmaps for assigned platforms, including obsolescence and aged-asset mitigation, technology upgrades and capability development.
  • Provide technical input to capital investment proposals, business cycle planning and cost-saving programmes.
  • Lead large, cross-functional engineering projects from concept through design, installation, commissioning, validation and ramp-up, including new product introductions, line conversions and capacity expansion.
  • Identify and lead cost, quality and technical improvement initiatives under the site continuous improvement programme, quantifying benefits and delivering to agreed timelines and budgets.
  • Apply robust project management governance, providing timely and accurate status reporting to stakeholders and leadership.
  • Evaluate emerging technologies and industry trends, and introduce those that deliver a measurable benefit to safety, quality, delivery and cost.
  • Ensure all engineering activities conform to corporate, franchise, statutory and regulatory requirements for Good Manufacturing Practices, environment, health and safety, and Quality, including change control, equipment qualification and process validation.
  • Own or support effective closure of Quality System actions such as corrective and preventive actions, non-conformances, audit actions and risk assessments.
  • Embed safety and environmental requirements in the purchase, modification and operation of new and existing equipment, including machine safety standards.
  • Create, review and approve technical documentation, including specifications, protocols, work instructions and troubleshooting guides.
  • Act as a subject matter expert during internal and external audits.
  • Partner with Operations, Quality, Research and Development, Supply Chain, Strategic Sourcing and Global Engineering to deliver value stream safety, quality, delivery and cost objectives.
  • Build relationships with other company sites, equipment vendors and external experts to share best practice and leverage learnings.
  • Mentor and coach Associate, Manufacturing and Senior Engineers, supporting their technical and career development.
  • Role-model the company's Credo and behavioural standards, and contribute to a high-performance, inclusive team culture.
  • Support the Engineering Manager in developing and implementing strategic engineering goals and objectives.
  • Minimise the environmental and health and safety impact of the work performed.

Desired Qualifications

  • A Master's degree in Engineering or a related discipline.
  • Experience with contact lens manufacturing, injection moulding, high-speed automated assembly or similar high-volume processes.
  • Six Sigma Green or Black Belt certification, or equivalent statistical problem-solving training.
  • Experience in FDA-regulated and ISO 13485 environments, including equipment validation.
  • Project management certification or training, such as J&J Flawless Project Execution or Project Management Professional certification.
  • Familiarity with data analytics and digital manufacturing tools is an advantage.

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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