Johnson & Johnson Posted November 10, 2026

Staff Manufacturing Engineer

Limerick, Ireland Full time
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Johnson & Johnson is the source of truth for this posting and owns the application process. We surface normalized context and market comparison you won't find on the original listing.

About this opportunity

At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at jnj.com .

As guided by Our Credo, Johnson & Johnson is responsible to our employees who work with us throughout the world. We provide an inclusive work environment where each person is considered as an individual. At Johnson & Johnson, we respect the diversity and dignity of our employees and recognize their merit.

Job Function:

Supply Chain Engineering

Job Sub Function:

Manufacturing Engineering

Job Category:

Scientific/Technology

All Job Posting Locations:

Limerick, Ireland

Job Description:

Job Position Summary

The Staff Manufacturing Engineer is a senior individual-contributor role providing technical leadership for manufacturing engineering within J&J Vision Care, Limerick. Working in a high-volume, fully automated and highly regulated contact lens manufacturing environment, the Staff Engineer leads complex, high-impact technical initiatives that improve equipment performance, process capability, yield and output, while ensuring operations remain safe, compliant and cost-effective.

The role acts as a subject matter expert and technical authority across one or more value streams, influences technical direction across Engineering, Operations, Quality, R&D and Global Engineering, and coaches and mentors engineers to raise the technical capability of the wider team. The Staff Engineer reports to the Manufacturing Engineering Manager and has no direct line management responsibility, but is expected to lead through influence.

Duties & Responsibilities

Technical Leadership

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 OEE, process capability, yield and output through structured problem solving, data analysis and Lean / 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.

Projects, NPI & Continuous Improvement

Lead large, cross-functional engineering projects from concept through design, installation, commissioning, validation and ramp-up, including new product introductions (NPI), 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.

Quality, Compliance & EHS

Ensure all engineering activities conform to corporate, franchise, statutory and regulatory requirements for GMP, EHS and Quality, including change control, equipment qualification and process validation.

Own or support effective closure of Quality System actions such as CAPAs, 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.

Collaboration, Coaching & Culture

Partner with Operations, Quality, R&D, Supply Chain, Strategic Sourcing and Global Engineering to deliver value stream safety, quality, delivery and cost objectives.

Build relationships with other J&J 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 Our Credo and JJVC behavioural standards, and contribute to a high-performance, inclusive team culture.

Support the Engineering Manager in developing and implementing strategic engineering goals and objectives.

All employees are responsible for minimising the environmental and health and safety impact of the work they perform.

Experience & Education

Essential

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.

Desirable

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 (e.g., J&J Flawless Project Execution, PMP).

Required Knowledge, Skills, Abilities, Certifications/Licences and Affiliations

Technical Knowledge

Deep knowledge of complex automated manufacturing equipment, including mechanical systems, pneumatics, vacuum, motion control and PLC-based controls.

Strong understanding of process control, statistical methods (e.g., DOE, SPC, 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, GMP, change control and machine safety standards.

Proficiency with engineering and data analysis tools, including CAD and Excel; familiarity with data analytics and digital manufacturing tools is an advantage.

Skills & Attributes

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.

Excellent 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.

#LI-CH5

Required Skills:

Preferred Skills:

Accelerating, Coaching, Compliance Risk, Critical Thinking, Facility Management, Good Manufacturing Practices (GMP), Lean Manufacturing Principles, Lean Supply Chain Management, Manufacturing Engineering, Performance Measurement, Product Design, Program Management, Project Engineering, Project Schedule, Robotic Automation, Safety-Oriented, Science, Technology, Engineering, and Math (STEM) Application, Technologically Savvy

The anticipated base pay range for this position is:

€64,300.00 - €102,925.00

Benefits:

In addition to base pay, we offer the following benefits*: an annual bonus with set target (% of pay) depending on pay grade / location, where the actual amount is based on the employees’ and companies’ performance of the previous calendar year, or sales commissions. Moreover, we offer vacation days, parental leave for a minimum of 12 weeks, bereavement leave, caregiver leave, volunteer leave, well-being reimbursement, programs for financial, physical and mental health. We also offer service anniversary and recognition awards, and subject to the terms of their respective plans, employees - and in some location’s eligible dependents - can participate in several insurance plans. For more information, visit Employee benefits | Supporting well-being & career growth | Johnson & Johnson Careers.

*This is for informative purposes only. Amounts and actual benefits may vary by location and are subject to change.

Job details

Seniority
Not listed
Function
Manufacturing & CMC
Therapeutic area
Not listed
Location
Limerick, Ireland
Employment type
Full time

How this role compares

Computed from every other active Manufacturing & CMC role in our database, not just this employer's listings.

We currently track 3432 comparable Manufacturing & CMC roles across 177 biopharma companies.

3432Comparable roles tracked
3080Currently active
177Companies hiring similar roles
61Countries represented

Salary context

816 of 3432 peers report a salary range (USD, annualized)

Peers share this role's job function. This posting doesn't list a seniority level, so peers aren't narrowed by seniority either -- the range below may span more levels than usual.

This roleSubject Not listed on this posting
Lowest disclosed · Alarm Room Monitor - First Shift · Genz. Therap Product LP $2,300/yr – $3,067/yr
Highest disclosed · Head of Analytical Development · ModernaTX, Inc. $272,200/yr – $490,100/yr
Peer group range $2,684 – $381,150 (median $128,400)

Where these roles are based

Top locations among the 3432 comparable roles

United States1578
Germany209
India160
France151
Ireland127
China123

+ 55 more countries

Seniority mix

1535 of 3432 peers have a known seniority level

Senior402
Manager360
Intern/Fellow/Postdoc216
Associate146
Principal134
Associate Director110
Director105
Senior Director55
Executive/VP7

Therapeutic area mix

19 of 3432 peers have a known therapeutic area; the rest are genuinely unlabeled, not hidden

Vaccines & Infectious Disease12
Dermatology & Aesthetics2
Oncology2
Respiratory1
Immunology1
Rare Disease1

Similar opportunities

The closest matches from our peer group, ranked by how similar they are, not how well you'd qualify for them -- treat this as market context, not a guaranteed shortlist; a weak match is labeled as one below.

40%similar
McDermott Laboratories Limited Northern Cross, Ireland Director
Same function Same country
40%similar
Mylan Teoranta Inverin, Ireland
Same function Same country
40%similar
Mylan Teoranta Inverin, Ireland
Same function Same country
40%similar
McDermott Laboratories Limited Northern Cross, Ireland
Same function Same country
40%similar
Mylan Teoranta Inverin, Ireland Director
Same function Same country
40%similar
Regeneron Ireland Limerick, Ireland
Same function Same country

Notify me about similar jobs

Get an email when we spot other openings like this one – same job function, comparable seniority, roles you'd actually want to see.

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How we calculate "similar"

No black box, no LLM guesswork: a deterministic score built from four normalized attributes. Here's this role's own peer group at different match levels, so you can see the mechanism, not just the result.

Every comparison starts from the same 100-point budget: 25 for working in the same function, 40 for the same therapeutic area, 20 for the same or adjacent seniority, 15 for the same country. A dimension we can't confirm on both sides contributes nothing, never a guess, never a free pass.

40%
Director, Combination Product Development
McDermott Laboratories Limited · Northern Cross, Ireland · Director
Function Therapeutic area Seniority Country
40%
Planning Master Data Analyst (12 month FTC)
McDermott Laboratories Limited · Northern Cross, Ireland · Seniority not listed
Function Therapeutic area Seniority Country
40%
Sr. Automation Engineer - Packaging
Amgen Technology (Ireland) UC · Dun Laoghaire, Ireland · Senior
Function Therapeutic area Seniority Country
40%
Warehouse Supervisor
AbbVie · Dublin, County Dublin · Seniority not listed
Function Therapeutic area Seniority Country
Unmatched or unknown dimensions score exactly the same: 0 points, never a partial guess. A role we know almost nothing about beyond its function bottoms out at 25%; it never inflates to 100% just because there's little to compare against. Seniority uses a defined ladder (Associate → Manager → Associate Director → Senior → Principal → Director → Senior Director → Executive/VP) so "Director" and "Senior Director" count as adjacent, but "Director" and "Executive/VP" do not.