Johnson & Johnson Posted October 9, 2026

Transcend Deployment Manager- MAKE Quality Management (QM)

Ringaskiddy, Ireland Full time
Quality Manager
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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:

Quality

Job Sub Function:

Digital Quality

Job Category:

Professional

All Job Posting Locations:

Latina, Italy, Leiden, Netherlands, Leiden, South Holland, Netherlands, Little Island, Cork, Ireland, Ringaskiddy, Cork, Ireland

Job Description:

About Innovative Medicine

Our expertise in Innovative Medicine is informed and inspired by patients, whose insights fuel our science-based advancements. Visionaries like you work on teams that save lives by developing the medicines of tomorrow. Join us in developing treatments, finding cures, and pioneering the path from lab to life while championing patients every step of the way. Learn more at https://www.jnj.com/innovative-medicine .

We are search for the best talent for Transcend Deployment Manager- MAKE Quality Managment (QM).

This hybrid role is located in Cork, Ireland. Alternate hybrid locations may be considered at other Innovative Medicine Supply Chain (IMSC) hubs location such as: Latina, Italy; Madrid, Spain; and Leiden, Netherlands. Other J&J Innovative Medicine manufacturing / principal locations may be considered for the ideal candidate.

Transcend is a global business transformation program that will modernize our foundational transactional processes and harmonize them into one “clean” ERP as a standardized platform for growth and efficiency gains.

The program will simplify the Innovative Medicine ERP landscape from 7 to 1, standardizing processes in order to have a cost effective, fit for purpose digital backbone that will enable us to support the Innovative Medicine business with agility. Additionally, the program will remediate the end-of-life system exposure that we risk towards the end of this decade.

The Transcend Deployment Manager - Quality Management provides advanced hands-on expertise supporting the global deployment of Quality Management capabilities within the Transcend SAP S/4HANA program.

From a Quality Management perspective, the role ensures full integration with NextGen QS to enable real-time control and disposition of non-conforming materials and batches across Source, Make, and Deliver.

The role is responsible for the end-to-end implementation of Quality processes supporting end-to-end release management, laboratory testing, manufacturing batch record review, and artwork (packaging material) key date management.

Global Batch Traceability is enabled through a single ERP backbone after full deployment, with the solution developed to support future integration of Global Batch Traceability (GBT) and Batch Record Hub (BRH).

The role also is responsible for the definition and deployment of batch determination rulesets, ensuring that only compliant and appropriate batches are used internally and released for shipment to customers across Make and Deliver.

Key Responsibilities:

Global Functional Ownership & Deployment

Implement and support the global deployment of SAP Quality Management capabilities integrated with NextGen QS, enabling real-time quality event handling and non-conformance management across Source, Make, and Deliver.

Ensure standard satellite system integrations enabling end-to-end release management, laboratory testing, manufacturing batch record review, and artwork (packaging material) key date governance.

Enable Global Batch Traceability through a single ERP backbone after full deployment and prepare the solution for future GBT and BRH integration.

Define and govern batch determination rulesets ensuring compliant batch usage for internal operations and customer shipment.

Leadership & Team Management

Act as senior functional authority supporting Quality Management functional SMEs and analysts, owning workload planning, prioritization, and delivery quality.

Provide functional leadership and coaching while remaining hands-on to ensure solution quality and regulatory compliance.

Act as the primary functional escalation point for QM-related topics within Transcend.

Solution Delivery, Testing & Hypercare

Support solution confirmation with Global Template Owners, Quality Assurance, and Regulatory collaborators.

Lead functional testing, validation support, and hypercare activities for QM capabilities in alignment with GxP and CSV expectations.

Ensure QM issues are resolved and lessons learned are incorporated into continuous improvement of the global template.

Cross-Functional Collaboration

Collaborate with Manufacturing, Supply Chain, Commercial Execution, IT, Validation, and Quality Assurance teams to ensure end-to-end quality integration.

Partner with system integrators and satellite system owners to ensure compliant, auditable, and sustainable integrations.

Qualifications:

Education

University degree or equivalent experience in Quality, Engineering, Life Sciences, or a related field.

Required

A minimum 6 years of proven experience.

Extensive experience in Quality Management processes within GxP-regulated manufacturing environments.

Strong functional expertise in SAP S/4HANA Quality Management (QM), including batch management, inspection processes, non-conformance handling, and release workflows.

Validated experience leading or supporting SAP implementations subject to Computer System Validation (CSV) and regulatory inspection.

Demonstrated people-management experience with accountability for functional delivery and quality outcomes.

Experience in Supply Chain (Plan, Source, Make, Deliver, Finance and/or Master Data as well as Data and Analytics).

Practical experience with ERP SAP Quality Management (QM) in J&J IM.

Experience in Business Processes related to ERP SAP Quality Management (i.e. Quality Inspection, Batch Release, Supplier Qualification, Process Validations etc.).

ERP SAP (ECC6 and/or S/4HANA) knowledge and practical application.

Experience with Comet, eLIMS or Manufacturing Execution System (MES) is an advantage.

Strong English verbal and written communication skills, including presentation skills.

Understanding the business process linkages in Supply Chain across Plan, Source, Make, Deliver, Finance, Master Data.

Practical experience in a pharmaceutical manufacturing/packaging environment.

Experience in Business Processes related to ERP SAP (ECC6 and/or S/4HANA) knowledge and practical application.

Preferred

Background in External / (Third Party / Contract Manufacturing) Quality, Market Quality, and/or Commercial Quality.

Experience in Master Data, Advanced Planning, Product Labelling, Materials Management, Serialization, Track & Trace or Process Order Management.

Experience working in a regional/global setting, or experience in a large-scale business transformation project.

Experience in Agile software as well as program deployment methodology including JIRA is an advantage.

Ability to negotiate and connect with both external and internal partners.

Experience in collaborating with business subject-matter experts.

Other

Ability to travel up to 50% of the time both domestically and internationally.

Required Skills:

Preferred Skills:

Coaching, Compliance Management, Controls Compliance, Digital Assurance, Human-Computer Relationships, Performance Measurement, Process Improvements, Process Optimization, Quality Control (QC), Quality Standards, Quality Validation, Regulatory Compliance, Researching, Stakeholder Engagement, Standard Operating Procedure (SOP), Subject Matter Experts (SME) Collaboration, Technical Credibility

The anticipated pay range for this position, in the primary posting location, is:

€70,100.00 - €121,210.00

The anticipated pay ranges for additional locations are:

Spain– The anticipated base pay range for this position is EUR61,800 – EUR106,260

Italy– The anticipated base pay range for this position is EUR56,100 – EUR96,945

Netherlands– The anticipated base pay range for this position is EUR68,600 – EUR119,600

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.

Additional information:

The NL: 8%.The annual base pay includes an 8% holiday allowance.

Job details

Seniority
Manager
Function
Quality
Therapeutic area
Not listed
Location
Ringaskiddy, Ireland
Employment type
Full time

How this role compares

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

We currently track 310 comparable Manager Quality roles across 81 biopharma companies.

310Comparable roles tracked
276Currently active
81Companies hiring similar roles
31Countries represented

Salary context

65 of 310 peers report a salary range (USD, annualized)

Peers share this role's job function and a matching or adjacent seniority level -- not necessarily the same therapeutic area or country.

This roleSubject Not listed on this posting
Lowest disclosed · Associate Quality Control Analyst (Virology) · Regeneron Pharmaceuticals, Inc (USA) $22/hr – $34/hr (≈ $45,302–$70,699/yr)
Peer group range $58,001 – $201,900 (median $163,000)

Where these roles are based

Top locations among the 310 comparable roles

United States150
China22
India17
Ireland16
Netherlands14
Germany14

+ 25 more countries

Seniority mix

310 of 310 peers have a known seniority level

Manager197
Associate73
Associate Director40

Therapeutic area mix

0 of 310 peers have a known therapeutic area; the rest are genuinely unlabeled, not hidden

No peers with a known therapeutic area yet.

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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.

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Function Therapeutic area Seniority Country
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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.