23 Jobs in Wicklow

By clicking the "Apply" button, I understand that my employment application process with Takeda will commence and that the information I provide in my application will be processed in line with Takeda's Privacy Notice and Terms of Use . I further attest that all information I submit in my employment application is true to the best of my knowledge.
**Job Description**
**Operational Excellence Lead**
As Operational Excellence Manager at Takeda's Bray site, you will play a key role in driving a culture of continuous improvement across our manufacturing operations. You will lead the site's Lean strategy and Agile Operating System (AOS) roadmap, coach cross-functional teams, and implement impactful process improvements. Working closely with Quality, Production, and Digital teams, you will help streamline operations, increase efficiency, and ensure sustainable performance improvements - all while upholding Takeda's high standards for safety, quality, and compliance.
**Responsibilities:**
+ Drive the site's Operational Excellence (OE) strategy and AOS (Agile Operating System) roadmap.
+ Lead Lean and Six Sigma (Green Belt level) initiatives to improve efficiency, quality, and cost performance.
+ Facilitate workshops (e.g. Kaizen events, value stream mapping, root cause analysis) to identify and implement improvement opportunities.
+ Coach and develop site teams in Lean methodologies, structured problem-solving, and continuous improvement practices.
+ Collaborate with cross-functional partners including Quality, Production, Engineering, and Digital (DD&T) to ensure alignment and integration of improvement initiatives.
+ Support digital transformation by identifying automation opportunities and data-driven process optimization.
+ Oversee the Six Sigma program, including mentoring Yellow/Green Belts and certifying Yellow Belt candidates.
+ Monitor and report performance metrics (KPIs), identify gaps, and lead corrective actions.
+ Apply Organizational Change Management (OCM) principles (e3+) to drive successful implementation of improvement projects.
+ Support strategic programs like Business Process of the Future and Factory of the Future.
+ Ensure all initiatives are aligned with safety, quality, and regulatory requirements.
**Skills & Qualifications:**
+ Bachelor's degree in a technical or scientific discipline; a master's degree (MBA or M.Sc.) is a plus.
+ 5-8 years of experience in manufacturing or operations with a focus on Lean, OE, or Continuous Improvement.
+ Lean/AOS and Six Sigma certification (Green Belt or higher); experience with Yellow Belt training/certification preferred.
+ Proven track record in leading cross-functional projects and delivering measurable improvements.
+ Strong project management, analytical, and problem-solving skills.
+ Experience in change management (ideally e3+) and coaching stakeholders at all levels.
+ Comfortable working in GMP-regulated environments; pharma experience is highly desirable.
+ Familiarity with tools such as SAP, MES, Minitab, and MS Office.
+ Excellent communication, collaboration, and leadership skills.
+ Fluent in English; strong interpersonal skills in a multicultural environment.
+ Willingness for occasional travel and active shopfloor presence.
**What you can look forward to with us:**
+ Competitive Salary: Including performance-based bonuses.
+ Retirement Plan: Employer contributions to your retirement plan.
+ Comprehensive Insurance: Employer-funded private medical insurance with dependants' cover, life insurance, and flexible options like dental insurance, partner life insurance, and serious illness protection.
+ Electric Charging Points: Available at parking locations.
+ Employee Assistance Program: Support for personal and professional challenges.
+ Wellbeing and Engagement: Dedicated teams to support your wellbeing.
+ Family-Friendly Policies: Supportive policies for a balanced work-life.
+ Generous Vacation: 26 vacation days plus additional days for service milestones and humanitarian volunteering leave.
+ Development Opportunities: Coaching, mentoring, educational programs, and formal training.
+ Subsidized Canteen: Enjoy meals at a reduced cost.
+ Flexible Benefits: Options like fuel card, bike to work, commuter ticket, and insurance deals.
**More about us:**
At Takeda, we are transforming patient care through the development of novel specialty pharmaceuticals and best in class patient support programs. Takeda is a patient-focused company that will inspire and empower you to grow through life-changing work.
Certified as a Global Top Employer, Takeda offers stimulating careers, encourages innovation, and strives for excellence in everything we do. We foster an inclusive, collaborative workplace, in which our teams are united by an unwavering commitment to deliver Better Health and a Brighter Future to people around the world.
**Empowering our people to shine:**
Takeda is proud in its commitment to creating a diverse workforce and providing equal employment opportunities to all employees and applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, gender expression, parental status, national origin, age, disability, citizenship status, genetic information or characteristics, marital status, or any other characteristic protected by law.
If you are interested in this opportunity, we look forward to receiving your application via our online tool!
**Locations**
Bray, Ireland
**Worker Type**
Employee
**Worker Sub-Type**
Regular
**Time Type**
Full time

By clicking the "Apply" button, I understand that my employment application process with Takeda will commence and that the information I provide in my application will be processed in line with Takeda's Privacy Notice and Terms of Use . I further attest that all information I submit in my employment application is true to the best of my knowledge.
**Job Description**
**Job Description**
**Manager Supply Chain, Planning and NPI**
As a Manager in Planning, Supply Chain, and NPI at Takeda's TIL Bray site, you will play a key role in ensuring the reliable and timely supply of pharmaceutical products to global markets. This position leads cross-functional teams and oversees critical supply chain, planning, and launch processes. It combines strategic thinking, operational execution, and close collaboration with internal and external stakeholders to support continuous improvement, product launches, and the achievement of performance targets.
**How You Will Contribute**
+ Lead and support Planning, Supply Chain, and Launch teams within Takeda's Supply Chain Department at the TIL Bray site.
+ Ensure global product supply in required quantities and timelines to meet customer demand across all markets.
+ Manage supply and demand planning processes, including replenishment planning, make-to-order strategies, and contract manufacturing (CMB) activities.
+ Maintain effective communication and alignment with Takeda LOCs, Oncology, external supply teams, suppliers, and internal departments.
+ Oversee production and QC planning, shift scheduling, scenario planning, and cost-related data for budgeting.
+ Drive the planning and execution of NPIs and sample orders while maintaining accurate SAP data.
+ Support continuous improvement initiatives across Planning & Supply Chain to enhance efficiency and implement best practices.
+ Monitor and report on supply chain KPIs (CSL, inventory, responsiveness, and launch excellence) and support cost-reduction initiatives.
+ Manage legal and operational processes related to stock holding, contracts, and license setups (e.g., TPIZ, TPIB).
+ Act as Supply Chain Director Designee when required.
+ Supervise the launch team and ensure timely introduction of new products and market transfers.
+ Collaborate closely with Manufacturing, Engineering, and Quality to ensure smooth launch processes.
+ Participate in audits, change controls, CAPAs, deviations, and ensure continuous inspection readiness.
+ Coordinate monthly reporting cycles (e.g., MRP, MYC, budgeting).
+ Represent TIL in cross-regional launch planning and communication, ensuring all deliverables are met.
**Skills & Qualifications**
+ Bachelor's degree in Supply Chain, Business Administration, Operations, Logistics, or a related field.
+ Minimum 5 years of relevant experience in the pharmaceutical industry, ideally including digital transformation and process innovation.
+ Strong knowledge of end-to-end supply chain processes and GMP/GxP compliance.
+ Technical expertise in supply planning and solid oral dosage manufacturing; SAP experience preferred.
+ Excellent coordination, analytical, and organizational skills with strong attention to detail.
+ Proven ability to manage cross-functional teams and influence internal and external stakeholders.
+ Strategic thinker with solid problem-solving and decision-making abilities.
+ Strong communication and interpersonal skills; confident working across global teams.
+ Experience managing KPIs, budgets, and performance targets.
+ Demonstrated leadership skills with a focus on collaboration, inclusivity, and team development.
+ Committed to continuous improvement, innovation, and maintaining a high-performance culture.
+ Willingness to engage with external industry forums to stay current with best practices.
**What you can look forward to with us:**
+ Competitive Salary: Including performance-based bonuses.
+ Retirement Plan: Employer contributions to your retirement plan.
+ Comprehensive Insurance: Employer-funded private medical insurance with dependants' cover, life insurance, and flexible options like dental insurance, partner life insurance, and serious illness protection.
+ Electric Charging Points: Available at parking locations.
+ Employee Assistance Program: Support for personal and professional challenges.
+ Wellbeing and Engagement: Dedicated teams to support your wellbeing.
+ Family-Friendly Policies: Supportive policies for a balanced work-life.
+ Generous Vacation: 26 vacation days plus additional days for service milestones and humanitarian volunteering leave.
+ Development Opportunities: Coaching, mentoring, educational programs, and formal training.
+ Subsidized Canteen: Enjoy meals at a reduced cost.
+ Flexible Benefits: Options like fuel card, bike to work, commuter ticket, and insurance deals.
**More about us:**
At Takeda, we are transforming patient care through the development of novel specialty pharmaceuticals and best in class patient support programs. Takeda is a patient-focused company that will inspire and empower you to grow through life-changing work.
Certified as a Global Top Employer, Takeda offers stimulating careers, encourages innovation, and strives for excellence in everything we do. We foster an inclusive, collaborative workplace, in which our teams are united by an unwavering commitment to deliver Better Health and a Brighter Future to people around the world.
**Empowering our people to shine:**
Takeda is proud in its commitment to creating a diverse workforce and providing equal employment opportunities to all employees and applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, gender expression, parental status, national origin, age, disability, citizenship status, genetic information or characteristics, marital status, or any other characteristic protected by law.
If you are interested in this opportunity, we look forward to receiving your application via our online tool!
**Locations**
Bray, Ireland
**Worker Type**
Employee
**Worker Sub-Type**
Regular
**Time Type**
Full time

By clicking the "Apply" button, I understand that my employment application process with Takeda will commence and that the information I provide in my application will be processed in line with Takeda's Privacy Notice and Terms of Use . I further attest that all information I submit in my employment application is true to the best of my knowledge.
**Job Description**
**About the Role:**
**A 9-month fixed-term offering candidates a chance to grow their Lean and Agile skills, lead impactful projects, and boost their career development.**
As an Operational Excellence Champion, you will play a key role in deploying Takeda's eAGILE Operating System (AOS) at site level. You will work closely with cross-functional teams to identify, support, and drive value creation initiatives aligned with site strategy. In this role, you'll actively support digital transformation, Lean thinking, and continuous improvement to help build a future-ready operation.
**Key Responsibilities:**
**eAGILE AOS Deployment & Value Creation:**
+ Establish a common understanding of the eAGILE Operating System (AOS) across the site.
+ Collaborate with workstream leads and owners to assess key programs for deployment and local relevance.
+ Support the Senior Operational Excellence Champion in the implementation of AOS elements at site level.
+ Participate in the site strategy deployment process and help translate strategy into a clear value creation roadmap.
+ Evaluate all project proposals for value creation potential, ensuring KPIs (baseline, plan, and actuals) are aligned with local finance.
+ Drive delivery of the value creation roadmap by managing the overall project portfolio and leading selected value creation projects.
+ Apply change management tools from the e3+ framework to support transformation efforts.
+ Ensure all value creation projects are tracked in the SPOT system and report on performance monthly.
+ Continuously build own capabilities in Operational Excellence through structured curricula.
**Digital, Data & Technology (DD&T):**
+ Act as an advocate for digital and automation adoption throughout the value stream as part of the site's DD&T community.
**Factory of the Future (FofF / FnoF):**
+ Develop expertise in Lean Value Stream Mapping and Business Process Management to support transformation initiatives.
+ Participate in Factory of the Future programs, including roadmap development, design sprints, project evaluation, prioritization, and execution.
**Collaboration & Continuous Learning:**
+ Work closely with local finance to develop financial acumen and validate value creation targets, forecasts, and results.
+ Partner with OE and OCM coaches, site-level influencers, and above-site stakeholders to ensure alignment and impact.
+ Collaborate with Site Business Excellence (BE) colleagues to co-develop the eAGILE AOS roadmap.
+ Serve as a "new pair of eyes" by offering and receiving constructive feedback.
+ Occasionally visit other sites to share, learn, and replicate best practices.
+ Support and mentor other Operational Excellence Champions and Yellow Belts.
+ Actively share best practises through eAGILE sharing tools and Community of Practice (CoP)
**Dimensions and Aspects**
**Technical / Functional Expertise**
+ Strong understanding of bio-pharmaceutical operations.
+ Logical, structured thinker with sound problem-solving and analytical skills.
+ Skilled in project/program management and implementation.
**Leadership**
+ Strong communicator able to influence and guide others through change.
+ Supports others through the change management process.
+ Aligns activities with vision, strategy, and business objectives.
**Decision-Making and Autonomy**
+ Contributes to key decision-making related to eAGILE deployment; final decisions rest with Business Excellence.
+ Develops decision-making capabilities and business acumen during the assignment.
+ Responsible for developing structured problem-solving skills.
**Interaction**
+ Engages with stakeholders at all organizational levels.
+ Builds effective relationships across Takeda's global network and eAGILE ecosystem.
+ Acts as a collaborative partner and integrator across functions and workstreams.
**Innovation**
+ Demonstrates an inquisitive mindset and passion for innovation.
+ Connects workstream activities to enhance the overall impact of eAGILE.
+ Openly shares knowledge and learns from others.
+ Embraces digital technology and seeks continuous improvement.
**Complexity**
+ Comfortable operating in a global, culturally diverse, and matrixed environment.
+ Adaptable and effective in complex and changing business contexts.
+ English language proficiency (or willingness to develop proficiency) required.
**Skills & qualifications required:**
+ Third-level degree in a Scientific or Engineering discipline.
+ Demonstrated passion for challenging the status quo and improving business outcomes.
+ Courage of conviction and openness to constructive feedback.
+ Recognized for strong and consistent performance with a high learning agility.
+ Natural leadership ability with a talent for networking and collaboration.
+ Proven project management, facilitation, and organizational skills.
+ Strong active listening and interpersonal communication abilities.
**What you can look forward to with us:**
+ Competitive Salary: Including performance-based bonuses.
+ Retirement Plan: Employer contributions to your retirement plan.
+ Comprehensive Insurance: Employer-funded private medical insurance with dependants' cover, life insurance, and flexible options like dental insurance, partner life insurance, and serious illness protection.
+ Electric Charging Points: Available at parking locations.
+ Employee Assistance Program: Support for personal and professional challenges.
+ Wellbeing and Engagement: Dedicated teams to support your wellbeing.
+ Family-Friendly Policies: Supportive policies for a balanced work-life.
+ Generous Vacation: 26 vacation days plus additional days for service milestones and humanitarian volunteering leave.
+ Development Opportunities: Coaching, mentoring, educational programs, and formal training.
+ Subsidized Canteen: Enjoy meals at a reduced cost.
+ Flexible Benefits: Options like fuel card, bike to work, commuter ticket, and insurance deals.
**More about us:**
At Takeda, we are transforming patient care through the development of novel specialty pharmaceuticals and best in class patient support programs. Takeda is a patient-focused company that will inspire and empower you to grow through life-changing work.
Certified as a Global Top Employer, Takeda offers stimulating careers, encourages innovation, and strives for excellence in everything we do. We foster an inclusive, collaborative workplace, in which our teams are united by an unwavering commitment to deliver Better Health and a Brighter Future to people around the world.
**Empowering our people to shine:**
Takeda is proud in its commitment to creating a diverse workforce and providing equal employment opportunities to all employees and applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, gender expression, parental status, national origin, age, disability, citizenship status, genetic information or characteristics, marital status, or any other characteristic protected by law.
If you are interested in this opportunity, we look forward to receiving your application via our online tool!
**Locations**
Grange Castle, IrelandBray, Ireland
**Worker Type**
Employee
**Worker Sub-Type**
Fixed Term (Fixed Term)
**Time Type**
Full time

By clicking the "Apply" button, I understand that my employment application process with Takeda will commence and that the information I provide in my application will be processed in line with Takeda's Privacy Notice and Terms of Use . I further attest that all information I submit in my employment application is true to the best of my knowledge.
**Job Description**
Are you looking for a patient-oriented, innovation-driven company that inspires you and promotes your career? Then take your future in your hands and become part of Takeda as a
**Quality Control Laboratory Apprentice**
This role offer unique opportunity to gain hands-on experience and comprehensive training in Quality Control (QC) practices within a cutting-edge pharmaceutical environment. Joining the team allows the applicant to develop crucial technical and soft skills while contributing to Takeda's commitment to innovation, quality, and patient-centric values. This apprenticeship fosters professional growth, teamwork, and meaningful work that impacts global healthcare.
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**You will be trained to possess the following skills:**
+ Demonstrating the ability to operate equipment and instruments effectively and according to standard operating procedures (SOPs).
+ Showing the ability to work effectively in a safe manner within the laboratory.
+ Communicating the theoretical knowledge of relevant sciences and technology.
+ Handling materials and equipment correctly paying due regard to safety and environmental protection regulations.
+ Capability to perform basic chemistry techniques to include but not limited to the use of: Pipettes, Auto-Titrators, pH, Weighing, Diluting to Volume, Volumetric Calculations, Karl Fischer, Thin Layer Chromatography, and Physical Testing.
+ Ability to identify and note equipment (foe sampling, testing and control) malfunction if it occurs, and informing the QC Team Leader.
**You will acquire the following knowledge:**
+ Understanding science fundamentals, basic chemistry, microbiology, and production processes (upstream/downstream).
+ Knowledge of cGMP, quality systems, GLP/GMP deficiencies, and data integrity principles.
+ Safe lab operations, housekeeping, proper labelling, calibration, and equipment use.
+ Handling, logging, and testing of samples e.g., water, raw materials, in-process, finished products.
+ Familiarity with pharmacopoeias and investigation processes e.g., OOS.
+ Awareness of QC purchase systems, supplier coordination, and proper reporting protocols.
**You will strengthen the following soft skills:**
+ Effective communication and team work.
+ Good technical writing skills.
+ Working independently and taking responsibility for initiating and completing tasks.
+ Understanding impact of work on others, especially where related to diversity and equality.
+ Time management and ability to complete work to schedule.
+ Ability to handle change and respond to change management processes.
**How you will contribute:**
+ Ensure that Accident Reports / Near Miss Forms are completed in a timely manner after an event.
+ Participate fully in any cross functional training initiatives.
+ Drive and promote the corporate values of Takeda-ism within the workplace.
+ Ensure timely completion of all SOP, reading, training and assessment.
+ Other duties as required and directed.
In this position you will report to the QC Team Leader.
**What you bring to Takeda:**
+ For entry into year 1 of Level 6 Quality Control Apprenticeship Programme you must have passed (Grade O6 or better) in five Leaving Certificate subjects, one of which must be math and one science related subject and gathered 250 CAO points **OR** you can also enter the Programme, if you have graduated relevant FETAC Level 5 or Level 6 and are a current employee with relevant experience and qualifications.
+ Before enrolment on the apprenticeship programme the apprentice must have SOLAS apprentice approval.
+ Health, Safety and Environmental awareness.
+ Ability to share knowledge and expertise with others.
+ Engage in teamwork.
+ Complete integrity and compliance programs.
+ Ability to work independently.
+ Problem solving & critical thinking.
+ Microsoft Office skills in MS Excel and MS Word.
+ Mathematics and statistics knowledge.
+ Proven continuous professional development.
**What Takeda can offer you:**
+ Flexible working arrangements, e.g., hybrid or shiftwork with shift allowance
+ 26 vacation days plus additional days for service milestones
+ Employee Assistance Program
+ Wellbeing and engagement teams
+ Development opportunities
+ Educational programs and formal training
+ Coaching and mentoring
+ Humanitarian volunteering leave options
+ Subsidized canteen
+ Electric charging points available at parking locations
**More about us:**
Takeda is focused on creating better health for people and a brighter future for the world. We aim to discover and deliver life-transforming treatments in our core therapeutic and business areas, including gastrointestinal and inflammation, rare diseases, plasma-derived therapies, oncology, neuroscience, and vaccines.
Takeda Ireland was established in 1997. Our story in Ireland is one of substantial growth, rapid change, and innovation. Over the past two years, Takeda Ireland has invested over 55 million in Ireland to develop our manufacturing sites. Solidifying our commitment in our people and contributing to the local economy. Takeda in Ireland has commercial operations, corporate services, and manufacturing facilities across four locations: Baggot St, Bray, Citywest, and Grange Castle. We have been certified as Top Employer for several consecutive years.
**How we will support you:**
Takeda is proud of its commitment to create a diverse workforce and to provide equal employment opportunities to all employees and applicants for employment without regard to ethnicity, color, religion, sex, sexual orientation, gender identity, gender expression, parental status, national origin, age, disability, citizenship status, genetic information or characteristics, marital status or any other characteristic protected by law. If you are living with disabilities, chronic illness, or neurodiversity, please feel free to let us know so that we can provide you with appropriate support during the application process.
**Locations**
Bray, Ireland
**Worker Type**
Employee
**Worker Sub-Type**
Apprentice / Trainee (Fixed Term) (Trainee)
**Time Type**
Full time

Our client, a rapidly expanding manufacturer of precision plastic components for the global MedTech sector, is seeking a Project Engineer to join their dynamic and high-performing team in Co. Wicklow. This is an exciting opportunity for an early-career engineer to gain broad project exposure within a regulated manufacturing environment, supporting both customer and internal engineering initiatives.

The successful candidate will play a key role in project coordination, schedule management, and technical documentation, while developing their skills alongside experienced engineers. This role suits someone with strong organisational abilities, a proactive mindset, and a keen interest in medical device manufacturing and process development.

Responsibilities Include but Are Not Limited to the Following:

• Support the engineering team with documentation, data analysis, technical reports, and validation protocols.

• Assist in preparing quotations and coordinating tasks across Quality, Operations, and Engineering functions.

• Help develop and maintain project schedules; monitor progress, update reports, and escalate risks where needed.

• Attend internal and customer-facing project meetings, taking minutes and tracking follow-up actions.

• Liaise with subcontractors and customers to ensure alignment on project deliverables and timelines.

• Contribute to the smooth handover of projects from development to production.

• Degree in Mechanical, Manufacturing, Process, or Biomedical Engineering.

• 1–2 years of experience in an engineering or manufacturing setting (internships or co-op experience considered).

• Exposure to project management tools such as MS Project or Gantt charts is desirable.

• Familiarity with regulated environments (medical device experience a plus).

• Strong communication and documentation skills with proficiency in Microsoft Office.

• Experience with SolidWorks or Minitab is an advantage.

• Understanding of Good Documentation Practices (GDP) is desirable.

Note: By applying for this position, you may also be considered by Pale Blue Dot® Recruitment for other relevant STEM roles.

Pale Blue Dot® Recruitment – The Experts in STEM Workforce Solutions

RecruitNet International Ltd specialises in Healthcare recruitment for Domestic and Overseas candidates for Hospitals, Nursing Homes, Home care and Community care.We are hiring a Clinical Nurse Manager  to lead a nursing home in Wicklow, Ireland. Responsibilities Ensure that the provision of a high standard of care to the residents and families in Name of Unit is consistent with the mission, vision, values, and strategic plan of the Nursing HomeDevelop relationships with residents, which facilitates resident autonomy, informed choice, and evidence-based decision-makingPromote and maintain resident safety and provide quality care by respecting the privacy, dignity, and rights of the residentAssist residents in maintaining their sense of identity and include them in decision-making whenever possibleEnsure the Nursing Home is operated in a manner that respects the age, gender, sexual orientation, disability, family status, civil status, race, religious beliefs and ethnic & cultural background of each residentPlan, assess and deliver resident care that maximises the resident’s capacity to exercise personal autonomy and choice, together with all members of the Multidisciplinary Care TeamRequirementsEligible to register or currently registered with the Nursing and Midwifery Board of Ireland (NMBI). Two to three years of minimum appropriate post-registration experience. Post-registration training in dementia care and/or gerontology is very desirable. Leadership, communication, organizational, and clinical expertise that may be demonstrated. Needed to be qualified to work in Ireland.BenefitsOngoing education and training programmesFlexible working hoursPaid breaksNight PremiumPremiums paid on Sundays and Public HolidaysComplementary meals provided on long day shiftsReferral bonusDiscounted uniformsCycle to work scheme with a repayment planFree Car ParkingPension SchemeDeath in Service benefitsPharmacy DiscountCommitted to providing and maintaining the highest standard of serviceModern custom built facilitatesRelocation Bonus available

RecruitNet International Ltd specialises in Healthcare recruitment for Domestic and Overseas candidates for Hospitals, Nursing Homes, Home care and Community care.We are hiring a Clinical Nurse Manager for a leading Nursing Home in Wicklow , Ireland.Responsibilities Make sure every employee does their utmost to support the nursing home's effective operation and the development of an environment that serves the interests of the residents. Engage with residents to make sure their medical needs are being satisfied and, if necessary, to address any issues. Discuss the residents' medical requirements with the district nurse. Report any resident illness and, if required, request a visit from a general practitioner or other professional. Make sure the resident's nutritional needs are satisfied and that there are enough healthy meals. Perform personal care and general nursing duties as needed. As directed by the NMBI and the company, administer prescribed medications and keep the required documentation.RequirementsRegistered on the NMBI live register.At least two years of experience in management or supervisionVerification of approval from the Garda Vetting UnitExcellent Leadership, Organizational and Communication skillsMinimum 2 years work experience in a Nursing Home environmentAbility to motivate self and others and work on own initiativeAbility to work well and promote a team environmentBenefitsCompetitive salaryBike to work schemeEmployee assistance programOn-site parkingBonus incentive schemeExcellent opportunity for career progressionLearning and Development OpportunitiesEmployee Assistance & Wellbeing ProgramCompany pension scheme

RecruitNet International Ltd specialises in Healthcare recruitment for Domestic and Overseas candidates for Hospitals, Nursing Homes, Home care and Community care.We are Hiring an Assistant Director Of Nursing for a leading Nursing home in Wicklow, Ireland.     Responsibilities To be a highly competent, knowledgeable practitioner in the care of the elderly.To participate in the Management Team actively. Maintain a high standard of professional and ethical conduct.To manage the development of the overall service plan and review the service against the plans.To assist with the direction and supervision of the nursing service to provide a high level of resident care and management.To provide innovative and effective leadership, support, and advice to nursing and allied staff at all levels.To guide all staff in the implementation of Centre policiesEnsure nursing staff adheres to standards and guidelines relating to professional nursing practice and behaviorThe involvement in discussions on the provision of services, e.g. catering, cleaning, and laundry services.To undertake other relevant duties as may be determined from time to time by the Director of NursingRequirementsIn the last six years, a qualified nurse with at least three years of management experience has provided care for elderly patientsA post-registration management degree in medicine or a similar field Demonstrated success in clinical management in healthcareSuperb organizational, communication, and leadership abilitiesAbility to make sound decisions and results-drivenCapacity to collaborate effectively and foster a team atmosphereA readiness to adjust and be adaptable to the demands of the businessBenefitsCompetitive Hourly Rates. Employee Assistance & Well-Being Programmes.Full and Part-Time Guaranteed Contracts.Free Parking.Uniform provided.Additional site-specific benefits.Company eventsOn-site parking

A rapidly expanding medical device manufacturer is seeking a Project Engineer II / Senior Project Engineer to join its high-performing team in Wicklow. This is a key engineering role focused on supporting new and existing manufacturing projects in a fast-paced, regulated environment.

The successful candidate will have strong project management skills, excellent communication abilities, and a proven track record within medical device manufacturing. This is an exciting opportunity to contribute to innovative product development and process improvement initiatives, with a focus on plastics and injection moulding.

Responsibilities include but are not limited to:

• Lead and support technical projects from concept through to validation and implementation on the manufacturing floor.

• Collaborate with cross-functional teams including Engineering, Quality, and Operations to execute project plans.

• Manage timelines, resources, and documentation to ensure projects are delivered on time and within scope.

• Interface with customers and external suppliers to ensure alignment with project requirements and manufacturing standards.

• Support process validation activities (IQ/OQ/PQ) in line with regulatory and quality expectations.

• Drive continuous improvement and problem-solving initiatives across processes and systems.

• Provide technical input on equipment selection, tooling design, and manufacturing methods.

• Ensure all project documentation, reports, and protocols meet internal and external standards.

• Degree in Engineering – Mechanical, Manufacturing, Process, or Biomedical preferred.

• Minimum of 4–5 years’ experience in a regulated medical device manufacturing environment (MNC or contract manufacturing).

• Demonstrated experience managing engineering or process development projects.

• Strong written and verbal communication skills — able to clearly present ideas, timelines, and technical information.

• Experience in injection moulding, tooling, and plastics manufacturing techniques.

• Solid knowledge of process validation practices and quality system requirements.

• Proficiency with Microsoft Office, including MS Project; knowledge of Minitab or equivalent is an advantage.

• Familiarity with CE Marking, GDP, and Lean/6 Sigma methodologies is desirable.

Immediate interviews available for suitable candidates

Note: By applying for this position, you may also be considered by Pale Blue Dot® Recruitment for other relevant STEM roles.

Pale Blue Dot® Recruitment – The Experts in STEM Workforce Solutions