27 Jobs in Wicklow

**Job Title:** Hospital Key Account Manager - Rheumatology
**Location:** Munster & Leinster, Republic of Ireland
**Position Type:** Field-based
An experienced Secondary Care Specialist is sought to join an established pharmaceutical sales team in the field of rheumatology. This strategic and promotional role focuses on driving product differentiation and uptake across key hospitals and clinical centres in Munster and Leinster.
The role involves leading product promotion to secondary care healthcare professionals, delivering professional presentations, and providing specialist medical education. The successful candidate will ensure that relevant decision-makers understand the clinical benefits of the products to support formulary access and funding.
A key aspect of the role is engaging and developing regional and national opinion leaders to build clinical experience and support therapy area education and access. The candidate will proactively communicate with customers through compliant channels including face-to-face visits, virtual meetings, phone calls, and emails. They will also collaborate with internal stakeholders to implement creative customer engagement initiatives aligned with business plans and strategic investments.
This position requires a high level of collaboration with the national sales and marketing teams and embraces the core values of the organization to contribute to a positive and impactful culture.
This is a great opportunity for an experienced Secondary Care Specialist, apply now!
Please note:
+ Sponsorship is not available for this opportunity.
+ Candidates attend interviews at their own cost. Unfortunately, expenses incurred to attend an interview are not covered by IQVIA.
#LI-DNI
#LI-CES
#LI-LK1
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide.
To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere. Thank you for your interest in growing your career with us.
EEO Minorities/Females/Protected Veterans/Disabled

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**
**Facilities and Utilities Engineering Lead**
**About the Role:**
The Facilities & Utilities Engineering Lead is responsible for the organization and leadership of the site engineering team, ensuring the availability, operation, optimization, and lifecycle management of facility and utility systems. The role includes oversight of the IFM provider, support of global sustainability objectives, and close collaboration with internal and external stakeholders. It combines leadership, technical expertise, and compliance responsibility to maintain high standards of safety, quality, and efficiency.
**Key Responsibilities:**
+ Lead, develop, and mentor the Facilities/Utilities Engineering team to high performance
+ Ensure reliable operation, optimization, and maintenance of facility and utility systems, including management of the IFM provider and external vendors
+ Conduct Root Cause Analyses of major failures, manage deviations/CAPAs, and implement corrective and preventive actions
+ Define and manage budgets, preventive maintenance plans, optimized maintenance strategies, spare parts lists, and bills of materials
+ Lead equipment lifecycle evaluations, forecast replacement needs, and ensure reliability, maintainability, and accessibility in new or modified designs
+ Represent the site in the global Carbon Community of Practice (CAPS) and support sustainability programs on carbon, energy, water, and waste reduction
+ Drive compliance with cGxP, GMP, and all local/global safety and quality standards
+ Act as consultant for Facility/Utility systems in investment projects and CAPEX initiatives
+ Collaborate with cross-functional teams (Engineering, Quality, Production, EHS, Vendors, Automation) to ensure alignment and effective execution
+ Support regulatory inspections, audits, and corporate reviews through active engagement with authorities and internal stakeholders
**What You Bring to Takeda:**
+ Degree in Engineering or equivalent (desired but not required) 7+ years of relevant experience, including 3+ years in a leadership role; trade background a Bonus
+ Proven expertise in facility and utility systems within pharmaceutical manufacturing, preferably oral solid dose plants
+ Strong knowledge of cGxP and GMP requirements, with experience in audits and regulatory inspections (FDA or equivalent)
+ Demonstrated leadership, project management, and organizational skills with strong communication, influencing, and negotiation ability
+ Advanced problem-solving, decision-making, and troubleshooting skills with experience analyzing complex technical issues
+ Proficiency in process improvement and reliability engineering methods (PDCA, LEAN, Six Sigma/DMAIC, FMEA)
+ Experience defining maintenance strategies, lifecycle assessments, and reliability-focused design requirements
+ Ability to manage budgets, prioritize under tight timelines, and deliver sustainable solutions
+ Strong interpersonal skills, natural team player, and proven ability to mentor and motivate technical teams
+ Track record of collaboration across departments and international stakeholders, embracing teamwork and continuous optimization
**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**
**Supply Chain Executive, Production Planner ( FTC 11 Months)**
As a Production Planner at Takeda's Bray site, you will be responsible for developing, coordinating, and maintaining robust production and packaging schedules that ensure the timely and efficient delivery of products to global markets. You will work cross-functionally with manufacturing, quality, supply chain, and technical teams to manage planning activities, support new product introductions (NPIs), and ensure resource alignment with strategic business objectives. This role requires strong analytical thinking, planning expertise, and the ability to manage competing priorities in a fast-paced environment.
**Responsibilities:**
+ Create monthly production plans based on fixed order data
+ Collaborate with technical departments to incorporate project, upgrade, or NPI impacts into schedules
+ Generate production shift plans for budget (MRP) and mid-year commitment (MYC); perform capacity analysis
+ Prepare business scenario plans for future opportunities or NPI rollouts
+ Ensure accurate product costing data is provided
+ Coordinate Material Review Board activities
+ Meet monthly reporting deadlines with internal stakeholders
+ Manage and maintain planning modules in SAP
+ Track and secure progress of NPIs and sample orders
+ Lead continuous improvement projects in the Planning & Supply Chain Department
+ Align closely with materials planners to ensure component availability
+ Manage packaging schedules to meet product launch timelines
+ Represent the planning function in key meetings (e.g. with SLT, Packaging)
+ Monitor and report on planning-related KPIs
+ Communicate with internal and external stakeholders (e.g., external supply, internal Takeda sites, GD&L)
**Skills & Qualifications:**
+ Bachelor's degree in Supply Chain, Business Administration, Logistics, or a related field
+ Minimum 5 years' relevant experience in pharmaceutical planning or supply chain roles
+ Strong knowledge of E2E supply chain processes and digital planning tools (SAP preferred)
+ Analytical mindset with the ability to interpret complex data and develop actionable plans
+ Strong decision-making and stakeholder management capabilities across local and regional levels
+ Effective communicator, confident in influencing cross-functional teams and managing diverse opinions
+ Experienced in supporting digital transformation and innovation within planning processes
+ Familiarity with GMP/GxP and pharmaceutical regulatory requirements
+ Strong organizational, prioritization, and time management skills
+ Comfortable working in a fast-paced, cross-functional environment
+ Committed to continuous improvement, collaboration, and driving results
This role plays a critical part in supporting Takeda's mission to ensure uninterrupted product supply and successful product launches while fostering a culture of operational excellence and innovation.
**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**
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**
**Manufacturing Packaging Manager**
**About the Role:**
The Manufacturing Packaging Manager ensures efficient packaging of finished goods, solving complex challenges, analyzing data, and collaborating with senior professionals. The role includes leading projects, representing the company values, liaising with senior stakeholders, and mentoring staff.
**Responsibilities**
+ Manage the packaging process to ensure efficiency and quality
+ Oversee the assembly of finished components or parts into finished products
+ Implement and monitor Good Manufacturing Practices (GMP) within the packaging department
+ Lead and mentor team members
+ Analyze and solve complex problems related to packaging and production
+ Ensure compliance with sanitation practices and quality control principles
+ Leading projects, representing the company values, liaising with senior stakeholders and mentoring staff
***
**What You Bring to Takeda:**
+ Degree in Life Sciences field
+ PMP or PRINCE2 certification preferred
+ 5+ years experience in Lead PM roles within the pharmaceutical industry.
+ Proficiency in project management processes and procedures.
+ Understanding of GMP procedures and practices.
+ Strong competency in organizing and managing complex project activities.
+ Excellent communication skills
+ Ability to work under pressure & managing conflicting tasks at the same time.
+ Problem Solving mindset with attention to detail.
+ Comfortable working in a fast-paced, dynamic environment.
+ Strong Knowledge of API processes preferred
**What you can look forward to with us:**
+ 3rd Level Degree (Bachelor's or higher), preferably in Science or Engineering
+ Minimum 5 years of managerial experience in pharmaceutical solid oral dosage production
+ Fully proficient in Good Manufacturing Practices (GMP), able to handle highly complex situations and mentor others
+ Basic understanding of sanitation and hygiene practices, able to perform routine tasks under supervision
+ Developing practical skills in arithmetic, able to perform basic calculations with ongoing coaching
+ Initial troubleshooting experience, understands key concepts and begins to solve simple problems with guidance
+ Excellent attention to detail, able to manage complex tasks independently and advise others on precision
+ Participates in team activities with basic understanding of team dynamics, requires continued guidance and support
+ Applies basic quality control principles in routine situations with some coaching, understands key terminology
+ Building practical experience in production scheduling, applying basic principles under close supervision
+ Basic knowledge of automation technologies, applying them in simple situations under guidance
+ Basic understanding of production equipment, able to perform simple tasks with guidance, requiring ongoing support
**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**
**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**
**People First** - At Takeda we are dedicated to improving the health and well-being of all people and bringing them the hope of a brighter future. It is our passion that transforms every job into meaningful action. Our people are the heart of Takeda.
For Takeda Ireland Ltd, we are looking for a
**Automation Engineer**
for a full-time permanent position at our location in Bray, Co. Wicklow, Ireland.
Are you passionate about cutting-edge technology and innovation? Join our team as an Automation Engineer, where you will be a Subject Matter Expert (SME) in Manufacturing Control Systems, Operational Technology, Machine Automation, and Digitalization. You will play a crucial role in ensuring the optimal performance of our automation systems and driving digital transformation projects.
**Your tasks in detail:**
+ Oversee automation systems to ensure maximum uptime and performance.
+ Manage system user access, backups, and restores.
+ Implement corrective actions and collaborate with vendor technical support.
+ Identify and execute small projects to enhance system performance.
+ Contribute to capital planning, project execution, and documentation.
+ Ensure all activities comply with site and corporate Quality Systems.
+ Create and maintain engineering deliverables and test scripts.
+ Develop and implement global automation strategies to standardize processes.
+ Maintain and optimize automation systems and infrastructure.
+ Develop solutions tailored to the manufacturing environment.
+ Drive automation projects, ensuring cost, schedule, and technical goals are met.
+ Stay updated with technology trends and benchmarks to keep Takeda at the forefront.
**Your profile:**
+ Degree in engineering (automation, robotics, computer science, etc.) or equivalent.
+ Minimum 5 years of work experience in GMP manufacturing, with expertise in automation. A broad understanding of pharmaceutical manufacturing processes and regulatory environments is essential. Experience in the pharmaceutical industry is advantageous.
+ Proficiency in automation solutions (Siemens, Omron, Mitsubishi, etc.). Knowledge of industry standards (GAMP, ANSI/ISA, 21 CFR Part 11, Annex 11) and GxP/QA. Familiarity with ANSI/ISA-99,100 standards is a plus.
+ Strong problem-solving and analytical skills, with experience in data analysis.
+ Ability to work in a team-based culture, engaging with internal and external stakeholders. Collaborate with Global Automation to implement best practices.
+ Contribute to the innovation roadmap and strategic planning. Mentor and train team members to enhance site expertise.
+ High communication skills, an analytical mindset, and the ability to work under pressure.
+ Fluent in written and spoken English
**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

Engineer Surveyor - Dublin
**Company**
HSB
**Location**
Wicklow
, Ireland
**Job title:** Engineer Surveyor
**Location:** Wicklow
**Salary:** 56,000
Are you ready to make a real impact with a company that leads in engineering inspection and insurance services? At HSB, we're on a mission to help businesses large and small stay safe, compliant, and operating at their best-and we're looking for exceptional Engineers to join us.
**What You'll Be Doing**
As an Engineer Surveyor at HSB, you'll play a key role in delivering expert inspections and advice that keep our customers' assets safe and compliant. From lifting equipment to minor pressure systems, you'll ensure everything meets legal and safety standards, giving our clients peace of mind-and helping them thrive.
You won't just be ticking boxes. You'll be empowered to use your technical know-how, professional judgement, and customer-first mindset to deliver the highest level of service. Your work will help build trust, loyalty, and long-lasting relationships with customers across.
**What Makes This Role Special**
+ Meaningful impact: Your work directly protects people, assets, and businesses.
+ Customer connection: Build strong relationships and become a trusted partner to clients.
+ Continuous growth: Access to first-class training and career development opportunities.
+ Trusted brand: Be part of a company known for technical excellence, integrity, and innovation. Part of the wider Munich Re Group.
**What You Bring**
+ Strong communication skills and a genuine drive to deliver outstanding service
+ A proactive, professional approach with high attention to detail
+ A flexible mindset and commitment to working safely and effectively across varied environments
**Why Join HSB?**
We don't just inspect-we protect. At HSB, you'll join a team with a clear purpose, strong values, and a supportive culture where your expertise is respected and your contributions matter. From flexible working to wellbeing support, we invest in you so you can bring your best self to work-every day.
Apply today and become part of a company that doesn't just engineer safety-but inspires trust.
**Typical examination may include, but is not limited to the following:**
+ Lifting equipment defined in LOLER 1998
+ Pressure system equipment defined in PSSR 2000
+ Other work equipment defined with PUWER 98 & subject to the contractual requirements of our client companies.
Our work locations vary greatly and can include but are not limited to.
+ Garage Equipment
+ Construction/plant equipment
+ Personnel Hoists and Tracks in domestic and other environments
+ Playground Equipment
+ Minor Pressure systems
Key Competencies:
+ Understanding clients needs
+ Self-starter
+ Flexible approach to delivering Great Service
+ Managing client relationships
+ Accepting change and taking initiative
+ Prioritising and bringing about decisions
+ Achieving Team targets
**Key Responsibilities:**
As an Engineer Surveyor, there is no fixed place of work, and you are required to attend the premises of the Company's clients to execute your duties.
+ Ensure full meaningful workdays by planning and arranging all work-related activities in an effective, timely and efficient manner, with an accurate account of all time involved being recorded.
+ Be familiar with the Health and Safety Regulations and Company policies and procedures applicable to the area of responsibility.
+ Be responsible for your own safety and that of the others whilst setting an example by using the appropriate health and safety procedure and appropriate use of PPE.
+ Understand and engage with the restricted competencies authorised and enhanced levels of supervision within their management plan.
+ Ensure that all plant on the Contract Schedule for the allocated service area is examined/ inspected in accordance with accepted codes of practice and applicable standards with reports compiled to the standard required in a timely manner.
+ So far as is reasonably practicable, ensure that safe systems of work are available, including application of appropriate Risk Assessments and Method Statements, both our clients and our own. Where safe systems of work are not deemed appropriate, the Regional Engineering Manager must be advised.
+ Provide, build and maintain excellent client relationships and ensure that all customer service standards are met
+ Maintain an awareness of developments in standards and legislation affecting the appropriate discipline and support change as required.
+ Maintains sufficient levels of CPD to maintain their professional competencies.
+ Provide advice as appropriate, on the operation of customers assets to ensure customers can derive further value from your inspection.
**Skills & Experience**
+ 3 Years of experience in general engineering environments.
+ Knowledge/ understanding of statutory regulations, such as, LOLER, PSSR, PUWER & relevant British Standards is desirable.
+ Ability to follow and apply statutory requirements and guidelines and company defined policies, processes and procedures.
+ Ability to communicate at all levels
+ Experience understanding client's needs and building/maintaining strong professional relationships
+ Able to work within a supervised environment reporting back to Technical Trainers, Principal Engineers or Line Managers.
+ Good IT skills (able to operate Microsoft packages and use an iPad)
**Qualifications and Educational Requirements:**
+ NVQ Level 4 minimum in an engineering based discipline or equivalent recognised qualification.
+ Or, a recognised relevant apprenticeship in lieu of an academic qualification.
**Personal Attributes**
+ Self-motivated, driven and able to take initiative
+ Organised
+ Confident
+ Customer focused
+ Holder of UK Driving licence, no more than 6 points.
+ Flexible approach to deliver great service
+ Good communicator
**Benefits:**
+ Stay connected with Mobile phone and tablet devices provided for work
+ Pension scheme with 4% employee contribution and 13% employer contribution
+ Access to our employee assistance program for confidential advice
+ Profit share bonus scheme
**Travel & Commuting:**
+ Travel time covered under working hours
+ Car Allowance or company car
+ Cycle to work scheme with tax and NI savings
**Health & Wellbeing:**
+ Free Aviva private healthcare scheme
+ Health and wellbeing program with regular events and activities
+ Occupational health support
+ Opportunity to join Bupa dental scheme
+ Well-being days
**Leave & Pay**
+ Enhanced maternity, paternity, and adoption leave
+ Enhanced sick pay
**Development & Support**
+ Bespoke training program
+ Reimbursement for professional membership subscriptions
**Rewards:**
+ Access to discounts at various retailers through Reward Gateway
**Diversity, Equity & Inclusion**
At HSB, Diversity, Equity, and Inclusion foster innovation and resilience and enable us to act braver and better. Embracing the power of DEI is at the core of who we are. We recognise diversity can be multi-dimensional, intersectional, and complex, so we want to build a diverse workforce that includes a wide range of racial, ethnic, sexual, and gender identities; economic and geographic backgrounds; physical abilities; ages; life, school, and career experiences; and political, religious, and personal beliefs. Additionally, we are committed to building an equitable and inclusive work environment where this diversity is celebrated, valued, and has equitable opportunities to succeed.
All candidates in consideration for any role can request a reasonable adjustment at any point in our recruitment process. You can request an adjustment by speaking to your Talent Acquisition contact.

Step Into a High-Impact Sales Role!
**Pharmacy Sales Representative, Midlands, Ireland**
Field-based across Carlow, Kildare, Laois, Wicklow, Offaly, Westmeath, Kilkenny & Wexford
Are you a seasoned pharmacy sales professional with a passion for healthcare and a business-owner mindset? We're looking for a resilient, driven, and strategic Pharmacy Sales Representative to champion leading consumer healthcare brands across the Midlands.
You'll be the face of innovation, building strong relationships with pharmacy stakeholders, driving sales, and delivering impactful campaigns that make a real difference to customers and communities.
**What You'll Do:**
+ Own your territory and drive brand uptake through smart, data-driven account planning.
+ Build lasting partnerships with pharmacies, delivering value through education, promotions, and commercial excellence.
+ Collaborate cross-functionally to unlock growth opportunities and overcome market challenges.
+ Be a role model for ethical business practices and agile decision-making.
**What You'll Bring:**
+ 5+ years of pharmacy-level experience in consumer healthcare.
+ A degree in Business, Marketing, Science or related field.
+ Exceptional communication, negotiation, and planning skills.
+ A valid driver's licence and the flexibility to travel.
**Why Join Us?**
Be part of a team that's shaping the future of pharmacy sales. We're committed to innovation, integrity, and impact-and we're looking for someone who's ready to make their mark.
**Ready to take the next step?**
Apply now and bring your energy, expertise, and entrepreneurial spirit to this exciting opportunity.
Please note:
+ Sponsorship is not available for this opportunity.
+ Candidates attend interviews at their own cost. Unfortunately, expenses incurred to attend an interview are not covered by IQVIA.
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IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide.
To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere. Thank you for your interest in growing your career with us.
EEO Minorities/Females/Protected Veterans/Disabled

Exclusivity: This position is being managed exclusively by Pale Blue Dot® Recruitment on behalf of our client. All applications and enquiries will be managed directly through ourselves.

Are you a driven and experienced Quality Engineer looking for your next big opportunity?

A leading medical device company based in Bray,  Wicklow is currently seeking a skilled and motivated  Senior Quality Assurance Engineer  to join their team. Are you a quality professional who’s ready to take on increased responsibility, mentor others, and drive excellence in a high-performing, regulated environment. This opportunity offers real career progression, exposure to a wide range of quality systems and activities, and the chance to make a meaningful impact in a company that values continuous improvement, innovation, and teamwork.

Responsibilities include but are not limited to:

• Lead and manage root cause investigations, ensuring timely and effective NCR and  CAPA implementation.

• Assist the QA Manager with the  day-to-day QMS management, ensuring compliance with ISO 13485 and all relevant regulatory requirements.

• Conduct and support internal audits, driving ongoing compliance and quality improvements.

• Support and oversee validation activities, including process validations, test method validations, and risk assessments.

• Provide hands-on quality support for manufacturing, ensuring product compliance and process control.

• Develop, implement, and maintain SOPs and work instructions to drive quality initiatives and support operations.

• Act as a key contact for customer quality concerns, complaints, and regulatory inquiries, leading investigations where required.

• Identify and lead continuous improvement projects to enhance efficiency and product quality.

• Mentor and support junior quality team members, contributing to a culture of learning and professional growth.

• Assist in supplier quality management, ensuring robust quality agreements and ongoing compliance.

• Own and manage the PM/Calibration schedule.

• Assist with the development of other quality personnel as required.

• A Bachelor’s degree in Engineering, Quality, Life Sciences, or a related discipline

• 5+ years’ experience in a medical device or regulated manufacturing environment

• Proven experience with root cause analysis, CAPA management, and failure investigations

• Training in ISO 13485 internal auditing (lead auditor certification preferred but not essential)

• Strong understanding of quality engineering tools and principles such as FMEA, SPC, risk management, and validation

• Excellent analytical and problem-solving skills, with a data-driven mindset

• Effective communication and interpersonal abilities, with a collaborative approach

• Proficiency in Microsoft Office Suite and quality management software

  Why Apply ?

• An opportunity to step up to senior-level responsibilities

• A forward-thinking, collaborative environment that encourages creativity, autonomy, and professional growth

• Direct influence on product quality, process improvements, and team development

• Join a company making a real difference in patients’ lives through high-quality medical device technology.

This is a fantastic opportunity to join a forward-thinking team and thrive in a collaborative, supportive environment that values creativity and teamwork!

Note: By applying for this position, you may also be considered by Pale Blue Dot® Recruitment for other or future related vacancies.

-Pale Blue Dot® Recruitment - The Resource for the MedTech Workforce-