10 Lab Manager jobs in Ireland

QC Manager - Sligo We are seeking a Quality Control (QC) Manager to an expanding team in Sligo.

This position plays a key role in leading a laboratory team responsible for QC testing, ensuring that products meet the highest standards of safety, quality, and compliance.

The role involves managing day-to-day laboratory activities, coordinating analytical testing of APIs and oral solid dosage (OSD) products, and aligning priorities with wider business needs.

Key Responsibilities Lead and support a QC laboratory team, ensuring all activities are carried out in line with data integrity, quality, and regulatory requirements.

Oversee and contribute to analytical testing for APIs and OSD products.

Coordinate sample management, inspection, and testing, ensuring schedules are met and priorities are aligned with project needs.

Act as a point of contact for audits, contributing to both preparation and follow-up of audit findings.

Compile and review technical reports, drive laboratory investigations, and ensure effective CAPA implementation.

Provide training, mentorship, and guidance to team members to support both short- and long-term objectives.

Communicate technical results to stakeholders to support timely and informed decision-making.

Report directly to the Senior QC Manager.

Qualifications & Experience Degree in Chemistry or a related scientific field.

At least 4 years' experience in a supervisory or management role within a pharmaceutical QC environment.

Strong technical knowledge of QC/QA practices and analytical testing methods for API and OSD.

Proven ability to write clear technical reports and deliver presentations.

Excellent communication and leadership skills, with a strong focus on quality and compliance.

Skills: QC Manager Analytical Leadership Science

**Work Schedule**
Standard (Mon-Fri)
**Environmental Conditions**
Adherence to all Good Manufacturing Practices (GMP) Safety Standards
**Job Description**
**Lab Manager - Biopharma**
At PPD, part of Thermo Fisher Scientific, you'll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our customers to make the world healthier, cleaner and safer.
We provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through research, development and delivery of life-changing therapies. With clinical trials conducted in 100+ countries and ongoing development of novel frameworks for clinical research, our work spans laboratory, digital and decentralised clinical trial services.
Your determination to deliver quality and accuracy will improve health outcomes that people and communities depend on - now and in the future.
**Location/Division Specific Information**
Our PPD® Laboratory Services team has a direct impact on improving patient health through the expertise of scientists, industry thought-leaders and therapeutic guides. As the world leader in serving science, our laboratory professionals bring their commitment to accuracy and quality to deliver groundbreaking innovations.
Labs - Analytical Services Division
Location: Athlone, Ireland, Biopharmaceutical Department
**Discover Impactful Work:**
The role of Lab Manager is to provide support to our Biopharma department by leading and coaching group leaders, scientists, and project managers in laboratory operations with tasks such as scheduling, resource management, technical and compliance related issues. They will plan, direct and implement improvements in systems, processes and procedures to increase efficiency, productivity and quality in the laboratory. They assist the division director in longer term planning, business development and expansion initiatives by providing mid-range (1-3 month) resource utilization predictions for a department
**A day in the Life**
+ Interacts with clients and business development on requests for proposals and project definition. Prepares, reviews and approves bids and proposals, scope of work and pricing. Negotiates with clients on timelines and pricing.
+ Leads/directs work responsibilities of group leaders as well as prioritize talks and resources.
+ Reviews data for technical quality and compliance to protocols, methods and SOPs. Reviews and approves laboratory investigation, deviations, and QA facility and data audits. Leads client and regulatory audits.
+ Prepares and updates revenue projection reports, reviews Partner and timesheet reports for revenue recognition and billing, evaluates resource utilization reports and project profitability.
+ Reviews and approves study protocols, project status reports, final study reports and other project related technical documentation.
+ Assists in technical sales and marketing, prepares technical marketing materials, and participates in poster and podium presentations in technical conferences.
+ Assists upper management in longer term planning, budgeting, new capabilities development and other responsibilities.
+ Prepares and implements PPD SOPs and company operational policies. Ensures adherence and makes recommendations to quality system improvements.
.
**Education and Experience**
+ Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to 10+ years) or equivalent and relevant combination of education, training, & experience.
+ 5+ years of management responsibility
+ Proven leadership skills
+ Years of experience refers to typical years of related experience needed to gain the required knowledge, skills, and abilities necessary to perform the essential functions of the job. Years of experience are not to be used as the only determining factor in establishing the job class or making employment selection decisions.
**Knowledge, Skills, Abilities**
+ Full understanding of laboratory requirements, PPD and client SOPs, ICH guidelines, USP requirements and FDA guidance
+ Proven technical troubleshooting analytical instrumentation and problem solving abilities
+ Excellent written and oral communication skills
+ Project and time management skills
+ Ability to implement quality systems and process improvements
+ Ability to provide guidance to clients on analytical issues and regulatory requirements
+ Knowledge of budgeting, forecasting and fiscal management
+ Demonstrated coaching and mentoring skills
+ Demonstrated longer term planning skill
+ Strong organizational agility and demonstrated drive for results
**Work Environment**
Thermo Fisher Scientific values the health and wellbeing of our employees. We support and encourage individuals to create a healthy and balanced environment where they can thrive. Below is listed the working environment/requirements for this role:
+ Able to communicate, receive, and understand information and ideas with diverse groups of people in a comprehensible and reasonable manner.
+ Able to work upright and stationary and/or standing for typical working hours.
+ Able to lift and move objects up to 25 pounds.
+ Able to work in non-traditional work environments.
+ Able to use and learn standard office equipment and technology with proficiency.
+ May have exposure to potentially hazardous elements, including infectious agents, typically found in healthcare or laboratory environments.
+ Able to perform successfully under pressure while prioritising and handling multiple projects or activities.
Our Mission is to enable our customers to make the world healthier, cleaner and safer. Watch as our colleagues explain 5 reasons to work with us. As one team of 100,000+ colleagues, we share a common set of values - Integrity, Intensity, Innovation and Involvement - working together to accelerate research, solve complex scientific challenges, drive technological innovation and support patients in need. #StartYourStory with PPD, part of Thermo Fisher Scientific, where diverse experiences, backgrounds and perspectives are valued.
**Apply today!** ** Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.
**Accessibility/Disability Access**
Job Seekers with a Disability: Thermo Fisher Scientific offers accessibility service for job seekers requiring accommodations in the job application process. For example, this may include individuals requiring assistance because of hearing, vision, mobility, or cognitive impairments. If you are a job seeker with a disability, or assisting a person with a disability, and require accessibility assistance or an accommodation to apply for one of our jobs, please submit a request by telephone at *. Please include your contact information and specific details about your required accommodation to support you during the job application process.
+ This telephone line is reserved solely for job seekers with disabilities requiring accessibility assistance or an accommodation in the job application process. Messages left for other purposes, such as not being able to get into the career website, following up on an application, or other non-disability related technical issues will not receive a response.
**_We welcome and encourage applicants from outside of Ireland. We can provide support with immigration and visa needs for successful applicants and dependents, tax consultations and other basic destination services. All other relocation costs are at the expense of the applicant._**
Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.

Company Description
AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas - immunology, oncology, neuroscience, and eye care - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at Follow @abbvie on X, Facebook, Instagram, YouTube, LinkedIn and Tik Tok ( .
Job Description
We are looking for a Lab Compliance Manager to join our team on our Manorhamilton Road site in Sligo. The Lab Compliance Manager drives project-related activities within the QC department, focusing on the introduction of innovative analytical techniques, automation, and the transition to a paperless lab environment. This role is pivotal in the implementation of the "Lab of the Future" concept and managing lab expansion projects.
Responsibilities:
+ Lead and manage all project-related activities in the QC department.
+ Oversee the introduction of new analytical techniques, focusing on automation and paperless laboratory systems.
+ Manage the implementation of the Lab of the Future initiative in the QC department.
+ Coordinate and oversee laboratory expansion projects.
+ Manage and oversee compendial reviews, documentation control for QC, maintenance and calibration of analytical instrumentation, analytical work orders on maximo and retain management.
+ Manage purchasing and budget control, including vendor managed inventory, laboratory cleaning services and capital requirements for QC.
+ Manage and ensure delivery of training curricula for QC via laboratory trainer role.
+ Lead operational excellence in QC delivering on various initiatives including reduced testing program for QC.
+ Liaise with PDS&T to ensure execution of reference standard interval testing program.
+ Lead inspection readiness in QC. Participate in internal and external audits and address audit findings.
+ Ensure compliance with data integrity policies and regulatory requirements.
+ Liaise with cross-functional teams to facilitate project goals and timelines.
+ Present project updates and technical data to stakeholders effectively.
+ Report to the Senior QC Manager.
Qualifications
+ M.Sc./B.Sc. in Chemistry or a related discipline.
+ Experience working in API and OSD QC laboratories.
+ Minimum 4 years of experience in people management within a QC lab setting.
+ Strong project management, presentation, and communication skills.
+ Innovative thinking, with a commitment to advancing laboratory practices and compliance.
Additional Information
AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community.  Equal Opportunity Employer/Veterans/Disabled.
US & Puerto Rico only - to learn more, visit & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:

Project Manager, Laboratory
ICON plc is a world-leading healthcare intelligence and clinical research organization. We're proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development.
We are currently seeking a Project Manager, Laboratory to join our diverse and dynamic team. As a Project Manager, Laboratory at ICON, you will play a pivotal role in designing and analyzing clinical trials, interpreting complex medical data, and contributing to the advancement of inNvative treatments and therapies.
**What you will be doing**
+ Ensure client satisfaction by acting as the Sponsor's main contact person in all matters regarding ICON services including the day-to-day management of studies.
+ Attend and represent ICON at Sponsor meetings.
+ Manage 10-15 studies in accordance with Good Clinical Practice.
+ Communicate with Sponsor's study progress in a responsible and professional manner and provide Sponsors with regular management reports.
+ Provide ICOLAB support to sponsor personnel.
**Your profile**
+ Bachelor's degree in a relevant field such as life sciences or healthcare.
+ Previous experience in project management within a laboratory or clinical research setting.
+ Strong communication and interpersonal skills, with the ability to represent the company at sponsor meetings.
+ Ability to manage multiple studies concurrently while ensuring adherence to regulatory standards and guidelines.
+ Detail-oriented with strong organizational skills to effectively manage study documentation and timelines.
**What ICON can offer you:**
Our success depends on the quality of our people. That's why we've made it a priority to build a diverse culture that rewards high performance and nurtures talent.
In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family.
Our benefits examples include:
+ Various annual leave entitlements
+ A range of health insurance offerings to suit you and your family's needs.
+ Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead.
+ Global Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized professionals who are there to support you and your family's well-being.
+ Life assurance
+ Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others.
Visit our careers site ( to read more about the benefits ICON offers.
At ICON, inclusion & belonging are fundamental to our culture and values. We're dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.
If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know or submit a request here ( in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless - there's every chance you're exactly what we're looking for here at ICON whether it is for this or other roles.
Are you a current ICON Employee? Please click here ( to apply

RecruitNet International Ltd specialises in Healthcare recruitment for Domestic and Overseas candidates for Hospitals, Nursing Homes, Home care and Community care. We are hiring  Clinical Nurse Manager II – Cath Lab  Posts for a hospital located in Tralee, Ireland.  Responsibilities  Have a lead role in the effective governance, operational management, and administration of the nursing and healthcare services with a particular emphasis on effective clinical leadership, providing a safe environment for patients and staff, while making the best use of resources. Development and delivery of auditing and reporting in line with relevant legislation and quality standards Engage with key stakeholders to ensure hygiene standards are maintained for patients, staff and visitors Adhere to and contribute to the development and maintenance of nursing standards, protocols, and guidelines consistent with the highest standards of care and in line with the Code of Professional Practice and Behaviours for Registered Nurses.Promote collaboration with the multidisciplinary team, inclusion health teams, and other partners.Ensure all relevant records are kept clear and up to date in the respective center relating to each service userRequirementsRegistered with NMBIMinimum 5-years post registration acute general hospital experience, 2 of which must be in the area of critical care nursing or cardiac catheterisation lab.  Qualification/Experience in Cardiac Catheterisation Lab is desirable  Effective Leadership and Communication skillsProven clinical, auditing and managerial experienceManagement experience and qualification desirableBenefitsTop pay and great working conditionsImmediate Start, Full-time PermanentGreat professional development opportunityContinued education and training.

RecruitNet International Ltd specializes in relocating qualified professionals throughout Ireland and overseas, we guide you through professional registration, job placement, visa and employment permit processing.We are hiring a  Clinical Nurse Manager (CNM II)  - Cath Lab in a Private Hospital in Galway, Ireland. (1 Year Fixed Term Contract)We will provide exceptional patient care in an environment where quality, respect, caring, and compassion are at the center of all we do. Key Responsibilities  Have a lead role in the effective governance, operational management, and administration of the nursing and healthcare services with a particular emphasis on effective clinical leadership, providing a safe environment for patients and staff, while making the best use of resources. Development and delivery of auditing and reporting in line with relevant legislation and quality standards Engage with key stakeholders to ensure hygiene standards are maintained for patients, staff and visitors Adhere to and contribute to the development and maintenance of nursing standards, protocols, and guidelines consistent with the highest standards of care and in line with the Code of Professional Practice and Behaviours for Registered Nurses.Promote collaboration with the multidisciplinary team, inclusion health teams, and other partners.Ensure all relevant records are kept clear and up to date in the respective center relating to each service userRequirementsRegistered nurse with NMBI registrationMinimum of 5 years post registration experience, of which 2 years is in a Cath. Lab with a postgraduate qualification in cardiology.Experience in management with excellent interpersonal, leadership & communication skillsBenefitsTop pay and great working conditionsImmediate Start, Full time PermanentGreat professional development opportunityContinued education and training.

RecruitNet International Ltd is specializing in relocating qualified professionals throughout Ireland and overseas, we guide you through the professional registration, job placement, visa and employment permit processing.We are hiring  Clinical Nurse Manager I  Cath Lab into a Private Hospital in Galway, Ireland.We will provide exceptional patient care in an environment where quality, respect, caring and compassion are at the centre of all we do. Key Responsibilities  Clinical nurse manager  will work closely with the CNMII, following their guidance and expertise.Coordinating and leading a team of dedicated staff members in the seamless implementation and delivery of exceptional patient careCommitted to ensuring that our patients receive the highest quality of care.The nurse in charge is responsible for ensuring the quality of patient care within their designated area. They are also tasked with effectively managing resources, providing leadership to the team, and assuming accountability for all nursing activities in their area.Provide support, assistance, and facilitation to colleagues in order to help them achieve the specific critical success factors that have been developed for the department. RequirementsRegistered nurse with NMBI registrationPreferred to have managerial experience with strong interpersonal, leadership, and communication abilities.A postgraduate cardiology qualification and at least three years of post-registration experience, two of which must be spent in a catheter lab, are preferred.Experience in management with excellent interpersonal, leadership, and communication skills is desirable.BenefitsTop pay and great working conditionsImmediate Start, Full time PermanentGreat professional development opportunityContinued education and training.

**Work Schedule**
Standard (Mon-Fri)
**Environmental Conditions**
Office
**Job Description**
**Laboratory Account Manager**
**Ideal Location:** Dublin (Remote) - Covering Ireland and N. Ireland
**How Will You Make an Impact?**
We believe in enabling our customers to make the world healthier, cleaner, and safer. As the global leader in serving science, our mission drives our teams to deliver innovative technologies, purchasing convenience, and comprehensive pharmaceutical services. Our brands-Thermo Scientific, Applied Biosystems, Invitrogen, Fisher Scientific, Unity Lab Services, and Patheon-are synonymous with excellence and reliability.
**About the Role:**
In this role, you will be instrumental in developing and implementing key account plans that drive sustained growth for our Phadia allergy and autoimmunity solutions. Reporting to the Head of Laboratory Sales UK, Netherlands & Ireland, you will collaborate closely with cross-functional teams to achieve your goals.
**Key Responsibilities:**
+ **Maintain and Grow Business:** Achieve targets by maintaining existing business and expanding the Allergy & Autoimmune market.
+ **Deliver Metrics:** Meet company and individual performance metrics consistently.
+ **Account Management:** Develop and maintain accurate account plans and customer details in Salesforce (SFDC) in collaboration with Marketing, Clinical, and Technical Services teams.
+ **Record Keeping:** Log all activities and meetings accurately and promptly in SFDC.
+ **Contract Negotiation:** Lead and negotiate Contracts, including Capital sales, Reagent Rentals, and Service Contracts, ensuring timely execution.
+ **Tender Management:** Lead tender responses and engage with Managed Service Providers (MSPs), conducting regular site visits and business reviews.
+ **Forecasting and Planning:** Participate in forecasting and planning activities using TFD tools such as SFDC and Power BI.
+ **Customer Support:** Conduct onsite stock checks for Cost Per Reportable (CPR) customers.
+ **Engage with Key Opinion Leaders:** Develop relationships with key opinion leaders across your territory.
+ **Market Intelligence:** Provide market feedback to Sales Manager, Marketing, and Finance.
+ **Effective Communication:** Ensure clear communication within all parts of the organization.
+ **Compliance:** Adhere to internal Quality Processes and CRM standards.
+ **Travel:** Spend the majority of time with customers face-to-face, with travel expected to be 50-75%.
+ **Event Attendance:** Attend internal and external meetings and events as required.
**Qualifications:**
+ Bachelor's or Master's degree in Life Sciences, e.g., Biomedical Science.
+ Relevant experience in Laboratory/Pathology Sales and/or product portfolio management.
+ Proficiency with Salesforce (SFDC).
+ Strong active listening and communication skills to build trust.
+ Flexible, self-motivated, and well-organized.
+ Teammate with a collaborative attitude.
+ Passionate professional with a proactive attitude.
+ Strong commercial competence to build and develop customer relationships and close sales.
+ Proven negotiation skills and the ability to influence others.
+ Analytical skills and experience working with data.
+ Understanding of business development principles.
+ Dedication to continuous personal and professional development.
+ Valid driver's license and willingness to travel approximately 75% of the time.
**Our Values:**
As part of our team of over 130,000 colleagues, you will share in our core values of Integrity, Intensity, Innovation, and Involvement. At Thermo Fisher Scientific, we celebrate diverse experiences, backgrounds, and perspectives.
**Apply Today!**
Start your story at Thermo Fisher Scientific by applying today!
We review applications on a rolling basis, so please apply as soon as possible.
Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.

Company Description
AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas - immunology, oncology, neuroscience, and eye care - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at Follow @abbvie on X, Facebook, Instagram, YouTube, LinkedIn and Tik Tok ( .
Job Description
We are currently looking for a Senior Manager of Quality Control Laboratories to join our team in Westport on a 12-month fixed-term contract. The Senior Manager of Quality Control is responsible for strategy, planning, and management of laboratory operations, ensuring compliance with FDA, HPRA, and EPA safety standards and budgetary constraints. This role supports the QA site head in achieving operational goals.
Responsibilities:
+ Manage and motivate employees, ensuring capacity aligns with business needs.
+ Develop and deliver business plans, manage departmental budget, and handle new product implementation.
+ Represent the company in client and regulatory meetings, ensuring GMP compliance.
+ Organize cross-functional activities to improve lab efficiencies.
+ Coordinate meetings and manage documentation and compliance tools.
Qualifications
+ Proven track record in people and operations management within Pharma/Medical Devices/Food industry.
+ Qualification in Pharmaceutical Science.
+ Excellent conflict resolution, planning, and communication skills.
+ Ability to manage in regulated environments and adapt to changes.
+ Strong commitment to AbbVie's values and business ethics.
Additional Information
AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community.  Equal Opportunity Employer/Veterans/Disabled.
US & Puerto Rico only - to learn more, visit & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more: