106 Lab Manager jobs in Ireland

Overview:

CLS is currently going through an unprecedented and exciting period of growth and development and is looking for dynamic, dedicated and solutions driven team members, who want to be part of the company's continued success.

Founded in 1994, Complete Laboratory Solutions (CLS) is the highest accredited contract laboratory in Ireland and the leading provider of sampling, analysis, and analysts to the pharmaceutical, medical device, food, and environmental industries.

As well as analysis and testing at our commercial laboratories, CLS builds strategic partnerships with its clients to deliver a flexible and managed quality solution (FlexiQ)by supplying organisations with highly skilled, work-ready quality professionals on a temporary, project-specific, or long-term basis. This service can be provided at a CLS site or directly at the client's location.

Job Title:

Microbiology Lab Manager

Job Responsibilities:

As the Microbiology Lab Manager, you will lead the microbiology function in a state-of-the-art pharmaceutical facility, ensuring high-quality, compliant, and efficient support for manufacturing operations. You will be responsible for managing a team of microbiologists and overseeing all laboratory testing activities to ensure product and environmental monitoring meet regulatory and company standards.

Key responsibilities include:

• Leading and managing the day-to-day operations of the microbiology laboratory.
• Overseeing testing programs for bioburden, endotoxin, sterility, and environmental monitoring.
• Ensuring all testing is performed in compliance with cGMP, SOPs, and regulatory requirements.
• Developing and maintaining microbial control strategies for the site, including cleanroom qualification and routine environmental monitoring.
• Leading laboratory investigations and implementing corrective and preventive actions (CAPAs).
• Driving continuous improvement initiatives in lab operations, quality systems, and safety.
• Coaching, mentoring, and developing the microbiology team, including performance management and training.
• Representing the microbiology lab in cross-functional meetings and regulatory inspections.
• Managing laboratory resources, including equipment qualification, maintenance, and procurement.
• Supporting method development, validation, and transfer activities.
• Ensuring adherence to the site's safety policies and promoting a culture of safety and quality.

Who You Are:

You are an experienced microbiology professional with strong leadership qualities and a passion for quality and compliance. You thrive in a fast-paced, regulated environment and are committed to developing your team and driving high standards. You are organized, analytical, and collaborative, with the ability to make sound decisions and influence others.

Where You Come From:

You have a degree in Microbiology, Biotechnology, or a related scientific discipline, along with at least 8 years' experience in a pharmaceutical or biopharmaceutical microbiology environment, including leadership or supervisory experience. You have:

• In-depth knowledge of aseptic processing, contamination control, and regulatory requirements (FDA, EMA, etc.).
• Experience managing microbiological testing programs, investigations, and audits.
• Strong technical expertise in microbiological methods and environmental monitoring.
• Excellent communication, team management, and problem-solving skills.

What We Offer:

• A leadership role in a world-class pharmaceutical manufacturing environment.
• The opportunity to shape and grow a high-performing microbiology team.
• Continuous professional development in a company that values innovation and quality.
• A collaborative and supportive culture focused on patient safety and operational excellence.
• A competitive salary.

Work Schedule
Standard (Mon-Fri)

Environmental Conditions
Adherence to all Good Manufacturing Practices (GMP) Safety Standards

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
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.

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.

Microbiology Lab Manager – Leadership Opportunity in Pharma

Are you a seasoned microbiology professional ready to lead in a cutting-edge pharmaceutical environment?

We're hiring a
Microbiology Lab Manager
to head up a high-performing team in a state-of-the-art facility. This is a unique opportunity to shape microbial control strategies, drive continuous improvement, and make a real impact in a regulated, quality-driven setting.

What You'll Do:

• Lead day-to-day operations of the microbiology lab
• Oversee bioburden, endotoxin, sterility & environmental monitoring programs
• Ensure compliance with cGMP, SOPs & regulatory standards
• Drive CAPAs, investigations & continuous improvement
• Coach and develop a talented team of microbiologists

What You Bring:

• Degree in Microbiology, Biotechnology or related field
• 8+ years in pharma/biopharma microbiology, including leadership experience
• Expertise in aseptic processing, contamination control & regulatory audits
• Strong communication, problem-solving & team management skills

What's On Offer:

• A leadership role in a world-class pharmaceutical setting
• Opportunity to grow and shape a dynamic team
• Supportive, quality-focused culture
• Competitive salary & professional development

Interested or know someone who might be? Let's connect

Planet Pharma is an equals opportunities Recruitment Business and Agency. We welcome applications from all suitably qualified candidates regardless of their race, sex, disability, religion/belief, sexual orientation, or age.

This job is with Thermo Fisher Scientific, an inclusive employer and a member of myGwork – the largest global platform for the LGBTQ+ business community. Please do not contact the recruiter directly.
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
Requirements
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
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.

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.

Lab Project Manager - Ireland, Dublin - 12 Month Contract
Our client, a globally recognised pioneer in Biotechnology, are recruiting for the position of Lab Project Manager. A leader in the industry, our client focuses on areas of high unmet medical need and leverages its expertise to stride for solutions. This is your chance to join them on their global mission to better the lives of those effected by disease and illness.

Responsibilities Include

• Manage project delivery through the full project life cycle from, design development, construction, equipment installation and CQV.
• Manage vendors
• Liaise and coordinate with cross functional teams to ensure successful project delivery
• Manage stakeholders and provide regular project updates.

* *Requirements:***

• Project management experience supporting either new Lab facility builds or existing lab refurbs/re-fits
• Strong cleanroom and lab equipment experience
• Construction project experience
• Experience managing projects through the full life cycle "from cradle to grave", including managing project schedules, budgets and vendors.
• Good communication and team-working skills

If this role is of interest, please apply now

We are looking for a dedicated Administrator who would be a key member of the company leadership team, responsible for ensuring that the service we provide is safe and compliant with all industry and certification regulations.

The candidate should have a "can-do" attitude that drives effective change and moves the company processes positively which will effectively lead to the provision of an optimum service to our clients.

We seek an effective coach and communicator who can skillfully create an empowered and engaged workforce culture.

The candidate should have knowledge of construction safety, quality and continuous improvement via effective data analysis and decision-making.

Key Responsibilities:

· Assure that all stakeholders are well trained in support of the I.M.S

· Manage and supervise I.M.S. administration and site activities

· Ongoing auditing to promote compliance with I.M.S. and H&S procedures

· Use effective negotiation skills to drive alignment and resolve conflict

· Provide coaching and constructive feedback

· Collaborate with team and cross-functional stakeholders

· Evaluate data, assess and develop ongoing improvements to the company I.M.S. and H&S procedures

Requirements:

· 3+ years of experience in quality management / Health & Safety

· Experience in business administration will be an advantage.

· In-depth knowledge of health & safety /quality control procedures and legal standards.

· Strong attention to detail, organisational, and leadership skills.

· Strong knowledge of data analysis, and statistical methods.

· Excellent communication and listening skills.

· Formal training in H&S and environmental monitoring and auditing will be an advantage

Job Types: Full-time, Permanent

Pay: €40,000.00-€50,000.00 per year

Benefits:

• Company pension
• On-site parking

Work Location: In person

Job Description
We have a great opportunity for a Quality Control Specialist to join our Carlow site. You will join a self-directed team and provide trouble shooting support. The quality control specialist will have the opportunity to be involved in and lead various exciting projects.

What you will do

Bring energy, knowledge, innovation and leadership to carry out the following

• Support new product introductions and provide quality expertise during product release.
• Generate, review, approve, and expedite QC GMP documentation, including Quality Notifications, Laboratory Investigations, CAPAs, Effectiveness Checks, SOPs, SWIs, change controls, Annual Product Reviews, Trend Reports, Out of Process Control Limit (OOPCL) events, and Compendial Assessments.
• Develop, revise, and roll out operational procedures and training materials.
• Lead and support batch release activities by completing timely investigations, quality notifications, OOPCL events, and generating interim/summary reports.
• Raise and investigate CAPAs and quality notifications using standard problem-solving tools (FMEA, Fishbone diagrams, 5 Whys), and implement corrective actions via change management.
• Provide coaching, mentoring, and guidance to lab teams
• Act as a document system expert review, approve, format, and facilitate documentation workflows.
• Lead or support projects and promote teamwork, open communication, and a high-performing, inclusive culture.
• Collaborate cross-functionally to ensure manufacturing, testing, and release processes comply with cGMP and regulatory standards.
• Support qualification/validation, technical transfers, and commercial operations with quality oversight.
• Perform laboratory testing and material inspections according to approved methods, including analytical, microbiological, environmental monitoring, and stability testing.
• Detect, report, investigate, and close out out-of-specification (OOS) and out-of-trend (OOT) results.
• Manage and monitor Quality Management Systems, generate performance and quality event reports.
• Provide quality support for supplier/material qualification, validation, risk management, and quality agreements.

Lab operates on a two-shift cycle pattern (7am-3pm/3pm-11pm)
In order to excel in this role, you will more than likely have

• Bachelor's degree or higher in Analytical Chemistry, Biochemistry, Biology, or a related discipline preferred.
• 5+ years' experience in a pharmaceutical laboratory, ideally in a similar role.
• Excellent troubleshooting, analytical, and problem-solving skills.
• Strong technical knowledge and scientific qualification relevant to the pharmaceutical environment.
• Strong experience with HPLC systems, bioassay methods, and associated software is desirable.
• Experience with cGMP, GLP, Quality Management Systems, method validation, and method transfer.
• Proficient in QC systems such as EN, LIMS, Trackwise, and Microsoft Office.
• Knowledge of Irish, European, and international regulatory codes and standards.
• Effective verbal and written communication skills with strong influencing capability.
• Commitment to maintaining a safe, compliant, and quality-focused culture.

As a company, we are committed to 'Inventing for Life' in all that we do. We keep the patient at the very heart of all that we do and strive to find solutions and treatments for some of the world's most challenging healthcare needs.

We are proud to be a company that embraces the value of bringing diverse, talented, and committed people together. The fastest way to breakthrough innovation is when diverse ideas come together in an inclusive environment.

So, if you are ready to
Invent solutions to meet unmet healthcare needs, Impact the future by driving one of the world's leading healthcare companies, and inspire your team to reach their full potential and push the boundaries of science and technology, please apply today.

Required Skills
Accountability, Accountability, Adaptability, Analytical Chemistry, Analytical Instrumentation, Analytical Method Development, Batch Releases, Biochemistry, Corrective Action Management, Data Integrity, Dissolution Testing, Driving Continuous Improvement, GMP Compliance, Ishikawa Diagrams, Karl Fischer Titrations, Laboratory Documentation, Laboratory Safety, Laboratory Testing, Management Process, Microbiological Analysis, Microbiological Test, Microsoft Office, Quality Control Management, Quality Management System Auditing, Quality Management System Improvement {+ 4 more}

Preferred Skills
Current Employees apply HERE

Current Contingent Workers apply HERE

Search Firm Representatives Please Read Carefully
Merck & Co., Inc., Rahway, NJ, USA, also known as Merck Sharp & Dohme LLC, Rahway, NJ, USA, does not accept unsolicited assistance from search firms for employment opportunities. All CVs / resumes submitted by search firms to any employee at our company without a valid written search agreement in place for this position will be deemed the sole property of our company. No fee will be paid in the event a candidate is hired by our company as a result of an agency referral where no pre-existing agreement is in place. Where agency agreements are in place, introductions are position specific. Please, no phone calls or emails.

Employee Status
Regular

Relocation
VISA Sponsorship
Travel Requirements
Flexible Work Arrangements
Not Applicable

Shift
Valid Driving License
Hazardous Material(s)
Job Posting End Date
10/17/2025

• A job posting is effective until PM on the day BEFORE the listed job posting end date. Please ensure you apply to a job posting no later than the day BEFORE the job posting end date.

Requisition ID
R