9 Manufacturing Companies jobs in Ireland

Within this role you will be responsible for the oversight of Quality Control support operations. As a Manager within Quality Control a typical day might include, but is not limited to, the following: Maintaining oversight of QC equipment lifecycle activities (including procurement, installation, qualification, maintenance, and decommissioning) Providing direction to Managers and staff that support the equipment Ensuring equipment qualification and maintenance programs are aligned with regulatory agencies requirements, qualified and available for QC laboratory usage Interacting with QC partner groups to establish internal requirements for equipment Leading QC equipment validation / qualification efforts through partnering and interaction with QA Validation and IT groups Managing oversight of the preventive and corrective maintenance monitoring program Managing oversight of the QC external laboratories activities and performance monitoring of external testing laboratories Supervising the issuance and approval of Quality agreements and SLAs with the contract labs Verifying that the site Manufacturing licence and global procedures reflect current contract lab utilization Identifying and calling out issues at contract laboratories to QC leadership Sourcing, co-ordinating and project management of GMP activities relating to new contract lab introduction Travel may be required in support of external contract laboratory testing activities Performing personnel management functions including time sheet submissions, scheduling of vacations, personnel development, and performance evaluations Responsibility for equipment automation and associated projects This role might be for you if you: Possess strong communication and interpersonal skills Demonstrate logical troubleshooting and problem-solving skills Have a detailed understanding of equipment qualification and maintenance activities and industry compliance norms Have the ability to communicate effectively with multiple partners Enjoy working in a fast-paced environment Demonstrate a collaborative and team-orientated approach To be considered for this opportunity you should have a BA/BS in chemistry, biology or related field with 8+ years' proven experience preferably in the pharmaceutical or biotechnology industry, and previous supervisory or leadership experience. Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive and diverse culture that provides comprehensive benefits, which often include (depending on location) health and wellness programs, fitness centers, equity awards, annual bonuses, and paid time off for eligible employees at all levels! Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business. For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U. positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location. Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.

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 QC Manager Projects to join our team on our Manorhamilton Road site in Sligo. The QC Manager Projects 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.
+ Ensure compliance with data integrity policies and regulatory requirements.
+ Liaise with cross-functional teams to facilitate project goals and timelines.
+ Participate in internal and external audits and address audit findings.
+ 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:

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

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 now hiring for the role of Quality Control (QC) Laboratory Supervisor at our state-of-the-art facility in Clonshaugh, Dublin. In this role, you will lead an experienced QC tech team, ensuring seamless daily operations in our QC laboratory. Your work will be pivotal in liaising with local and global teams to facilitate the successful transfer of products to our site and laboratory.
Key Responsibilities:
+ Lead and Develop Teams: Cultivate a supportive environment and set clear expectations to ensure team capability in meeting performance goals. Invest in personal development through coaching, mentoring, and tailored growth plans for career advancement.
+ Oversee Laboratory Operations: Manage daily lab operations, ensuring personnel strictly adhere to regulatory guidelines and execute their duties efficiently.
+ Production Support & Coordination: Actively participate in daily Tier 0 and Tier 1 meetings, aligning laboratory initiatives with production schedules and objectives to achieve quality goals on time.
+ Sample & Data Management: Direct management of samples for analytical testing, ensuring both internal and contract laboratories deliver accurate and timely results in accordance with cGMP standards.
+ Compliance and Process Improvement: Monitor laboratory metrics and drive continuous process improvement initiatives, fostering innovation and efficiency in the laboratory.
+ Training and Method Implementation: Provide or schedule comprehensive training sessions, ensuring all staff maintain requisite skills for safe and compliant operations. Lead the introduction and qualification of new methods in line with regulatory requirements
Qualifications
+ Minimum 3-5 years of relevant Quality Control experience within the pharmaceutical industry.
+ Proven leadership experience with at least 2 years in a supervisory role or demonstrated mentoring capability.
+ Strong analytical laboratory skills with expertise in troubleshooting and method validation/transfer.
+ Ability to align individuals and teams with broader business objectives and manage performance using metrics.
+ In-depth understanding of pharmaceutical manufacturing operations and regulatory requirements.
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:

Quality Control Assistant Manager Irish Food Manufacturing Location: (Baldoyle Dublin 13) Sector: Food & Beverage Manufacturing Job Type: Full-Time | Permanent Salary: Competitive, DOE About the Role We are currently recruiting for a Quality Control Assistant Manager to join our Quality team at a leading Irish food production facility. This role supports the Quality Manager in maintaining and developing robust Food Safety and Quality Management Systems in line with Irish and EU food legislation and leading retailer and GFSI audit schemes (e.g. BRCGS). This is a fantastic opportunity for an experienced quality professional looking to further their career in the Irish food industry, one of Irelands most important and dynamic sectors. What You'll Be Doing Support the Quality Manager in overseeing site-wide QMS and FSMS, including HACCP, GMP, and traceability in line with Irish food law. Act as site lead for BRCGS certification, EHO inspections, and customer audits. Provide leadership to the QA team and act as Deputy Quality Manager during absences. Manage internal audit schedules, handle non-conformances, and lead investigations into quality and food safety issues. Liaise with Production, Engineering, and NPD to continuously improve Irish and export product quality. Coordinate site cleaning and hygiene programmes, ensuring validated and documented practices. Lead training in pest control, allergen management, food defence, and food safety culturekey areas under Irish and EU regulations. Foster a proactive food safety culture in line with values and retailer standards. Why Work With Us? Be part of a respected Irish food manufacturing company serving both domestic and export markets. Engage in meaningful work aligned with Irelands globally recognised food standards. Work in a collaborative team environment that values continuous improvement and food innovation. Real opportunity for career development and training in one of Irelands core industries. Skills: Qusality Control Assistant manager Benefits: Career development

LSC have a great opportunity for a Quality Control NPI Associate to join a South Dublin-based Biopharmaceutical company that specializes in secondary manufacturing activities such as Formulation, Fill Finish and Packaging. If you have 2+ years of experience in construction management/engineering within the pharmaceutical or biotechnology industry and are ready for your next challenge, this could be the perfect project for you! ABOUT THE PROJECT - KEY RESPONSIBILITIES: QC Representative for NPI activities and routine Product meetings Plan and perform non-core testing related to NPI activities Manage all sample management activities related to NPI activities throughout the site Create/own and approve protocols, sample plans, SOP and documentation related to NPI QC Representative responsible for Method Validation and Transfers co-ordination and readiness Sample shipments and temperature monitoring activities for NPI activities ABOUT YOU - ARE YOUR SKILLS A MATCH? Bachelor's degree in science discipline. 2-3 years of biopharmaceutical QC experience or related quality control or GMP laboratory experience in the pharmaceutical or medical device industry. Strong background in Chemistry and Analytical testing is required. Experience with regulatory compliance in cGMP manufacturing and testing of pharmaceutical products. Applicants interested in our contracting opportunities within the pharmaceutical sector in Ireland are required to have a Stamp 1G or a Stamp 4 visa. Please note that we are unable to provide visa sponsorship. Thank you for your understanding. Apply via this advert or contact Grinne Hodnett on if you have any more questions about this opportunity! Skills: GMP NPI Method Validation Tech transfer

Quality Control NPI Senior Associate Purpose Under minimal supervision, responsible for contributing to the team by ensuring the quality of the tasks/services provided by self and contributes to the completion of milestones associated with specific projects or activities within team. This role will support QC and manufacturing operations, as such some extended hours and weekend work flexibility may be necessary as required. Responsibilities QC Representative for NPI activities and routine Product meetings Assist with activities related to QC projects and/or QC tasks within Site projects Plan and perform non-core testing related to NPI activities Manage all sample management activities related to NPI activities throughout the site Create/own and approve protocols, sample plans, SOP and documentation related to NPI QC Representative responsible for Method Validation and Transfers co-ordination and readiness Responsible for their own training and safety compliance. Sample shipments and temperature monitoring activities for NPI activities LIMS data coordination of non-core (NPI) activities. Plan and perform analyses with great efficiency and accuracy. Plan and perform multiple, complex routine/ non-routine methods and procedures and a large variety of assays. Report, evaluate, back-up/archive, trend and approve analytical data. Create APPX data files and randomisation memo to facilitate data analysis. Participate in audits, initiatives and projects that may be departmental or organizational in scope. Write protocols and perform assay validation and equipment qualification/ verification. Introduce new techniques to the lab, including method transfers, reports, validations and protocols. Qualifications Bachelors degree in a science discipline. 2-3 years of biopharmaceutical QC experience or related quality control or GMP laboratory experience in the pharmaceutical or medical device industry. Strong background in Chemistry and Analytical testing is required. Experience with regulatory compliance in cGMP manufacturing and testing of pharmaceutical products. Understanding and application of principles, concepts, theories, and standards of GMP QC analytical laboratories. Deepens technical knowledge through exposure and continuous learning Knowledge of related regulatory/industry considerations, compliance issues and/or scientific discovery Applies analytical skills to evaluate and interpret complex situations/ problems using multiple sources of information Anticipates and prevents potential problems Skills: Quality Control

Quality Control Technician - 23 Month Contract Do you want to join us in helping to fight the world's most threatening diseases and enabling access to care for more people around the world? At Siemens Healthineers, we pioneer breakthroughs in healthcare. For everyone. Everywhere. Sustainably. We offer you a flexible and dynamic environment with opportunities to go beyond your comfort zone in order to grow personally and professionally. Sound interesting? Then come and join our global team as Quality Technician at our facility in Swords, Dublin Your tasks and responsibilities: You will be responsible for the technical inspection of electro-mechanical parts & large in-vitro diagnostic instrumentation in a low volume, high complexity & highly regulated technology environment. You will support the quality control aspects of instrument manufacture & support resolution of issues in a timely manner to ensure daily output targets are achieved. You will compile, maintain & review all necessary paperwork and test data for each system/module to ensure that accurate Quality records are available leading to the final assessment of our devices prior to shipment. Develop, improve & maintain good manufacturing practices & workmanship standards and drive improvements back into production with a quality & process robustness focus. To find out more about the specific business, have a look at Siemens Healthcare Diagnostics Manufacturing Limited - Swords (siemens- Your qualifications and experience: You will have a minimum of a QQI Level 6 qualification (Diploma or higher) in Engineering or Science Discipline (Bio-Chemistry, Chemical, Science, Mechanical, Electrical, Electronic or other relevant technical background) or Diploma / Trade qualification with relevant experience in automation / system manufacturing or support. You will possess relevant experience in Quality Control and complex instrumentation inspection. You will have a minimum of 2 years-experience in a similar role in a manufacturing environment being a part of a teams with good communications skills, written & verbal. Your attributes and skills: You must have strong trouble shooting skills & practical experience with instrument(s) and an ability to analyze data outputs for quality trends. You should have a willingness to learn and lhave the possibility of shift work to meet supply demand. You should ideally possess relevant experience in Quality Control and complex instrumentation inspection. Our global team: We are a team of more than 70,000 highly dedicated employees across more than 70 countries passionately pushing the boundaries of what's possible in healthcare to help improve people's lives around the world. As a leader in the industry, we aspire to create better outcomes and experiences for patients no matter where they live or what health issues they are facing. Our portfolio, spanning from in-vitro and in-vivo diagnostics to image-guided therapy and innovative cancer care, is crucial for clinical decision-making and treatment pathways. Our culture: We are part of an incredible community of scientists, clinicians, developers, researchers, professionals, and skilled specialists pushing the boundaries of what's possible, to improve people's lives around the world. We embrace a culture of inclusivity in which the power and potential of every individual can be unleashed. We spark ideas that lead to positive impact and continued success. Check our Careers Site at Jobs at Siemens Healthineers (siemens- #Siemens Please note: For candidates applying through Irishjobs, please ensure that you complete your application fully all the way through to Avature. Failure to fully complete your application may result in Siemens not being able to view your CV. Please find Avature link to this role below. As an equal opportunity employer, we welcome applications from individuals with disabilities. We care about your data privacy and take compliance with GDPR as well as other data protection legislation seriously. For this reason, we ask you not to send us your CV or resume by email. We ask instead that you create a profile in our talent community where you can upload your CV. Setting up a profile lets us know you are interested in career opportunities with us and makes it easy for us to send you an alert when relevant positions become open. Click here to get started. To be considered for this role you will be redirected to and must complete the application process on our careers page. To start the process, click the Apply button below to Login/Register.