75 Quality Control Inspector jobs in Ireland

Overview The primary function of this role is the inspection of raw materials (IQC), finished devices (FQC), packaged devices (PKQC) , sterilised devices (PSQC) and device history records (Batch Release) ensuring that inspection procedures are followed at all times and that all product and paperwork passes specified quality control requirements before shipping to customers.

Reporting to: Supervisor, Quality Control Find out more about Cook Medical here Responsibilities Ensure that all products which are manufactured at Cook Medical are inspected as per the relevant FQC instructions and that it meets the required quality control specifications before it is shipped to customers.

Ensure that all raw materials received on site at Cook Medical are inspected as per the relevant IQC instructions and that they meet the required quality control specifications before release for use in manufacturing.

Ensure that finished goods packaged at Cook Medical are inspected as per the relevant packaging quality control instructions and that they meet the required quality control specifications.

Ensure that product which has completed the sterilisation cycle is inspected as per the relevant instructions and that its meets the quality control specifications before it is shipped to customers.

Ensure that all device history records are reviewed in line with Batch Release procedures and are compliant before product is released to stock.

Ensure compliance with GMP practices i.e.

gowning correctly, adhering to CMA rules, adhering to relevant line clearance procedures, following procedures and completion of paperwork accurately.

Highlight any potential issues to Team Leaders.

Contribute to attainment of overall KPI targets for the QC group by achieving daily/weekly quality and output targets.

Working as part of a QC team within the Controlled Manufacturing Areas.

Ensure that Cook's Code of conduct is considered in all business matters carried out on Cook's behalf.

Qualifications Experience in a manufacturing environment/QC inspection role.

Previous experience in medical devices, while not essential is advantageous.

Good communication and inter-personal skills.

Ability to work as part of a team.

Some flexibility as regards working hours/days.

Willingness and availability to travel on company business.

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Associate Director Manufacturing & Quality Technical Learning & Development Our client, a global pharma company, are currently recruiting for an Associate Director Manufacturing & Quality Technical Learning & Development to join their team on a permanent basis. AsAssociate Director for Technical Learning & Development, you will lead site-level learning strategies for Manufacturing, Quality, Health & Safety, and Central Functions. This role offers the opportunity to shape workforce development and learning in a cutting-edge, next-generation drug substance manufacturing facility. Responsibilities: Serve as the site lead for technical Learning & Development, aligning with global frameworks while addressing local needs Partner with senior leaders and the global Centre of Excellence to deliver future-focused learning solutions Design and implement site-specific site technical Learning initiatives that support compliance, manufacturing excellence, and employee development Ensure governance, compliance, and audit/inspection readiness at all times and proactively address training gaps and regulatory expectations Champion modern, technology-enabled learning (digital, interactive, experiential) Lead and develop the site L&D team, fostering innovation and continuous learning Design and implement training programs that strengthen compliance and workforce capability Collaborate cross-functionally with Operations, Quality, HR, and SMEs Use data and analytics to measure training impact and drive improvements Requirements: Bachelors degree minimum Minimum 5 years of experience in Learning & Development, Talent Development Manufacturing Training with a focus on regulated environments Strong knowledge of GMP and compliance training Proven leadership of L&D teams in a manufacturing or regulated setting Experience in governance, audit readiness, and inspection preparation Familiarity with modern learning methods (competency-based, digital, AI-driven) Strong stakeholder management and cross-functional collaboration skills Excellent communication, project management, and change management experience Ability to analyse data and provide strategic insights For more information please contact Sinéad Cullen on or

Associate Director Manufacturing & Quality Technical Learning & Development Our client, a global pharma company, are currently recruiting for an Associate Director Manufacturing & Quality Technical Learning & Development to join their team on a permanent basis.

As Associate Director for Technical Learning & Development, you will lead site-level learning strategies for Manufacturing, Quality, Health & Safety, and Central Functions.

This role offers the opportunity to shape workforce development and learning in a cutting-edge, next-generation drug substance manufacturing facility.

Responsibilities: Serve as the site lead for technical Learning & Development, aligning with global frameworks while addressing local needs Partner with senior leaders and the global Centre of Excellence to deliver future-focused learning solutions Design and implement site-specific site technical Learning initiatives that support compliance, manufacturing excellence, and employee development Ensure governance, compliance, and audit/inspection readiness at all times and proactively address training gaps and regulatory expectations Champion modern, technology-enabled learning (digital, interactive, experiential) Lead and develop the site L&D team, fostering innovation and continuous learning Design and implement training programs that strengthen compliance and workforce capability Collaborate cross-functionally with Operations, Quality, HR, and SMEs Use data and analytics to measure training impact and drive improvements Requirements: Bachelors degree minimum Minimum 5 years of experience in Learning & Development, Talent Development Manufacturing Training with a focus on regulated environments Strong knowledge of GMP and compliance training Proven leadership of L&D teams in a manufacturing or regulated setting Experience in governance, audit readiness, and inspection preparation Familiarity with modern learning methods (competency-based, digital, AI-driven) Strong stakeholder management and cross-functional collaboration skills Excellent communication, project management, and change management experience Ability to analyse data and provide strategic insights For more information please contact Sinéad Cullen on or

**Have you ever wanted to make a difference?**
At Abbott, you will play a crucial role to help people live more fully at all stages of their lives. Abbott is a global healthcare leader and our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritional products and branded generic medicines. Our 113,000 colleagues have a daily impact on the life of people in more than 160 countries.
**Abbott Ireland**
In Ireland, Abbott employs over 6,000 people across ten sites. We currently have six manufacturing facilities located in Clonmel, Cootehill, Donegal, Longford and Sligo and a third-party manufacturing management operation in Sligo. Abbott also has commercial, support operations and shared services in Dublin and Galway. We have been making a difference in the lives of Irish people since 1946.
**Vascular Division Clonmel**
Abbott Vascular is one of the world's leading vascular care businesses. Abbott Vascular is uniquely focused on advancing the treatment of vascular disease and improving patient care by combining the latest medical device innovations with world-class pharmaceuticals, investing in research and development, and advancing medicine through training and education. Our broad line of vascular devices-which includes vessel closure, endovascular and coronary technologies-are used to treat vessel diseases of the heart, carotid arteries, and peripheral blood vessels. These vessel diseases can lead to heart attack, stroke, critical limb ischemia, and other serious vascular conditions.
**We are currently looking for Manufacturing Engineers and Quality Engineers to join our modern site in Clonmel.**
**This is how you will make a difference:**
As a Manufacturing Engineer, you will be responsible for engineering support of manufacturing operations, which will involve key engineering metric management and process optimization activities including Manufacturing Yield improvement, product quality monitoring, lean manufacturing design and material/equipment/process troubleshooting using continuous improvement tools and methodology. Working as part of the operations support team, the manufacturing engineer will liaise with operations, quality, R&D and materials & purchasing departments to ensure quality and efficient manufacturing operations.
**Main responsibilities**
+ Initiates and completes technical activities leading to new or improved products or process, for current programs, next generation programs and to meet strategic goals and objectives of the company.
+ Prepares reports, publishes, and makes presentations to communicate findings.
+ Analyses and solves problems from basic engineering principles, theories and concepts through to a wide range of complex and advanced problems which require novel and new innovative approaches or a major breakthrough in technology.
+ Understands engineering principles theories, concepts, practices and techniques.
+ Understands the business needs of the company, and has knowledge of the customer needs of our business.
+ Understands the business cycle and foresight of emerging technologies trends.
+ Cultivates internal and external network of resources to complete tasks. Serves as a resource in the selection orientation and training of new engineers and employees.
+ May lead a project team, determining goals and objectives for the projects.
+ Mentors employees by sharing technical expertise and providing feedback and guidance.
+ Interacts cross functionally and with internal and external customers.
+ Serves as a consultant for engineering or scientific interpretations and advice on significant matters.
+ Acts as a spokesperson to customers on business unit current and future capabilities.
+ Participates in validation activity. Role may vary between providing input to owning activities such as protocol/report writing and managing execution of validation activities.
**Experience, Education and Skills Required - Manufacturing Engineer:**
+ National Framework of Qualifications (NFQ) level 7 qualification in a relevant discipline.2+ years of related work experience, or an equivalent combination of education and work experience.
+ Basic technical knowledge of concepts, practices and procedures. Limited understanding of business unit/group function.
+ Learns to use professional concepts and company policies and procedures to solve routine problems.
+ Developing a network of internal resources to facilitate completion of tasks.
**JOB DESCRIPTION:**
**About Abbott**
Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 109,000 colleagues serve people in more than 160 countries.
**Abbott Ireland Vascular Division Clonmel**
Abbott Vascular is one of the world's leading vascular care businesses. Abbott Vascular is uniquely focused on advancing the treatment of vascular disease and improving patient care by combining the latest medical device innovations with world-class pharmaceuticals, investing in research and development and advancing medicine through training and education.
Our broad line of vascular devices-which includes vessel closure, endovascular and coronary technologies-are used to treat vessel diseases of the heart, carotid arteries and peripheral blood vessels. These vessel diseases can lead to heart attack, stroke, critical limb ischemia and other serious vascular conditions.
**Purpose Statement:**
Provide Process/Quality Engineering support to manufacturing, helping to ensure delivery of highest quality product to the customer. Provide Process/Quality Engineering support to product development teams, helping to ensure development of highest quality new products.
Shift Role: 2-cycle shift (8-16:30 and 16:30-00:30)
**Key Responsibilities - Quality Engineer:**
1. Identifies manufacturing process defects (scrap, non-conforming material, customer complaints) by dispositioning non-conforming material, identifying primary root causes and suggesting corrective and preventative actions. May be responsible for querying and bounding data to support implementation of basic product stops.
2. Assists in development of product quality plans, documents and systems by providing input to product specifications, quality specifications, quality plans, risk analyses, Failure Mode Effect Analysis (FMEA) in conjunction with other product development team members. May be responsible for providing input to risk analyses and Failure Mode Effect Analysis' (FMEAs).
3. Becomes skilled at using process monitoring systems by starting to identify critical process steps and applying basic methods to reduce process variation to reduce/eliminate the cause of defects.
4. Assists product/process improvement efforts (example, scrap, nonconforming product, customer complaints) by systematically gathering quality metric data based on previous program templates and by assisting in the appropriate analysis methods to enhance sustaining product design and new product development.
5. Becomes skilled at using quality tools and training materials by working with existing quality tools and training materials and by understanding evolution/history of tools in use.
6. Participates in validation activity. Role may vary between providing input to owning activities such as protocol/report writing and managing execution of validation activities.
7. Participates in corrective and preventive action activity.
8. Participates in Field Discrepancy Notification (FDN) investigations.
**Education & Job Skills - Quality Engineer**
+ (Education/ Experience) National Framework of Qualifications (NFQ) level 7 qualification in a relevant discipline. 2+ years of related work experience, or an equivalent combination of education and work experience.
+ (Technical/Business Knowledge (Job Skills)) Working technical knowledge and application of concepts, practices and procedures. General understanding of business unit/group function. Will perform this job in a quality system environment. Failure to adequately perform tasks can result in noncompliance with governmental regulations.
+ (Cognitive Skills) Works on problems of moderate scope where analysis of situations or data requires a review of identifiable factors. Exercises judgment within defined procedures and practices to determine appropriate action. Has a broad knowledge of technical alternatives and an understanding of their impact on the systems environment.
+ (Influence/Leadership) Cultivates a wide range of internal networks and begins to develop an extensive external network of resources to facilitate completion of tasks. May lead a project team of moderate scope. Provides guidance to less experienced staff. Acts as a mentor to lower level individual contributors. Influence exerted at peer level and occasionally at first levels of management.
+ (Planning/Organisation) Plans, organises, and prioritises own daily work routine to meet established schedule.
+ (Decision Making/Impact) Exercises authority and judgment within defined limits to determine appropriate action. Failure to achieve results or erroneous decisions or recommendations may cause delays in program schedules and may result in the allocation of additional resources.
+ (Supervision Provided) May provide limited work direction and guidance to exempt and/or skilled nonexempt levels of employees, may be asked to evaluate performance of and assist in career development planning for subordinates.
An Equal Opportunity Employer
Abbot welcomes and encourages diversity in our workforce.
We provide reasonable accommodation to qualified individuals with disabilities.
To request accommodation, please call or email

At Zimmer Biomet, we believe in pushing the boundaries of innovation and driving our mission forward. As a global medical technology leader for nearly 100 years, a patient's mobility is enhanced by a Zimmer Biomet product or technology every 8 seconds.
As a Zimmer Biomet team member, you will share in our commitment to providing mobility and renewed life to people around the world. To support our talent team, we focus on development opportunities, robust employee resource groups (ERGs), a flexible working environment, location specific competitive total rewards, wellness incentives and a culture of recognition and performance awards. We are committed to creating an environment where every team member feels included, respected, empowered and recognised.
**What You Can Expect**
The purpose of this position is to provide direct user support for Manufacturing systems, such as MES and Delmia. Duties include updating of functional specifications, software, data, workflows and trouble shooting. The person will act as a cross-functional, inter-business unit resource which ensures our automated quality processes are compliant with all applicable regulations. As such, the incumbent must be technically knowledgeable in multiple disciplines including information technology, quality, and GxP processes.
**How You'll Create Impact**
+ Facilitates and / or provides support for all application users, including training and trouble shooting.
+ Act as technical expert for system requirements and updates.
+ Ensure systems are available, globally 7x24. Includes troubleshooting and problem resolution.
+ Support activities for process and system improvements, focusing on compliant, yet lean initiatives.
+ Manage and confront issues as they arise.
+ Formulate cross-functional teams, gaining consensus of requirements and approach and global teams
+ Prepares and assures completion of required personnel training.
+ Proactively works to ensure automated systems related to quality systems meet or exceed all applicable regulations and standards.
+ Lead procedures and validation activities for any manufacturing software system tools
**What Makes You Stand Out**
+ Ideally possesses a broad business perspective, including understanding the processes used within the respective areas, project management and Zimmer business goals of cost, quality and customer satisfaction
+ Must work well with others and interact effectively with all levels, technical information, outside contacts and support personnel.
+ Must be creative in solving problems with new products to maintain scheduled completion dates.
+ Must possess an understanding of GxP regulations, state of the art validation techniques.
+ Must be able to develop, implement, and execute system protocols.
+ Requires an understanding of process, equipment, software, and infrastructure, with an emphasis on software.
+ Requires knowledge of Systems.
**Your Background**
+ Bachelor's degree in computer science or an appropriate engineering discipline
+ A minimum of one year of experience supporting applications is required
+ Familiarity with Good Manufacturing Practices and QSR/ISO standards required.
+ 5-7 years plus professional work experience required.
EOE/M/F/Vet/Disability

At Zimmer Biomet, we believe in pushing the boundaries of innovation and driving our mission forward. As a global medical technology leader for nearly 100 years, a patient's mobility is enhanced by a Zimmer Biomet product or technology every 8 seconds.
As a Zimmer Biomet team member, you will share in our commitment to providing mobility and renewed life to people around the world. To support our talent team, we focus on development opportunities, robust employee resource groups (ERGs), a flexible working environment, location specific competitive total rewards, wellness incentives and a culture of recognition and performance awards. We are committed to creating an environment where every team member feels included, respected, empowered and recognised.
**What You Can Expect**
The purpose of this position is to provide direct user support for Manufacturing systems, such as MES and Delmia. Duties include updating of functional specifications, software, data, workflows and trouble shooting. The person will act as a cross-functional, inter-business unit resource which ensures our automated quality processes are compliant with all applicable regulations. As such, the incumbent must be technically knowledgeable in multiple disciplines including information technology, quality, and GxP processes.
**How You'll Create Impact**
+ Facilitates and / or provides support for all application users, including training and trouble shooting.
+ Act as technical expert for system requirements and updates.
+ Ensure systems are available, globally 7x24. Includes troubleshooting and problem resolution.
+ Support activities for process and system improvements, focusing on compliant, yet lean initiatives.
+ Manage and confront issues as they arise.
+ Formulate cross-functional teams, gaining consensus of requirements and approach and global teams
+ Prepares and assures completion of required personnel training.
+ Proactively works to ensure automated systems related to quality systems meet or exceed all applicable regulations and standards.
+ Lead procedures and validation activities for any manufacturing software system tools
**What Makes You Stand Out**
+ Ideally possesses a broad business perspective, including understanding the processes used within the respective areas, project management and Zimmer business goals of cost, quality and customer satisfaction
+ Must work well with others and interact effectively with all levels, technical information, outside contacts and support personnel.
+ Must be creative in solving problems with new products to maintain scheduled completion dates.
+ Must possess an understanding of GxP regulations, state of the art validation techniques.
+ Must be able to develop, implement, and execute system protocols.
+ Requires an understanding of process, equipment, software, and infrastructure, with an emphasis on software.
+ Requires knowledge of Systems.
**Your Background**
+ Bachelor's degree in computer science or an appropriate engineering discipline
+ A minimum of one year of experience supporting applications is required
+ Familiarity with Good Manufacturing Practices and QSR/ISO standards required.
+ 5-7 years plus professional work experience required.
EOE/M/F/Vet/Disability

**Have you ever wanted to make a difference?**
At Abbott, you will play a crucial role to help people live more fully at all stages of their lives. Abbott is a global healthcare leader and our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritional products and branded generic medicines. Our 115,000 colleagues have a daily impact on the life of people in more than 160 countries.
**Abbott Ireland**
In Ireland, Abbott employs over 6,000 people across ten sites. We currently have six manufacturing facilities located in Clonmel, Cootehill, Donegal, Longford and Sligo and a third-party manufacturing management operation in Sligo. Abbott also has commercial, support operations and shared services in Dublin and Galway. We have been making a difference in the lives of Irish people since 1946.
**Vascular Division Clonmel**
Abbott Vascular is one of the world's leading vascular care businesses. Abbott Vascular Clonmel is uniquely focused on advancing the treatment of vascular disease and improving patient care by combining the latest medical device innovations with world-class pharmaceuticals, investing in research and development and advancing medicine through training and education. Our broad line of vascular devices Manufactured in Clonmel includes vessel closure, endovascular and coronary technologies-These devices are designed to treat heart attack, stroke, critical limb ischemia and other serious vascular conditions.
Abbott Vascular Clonmel is the largest Abbott Manufacturing facility in Ireland focusing on both manufacturing and research and development of next generation vascular products.
**We are currently on the look out for both Manufacturing Technicians and Quality Technicians.**
**As the Quality Technician, you will:**
+ Assist engineering in providing manufacturing support by reviewing and analysing data to determine manufacturing issues and trends. You may also train operators on processes and engineering changes, and perform operator certification on-the-job training and testing.
+ Resolve and prevent manufacturing issues by assisting engineering in determining root cause and implementing corrective and preventative action.
+ Review and disposition non-conforming material by utilising quality tools and by developing knowledge of manufacturing practices and procedures.
+ Develop and implements process improvements by assisting engineering in researching and validating changes in processes/equipment and test methods to improve yield and/or reduce cycle time per established procedures.
+ Support process development during new product introduction by defining traceability and inspection requirements, developing statistical process control criteria, developing manufacturing instructions, and creating training sheets and certifications.
+ Provide input to engineering, qualification, and validation studies and reports by collecting, compiling, measuring, organising and recording data, and by writing procedures. May keep lab notebook.
**EDUCATION & COMPETENCIES - QUALITY TECHNICIAN:**
+ (Education/ Experience) National Framework of Qualifications level 6 qualification in a relevant discipline and 4+ years of related work experience or an equivalent combination of education and work experience.
+ (Technical/Business Knowledge (Job Skills)) Applies extensive knowledge of advanced technical concepts and practices, and a complete understanding of product or systems fundamentals in a functional area, and working knowledge of other related disciplines. Utilises/interprets advanced numerical and statistical data and computer software programs to present documentation and analysis and resolve complex problems. Will perform this job in a quality system environment. Failure to adequately perform tasks can result in noncompliance with governmental regulations.
+ (Cognitive Skills) Performs complex technical assignments usually without established procedures. Assists in the design, development, evaluation or modification of all area-specific equipment, materials, systems, and/or product. May determine types of tests or develop preventative maintenance plans. Assignments require considerable judgment, initiative, creativity and leadership in troubleshooting, suggesting alternatives, and making recommendations for continuous quality improvement methods.
+ (Influence/Leadership) Mentor less senior employees in work group and offer counsel. Leads cross functional teams to resolve technical issues as required. Establishes effective channels of communication cross shift, site and functional groups.
+ (Planning/Organisation) Plans and organises non-routine tasks with approval. Initiates or maintains work schedule. Establishes priorities of work assignments.
+ (Decision Making/Impact) Solves a wide range of complex problems requiring advanced interpretation of generally defined procedures and practices. Selects methods and practices to obtain imaginative, thorough, and practical solutions to questions. Understands organisational structure and positions of key employees. Maintains general knowledge of products/services associated with the company and employees involved with specific product lines and services. Maintains confidentiality in handling sensitive information or documents.
+ (Communication) Regularly presents findings to cross-functional teams and begins to win support for ideas. Can adequately write procedures and product disposition documentation that may be presented to external auditing bodies.
+ (Supervision Received) Limited supervision. Receives no instruction on routine work and general instruction on new lines of work or special assignments.
**As the Manufacturing Technician, you will:**
+ Observe and comply with all safety rules and regulations. This includes Quality Systems Registrars (QSR) and International Organisation for Standardisation (ISO) Standards.
+ Identify and implement corrective actions for manufacturing related issues.
+ Performs equipment setup and corrective, preventive and calibration maintenance as necessary.
+ Install and validate equipment and processes in the production area to improve yield and/or reduce cycle time following the established validation procedure.
+ Evaluate operating data to conduct on-line adjustments to products, instruments, or equipment. May develop or revise documents and procedures.
+ Certify manufacturing associates in the production processes.
+ Evaluate and order necessary equipment, tools and fixtures.
**EDUCATION & COMPETENCIES - MANUFACTURING TECHNICIAN:**
+ (Experience/Education) National Framework of Qualifications (NFQ) level 6 qualification in a relevant discipline. Relevant work experience advantageous but not essential or an equivalent combination of education and work experience.
+ (Technical/Business Knowledge (Job Skills)) Applies limited knowledge of basic technical concepts and practices and a basic understanding of product or systems fundamentals. Utilises basic knowledge of numerical and/or statistical data and computer software programs to resolve routine problems. Will perform this job in a quality system environment. Failure to adequately perform tasks can result in noncompliance with governmental regulations.
+ (Cognitive Skills) Performs routine technical tasks working from detailed written or verbal instructions. Performs routine set-up, testing, repair, inspection, and/or maintenance of certain area-specific equipment, materials, systems, and/or product. Assignments require limited judgment in troubleshooting proven processes.
+ (Planning/Organisation) Completes daily work to meet established schedule with guidance from supervisor on prioritisation of tasks.
+ (Decision Making/Impact) Solves problems of limited scope and complexity requiring basic interpretation of well-defined procedures and practices. Maintains confidentiality in handling sensitive information or documents.
An Equal Opportunity Employer
Abbot welcomes and encourages diversity in our workforce.
We provide reasonable accommodation to qualified individuals with disabilities.
To request accommodation, please call or email

Job Description Our client in Galway require experienced Manufacturing Engineers to support an upcoming project. This role will focus on manufacturing process validation, quality system updates, and documentation remediation. You will be based onsite and work directly with manufacturing and quality process owners to identify compliance gaps, implement corrective actions, and ensure documentation is accurate and audit-ready. Key ResponsibilitiesAnalyse process, product, material or equipment specifications and performance requirementsUnder broad supervision / guidance compile and analyse operational, test and experimental data to establish performance standards for newly implemented or modified products / processesSummarise, analyse and draw conclusions from test results leading to effective technical resolutionTroubleshoot new products / process working closely with product developmentContinually seek to drive / improvements in process design, layout and operational performanceDemonstrate good working knowledge and application of validation techniques and associated regulatory requirementsActively promotes and participates in a cross -functional teamwork environmentEvaluates in conjunction with EHS new equipment/processes/chemicals for environmental impact/effect to eliminate or lessen such impacts/effectsUnderstands and comply with all the regulations governing the quality systems Key RequirementsEngineering or Quality degree with 2-3 years' relevant industry experienceBackground in remediation, process validation, CAPA, NCRs.Strong technical writing and documentation skills.Knowledge of 21 CFR Part 820, ISO 13485. BenefitsCompetitive and attractive employee compensation packagePension contributionsHealth insurancePaid public holidays Location: Galway, Ireland | onsite

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 Assurance Student_**
Working with the Quality team to help maintain quality standards throughout the company. The brief requires knowledge of Good Manufacturing Practice, current FDA and EMEA regulations for solid oral dosage pharmaceuticals for human use and a good working knowledge of manufacturing processes and packaging processes used in the pharmaceutical industry in Bray.
**_How you will contribute_** **_:_**
+ To assist in the investigation into non-conformances, participate in root cause analysis and carry out quality review of non-conformances.
+ To assist in preparation of communication to external partners
+ Preparation and revision of cGMP documentation as required including;
+ Annual Product Reviews
+ Standard Operating Procedures
+ GMP forms
+ Product specification
+ Technical Reports and Protocols
+ Preparation of Certificate of Analysis
+ Support the site Quality Management systems including;
+ Non-Conformance and CAPA Management systems
+ Change Control system
+ Internal Auditing programs
+ GMP Training
+ Customer Complaints
+ Vendor Management program.
+ Participate in and facilitate continuous improvement projects as required
+ Control/storage of retain samples, including periodic retain inspection
+ Archiving GMP documents
In this position you will report to the **Quality Executive** **.**
**_What you bring to Takeda_** **:**
+ Participate fully in any cross functional training initiatives.
+ Drive and promote the corporate values of Takeda-ism within the workplace.
+ Participate in driving Quality Culture within workplace.
+ Actively foster, in cooperation with other TIL staff, an ethos and culture of safety awareness where safety is accepted as an integral part of the overall business.
+ Excellent verbal and written communication skills.
+ Be self-motivated, flexible, organized and a good team player with the ability to prioritize own work based on departmental and site requirements.
+ Experience in the pharmaceutical industry would be preferable but is not essential
**_What Takeda can offer you:_**
+ Flexible working arrangements
+ 26 vacation days plus additional days for service milestones
+ Employee Assistance Program
+ Wellbeing and engagement teams
+ Development opportunities
+ 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 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**
Paid Intern (Fixed Term) (Trainee)
**Time Type**
Full time