Find Patient safety manager Jobs in Dublin, D

Senior Manager, Process Validation
West Pharmaceutical Services —Dublin, County Dublin
- €100,900–€130,200 a year
- Computer Science
- No degree
- Manufacturing
Clinical Development Director - Renal
Novartis —Dublin, County Dublin
- €90,300–€167,700 a year
- Full-time
- Doctoral degree
- Writing skills
- No degree
Manager Procurement Technology & Program
West Pharmaceutical Services —Dublin, County Dublin
- €80,960–€103,040 a year
- Microsoft Powerpoint
- Microsoft Excel
- Project management
1d
GMDP Quality Assurance Manager
WEP Clinical —Dublin, County Dublin
- Full-time
- Hybrid work
- Microsoft Word
- Microsoft Excel
- Microsoft Outlook
Clinical Trials Manager (12-month contract)
Zymeworks Inc. —Swords, County Dublin
- Full-time
- Hybrid work
- Bachelor's degree
- Organisational skills
- Communication skills
- Annual leave
Quick apply
Manufacturing Process Technician
Amgen —Dún Laoghaire, County Dublin
- €39,477.40–€53,410.60 a year
- English
- Leaving certificate
- No degree
14d
EHS Associate Manager
Viatris —Northern Cross, County Dublin
- Full-time
- Engineering
- Bachelor's degree
- Communication skills
Finance Operations Manager
Mater Private Network —Dublin, County Dublin
- Full-time
- Microsoft Excel
- Microsoft Office
- Analysis skills
Quick apply
7d
Bioprocess Technician
Amgen —Dún Laoghaire, County Dublin
- €39,477.40–€53,410.60 a year
- Leaving certificate
- No degree
- Manufacturing
Haemovigilance Officer
Beacon Hospital —Dublin, County Dublin
- Full-time
- Microsoft Powerpoint
- Microsoft Excel
- IT
Quick apply
Creative Account Manager
Perigord Premedia Limited —Blanchardstown, County Dublin
- From €60,000 a year
- Full-time
- Hybrid work
- Project management
- No degree
- Organisational skills
- Employee assistance program
Quick apply
Director, Combination Product Development
Viatris —Northern Cross, County Dublin
- Full-time
- Engineering
- Organisational skills
- Leadership
Quality Engineer (NPI)
West Pharmaceutical Services —Dublin, County Dublin
- €51,000–€59,000 a year
- Engineering
- Manufacturing
- Communication skills
Senior Accountant, GFS
West Pharmaceutical Services —Dublin, County Dublin
- €63,100–€80,200 a year
- ERP systems
- Microsoft Office
- Finance
CSSD Technician
Blackrock Health Blackrock Clinic —Blackrock, County Dublin
- Full-time
- Clinic
- Operating room
- Communication skills
- Annual leave
- Employee assistance program
Quick apply
Interim Chief Operations Officer/Príomhoifigeach Oibríochtaí Eatramhach
Incorporated Orthopaedic Hospital Of Ireland —Dublin, County Dublin
- Full-time
- No degree
- Rehabilitation centre
- Leadership
7d
Customer Service Supervisor
Air Liquide —Dublin, County Dublin
- Full-time
- Customer service
- Analysis skills
- In-person
- Annual leave
- Employee assistance program
Facilities and Sustainability Manger
United Drug —Citywest, County Dublin
- Full-time
- Project management
- Bachelor's degree
- Communication skills
- Employee assistance program
- Employee discount
Quick apply
Technical Product Manager - (Clinical Integrations) - Ireland
Heidi —Dublin, County Dublin
- Full-time
- Hybrid work
- Master's degree
- Bachelor's degree
- EMR systems
- Work from home
Senior Art Therapist
St Patrick's Hospital —Dublin, County Dublin
- €65,200–€76,770 a year
- Part-time
- Hybrid work
- Microsoft Word
- Microsoft Excel
- Microsoft Outlook
- Annual leave
4d

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Senior Manager, Process Validation

West Pharmaceutical Services -
Dublin, County Dublin

Apply Now

Job details

€100,900–€130,200 a year

Qualifications

Computer Science
Lean
Manufacturing
Communication skills
ISO 13485

Full job description

Requisition ID: 73131
Date: Jun 22, 2026

Location:
Dublin, IRL, IE Dublin, L, IE

#job-location.job-location-inline { display: inline; }
Department: Engineering

Description:
At West, we’re a dedicated team that is connected by a purpose to improve patient lives that has been at the center of our Company for more than a century. Our story began when Herman O. West solved the problem of supplying penicillin in mass quantities to the US Government during World War 2. Through our work to deliver thousands of life-saving and life-enhancing injectable medicines to millions of patients daily, West’s indelible mark on the healthcare industry has just begun. A name started our story. How will yours help write our future?

There’s no better place to join an inclusive community of professionals with opportunities for lifelong learning, growth and development. Supported by benefit programs, we empower the physical, mental, emotional and financial health of our team members and their families.

We believe in giving back to help those in need in the communities where we live and work. And are equally committed to creating a healthier environment and planet through our sustainability efforts.

Job Summary

Reporting to the Director of Global Validation and Metrology Services, this role is responsible for contributing to the development and implementation of the validation engineering strategy for West Global Technical Operations whilst ensuring the qualification and validation of equipment, facilities, utilities, automated systems, processes and process cleaning procedures are carried out in accordance to GMP and relevant guidelines. This role will direct the application of resources within and across its functional responsibility to assist global sites in improving the manufacturing of products and develop the most optimum processes and solutions which meet or exceed West and/or customer requirements.

Essential Duties and Responsibilities
Provide technical leadership and direction to a globally dispersed Validation Engineering team with responsibility for defining strategy, planning and execution of Validation activities within the Global Technical Operations network.
Provide strategic leadership of long-term and intermediate goals the Global Technical Operations Network.
Direct resources from functional responsibility for Validation in support of programs within the Global Technical Operations Network.
Participate in the harmonization and implementation of Validation standards and procedures across the Global Technical Operations network based on current regulations, industry standards and industry practices.
Drive innovative and efficient approaches to validation incorporating science and risk-based approach.
Oversee the preparation, review, and approval of Site Validation Master Plans.
Review and or approval of qualification and/or validation documentation (specifications, protocols, reports etc.) in relation to instrument, equipment, facilities, utilities, automated systems, manufacturing processes and cleaning processes including FAT, SAT, IQ, OQ, PQ phases in conjunction with program Quality representation.
Oversight of third party generated protocols and reports in conjunction with program Quality representation.
Fosters and encourages shared learning’s across the organisation e.g. system and technology best practices.
Chair, schedule and minute validation meetings and participate in meetings when required.
Perform periodic reviews of systems in order to maintain validation status.
Support the set-up and maintenance of electronic validation documentation while ensuring the archiving and
filing of hard copy validation documentation across all programs is compliant with site policies.
Oversee the implementation of site validation strategies to meet customer and West needs.
Work with all departments across the business to ensure that new processes meet their requirements.
Play a key part in Global Technical Operations transfer programs to ensure flawless transition into Operations.
Represent West at customer meetings to ensure that the needs of the business are met.
Assist with the training and development of personnel at all levels of West on new processes or systems introduced to the company.
Ensure that the procedures and systems are in place to facilitate the introduction of new processes and equipment.
Lead and manage a high performing team to deliver the defined business goals & objectives.
Perform additional duties at the request of the direct supervisor.
Education
Must have a third level qualification, at a minimum to degree level, in Computer Science, Engineering or related fields.
Work Experience
Must have 10 years of validation engineer experience in a cGMP regulated industry.
Must have a minimum of 10 years post graduate experience of working in a high-volume manufacturing environment ideally in the Medical Device / Pharmaceutical sector.
Preferred Knowledge, Skills and Abilities
Must have in-depth / working knowledge of: ISO 13485; EU GMP, CFR Part 820.
An excellent understanding of plastic process manufacturing, computer validation, analytical methods and testing and documentation systems is desired.
Must have dealt with customers in a previous employment.
Must have excellent written and verbal communication skills as well as the ability to accurately document work performed.
Demonstrated ability to lead, influence and train others.
Must be able to work in a fast paced environment.
Must be able to travel as required by the position.
Must be able to organize and prioritize tasks; must be detail orientated and self-motivated.
An ability to collaborate across functional teams and work effectively in a matrixed team environment.
Must be able to work independently on own projects while working concurrently with all departments.
Previous people management experience required.
Support and contribute in Lean Sigma programs and activities towards delivery of the set target
Able to comply with the company’s safety policy at all times
Able to comply with the company’s quality policy at all times.
Travel Requirements
5%: Up to 13 business days per year

Pay Transparency:
The annual base salary range for this position is €100,900.00 - €130,200.00. Total target compensation is determined using objective and gender-neutral criteria, including relevant experience, qualifications, skills, market benchmarks, geographic location, and the scope and responsibilities of the role.

This position may be eligible for variable compensation and other incentive programs in accordance with the terms of the applicable plans within the country of employment. In addition, team members are eligible to participate in the company’s benefits and total rewards programs applicable to their location and employment status. #LI-Hybrid #LI-BC

West is an equal opportunity employer and we value diversity at our company. We do not discriminate on the basis of race, religion, color, national origin, gender, sex, gender identity, sexual orientation, age, marital status, veteran status, or disability status. If you have a special need that requires accommodation in order to apply to West, please send an email to [email protected]. Where permitted by law, an offer of employment with West Pharmaceutical Services, or any of its subsidiary or affiliate companies, is contingent upon the satisfactory completion of background screening.

Apply Now

Refine Your Search

patient safety manager jobs in dublin, d

Senior Manager, Process Validation

Clinical Development Director - Renal

Manager Procurement Technology & Program

GMDP Quality Assurance Manager

Clinical Trials Manager (12-month contract)

Manufacturing Process Technician

EHS Associate Manager

Finance Operations Manager

Bioprocess Technician

Haemovigilance Officer

Creative Account Manager

Director, Combination Product Development

Quality Engineer (NPI)

Senior Accountant, GFS

CSSD Technician

Interim Chief Operations Officer/Príomhoifigeach Oibríochtaí Eatramhach

Customer Service Supervisor

Facilities and Sustainability Manger

Technical Product Manager - (Clinical Integrations) - Ireland

Senior Art Therapist

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