(Only 24h Left) Validation Engineer
4 weeks ago
Select how often (in days) to receive an alert: Create Alert
Would you like to join an international team working to improve the future of healthcare? Do you want to enhance the lives of millions of people? Grifols is a global healthcare company that since 1909 has been working to improve the health and well-being of people around the world. We are leaders in plasma-derived medicines and transfusion medicine and develop, produce and market innovative medicines, solutions and services in more than 110 countries and regions.
At Grifols, we believe that diversity adds value to our business, our teams, and our culture. We are committed to equal employment opportunities that foster an inclusive environment.
POSITION SUMMARY:
Write, review and execute Validation Plans, Protocols and Reports for Albumin Projects ensuring compliance to all relevant global and local quality and validation procedures /standard.
Initial requirements to focus on the areas Equipment Qualification, Temperature Mapping (steam sterilisation), Aseptic Process Validation, Cleaning Validation and Process Validation to follow.
Represent Validation at technical forum include external and internal audits.
KEY RESPONSIBILITIES
- Write, review and execute Validation Protocols and Reports for Equipment Qualification, Aseptic Process Validation, Cleaning Validation, Process Validation, Temperature Mapping (steam sterilisation) and Equipment Software Validation, ensuring compliance to all relevant global and local quality and validation procedures/standards
- Represent Validation at both internal and external audits by regulatory agencies, including HPRA and FDA.
- Generation and review of project documentation (User Requirement Specifications, validation protocols, reports etc.) and Standard Operating Procedures.
- Supporting validation activities including review of documentation and hands-on execution of validation activities (FAT, SAT, IQ, OQ, PQ etc) to ensure equipment meets current GMP requirements and industry standards.
- Development and execution of Process Validation protocols and reports (Cleaning Validation, APS, Process Validation and Continuous Process Verification).
- Demonstrates technical knowledge and ability to adapt to changing circumstances. Works with other departments Operations, Quality, and Maintenance) to execute qualification and validation efforts in support of site projects.
- Completion of risk assessments, closure of corrective and preventive actions (CAPA’s)
- Investigates and troubleshoots problems and determines solutions or recommendations for changes and/or improvements
- Performs other validation associated activities as defined by Manager or Director.
KEY COMPETENCIES
- Cleaning Validation.
- Process Validation
- Aseptic Process Validation
- Commissioning and Qualification
- Documentation (Writing SOPs, Protocols, Reports)
- Auditing
PERSON SPECIFICATION
- Qualifications
- Project Management Experience
- Hands-on knowledge of execution of Validation (Min 2 years)
- Experience in a Quality or Validation Role within Pharma sector
- Experience within aseptic manufacturing environment
- Familiarity with Annex 1 (Manufacture of Sterile Medicinal Products)
- Excellent Technical Writing and analytical skills.
- Familiarity with cGMPs and industry and federal guidelines required.
- Experience with Word, Excel and Access computer applications.
- Strong interpersonal skills for interactions with other departments.
- Degree in Science/Engineering and/or Min 2 years Validation experience
- Experience in representing client companies during internal (Corporate) audits and external (FDA and HPRA) audits
- Working knowledge of HTM 01 (Part C, Steam Sterilization) Autoclaves
- Familiarity with ISO-14644 (Cleanrooms and Associated Environments)
- Experience with Software validation for manufacturing
Our Benefits Include:
- Highly competitive salary
- Group pension scheme - Contribution rates up to 7%
- Private Medical Insurance for the employee
- Ongoing opportunities for career development in a rapidly expanding work environment
- Succession planning and internal promotions
- Wellness activities - Social activities eg. Golf, Padel, Summer Events
We understand that self-doubt can hold talented individuals back from applying for opportunities. We encourage everyone who meets the qualifications to apply – we're excited to hear from you.
#J-18808-Ljbffr
-
(Only 24h Left) DevOps Engineer
1 week ago
Dublin Pike, Ireland Cognitive Group | Part of the Focus Cloud Group Full timeOverview Cybersecurity & Cloud / Infrastructure Lead Europe @Cognitive (part of the Focus Cloud Group). DevOps Engineer, freelance, Spain or Ireland, 3-year project. Unique opportunity to join an human size international team that constantly innovates in its sector. You will play a leading role in supporting infrastructure, CI/CD pipelines, and cloud...
-
[Only 24h Left] Director, Operations
3 weeks ago
Dublin, Ireland SS&C Full timeDirector, Operations page is loaded## Director, Operationslocations: Dublin, Irelandtime type: Full timeposted on: Posted Todaytime left to apply: End Date: October 24, 2025 (13 days left to apply)job requisition id: R38070As a leading financial services and healthcare technology company based on revenue, SS&C is headquartered in Windsor,...
-
Only 24h Left: Commissionaire
4 weeks ago
Dublin, Ireland The Merrion Hotel Full timeThe Merrion, one of Dublin's finest luxury hotels, a member of the Leading Hotels of the World is recruiting for full time Commissionaire to join our professional and friendly Concierge Team . Centrally located in Dublin within easy reach of public transport, this role will offer you the opportunity to work in a beautiful hotel where the highest of standards...
-
Validation Engineer
3 weeks ago
Dublin, Ireland Ascend Project Management Full timeClient Services Manager | Life Science & EngineeringAscend PM are hiring a Validation Engineer to join our client team, a biopharmaceutical company based in Dublin.This is a great contract opportunity to join a growing team.Contact or email CV to to find out more.OverviewAn exciting opportunity has arisen for a Validation Engineer to support Tech Transfers/...
-
Dublin, Ireland CPL Full timeCompany Profile: Our long-standing client a leading medical device company are seeking an experienced Process Engineer to join their global device engineering team on an initial 12-month contract. The company possess a significant manufacturing and R&D presence that's been maintained via astute and robust capital investment. The site prides itself on being...
-
Dublin, Ireland Boeing Full timeMarketing and Sales Representative page is loaded## Marketing and Sales Representativelocations: IRL - Dublin, Irelandtime type: Full timeposted on: Posted Todaytime left to apply: End Date: November 6, 2025 (13 days left to apply)job requisition id: JR2025479877Marketing and Sales Representative**Company:**Boeing Ireland LimitedBoeing Global...
-
Validation Engineer
4 weeks ago
Dublin, Ireland Impact Iel Full timeImpact Engineering Ltd is a trusted automation partner based in Dublin, focusing on business transformation, digitalisation, automation projects, and targeted automation training.We offer a range of services including consultancy, system upgrades, process optimization, and automation front line support.Our mission is to deliver innovative, cost-competitive,...
-
Validation Engineer
4 weeks ago
Dublin, Ireland Quanta Consultancy Services Ltd Full timeValidation Engineer- Dublin, Ireland - 12 Months Contract Our client, a globally recognised pioneer in Biotechnology, are recruiting for the position of Validation Engineer. 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...
-
Test Technician
1 week ago
Dublin, Ireland Link Personnel Services Full timeOur Client, a large medical device company based in North County Dublin, requires a Test Technician for a 23 Month Contract. The Salary for the role is €42k + Benefits. This is a DAY SHIFT role, but some night shift work may be required during the contract (shift allowance will apply). OVERTIME is available. There is a possibility for permanency...
-
15h Left: Validation Specialist
1 week ago
Dublin, Ireland Noel Group Full timeRole: Validation Specialist Reporting to: Engineering and Facilities Manager Location: Dublin 15 Employment Type: Full Time Industry: Logistics and Supply Chain About Us: Noel Group are partnered with a unique supply chain management company with a strong service portfolio within the areas of Transportation, Refrigeration, Storage and Value-Added Services....