
Senior Validation Specialist
7 days ago
We are seeking a skilled Commissioning, Qualification and Validation (CQV) engineer to join our team. As a CQV engineer, you will play a critical role in ensuring the safety and efficiency of our operations.
Job Responsibilities:- Lead and conduct CQV activities with a focus on safety.
- Manage the C&Q documentation and execution lifecycle from SLIA generation through to OQ completion.
- Create C&Q procedures for projects.
- Approve Test Operating Procedures (TOPs).
- Foster collaboration with stakeholders to plan commissioning spares and consumables.
- Deliver CQV activities as required to meet project schedules.
- Track progress of CQV activities as needed.
- Prepare comprehensive Qualification Summary Reports (QSR), and manage Requirement Traceability Matrix (RTM)
- Execute design reviews, shakedown, commissioning, FAT's, IQ, OQ, PQ activities.
- Oversee aspects of C & Q, verification as requested i.e., Change Controls, Management of Contractors and Vendors, document control, punch list management.
- Collaborate with project contractors and equipment vendors to execute required tests.
- Allocate project resources efficiently to deliver project objectives.
- Bachelor's or Master's degree in a relevant science or engineering field.
- At least 3 years of experience in CQV roles, preferably in life sciences Clean Utilities/Filling.
- Excellent communication and problem-solving skills.
- A customer-focused approach.
- Proficiency in life science manufacturing processes.
- Ability to travel domestically and internationally if required.
This is an exciting opportunity to work in a dynamic and growing industry. We offer a collaborative and inclusive work environment, with opportunities for professional growth and development.
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Isolator Validation Engineer
3 weeks ago
The Municipal District of Carlow, Ireland QCS Staffing Full timeIsolator Validation Engineer - Ireland, Carlow - 11 Month ContractEssential Duties and Responsibilities for this role include, but are not limited to, the following:Design/Author/Review/Approve/Execute qualification/validation documentation and cycle development studies in line with the standard approval process.Design/Author/Review/Approve/Execute...
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CQV/Validation Engineer
7 days ago
The Municipal District of Carlow, Ireland CAI Full timeAbout CAICAI is a 100% employee-owned company established in 1996, that has grown year over year to nearly 700 people worldwide. We provide commissioning, qualification, validation, start-up, project management and consulting services related to operational readiness to FDA regulated and other mission critical industries.About CAICAI is a 100% employee-owned...
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Pharmaceutical Validation Specialist
1 week ago
Carlow, Ireland beBeeValidation Full time €85,000 - €110,000Job Opportunity:We are recruiting for a position with a multinational organization.This is an excellent opportunity to join a company renowned for its excellence in the industry.Duties and Responsibilities:Develop and qualify cleaning cycles, execute equipment qualification.Coordinate validation strategies, write protocols, submit samples, analyze test...
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Cleaning Validation Specialist
1 week ago
Carlow, Ireland Scientificjobs Full timeWe're currently recruiting for an exciting opportunity with a Pharmaceutical organization based in Carlow. This is an excellent position for anyone who is looking to join a leading multinational who are one of the best at what they do. DutiesExecute cleaning cycle development and PQ of equipment.Writing and adhering to validation strategies, coordinating...
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Cleaning Validation Specialist
3 days ago
Carlow, Ireland Scientificjobs Full timeWe’re currently recruiting for an exciting opportunity with a Pharmaceutical organization based in Carlow. This is an excellent position for anyone who is looking to join a leading multinational who are one of the best at what they do. Duties Execute cleaning cycle development and PQ of equipment.Writing and adhering to validation strategies, coordinating...
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Senior Validation Specialist
2 weeks ago
Carlow, Ireland beBeeValidation Full time €60,000 - €90,000Valuation Engineer PositionThis is an excellent opportunity to join a leading multinational in the Biopharmaceutical industry based in Carlow.Design, author, review, approve and execute qualification/validation documentation and cycle development studies in line with the standard approval process.Develop and execute change controls to ensure compliance and...
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Validation Professional
1 week ago
Carlow, Ireland beBeePharmaceutical Full time €60,000 - €80,000We're recruiting for an exciting opportunity in the pharmaceutical industry.About the RoleDevelop and execute cleaning cycle development and process qualification of equipment to ensure compliance with regulatory guidelines.Write and adhere to validation strategies, coordinating with vendors, writing protocols independently, submitting samples, analyzing...
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Expert Process Validation Specialist
6 days ago
Carlow, Ireland beBeeTechnical Full time €70,000 - €85,000Are you looking for a challenging opportunity in process engineering?Senior Technical Transfer EngineerWe are seeking an experienced Senior Technical Transfer Engineer to lead and execute process engineering and validation activities.This includes managing multiple technical projects, improving processes, capital projects, and Lean projects across...
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Senior Validation Specialist
2 weeks ago
Castlebar Municipal District, Ireland beBeevalidation Full time €80,000 - €120,000We are currently recruiting for a Validation Engineer to join our client's state-of-the-art biopharmaceutical facility. This is an excellent opportunity to work with cutting-edge technology and be part of a team that is dedicated to delivering high-quality products.
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Validation Expert Wanted
7 days ago
Carlow, Ireland beBeePharmaceutical Full time €60,000 - €80,000Validation Expert SoughtWe are seeking a skilled Validation Expert to join our team in the Pharmaceutical industry.Duties and ResponsibilitiesClean equipment and execute periodic reviews, cleaning periodic review, CAPAs, deviations, change control, risk assessments.Coordinate with vendors, write protocols independently, submit samples, analyse test results,...