Find Commissioning qualification validation Jobs in Cork, C

QA Validation Associate
PSC Biotech —Cork, County Cork
- Full-time
- Bachelor's degree
- No degree
- Typing
Sr QA Validation Associate
PSC Biotech —Cork, County Cork
- Bachelor's degree
- No degree
- Typing
Commissioning Maintenance Technician
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- Full-time
- Microsoft Powerpoint
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- Employee assistance program
Quick apply
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Lab IT Desktop Support Engineer
Catalyx —Cork, County Cork
- Full-time
- Organisational skills
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Cognizant —Cork, County Cork
- Full-time
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- Bachelor's degree
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R&D Technician
Alcon —Cork, County Cork
- Full-time
- Engineering
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4d
Installation & Commissioning Engineer
Catalyx —Cork, County Cork
- Full-time
- Hybrid work
- AutoCAD
- CAD
- Engineering
Quick apply
21h
2024 Graduate Architectural Technologist – Cork
DPS Group —Cork, County Cork
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CQV Engineers - Senior / Lead / Managers- Opportunities 2026
PM Group —Cork, County Cork
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Building Services Engineer
Controlled environment solutions —Cork, County Cork
- Full-time
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Foxboro I/A System Administration Engineer
PACIV —Cork, County Cork
- Full-time
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Project Manager
IPS-Integrated Project Services —Cork, County Cork
- Full-time
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10d
Electrician / BMS Engineer
Sygma Automation —Cork, County Cork
- Full-time
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DELTAV AUTOMATION ENGINEER
Réalta Technologies (RT) —Cork, County Cork
- Full-time
- Communication skills
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Construction Manager
IPS-Integrated Project Services —Cork, County Cork
- Engineering
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10d
MES Engineer (POMSnet)
NeoDyne —Cork, County Cork
- Overtime
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Senior Quantity Surveyor
IPS-Integrated Project Services —Cork, County Cork
- Full-time
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QA Validation Associate

PSC Biotech -
Cork, County Cork

Apply Now

Job details

Full-time

Qualifications

Bachelor's degree
Typing

Full job description

Job Information

Date Opened

05/29/2026

Job Type

Full time

Industry

Pharma/Biotech/Clinical Research

Work Experience

4-5 years

City

Cork city

State/Province

Cork

Country

Ireland

Job Description

About PSC Biotech

Who are we?

PSC Biotech is a leading Biotech Consultancy firm founded in 1996, headquartered in Pomona, California, USA, with Global operations in Ireland, India, Singapore, Australia and the US, serving 350 clients in more than 23 countries worldwide. We provide cloud-based software solutions for Quality Management and Regulatory Inspections, pharmaceuticals contract manufacturing professionals, and metrology services to our clients.

‘Take your Career to a new Level’

PSC Biotech disrupts the conventional consultancy model by aligning our EVP as one of the unique selling point which includes the opportunity to work with the most talented cohort of like-minded professionals operating in the Pharma/ Biotech Industry. We offer a permanent contract of employment giving exposure of working in Top Pharmaceutical client sites in a diverse-cultural work setting.

Employee Value Proposition

Employees are the “heartbeat” of PSC Biotech, we provide unparalleled empowering career development though Learning & Development in-house training mentorship through constant guidance to facilitate career progression. We believe in creating high performing teams that can exceed our client’s expectations with regards to quality of all scalable and business unit deliverables, staying under budget and ensuring timelines for our deliverables are being met.

the client are a high-performing, team based organization, where colleagues are flexible, multi-skilled and empowered to make decisions.

A high level of initiative, energy and motivation are key role requirements, as well as organizational skills.

This position is responsible for the quality oversight of validation activities in a GMP regulated environment, incorporating implementation, requalification and decommissioning of manufacturing processes, equipment, computer systems, laboratory systems and changes to existing equipment.

RESPONSIBILITIES

Provide quality oversight for validation activities related to products and facilities, utilities, equipment (FUE).
Support the development of validation plans for specific system implementation projects.
Supporting and reviewing/approving (project lifecycle documentation (URS, RA, Commissioning, Qualification Protocols)) validation activities related to the implementation of facilities, utilities, equipment changes while exercising judgment within broadly defined procedures and practices to establish approval criteria, and identify and implement solutions.
Support validation policies, through development, generation and implementation of validation master plans, guideline documents and SOP’s.
Maintain current knowledge of industry standards and regulatory requirements for products developed or manufactured by the client validation techniques/approaches and systems utilized
Lead and represent QA Validation in multi-departmental meetings & project teams.
Identifies and implements improvements to the QA Validation systems.
Participation in the change control program for modifications to qualified systems.
Quality oversight for the Revalidation Evaluation program.
Identify, track and resolve issues through robust root cause analysis in a timely manner working with relevant SMEs as required. Apply a risk management approach to identify, categorise, prioritise, mitigate and establish contingency plans associated with qualification / validation and system risks

Requirements

DUCATION

Bachelor of Sciences degree, or higher, in a technical discipline (physical, engineering, chemical or biological sciences) is required.

EXPERIENCE

+3 years’ experience in a cGMP regulated manufacturing environment, with knowledge of equipment and utility validation, and laboratory systems / validation.
Organizational and management skills to coordinate multi-discipline project groups
Ability to speak, present data, and defend approaches in front of audiences and inspectors.
Ability to comprehend technical information related to equipment, processes, and regulatory expectations.
Experience with participation in regulatory inspections presenting or defending departmental functions in audits or regulatory inspections.
Understanding and familiarity with FDA & European regulatory requirements, guidelines, and recommendations for equipment validation expectations.
Proficiency with technical summary report generation required, with exceptional organizational, spelling, grammar, and typing skills preferred.

#LI-KV1

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Refine Your Search

commissioning qualification validation jobs in cork, c

QA Validation Associate

Sr QA Validation Associate

Commissioning Maintenance Technician

Lab IT Desktop Support Engineer

CSV Automation Engineer

R&D Technician

Installation & Commissioning Engineer

2024 Graduate Architectural Technologist – Cork

CQV Engineers - Senior / Lead / Managers- Opportunities 2026

Building Services Engineer

Foxboro I/A System Administration Engineer

Project Manager

Electrician / BMS Engineer

DELTAV AUTOMATION ENGINEER

Construction Manager

MES Engineer (POMSnet)

Senior Quantity Surveyor

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