Find Master, data science & analytics Jobs in Midleton, C

QA Validation Associate
PSC Biotech —Cork, County Cork
- Full-time
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Sartorius —Cork, County Cork
- Full-time
- Doctoral degree
- Master's degree
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Forcepoint International Technology Limited —Cork, County Cork
- Full-time
- Master's degree
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OTC Analyst - FTC 6 months
Grant Thornton —Cork, County Cork
- Full-time
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AP Analyst - FTC 18 months
Grant Thornton —Cork, County Cork
- Full-time
- Microsoft Powerpoint
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Dell Technologies —Cork, County Cork
- Full-time
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Qumulo —Cork, County Cork
- Full-time
- Hybrid work
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DIGITAL ENGINEER
Réalta Technologies (RT) —Cork, County Cork
- Full-time
- Computer Science
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IT Manager
Citco —Cork, County Cork
- Full-time
- Doctoral degree
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Auto QA Engineer
Xanadu —Cork, County Cork
- Computer Science
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Chief Medical Scientist (Biochemistry)
Mater Private Network —Cork, County Cork
- Full-time
- Master's degree
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Quick apply
German-Speaking Senior Engineer, Technical Support– PowerMax Support
Dell Technologies —Cork, County Cork
- Full-time
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Global Travel, Expense & Card Programs – Senior Specialist
Gilead Sciences —Cork, County Cork
- Full-time
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4d
IT Project Manager
G MASS —Cork, County Cork
- Hybrid work
- Computer Science
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Lead AI Developer
OpenText —Cork, County Cork
- On call
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Business Process Re-engineer
Apple —Cork, County Cork
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2d
Financial Specialist II
Gilead Sciences —Cork, County Cork
- Full-time
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Recurring Revenue Management IT Product Owner
Logitech —Cork, County Cork
- Full-time
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Qualified Person
Hovione —Cork, County Cork
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Senior Data Engineer
Datavant Ireland —Cork, County Cork
- Remote
- Azure
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11d

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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

master, data science & analytics jobs in midleton, c

QA Validation Associate

Field Application Specialist - Fluid Management Technologies

UX Product Designer

OTC Analyst - FTC 6 months

AP Analyst - FTC 18 months

German-Speaking Principal Engineer, Technical Support– PowerMax Support

Senior Data Engineer (Cork)

DIGITAL ENGINEER

IT Manager

Auto QA Engineer

Chief Medical Scientist (Biochemistry)

German-Speaking Senior Engineer, Technical Support– PowerMax Support

Global Travel, Expense & Card Programs – Senior Specialist

IT Project Manager

Lead AI Developer

Business Process Re-engineer

Financial Specialist II

Recurring Revenue Management IT Product Owner

Qualified Person

Senior Data Engineer

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