Validation Engineer
Contract
contract
30 Oct 2025
Cork
Verified by Turrior
Content + Source + Freshness • 16 Dec 2025 • 95% confidence
85 / 100
Offer value
High value attributed to the role's critical impact in validation processes, attractive contract position, and competitive salary potential.
- Significant influence in quality control within manufacturing
- Attractive contract with potential extension
- Strong market demand for validation expertise
Pros
- Opportunity to impact manufacturing quality in a high-stakes industry.
- Possibility for contract extension and competitive pay.
- Work within a growing team, enhancing professional skills.
Cons
- Contract position may lack long-term stability.
- Needs significant industry experience (4+ years).
- Intensive responsibilities with strict regulatory adherence.
Who it's for
Mid-level • On-site
Good fit
- Experienced validation engineers
- Quality assurance specialists
- Professionals aiming to work in high-impact industries
Not recommended for
- Fresh graduates without engineering experience
- Candidates unaccustomed to contract positions
- Individuals who struggle with self-management
Motivation fit
Desire to work in quality assurance within the medical field.Interest in leading improvement projects.Ability to work under pressure with a focus on compliance.
Key skills
Validation of manufacturing processesKnowledge of regulatory standardsEffective project management
Score: 85/100 AI verified analysis
About the job
We are looking for an experienced Validation Engineer ready to drive critical qualification programmes and contribute directly to a world-class manufacturing operation. This is an exciting chance to join a growing, high-impact team.
This is a 12 month contract position.
Key Responsibilities:
- Take ownership of process, systems, and equipment validations in accordance with Validation Master Plans and project schedules.
- Participate in cross-functional teams to establish robust validation strategies and objectives, supporting process and equipment changes.
- Prepare, execute, and complete Validation Protocols and Reports, ensuring strict compliance with all relevant Quality standards and Regulatory requirements.
- Maintain expertise in applicable regulations and guidance documents. Review existing practices, identify opportunities for continuous improvement, and lead improvement projects.
- Monitor the progress of validation projects, ensuring adherence to schedule, and provide regular stakeholder updates.
- Ensure all relevant departments understand and comply with validation programme requirements, providing necessary training.
- Lead thorough investigation of Quality and Validation issues using Root Cause Analysis (RCA) and implement robust Corrective and Preventative Actions (CAPA).
- Lead and coordinate Risk Mitigation initiatives such as FMEA (Failure Modes and Effects Analysis) and Risk Assessments.
- Adhere to all EHS guidelines and Quality procedures.
Skills, Attributes & Experience
- Degree in Engineering or related discipline.
- Minimum of 4 years + experience working in a Quality Engineer or Validation role within Pharmaceuticals or Medical Device.
- Experience generating validation documents - IQ, OQ & PQ.
- The successful candidate must demonstrate strong time management and organisational skills.
- Excellent communication is essential.
