Validation software tools jobs

Senior Specialist, Engineering Commissioning, Qualification & Validation

Bristol Myers Squibb · Posted Nov 4, 2026

Open

Ireland
Hybrid
Full-time · Senior

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Senior Specialist, Engineering Commissioning, Qualification & Validation

Bristol Myers Squibb · Posted Nov 4, 2026

Open

Ireland
Hybrid
Full-time · Senior

Apply with Referso

Senior Specialist, Engineering Commissioning, Qualification and Validation (CQV)

Bristol Myers Squibb · Posted Nov 4, 2026

Open

Cruiserath, Ireland
On-site
Full-time · Senior

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Lead qualification and validation of process and utility equipment and computerised systems across BMS’s MPCC and SDPF facilities.

Compensation

You’ll get a competitive salary and a great benefits package including an annual bonus, pension contribution, family medical allowance, 27 days of annual leave, life assurance and on-site gym

Responsibilities

Plan and execute risk-based protocols for equipment and systems
Author and manage IQ, OQ, PQ protocols and CSV deliverables
Ensure compliance with regulatory requirements and industry standards
Maintain audit-ready validation documentation
Support regulatory inspections and root cause analysis

Requirements

Bachelor's degree in Engineering, Life Sciences, Chemistry or a related field
Nice to have: biologics or pharmaceutical manufacturing experience
Nice to have: biologics start-up facility familiarity
Nice to have: experience with DeltaV, MES or SAP

Skills

equipment qualification (IQ/OQ/PQ)computer systems validation (GAMP 5, 21 CFR Part 11, Annex 11)risk-based validation approaches

Senior Specialist, Engineering Commissioning, Qualification & Validation

Bristol Myers Squibb · Posted Nov 4, 2026

Open

Ireland
Full-time · Senior

Apply with RefersoAI Apply on careers page

Lead qualification and validation of process and utility equipment and computerised systems across the MPCC and SDPF facilities.

Compensation

You’ll get a competitive salary and a great benefits package including an annual bonus, pension contribution, family medical allowance, 27 days of annual leave, life assurance and on-site gym

Responsibilities

Develop commissioning, qualification and validation plans and risk-based strategies for new and existing process and utility equipment and computerised systems.
Author, execute and report IQ, OQ and PQ protocols for equipment, including functional testing, troubleshooting and support for start-up activities.
Author and manage CSV deliverables across the system lifecycle in line with GAMP 5, including URS, FS, DS, IQ/OQ/PQ and traceability matrices.
Ensure computerised systems comply with 21 CFR Part 11, EU Annex 11 and data integrity requirements.
Ensure all qualification and validation activities meet applicable regulatory requirements (FDA, EMA, ICH) and industry standards (GAMP 5, ASTM).

Requirements

Bachelor's degree in Engineering
Bachelor's degree in Life Sciences
Bachelor's degree in Chemistry
Nice to have: experience in biologics or pharmaceutical manufacturing
Nice to have: experience in a biologics start-up facility

Skills

equipment qualification (IQ/OQ/PQ)

Senior Specialist, Engineering Commissioning, Qualification & Validation

Senior Specialist, Engineering Commissioning, Qualification & Validation

Compensation

Responsibilities

Requirements

Skills

Benefits

Senior Specialist, Engineering Commissioning, Qualification and Validation (CQV)

Compensation

Responsibilities

Requirements

Skills

Senior Specialist, Engineering Commissioning, Qualification & Validation

Compensation

Responsibilities

Requirements

Skills

Benefits

Benefits