CQV Engineer

Life Science Recruitment; Athlone; On-site; EUR 90,000 - 120,000; Full time

Job summary

Life Science Recruitment advertises an exciting CQV Engineer role in Athlone within an award-winning pharmaceutical organization. The role focuses on life cycle qualification documentation for process equipment in a solid dosage environment and requires leadership of commissioning activities.

The candidate will manage CQV strategy, schedule, quality, safety and compliance across commissioning lifecycle, and will have a minimum of seven years in pharma commissioning with strong risk-based

Qualifications

• Degree in Engineering, Science or related discipline.
• Minimum 7 years GMP experience in pharma commissioning.
• Proven track record managing commissioning partners and contractors.

Responsibilities

• Develop and own CQV activities aligned to project schedule and GMP requirements.
• Act as Client C&Q Lead for the project.
• Coordinate all CQV activities and serve as single point of contact for CQV interfaces.
• Plan and lead system commissioning and qualification of equipment per schedule.
• Oversee and coordinate commissioning sub-contractors and partners.
• Interface with Quality, Manufacturing, EHS, QC and other stakeholders.
• Provide CQV status reporting to Senior Project Manager and governance forums.
• Manage risk registers and mitigation for the CQV lifecycle.
• Support turnover activities and handover to CQV and Operations with documentation.

Skills

CQV

Commissioning

Qualification

Validation

GMP

Stakeholder mgmt

Education

Engineering degree

Science degree

Job description

We're currently recruiting for an exciting opportunity with an award-winning Pharmaceutical organization based in Athlone. 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. The CQV Engineer will be responsible for life cycle qualification documentation. This specific role is for Process Equipment in a solid dosage environment. They will work with the Equipment Project Lead to ensure the system is commissioned and qualified as expected. The role is client-side, and will be accountable for commissioning strategy, schedule, quality, safety, and compliance during the commissioning & qualification lifecycle of the project. Candidates must have minimum 7 years experience in pharma commissioning, proven management of commissioning partners and contractors as well as strong understanding of science and risk-based verification of facilities, utilities and process equipment.

Duties:

• Develop and own the Commissioning, Qualification & Validation (CQV) activities associated with your project, aligned to project schedule and GMP requirements up to Performance Qualification of all systems and equipment.
• Act as Client C&Q Lead for the project.
• Throughout execution; coordinate all commissioning and qualification activities and act as single point of contact for CQV interfaces.
• Plan and lead execution of system commissioning and qualification of equipment in accordance with project schedule and phased release of areas.
• Oversee and coordinate Commissioning Partner and commissioning sub-contractors; manage performance against scope and programme.
• Commissioning partner responsible for commissioning of utility and facility systems.
• Interface with internal stakeholders including Quality, Manufacturing, Operational Readiness, Engineering, EHS, QC.
• Good knowledge of GMP, validation lifecycle, CSV (computer system validation) fundamentals, and regulatory expectations for qualification documentation Provide regular CQV status reporting (commissioning progress, qualification status, open actions, risks) to the Senior Project Manager.
• Own risk management for your project: identify, evaluate and mitigate risks; maintain and report risk registers.
• Collaboration during turnover activities and ensure successful system handover to CQV and Operations including documentation, training and punchlist closure.
• Ensure best-practice quality management and documentation for GMP and GEP compliance(CTOP, VTOP, test packs, deviation reports).
• Manage resolution of CQV issues, deviations, and change controls

Education and Experience:

• Degree qualification in Engineering, Science, related discipline or relevant experience
• Relevant experience in pharmaceutical and GMP regulated manufacturing environments.
• Minimum 7 years GMP experience, with demonstrable experience.
• Proven track record of commissioning and qualification involving solid dosage process equipment installation.
• Experience planning and delivering complex commissioning and qualification of systems.
• Excellent stakeholder management and reporting skills; able to present to senior leadership and governance forums.