Dillon Engineering Services Hiring for CQV Lead Job at Remote , Ireland Full Time

Dillon ES is seeking to hire a number of experienced CQV Leads and Engineers for an upcoming pharmaceutical expansion project in Tullamore, Offaly.

These openings provide a great opportunity for someone who is looking for a longterm contract in the midlands. 24 months work on offer and hybrid/remote working on offer until Jan 2023.

Our client is a global leader within the life science engineering and design space, and they are the selected construction vendor for this major project.

Responsibilities:

• Manage team of C&Q Engineers on high profile client site throughout the project lifecycle.
• Strong experience with Validation Master Plan, Commissioning Master Plan, project procedures and commissioning and qualification protocols (SAT/Commissioning, IQ and OQ)
• Design Review (DR) process and GMP Risk Assessment (FMEA) experience
• Identify the appropriate Commissioning and Qualification strategy to apply on specific project and define the list of activities required
• Review and follow-up technical documentation from the early design phase in order to ensure alignment with GMP and CQV requirements
• Investigate and resolve technical issues with assistance from Jacobs engineers and/or suppliers
• Ensure site project execution is undertaken in compliance with company guideline, department procedures and safety standards
• Be familiar with the Mechanical Completion procedure and Construction scope of work (Walkdown, system acceptance, punch list and follow up)
• Schedule preparation and progress review
• Organize and review daily activities of other CQV Engineers assigned to the project
• Project management principles to coordinate CQV activities and reporting to Jacobs and Clients PM
• Contractors and Vendors management and coordination
• Final Handover reports to the Client user
• The Lead CQV Engineer reports to the department manager / site commissioning manager and is accountable to coordinate CQV resources, deliverables and activities from the validation approach definition, design review, turn-over systems definition and C&Q activities at site.

Required Experience and Qualifications:

• Degree or equivalent in an engineering related discipline
• 7+ years of experience in commissioning and qualification activities for pharmaceutical facilities
• Strong leadership and team player ability, liaising directly with client and other project key functions
• Previous experience as manager/leader of C&Q team
• Strong knowledge of ISPE and ASTM E2500
• Proven experience with international pharmaceutical projects
• Mentor for junior staff members

To explore this role in strict confidence please contact Diarmaid directly on 085-1187741.

IND004

Job Types: Full-time, Fixed term
Contract length: 24 months

Salary: €80.00-€100.00 per hour

Additional pay:

• Overtime pay

Schedule:

• Monday to Friday
• No weekends

Ability to commute/relocate:

• Remote: reliably commute or plan to relocate before starting work (required)

Experience:

• process equipment or utilities: 5 years (required)
• pharma: 5 years (required)
• CQV: 5 years (required)

Work authorisation:

• Ireland (required)