Website Asset Recruitment

Asset Recruitment

#00993

Lead CQV Engineer

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 the site.

Responsible for leading a team for Upstream equipment including Single-use bioreactors, single-use mixers, depth filtration, centrifuges, and solution prep.

Responsibilities:
• Manage a 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 users

Requirements:
• Bachelor’s Degree in Engineering or relevant field
• 8+ years of experience in GMP pharmaceutical commission, qualification, validation & start-up.
• Strong leadership and team player ability, liaising directly with client and other project key functions
• Previous experience as manager/leader of C&Q team
• Proven experience with international pharmaceutical projects will be an advantage
• Knowledge and experience with facility start-up projects (brown field or green field

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