C&Q Consultant for Pharma Industry
Core
Commissioning and Qualification Consultant supporting Life Science companies in Portugal to ensure GMP compliance and equipment validation.
Role type
Commissioning & Qualification Consultant
Builds
Commissioning and Qualification Plans, Protocols, VMP, URS, RA, DQ, IQ, OQ, PQ, Traceability Matrix
Domain
Life Sciences / Pharmaceutical Manufacturing
Required skills
Equipment and utilities qualification, GMP regulations, Validation principles, Project planning and management, Technical documentation preparation, Test execution, Client collaboration
Preferred skills
Engineering or related degree background, Analytical skills, Proactive approach, Dynamic attitude, Travel availability
Technologies
GMP, Validation, Commissioning, Qualification, URS, DQ, IQ, OQ, PQ
Responsibilities
Lead commissioning and qualification projects, Plan and manage project activities per regulatory requirements, Prepare and review key project documentation, Execute qualification tests and support technical investigations, Collaborate with client teams to define strategies and ensure delivery, Contribute to continuous improvement of internal processes
Seniority
Junior to Mid-level (0-2 years experience)