On behalf of one of our Pharmaceutical clients at RED we are currently recruiting for a Quality Control - CSV Consultant with One Lab or Lab X experience
This is an exciting opportunity to work at the intersection of Quality Control, laboratory automation, digital transformation, and GxP compliance, supporting projects across multiple sites and international stakeholders.
Role
QC CSV Consultant
Duration
ASAP till end of the year with extensions
Location
100% Remote role
Roles & Responsibilities
5+ years of QC laboratory experience, ideally including microbiology workflows
Strong understanding of QC laboratory operations and analytical workflows
Hands-on expertise with laboratory automation, particularly OneLab
Experience with LabX and/or laboratory software administration is highly desirable
Strong knowledge of GxP, CSV, data integrity, and regulated computerized systems
Experience developing validation documentation and executing UAT
Experience managing multi-site laboratory system implementation projects
Knowledge of Power BI and dashboard/report development
Experience with ALM, JIRA, Confluence, or similar information/project management tools
Excellent stakeholder management and communication skills
Ability to work effectively with international teams and manage competing priorities
Strong analytical, problem-solving, and project management capabilities
Professional working proficiency in English
You’ll play a key role in the digital transformation and automation of global QC laboratories, helping to standardize processes, improve efficiency, strengthen data integrity, and ensure compliant laboratory operations.
If you are looking for a new role , apply on this link or send me your CV at npawar@redglobal.com
Thanks,
Nisha