Requalification Lead

EFOR

Spain

Remote

EUR 90,000 - 150,000

Full time

48 hours ago
Be an early applicant

A complete application in a minute

Tailored resume and cover letter, ready to send.

Get past ATS filters

Job summary

EFOR is seeking a Requalification Lead to drive the strategy, execution, and oversight of equipment and facility requalification activities. You will maintain the validated state of GMP facilities in line with FDA/EMA/PIC/S, define review cycles, and lead risk-based strategies across a broad portfolio of assets.

Responsibilities include developing IQ/OQ/PQ programs, qualifying process support equipment and clean utilities, and ensuring inspection readiness while maintaining data integrity across

Qualifications

  • Bachelor's degree in a relevant field (Engineering/Life Sciences)
  • Minimum 10 years of GMP equipment qualification experience
  • Deep understanding of FDA, EMA, and PIC/S requirements
  • Experience with CTU qualification and continued process verification
  • Proven leadership and cross-functional collaboration skills

Responsibilities

  • Develop, implement, and oversee the equipment requalification lifecycle (IQ/OQ/PQ) and continued process verification
  • Establish qualification protocols and schedules for process support equipment and utilities
  • Lead requalification efforts for clean utilities and environmental monitoring
  • Ensure inspection readiness and data integrity across qualification documentation
  • Perform risk assessments to prioritize systems and define requalification strategies
  • Collaborate with QA, Engineering, and Validation to ensure regulatory compliance
  • Support global site qualification with remote work and travel as needed
  • Identify gaps and drive corrective actions for qualification issues

Skills

GMP knowledge
Equipment qualification
IQ/OQ/PQ
Risk assessment
Regulatory compliance
Leadership

Education

Bachelor's degree in Engineering/Life Sciences

Job description

The Requalification Lead will drive the strategy, execution, and oversight of equipment and facility requalification activities. This position is responsible for maintaining the validated state of GMP facilities, ensuring compliance with FDA, EMA, and PIC/S regulations, and supporting continuous process verification. The candidate must be capable of establishing the overall requalification approach, defining review cycles and assessment methodologies, prioritizing systems based on risk, and ensuring continued maintenance of the validated state across a broad portfolio of equipment, facility, and utilities.

Key Responsibilities
  • Develop, implement, and manage the equipment requalification lifecycle (IQ/OQ/PQ), including CTU qualification and continued process verification.
  • Establish and maintain qualification protocols and schedules for process support equipment (autoclaves, sterilizers, washers, refrigerators, freezers, cold storages, incubators).
  • Lead requalification efforts for clean utilities (WFI, Purified Water, Clean Steam, Process air/gas).
  • Oversee cleanroom environmental monitoring (EM) requalification and inspection readiness.
  • Conduct risk assessments to prioritize systems and define appropriate requalification strategies.
  • Collaborate with cross-functional teams (Quality Assurance, Engineering, Validation) to ensure alignment and compliance.
  • Maintain and ensure data integrity throughout all qualification documentation and processes.
  • Facilitate inspection readiness in accordance with FDA, EMA, and PIC/S regulatory expectations.
  • Identify gaps, develop action plans, and lead initiatives to resolve qualification-related issues.
  • Support facility and utility qualification and requalification across global sites (remote work, with ad hoc travel as needed).
Required Qualifications
  • Bachelor's degree (or higher) in Engineering, Life Sciences, or related field.
  • Minimum 10 years' experience in GMP equipment qualification and lifecycle management.
  • Extensive knowledge of equipment requalification, IQ/OQ/PQ, CTU qualification, and continued process verification.
  • Deep understanding of GMP compliance, data integrity principles, and regulatory expectations (FDA, EMA, PIC/S).
  • Hands-on experience with process support equipment, clean utilities, cleanrooms, and environmental monitoring.
  • Strong risk assessment and management skills.
  • Demonstrated leadership in defining requalification strategies and inspection readiness.
  • Exceptional written and verbal communication skills.
  • Ability to work independently in a remote setting, with willingness to travel as required.
  • Proven success in cross-functional collaboration and change management.
Get your free, confidential resume review.

or drag and drop your file here.

Similar jobs

Similar jobs worth comparing

Senior Requalification Lead - GMP Facilities (Remote)
Senior Requalification Lead - GMP Facilities (Remote)

EFOR • Spain

Remote
EUR 90,000 - 150,000
Equipment Qualification & Validation Specialist
Equipment Qualification & Validation Specialist

QbD Group • Barcelona

On-site
EUR 52,000 - 76,000
Mechanical Designer
Mechanical Designer

Hitachi Energy Ltd. • León

Remote
EUR 24,000 - 42,000
Life Sciences Equipment Qualification Specialist
Life Sciences Equipment Qualification Specialist

QbD Group • Barcelona

On-site
EUR 52,000 - 76,000
Maintenance Manager
Maintenance Manager

Werfen Immunoassay • Lliçà d'Amunt

On-site
EUR 60,000 - 90,000
CQV Lead - Biotech Equipment Validation & GMP
CQV Lead - Biotech Equipment Validation & GMP

PQE Group • Barcelona

On-site
EUR 36,000 - 44,000
Global QA Manager
Global QA Manager

AdQualis Human Results • Cataluña

On-site
EUR 90,000 - 120,000
Interim Quality Manager
Interim Quality Manager

Barrington James • Barcelona

On-site
EUR 65,000 - 85,000
Competitive compensation
Professional development opportunities
Engineering Project Manager
Engineering Project Manager

PQE Group • Madrid

On-site
EUR 70,000 - 90,000
Qualification & Validation Specialist
Qualification & Validation Specialist

QbD Group • Barcelona

On-site
EUR 35,000 - 50,000
Attractive and competitive salary package
Continuous learning and development opportunities
Job security and meaningful connections