QA Validation Consultant
AKKODIS Belgium is looking for an experienced person in a pharmaceutical environment in the field of Validation.
What are your responsibilities?
Provide a compliance expertise in validation
Ensure QA oversight in validation activities (IQOQ / PQ / PV…)
Review/Approve the validation documentation regarding the GMP requirements and internal procedures
Ensure that production practice are aligned with validation conclusion
Escalate to Management of critical issues during validation
Contribute to deviation process providing QA expertise
Identify potential quality and compliance risks
Define the validation strategies
Write and implement validation documentation (Validation
Plan, Validation Summary Report, Risk Assessment, Gap Analysis , Periodic review ….)
Profile
Who are you?
University degree (Biotechnology, Agronomy, Chemistry or Pharmacy, etc.)
Former relevant industrial experience in Validation
Knowledge of GMP / CFR / EudralexEU, cGMP, PMDA, ICH, PIC/S, WHO
Good teamwork and organizational skills. Must have strong, organization and analytical skills.
Facilitator, influencer and planner
Problem solving and achievement oriented
Good oral and written communication skills in French & English
What’s the offer you can’t refuse?
As an AKKODIS Team Member, you will be:
• Onboarded in your position via a buddy process
• Supported in your career by your Business Manager
• Actor of your training plan and your personal and professional development
• Benefiting from a permanent contract
• Benefiting from a competitive salary package including several extra-legal benefits
Interested? I invite you to send me your resume to the following mail adress: marie.defruit@akkodis.com