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 ….)

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