Medior Cleaning Validation Consultant

Avertim; Antwerpen; Sur place; EUR 70 000 - 95 000; Plein temps

Avantages offerts par ce poste

Company car

Hospitalization insurance

Bonus plan

Meal vouchers

Eco-cheques

Résumé du poste

Avertim is seeking a Medior Cleaning Validation Consultant to support validation and qualification activities in GMP environments. You will define, execute, and maintain cleaning validation strategies, collaborating with cross-functional teams and global stakeholders for a leading Life Sciences client.

Responsibilities include developing Master Plans, establishing acceptance criteria, and supporting ongoing monitoring programs, while ensuring regulatory compliance and process improvements

Qualifications

• Master’s degree in a life sciences or engineering field.
• Minimum 5 years’ experience in pharmaceutical or food industries.
• Proven experience in Cleaning Validation in regulated environments.
• Strong GMP knowledge and regulatory awareness.
• Experience with CIP/SIP and validation lifecycles.
• Excellent analytical and problem-solving skills.
• Strong communication and stakeholder management.
• Ability to work autonomously in cross-functional teams.
• Fluent English and Dutch.

Responsabilités

• Develop, review, and execute Cleaning Validation Master Plans, protocols, and reports.
• Define cleaning validation strategies and acceptance criteria based on risk assessments and product characteristics.
• Support cleaning process verification activities and ongoing monitoring programs.
• Perform data analysis and assess cleaning validation results.
• Investigate deviations, non-conformities, and OOS related to cleaning activities.
• Ensure GMP compliance and regulatory guidelines.
• Collaborate with QA, Manufacturing, Engineering, Validation, and Technical Services teams.
• Support inspections and audits by authorities and customers.
• Participate in continuous improvement of cleaning processes.

Connaissances

Cleaning Validation

GMP knowledge

Risk assessment

Data analysis

Stakeholder management

Autonomy

Multidisciplinary teamwork

English & Dutch

Formation

Master's degree in Life Sciences

Master's degree in Engineering

Outils

CIP (Clean-In-Place)

SIP (Sterilize-In-Place)

Description du poste

Your Role:

As a Medior Cleaning Validation Consultant, you will support validation and qualification activities within highly regulated GMP environments. You will collaborate with cross-functional teams and global stakeholders to define, execute, and maintain cleaning validation strategies, ensuring compliance with industry regulations and quality standards. Your expertise will contribute to the reliability and efficiency of manufacturing processes and cleaning systems for a leading client in the Life Sciences sector.

What will you do?

• Develop, review, and execute Cleaning Validation Master Plans, protocols, and reports
• Define cleaning validation strategies and acceptance criteria based on risk assessments and product characteristics
• Support cleaning process verification activities and ongoing monitoring programs
• Perform data analysis and assess cleaning validation results
• Investigate deviations, non-conformities, and out-of-specification results related to cleaning activities
• Ensure compliance with GMP requirements and applicable regulatory guidelines
• Collaborate with QA, Manufacturing, Engineering, Validation, and Technical Services teams
• Support inspections and audits by regulatory authorities and customers
• Participate in continuous improvement initiatives related to equipment cleaning and validation processes
• Provide technical expertise throughout the lifecycle of manufacturing and cleaning systems

Your Profile:

• Master’s degree in Engineering, Pharmacy, Biotechnology, Life Sciences, or a related scientific field
• Minimum 5 years of relevant industrial experience within the pharmaceutical and/or food industry
• Demonstrated experience in Cleaning Validation activities within regulated environments
• Strong knowledge of GMP standards and applicable regulatory requirements
• Experience with implementation, qualification, and validation of CIP (Clean-In-Place) and/or SIP (Sterilize-In-Place) systems
• Experience in risk assessment methodologies and validation lifecycle management
• Excellent analytical and problem-solving skills
• Strong communication and stakeholder management capabilities
• Ability to work autonomously while thriving in multidisciplinary project teams
• Professional proficiency in English and Dutch

About Avertim

We are a trusted partner for complex transformation programs. From strategy to operations, our consultants help clients perform, innovate, and comply, delivering sustainable change across Life Sciences & Chemicals, Banking & Insurance, Transport & Mobility, Energy & Utilities, and Telecom & Media.

What Avertim Offers

• High impact assignments with European clients in our core sectors
• A culture of experience, excellence, and diversity, working alongside subject-matter experts
• Learning & development tracks with mentoring, internal academies, and access to external trainings/certifications
• The opportunity to drive initiatives that perform, innovate, and comply with a sustainable mindset
• Salary package in line with your experience with extra-legal advantages (ex. company car, hospitalization insurance, bonus plan, meal vouchers, eco-cheques, and more)