QA Validation Lead

Chiesi Group; Nerviano; In loco; EUR 70.000 - 100.000; Tempo pieno

Descrizione del lavoro

A leading company in the pharmaceutical industry is seeking a Validation Manager to oversee validation processes ensuring regulatory compliance and quality standards. The ideal candidate will lead a team, develop validation protocols, and collaborate with cross-functional teams. Candidates should have extensive experience in validation and quality assurance, with a strong focus on leadership to drive continuous improvement and compliance with GxP requirements.

Servizi

Flexible working approach

Remote working support

Continuous training and development

Tax assistance for foreign colleagues

Competenze

• Minimum of 10 years pharmaceutical quality assurance experience.
• At least 5 years in a leadership role.
• Extensive validation and qualification processes expertise.

Mansioni

• Lead validation team and ensure compliance with regulations.
• Develop and maintain validation protocols.
• Manage the quality budget and resources effectively.

Conoscenze

Project Management

Communication

Problem Solving

Decision Making

Leadership

Formazione

Bachelor’s or Master’s degree in scientific discipline

Advanced degree preferred

Descrizione del lavoro

The ideal candidatewill be responsible for overseeing all validation activities, ensuring compliance with regulatory requirements, and maintaining the highest standards of quality. This role requires extensive experience in validation processes, including equipment, process, and facility validation and is crucial for maintaining the integrity and quality of pharmaceutical products, ensuring they meet all regulatory and safety standards.

Main Responsibilities

• Leadership : Lead and manage the validation team to ensure all validation activities are conducted in compliance with regulatory requirements and industry standards. Provide leadership and guidance on validation-related issues, including troubleshooting and problem-solving.
• Documentation : Develop, implement, and maintain validation protocols and procedures for equipment, processes, and facilities. Ensure timely and accurate documentation of all validation activities and results. Prepare and present validation reports to senior management and regulatory authorities.
• Qualification : Oversee the execution of validation studies, including Installation Qualification (IQ), Operational Qualification (OQ), and Performance Qualification (PQ).
• Issue Resolution : Investigate validation and qualification failures, and deviations, ensure timely and effective resolution, and implement corrective and preventive actions.
• Risk Assessments : Conduct risk assessments and develop mitigation strategies for validation-related issues.
• Collaboration : Collaborate with cross-functional teams, including quality assurance, manufacturing, and engineering, to support validation efforts.
• Continuous Improvement : Ensure continuous improvement of validation processes and procedures. Design and execute initiatives to enhance compliance, efficiency, and cost-effectiveness.
• Regulatory Compliance : Ensure the validation and qualification activities and documentation is suitable for regulatory inspections.
• Budget Management : Prepare and manage the site quality budget for validation activities, ensuring expenditures align with projections.
• Resource Management : Ensure adequate resources, including manpower, to maintain compliance with GxP requirements for validation and qualification activities.
• Governance : Prepare and present validation strategies to Chiesi senior management
• Development : Stay current with industry trends and regulatory changes to ensure the site remains compliant with all applicable requirements.

Experience Required

• Minimum of 10 years of experience in pharmaceutical quality assurance, with at least 5 years in a leadership role.
• Extensive experience in validation and qualification processes, including equipment, process, and facility validation.
• In-depth knowledge of regulatory requirements (e.g., FDA, EMA, ICH) and industry standards (e.g., GMP) and quality systems.

Education

Bachelor’s or Master’s degree in a scientific discipline (e.g., Chemistry, Biology, Pharmacy) or related field. Advanced degree preferred.

Languages

• Fluent in English spoken language
• Proven ability to write clear, concise, and grammatically correct content in English

Skills & Abilities

• Excellent project management and organizational skills.
• Exceptional communication, problem-solving skills and decision-making abilities, with the ability to collaborate effectively with cross-functional teams.
• Strong leadership and management skills, with the ability to effectively lead and motivate a team.
• Ability to work cross-functionally and build strong relationships with diverse teams.

Soft Skills

• Planning and organizational skills
• Problem solving
• Decision making
• Leadership and social influence

What we offer

You would join a dynamic, fast-growing, challenging and friendly environment.

In Chiesi we firmly believe that our people are our most valuable asset , that is why we invest in continuous training, learning and development. Therefore, we strive to continuously promote and satisfy development needs, paying particular attention to the quality of our working environment and to collective well-being.

We want our people to come to work happy every day , and we know how important it is to find the right work-life balance in order to be able to give our best. That is why we offer flexible working approach, remote working, support in the relocation process, tax assistance service for foreign colleagues and many other people-care services.