Senior Director Quality Assurance, Data Integrity, Technology & Data

TN United Kingdom; United Kingdom; Hybrid; GBP 60,000 - 100,000; Full time

Job summary

An established industry player is seeking a Senior Director of Quality Assurance to lead data integrity and compliance efforts. This role involves ensuring global compliance for computer system validation and fostering strategic partnerships within the organization. With a focus on innovative science and patient-centric solutions, this position offers a unique opportunity to influence quality standards across R&D and commercial operations. The flexible hybrid working model allows for a balanced work-life dynamic, making it an attractive opportunity for seasoned professionals in the pharmaceutical sector.

Qualifications

• Extensive experience in pharmaceutical quality assurance.
• Proven leadership skills in a matrix organization.

Responsibilities

• Ensure compliance with global data integrity regulations.
• Oversee computer systems and data management processes.

Skills

Pharmaceutical QA Experience

Leadership in a Global Environment

Data Integrity Expertise

Audit Management

Stakeholder Engagement

Education

Degree in IT, Science, Biotechnology, or related field

Job description

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Senior Director Quality Assurance, Data Integrity, Technology & Data, United Kingdom

Job Details:

• Client:
• Location: London, UK
• Job Category: Other
• EU work permit required: Yes
• Job Reference: 7ae150895aa9
• Job Views: 14
• Posted: 05.05.2025
• Expiry Date: 19.06.2025

Job Description:

About Astellas: At Astellas, we are a progressive health partner committed to delivering value and outcomes. We focus on innovative science, prioritizing areas with high patient need, including rare and life-threatening diseases. We work closely with patients, healthcare professionals, and regulatory bodies to ensure patient-centric solutions.

The Opportunity: You will ensure global compliance for computer system validation, data integrity, information systems, and electronic records supporting R&D, clinical, manufacturing, and commercial operations. You will develop strategic partnerships with leadership to promote excellence in data integrity and compliance.

Hybrid Working: Our flexible hybrid model allows working from home or in-office, with approximately 1 day per quarter in London.

Key Responsibilities:

1. Ensure compliance with global data integrity regulations and standards.
2. Oversee computer systems and data management for clinical and manufacturing processes.
3. Provide QA oversight for validation and compliance of all systems supporting various operations.
4. Partner with management to monitor quality, identify risks, and lead improvements.
5. Contribute to the QA strategic plan and provide global oversight.

Essential Knowledge & Experience:

• Extensive pharmaceutical QA experience.
• Proven leadership in a global, matrix environment.
• Expertise in Data Integrity and computer system validation standards.
• Experience managing audits and regulatory inspections.
• Strong communication and stakeholder engagement skills.

Preferred Qualifications:

• Excellent communication and problem-solving skills.
• Ability to build industry relationships.

Education:

• Degree in IT, Science, Biotechnology, or related field, or equivalent.
• Fluency in English.

Additional Information:

• Permanent, full-time position.
• Based in London, UK.
• Hybrid working model with flexibility.

We are an equal opportunity employer, welcoming applicants regardless of race, color, religion, sex, national origin, disability, veteran status, or other protected characteristics.