Principal QA Specialist - UK

BioTalent; Slough; On-site; GBP 40,000 - 70,000; Full time

Job summary

An established industry player is seeking a dedicated Quality Assurance professional to support the global implementation of quality management systems. This role will serve as a crucial link between global quality teams and local needs, ensuring robust documentation processes and effective stakeholder alignment. The ideal candidate will have a strong background in the pharmaceutical industry, with advanced skills in IT PQS systems, particularly Veeva Vault. If you are detail-oriented and passionate about promoting a quality culture, this opportunity is perfect for you. Join a dynamic team and make a significant impact in the pharmaceutical manufacturing sector.

Qualifications

• 5-10 years' experience in QA roles within the pharmaceutical industry.
• Advanced experience implementing IT PQS systems.

Responsibilities

• Lead enrolment and maintenance for global standards processes.
• Manage documentation processes and quality records.

Skills

Documentation Writing

Communication Skills

Collaboration Skills

Quality Assurance

Stakeholder Management

Organizational Skills

GMP Compliance Knowledge

Ability to Manage Ambiguity

Detail-oriented

Education

Bachelor's degree in Science or QA discipline

Tools

Veeva Vault

Job description

You'll support the global implementation of quality management systems, ensuring robust documentation processes and effective stakeholder alignment. This role serves as a key liaison between global quality teams and local implementation needs. The role will be working onsite in Slough, starting in May for an initial 12 month contract.

Key Responsibilities

• Lead enrolment and site maintenance for global standards processes
• Manage documentation processes and quality records
• Support implementation of global QMS systems including validation, qualification, and training
• Serve as point of contact for new system inquiries
• Ensure timely project execution through alignment with global teams
• Promote quality culture across the organization

Required Qualifications

• Bachelor's degree in Science or QA discipline (or equivalent experience)
• 5-10 years' pharmaceutical industry experience in QA roles
• Advanced experience implementing IT PQS systems (particularly Veeva Vault)
• Excellent documentation writing capabilities
• Strong communication and collaboration skills
• Deep understanding of GMP compliance requirements
• Ability to manage ambiguity and drive results
• Detail-oriented with strong organizational skills
• Collaborative team player with stakeholder management abilities

Seniority level

Associate

Employment type

Contract

Job function

Quality Assurance

Industries

Pharmaceutical Manufacturing