QA Compliance Officer
Job Description
About the Role
A leading pharmaceutical development and manufacturing organisation is seeking a QA Compliance Officer to support the governance and compliance of its Pharmaceutical Quality Management System (PQS). This role plays a key part in maintaining regulatory compliance across international standards including UK/EU/US GMP/GDP and ICH guidelines.
Please note, this is a site based role in central Scotland so you must be comfortable with on site working.
Key Responsibilities
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Support quality system elements such as QMS monitoring, supplier qualification, and audits.
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Assist in maintaining and updating regulatory registrations, licences, and certifications.
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Track site compliance commitments and regulatory trends.
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Collaborate with site functions to reduce compliance issues and implement improvements.
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Review QMS documentation in line with global regulatory guidance.
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Lead Quality Management Review meetings.
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Support investigations and develop effective CAPA.
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Prepare for regulatory and customer audits and support follow-up.
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Escalate significant compliance concerns to Quality Management.
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Build strong working relationships with stakeholders.
Essential Qualifications & Experience
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Degree or relevant qualification in a scientific, business, or engineering discipline.
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Minimum 2 years' experience in QA within a GMP environment.
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Experience conducting internal or supplier audits.
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Experience with QMS documentation (SOPs, deviations, investigations, CAPA).
Desirable Experience
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Certified Auditor training.
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Supplier/vendor/material approval experience.
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Experience supporting regulatory audits.
Key Competencies
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Strong attention to detail
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Problem-solving skills
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Excellent communication
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Proficiency in Microsoft Office applications
What is on Offer
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Excellent benefits package including enhanced pension, healthcare and flexi-time.
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Development and learning opportunities.
Guidant, Carbon60, Lorien & SRG - The Vertage Group Portfolio are acting as an Employment Business in relation to this vacancy.
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