Senior Quality Assurance Officer

Science Solutions Recruitment Ltd; Manchester; Sur place; GBP 45 000 - 65 000; Plein temps

Résumé du poste

Smart4 Sciences, partnering with a pharmaceutical business, invites applications for a Senior QA Officer to join its Quality team in Manchester. You will support operations, maintain robust quality systems, and ensure GMP, GDP and internal procedures are followed.

This role suits a scientifically qualified professional with strong organisational skills, a meticulous eye for detail, and a proactive, quality-focused mindset. Experience with audits and regulatory readiness is advantageous.

Qualifications

• Degree in a scientific discipline (Pharmaceutical Sciences, Chemistry or related).
• Experience in an administrative or office-based role.
• Excellent organisational, communication and interpersonal skills.
• Strong attention to detail and ability to manage competing priorities.
• Proficiency in Microsoft Word, Excel and PowerPoint.
• Ability to work independently and collaboratively while meeting deadlines.
• A proactive, flexible and quality-focused approach.

Responsabilités

• Review finished batch records and GMP release documentation.
• Maintain QMS including CAPAs, deviations, change controls and non-conformances.
• Prepare, review, issue and control SOPs, forms and batch records.
• Investigate quality issues, customer complaints, deviations and recalls.
• Maintain quality databases, master lists and performance metrics.
• Support regulatory licence approvals and inspection readiness.
• Liaise with suppliers for quality and regulatory documentation.
• Assist with internal and external audits and regulatory inspections.
• Prepare quality reports, analyse data and identify improvements.
• Collaborate with cross-functional teams to maintain compliance and drive improvement.

Connaissances

Organisational skills

Attention to detail

Communication skills

Microsoft Office

Independent and collaborative working

Quality-focused mindset

Proactive

Formation

Degree in Pharmaceutical Sciences or related field

Outils

Microsoft Word

Microsoft Excel

PowerPoint

Description du poste

About the Role

Are you a detail-oriented quality professional looking to develop your career within the pharmaceutical industry?

Smart4 Sciences is partnering with a pharmaceutical business seeking a proactive Senior QA Officer to join its Quality team. The role involves supporting pharmaceutical operations, maintaining robust quality systems, and ensuring compliance with GMP, GDP, and internal quality procedures.

This is an excellent opportunity for a scientifically qualified professional with strong organisational skills and an interest in Quality Assurance, quality systems, and regulatory compliance.

Key Responsibilities

• Review finished batch records and GMP release documentation.

• Maintain and manage Quality Management Systems (QMS), including CAPAs, deviations, change controls, and non-conformances.

• Prepare, review, issue, and control SOPs, forms, and batch manufacturing records.

• Investigate quality issues, customer complaints, deviations, and product recalls.

• Maintain quality databases, documentation, master lists, and performance metrics.

• Support regulatory licence approvals and ensure inspection readiness.

• Liaise with suppliers to obtain quality and regulatory documentation.

• Assist with internal and external audits and regulatory inspections.

• Prepare quality reports, analyse data, and identify opportunities for improvement.

• Collaborate with cross-functional teams to maintain compliance and drive continuous improvement.

Requirements

Essential:

• A degree in a scientific discipline, preferably Pharmaceutical Sciences, Chemistry, or a related field.

• Experience in an administrative or office-based role.

• Excellent organisational, communication, and interpersonal skills.

• Strong attention to detail and the ability to manage competing priorities.

• Proficiency in Microsoft Word, Excel, and PowerPoint.

• The ability to work independently and collaboratively while meeting strict deadlines.

• A proactive, flexible, and quality-focused approach.

Desirable:

• Previous experience within the pharmaceutical industry.

• Experience with product release and batch documentation.

• Knowledge of GMP guidelines and Regulatory Affairs.

• Familiarity with QMS processes, CAPAs, deviations, and change controls.

• Experience in problem-solving, investigations, and root cause analysis.

Why Apply?

• The opportunity to develop your career within a growing pharmaceutical group.

• Exposure to a broad range of Quality Assurance and regulatory activities.

• A collaborative and supportive working environment.

• Ongoing training and professional development opportunities.