QA Officer

SLS Services Limited; Birmingham; On-site; GBP 28,000 - 36,000; Full time

Job summary

SLS Services Limited in Birmingham is seeking a quality professional to ensure GMP/GDP compliance and oversee the company's Quality Management System within a fast-paced pharmaceutical environment. You will perform internal audits, manage CAPA, approve materials, and maintain manufacturing documentation, contributing to product quality and patient safety.

This onsite, full-time role requires a degree in Pharmaceutical Sciences and at least six months' GMP experience, with MHRA standards

Qualifications

• Bachelor's degree in Pharmaceutical Sciences or related discipline.
• Minimum 6 months’ experience in a GMP-regulated pharmaceutical environment.
• Solid understanding of QMS, SOPs, validation protocols, and regulatory guidelines.
• Experience with internal audits, supplier assessments, and CAPA systems.

Responsibilities

• Ensure compliance with statutory regulations and GMP/GDP requirements. Implement and maintain the company’s Quality Management System.
• Investigate non-compliance issues and manage corrective actions.
• Approve raw materials, intermediates, and finished products.
• Organize and audit manufacturing documentation and records.
• Perform internal audits and manage change control procedures.
• Oversee validations for equipment, facilities, and processes.

Skills

GMP Compliance

QMS Knowledge

Internal Audits

CAPA Management

Documentation Review

Regulatory Awareness

HVAC Knowledge

Education

Bachelor's degree in Pharmaceutical Sciences

Tools

HVAC Systems

Job description

Join a highly respected pharmaceutical organization renowned for its commitment to quality, safety, and innovation. With an emphasis on compliance and excellence, this company offers an inclusive and supportive environment where your expertise will directly contribute to patient safety and product quality. You’ll have the chance to work alongside dedicated professionals and develop your career in a business that values integrity and growth.

Onsite full-time - 10am - 7pm working hours

Responsibilities / Role

In this role, you will:

• Ensure compliance with statutory regulations and GMP/GDP requirements. Implement and maintain the company’s Quality Management System.
• Investigate non-compliance issues and manage corrective actions.
• Approve raw materials, intermediates, and finished products.
• Organize and audit manufacturing documentation and records.
• Perform internal audits and manage change control procedures.
• Oversee validations for equipment, facilities, and processes.

Qualifications & Experience

• Degree in Pharmaceutical Sciences (minimum BSc) or related discipline.
• At least 6 months’ experience within a GMP-regulated pharmaceutical environment.
• Solid understanding of Quality Management Systems, SOPs, validation protocols, and regulatory guidelines.

Additional Skills

• Strong knowledge of QMS and validation protocols.
• Ability to review and approve technical documentation.
• Experience with internal audits, supplier assessments, and CAPA systems.
• Familiarity with raw material testing and compliance standards.
• Experience with HVAC systems operation.
• Knowledge of MHRA requirements and product recalls.
• Proficiency in environmental monitoring techniques.