Quality Assurance Specialist

1Tech Staffing Limited; Birmingham; On-site; GBP 30,000 - 40,000; Full time

Job summary

A leading pharmaceutical logistics company is seeking a Quality Assurance Specialist in Birmingham. The role involves maintaining the Quality Management System in compliance with ISO standards and ensuring adherence to EU GDP guidelines. Candidates should have proven experience in a regulated environment and strong knowledge of relevant standards. Excellent organizational and communication skills are essential for this mid-senior level position.

Qualifications

• Proven experience in a GMDP or similar regulated environment.
• Strong knowledge of GDP, GMP, ISO 9001, and ISO 13485 standards.

Responsibilities

• Maintaining and enhancing the QMS to meet regulatory requirements.
• Supporting audits and managing CAPA plans.
• Driving a culture of quality excellence across the business.

Skills

Organizational Skills

Communication

Stakeholder Management

Quality Promotion

Education

Experience in GMDP or regulated environment

Knowledge of GDP, GMP, ISO 9001, ISO 13485

Tools

MS Office

Job description

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1Tech Staffing Limited provided pay range

This range is provided by 1Tech Staffing Limited. Your actual pay will be based on your skills and experience — talk with your recruiter to learn more.

Base pay range

Direct message the job poster from 1Tech Staffing Limited

Recruitment Consultant - UK & US Azure Infrastructure Talent Solutions

Quality Assurance Specialist

Birmingham

Up to £40,000

We are seeking a Quality Assurance Specialist to join a leading pharmaceutical logistics company. This role focuses on supporting the implementation and maintenance of the Quality Management System (QMS) in line with ISO 9001 and ISO 13485 standards, and ensuring compliance with EU GDP guidelines.

Key Responsibilities:

• Maintaining and enhancing the QMS to meet regulatory, ISO, and client requirements.
• Supporting audits (regulatory, ISO, client, supplier) and managing CAPA plans.
• Driving a culture of quality excellence across the business.
• Conducting supplier audits, internal inspections, and management reviews.

Key Requirements:

• Proven experience in a GMDP or similar regulated environment.
• Strong knowledge of GDP, GMP, ISO 9001, and ISO 13485 standards.
• Excellent organizational, communication, and stakeholder management skills.
• A positive attitude toward promoting quality across all departments.
• Proficiency in MS Office applications (Word, Excel, PowerPoint, Teams).

If you have the skillset required and looking for your next career move, please apply for immediate consideration.

Seniority level

• Seniority level

  Mid-Senior level

Employment type

• Employment type

  Full-time

Job function

• Job function

  Quality Assurance

• Industries

  Pharmaceutical Manufacturing

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