Quality Assurance Speciliast

1 Tech Staffing Ltd; Birmingham; On-site; GBP 34,000 - 40,000; Full time

Job summary

A leading company in pharmaceutical logistics is seeking a Quality Assurance Specialist in Birmingham. The role involves maintaining quality systems per industry standards, fostering a positive quality culture, and ensuring compliance. Successful candidates will demonstrate expertise in GMP, GDP, and ISO regulations and bring strong organizational skills to the team.

Qualifications

• Experience and knowledge of GDP, GMP, GPhC regulations.
• Proven experience with ISO 9001 and ISO 13485 standards.
• Ability to work under pressure and meet deadlines.

Responsibilities

• Implementation and upkeep of the Quality Management System.
• Ensure compliance with industry standards and company policies.
• Participate in audits and manage CAPA plans.

Skills

Organizational skills

Communication skills

Attention to detail

Initiative

Collaboration

Tools

Microsoft Office

Job description

Quality Assurance Specialist
Birmingham (Office Based)

Up to GBP40,000 doe

We are seeking a Quality Assurance Specialist for a leading company specialising in pharmaceutical logistics. Their clients include some of the most well-known pharmaceutical brands globally.

The successful candidate will work within the Quality department and support the Head of QA and other key personnel in maintaining and implementing the Quality Management System. This will be in line with ISO 9001 and ISO 13485 standards and in compliance with EU GDP guidelines. Ideally, you will have experience working in a GMDP environment and a proactive approach to improving quality systems across the business.

Key Responsibilities:

• Assist in the implementation and upkeep of the Quality Management System, adhering to GMP, GDP, and ISO standards.
• Ensure ongoing compliance with industry standards, regulations, and company policies.
• Foster a positive quality culture within the organization, supporting continuous improvement efforts.
• Contribute to Quality System Management Reviews, preparing inputs, attending, presenting at meetings, and managing outcomes.
• Participate in audits (Regulatory, ISO, Client, Supplier, and internal) and manage CAPA plans.

Skills and Experience:

• Proven experience and good working knowledge of GDP, GMP, and GPhC regulations, as well as ISO 9001 and ISO 13485 standards.
• Strong organizational and communication skills, with excellent attention to detail.
• Ability to take initiative and work under pressure to meet deadlines.
• Experience fostering collaborative relationships within QA teams and across the business.
• Proficiency in Microsoft Office (Word, Outlook, Excel, PowerPoint, Teams).

Interviews are taking place w/c 21st October so please apply for immediate consideration.