SRG - QA Specialist

Bionow; England; On-site; GBP 36,000 - 42,000; Full time

Job summary

A growing pharmaceutical manufacturer in Kent is seeking a Quality Assurance Specialist to enhance their Pharmaceutical Quality System. This role involves ensuring compliance with GMP standards, managing audits, and leading continuous improvement initiatives, as well as mentoring team members. Ideal candidates will possess a relevant degree and proven QA experience in a GMP environment.

Qualifications

• Proven QA experience in a GMP environment.
• Experience in supporting or leading audits is a must.
• Validation experience is highly advantageous.

Responsibilities

• Maintain the Pharmaceutical Quality System (PQS) and manage change controls.
• Support and prepare for audits and regulatory inspections.
• Mentor QA Officers and support staff training in GMP/GDP matters.

Skills

Attention to detail

Ability to manage multiple priorities

Education

Degree in Chemistry, Pharmaceutical Sciences, or related field

Job description

Job Title: Quality Assurance Specialist
Location: Kent
Salary: £36,000 – £42,000

SRG is recruiting a Quality Assurance Specialist to join a growing pharmaceutical manufacturer based in Kent. This company specializes in the production and distribution of a diverse range of medicinal products, emphasizing quality, compliance, and innovation.

The Role:
As a Quality Assurance Specialist, you will be crucial in maintaining and improving the Pharmaceutical Quality System (PQS). You will support compliance with GMP/GDP standards and regulatory frameworks, and contribute to the development of QA staff. Your role is vital in ensuring the company's high standards are met and continuously enhanced.

You will:

• Act as a Quality Specialist for the Business Unit, maintaining the QMS, managing change controls, deviation investigations, and the implementation & review of CAPAs.
• Support and prepare for audits, including regulatory inspections and supplier assessments.
• Oversee batch record and label generation in line with production schedules.
• Lead quality and continuous improvement projects.
• Mentor QA Officers and support staff training in GMP/GDP matters.

Requirements:

• A Degree in Chemistry, Pharmaceutical Sciences, or a related field, or equivalent practical experience.
• Proven QA experience in a GMP environment.
• Experience in supporting, preparing for, or leading internal/external audits.
• Validation experience is highly advantageous.
• Attention to detail and the ability to manage multiple priorities.