QA Manager-Pharma Biotech (Sterile)

Russell Taylor Group Ltd; Alderley Edge; On-site; GBP 50,000 - 70,000; Full time

Job summary

A growing SME in the pharmaceutical sector is seeking a QA Manager to oversee the Quality Management System and ensure compliance with GMP standards. The ideal candidate will have experience managing teams and driving continuous improvement initiatives. This onsite role is based in Alderley Edge, offering a competitive salary and benefits including 25 days of holiday, private medical care, and a company pension.

Benefits

25 days holiday + BH

Private medical care

Share options scheme

Company pension

Qualifications

• Proven experience in QA management within pharmaceutical or biotech industries.
• Experience managing teams and familiar with GMP standards.
• Direct experience of CAPA, Change control, root cause analysis, and deviations.

Responsibilities

• Manage and improve the Quality Management System (QMS).
• Ensure compliance with MHRA and other regulatory requirements.
• Drive quality culture and support training initiatives.

Skills

Quality Management System (QMS)

Regulatory compliance

Leadership

Problem-solving

Communication

Education

Degree in Life Sciences or related discipline

Job description

Overview

Role: QA Manager-Pharma Biotech (Sterile)
Location: Alderley Edge onsite only
Salary: Competitive salary (DOE)
Hours: Days (Monday - Friday) 40 hours per week
Benefits: 25 days holiday + BH, private medical care, share options scheme & company pension

Russell Taylor Group have a fantastic opportunity for a QA Manager with sterile experience to join a continually growing SME in Cheshire. Our client requires someone who has experience managing a team and QMS. This position plays a leading role in improving the QA function and ensuring compliance to GMP standards. Experience of internal audits, CAPAs, deviations, root cause analysis and change control are essential for this role.

Key Responsibilities

• Manage and improve the Quality Management System (QMS).
• Ensure compliance with MHRA and other regulatory requirements.
• Driving continuous improvement and fostering a strong quality culture.
• Lead audits- manage CAPA and change control processes.
• Oversee batch record reviews, deviation investigations, and release documentation.
• Provide QA oversight for manufacturing, testing, and validation activities.
• Support training and continuous improvement in quality culture.
• Liaise with regulatory bodies, suppliers, and cross-functional teams.
• Manage a small team of 6- conducting regular one to one appraisals and performance reviews.
• Provide monthly KPI metrics in relation to quality.

Requirements

• Degree in Life Sciences or related discipline.
• Proven experience in QA management within pharmaceutical, biotech, or medical manufacturing- experience of directly managing individuals is essential for this role.
• Previous direct experience of CAPA, Change control, root cause analysis & deviations
• Experience in a sterile environment.
• Strong knowledge of GMP and quality system regulations.
• Excellent communication, leadership, and problem-solving skills.
• Audit and regulatory inspection experience.

Important Information

We endeavour to process your personal data in a fair and transparent manner. In applying for this role, Russell Taylor will be acting within your interest and will contact you in relation to the role, either by email, phone or text message. For more information see our on our website. It is important you are aware of your individual rights and the provisions the company has put in place to protect your data. If you would like further information on the policy or GDPR please get in touch with us