QC Team Lead

The One Group; South Cambridgeshire; On-site; GBP 45,000; Full time

Job summary

An established industry player is seeking a dynamic QC Team Lead to spearhead a high-performing team in a fast-paced environment. This role combines hands-on leadership with technical expertise, focusing on continuous improvement and quality objectives. You will oversee QC systems, manage training, and ensure compliance with GMP standards while nurturing a culture of safety and excellence. With a competitive salary and attractive benefits, this opportunity is perfect for those passionate about driving change and fostering team development. Join a company that values your contributions and offers a supportive environment for professional growth.

Benefits

25 days holiday + bank holidays

Medical & Dental Care

Subsidised restaurant

Pension scheme

Discretionary bonus scheme

Voucher scheme

Qualifications

• Proven experience in people management and leadership.
• Strong technical knowledge in analytical validation and method transfer.

Responsibilities

• Lead and manage the QC team, driving performance and setting objectives.
• Oversee QC systems and ensure compliance with GMP standards.

Skills

People Management

Analytical Validation

Method Transfer

Communication Skills

Continuous Improvement

Education

Degree in a relevant science discipline

Tools

HPLC

GC

FTIR

UV Spectroscopy

Job description

Are you an experienced QC professional with a passion for team leadership and process improvement?

We are looking for a talented QC Team Lead to lead and develop a high-performing team, ensuring the delivery of quality objectives while driving continuous improvement in a dynamic environment. This hands-on leadership role requires a blend of technical expertise and strong people management skills.

On a day to day basis you will:

• Lead and manage the QC team, setting clear objectives and driving individual and team performance.
• Oversee and improve QC systems and processes, ensuring compliance with GMP standards.
• Lead technical assessments, independently determining the best approach for method validation, transfer, and verification across multiple techniques
• Nurture a culture of continuous improvement, ensuring high-quality results while promoting safety and environmental standards.
• Develop team capabilities and manage training requirements to maintain technical proficiency.
• Prepare and review technical reports, providing detailed analysis and recommendations.
• Take ownership of lab error investigations, ensuring thorough and timely resolutions.
• Support audits and inspections to ensure ongoing inspection readiness.

What do we need from you?

• A degree in a relevant science discipline.
• Proven experience in people management, performance development, and leadership.
• Strong technical knowledge in analytical validation, method transfer, and verification principles
• Wide knowledge of analytical techniques (HPLC, GC, FTIR, UV, etc.).
• Demonstrable pharmaceutical experience with QC process (sample management, stability management, reference and retains sample management)
• In-depth understanding of GMP and the ability to assess and address technical challenges independently.
• Excellent communication skills, including the ability to prepare and present detailed technical reports in writing and verbally to stakeholders.
• A proactive approach to driving development, change, and continuous improvement within the team.

What can you expect in return?

• Salary £45,000
• 25 days holiday + bank holidays
• Medical & Dental Care
• Subsidised restaurant
• Pension scheme
• Discretionary bonus scheme
• Voucher scheme

Interested to learn more? Get in touch with your CV today!