Quality Manager (Release)

Quantum Pharmaceutical Limited; Luton; On-site; GBP 40,000 - 60,000; Full time

Job summary

Quantum Pharmaceutical Limited seeks a Quality Manager (Release) to lead a quality team in their aseptic manufacturing unit. The role includes ensuring compliance with GMP practices, overseeing quality control activities, and developing strategies. Ideal candidates will have relevant experience in aseptic environments and strong leadership skills. Join a company dedicated to improving patient outcomes and be part of a team that truly matters.

Benefits

Competitive Salary (Negotiable DOE)

Flexible shift patterns

Free food and drink at work

Strong Social Committee

Eye care vouchers

Cycle to work scheme

EV Scheme

Qualifications

• Proven experience in aseptic manufacturing and quality management.
• At least 5 years of relevant GMP experience.
• Strong interpersonal skills and high computer literacy.

Responsibilities

• Lead a quality team and monitor compliance with GMP.
• Drive microbiology testing and oversee batch-releasing activities.
• Investigate quality trends and oversee inspections.

Skills

Leadership

Quality Control

GMP Knowledge

Interpersonal Skills

Computer Literacy

Education

Degree in Life Sciences

Job description

At Target Healthcare Group, we are at the forefront of pharmaceutical innovation and manufacturing. As a pioneering force in the industry, we are committed to revolutionising healthcare and improving patient outcomes.

Quantum Pharmaceutical, a vital part of our Group, stands as the UK’s premier manufacturer and supplier of compounded chemotherapies to the NHS and Private Hospitals. Our relentless dedication to helping patients, has propelled us to become one of the fastest-growing companies in the UK.

In line with our exciting growth within Aseptic Services, we have recently built a state-of-the-art dedicated aseptic manufacturing facility. We are currently looking for a motivated QualityManager (Release) to join our dynamic Aseptic Services team.

This isn’t just a job - it’s a chance to contribute to a mission that truly matters, to develop professionally and personally, and to be part of a team that values growth and advancement.

In this vital role, you will:

• Lead and Inspire: Build and manage a high-performing, collaborative quality team that embodies our Group’s values.
• Drive Excellence: Develop, implement, and monitor the microbiology testing and environmental monitoring program.
• Ensure Quality: Oversee a team of batch-Releasing Officers and Quality Control Assistants to maintain the highest standards for aseptically compounded medicines.
• Monitor Trends: Investigate trends in quality KPIs, including fails, rework, and complaints, and report findings to management.
• Promote Best Practices: Educate colleagues on GMP (Good Manufacturing Practices) and ensure compliance.
• Support Inspections: Assist the Head of Quality Assurance in leading and closing MHRA and Home Office inspections.
• Strategise for Success: Work with Executive Directors to develop a strategy for the Quality Department, ensuring ongoing regulatory compliance and alignment with business development goals.
• Collaborate and Communicate: Provide quality input for management reviews, address outstanding issues, and support other departments with quality information for new business, product, and service tenders.

About you:

We’re looking for an experienced, forward-thinking individual who meets the following criteria:

• Proven experience in a similar role, ideally in aseptic manufacturing
• A degree in a life sciences discipline (e.g., pharmacy, microbiology, chemistry).
• At least 5 years of relevant GMP experience within a licensed facility or under a section 10 exemption.
• Comprehensive, up-to-date knowledge of GMP practices.
• A self-starter with a demonstrated ability to work autonomously and make decisions confidently.
• Strong interpersonal skills with the ability to engage with colleagues at all levels.
• High computer literacy, particularly with Microsoft Office software.
• A recognised management qualification is desirable but not essential.

What We Offer:

Join us, and you’ll become part of a high performing team in a diverse and inclusive environment that encourages personal and professional growth.

Enjoy benefits like:

• Competitive Salary (Negotiable DOE)
• Flexible shift patterns
• Free food and drink at work
• Strong Social Committee
• Eye care vouchers
• Cycle to work scheme
• EV Scheme

Please note: All applicants are subject to online psychometric assessments and a DBS check

Join us at Quantum and be a part of something bigger – apply today to start your career journey with us!

🔠Important:

Aseptic manufacturing facilities operate under highly controlled conditions to ensure the production of sterile products without contamination. These working conditions are governed by strict regulations and guidelines.

The work environment and requirements described below are representative of those an employee encounters while performing the essentials of this role. Reasonable adjustments may be made to perform the essential functions:

Attention to detail: Our Aseptic environment requires precision and adherence to legislation at all times.

Workers will be required to detect any minor imperfections, such as: Particles or contaminants in solutions, scratched or damage to sterile containers and misalignment in machine components.

Discipline and Focus: Adhering to strict guidelines without shortcuts is essential.

Physical demands: The role often involves repetitive processes and being stationary for prolonged periods, working in protective clothing and maintaining aseptic techniques under demanding conditions.

High levels of concentration are equally important to avoid errors

Ability to follow instructions: Workers must follow standard operating procedures (SOPs) meticulously without deviation.

Commitment to hygiene and cleanliness: A strong personal commitment to cleanliness is critical, including strict adherence to handwashing, gowning and personal hygiene protocols.

Resilience under pressure: Aseptic manufacturing can involve working under tight deadlines and regulations

Technical Aptitude: Familiarity with machinery and aseptic processes is valuable for understanding and troubleshooting equipment

Comfort with using monitoring systems and understanding documentation is required

📢 Be Part of Something Bigger!
Join Quantum Pharmaceutical and start your journey with a team that truly makes a difference. Apply today!