Quality Manager UK

Ellab; Ellesmere Port; On-site; GBP 40,000 - 60,000; Full time

Job summary

Join a leading company in compliance solutions as a Quality Manager in Ellesmere Port. This role involves managing quality standards, driving ISO9001 and ISO17025 implementations, and collaborating with a local team to enhance quality processes. If you're passionate about quality and ready to take on a dynamic challenge, apply now!

Benefits

Opportunity for career development

Collaborative work environment

Influence your own tasks and responsibilities

Qualifications

• Minimum 2-3 years of relevant experience in quality management.
• Profound knowledge of ISO9001 and ISO17025.
• Hands-on experience with quality processes and audits.

Responsibilities

• Manage, evaluate and improve quality processes in the UK.
• Establish documented processes and manage nonconformities.
• Conduct internal audits and provide quality training.

Skills

Communication

Collaboration

Proactivity

Analytical Thinking

Education

Relevant science or technical degree

Job description

Quality Manager UK

Direct message the job poster from Ellab

Do you have a passion for quality and thrive in dynamic environments? Are you a motivated and passionate Quality professional looking for an exciting new challenge?

If so, you might be the perfect fit for our Team at Ellab UK – Ellesmere Port!

About the role

Ellab, a leading provider of innovative compliance solutions for the pharmaceutical and biotech industries, is experiencing rapid growth. We are looking for an enthusiastic, skilled and self-driven Quality Manager who is eager to contribute to our company's journey and ensure the highest standards of quality in our operations. You will become an integral part of a dedicated Global Quality team and, with the responsibility for Quality management in the UK you will work very closely with the local team. Reporting directly to the Senior Quality Manager for UK & Ireland, located in Ireland, you will play a crucial role in maintaining and enhancing our quality standards. We offer a collaborative and dynamic environment where independence, fresh ideas and adaptability are highly valued. Professionalism, mutual support and respect form the core of our team culture.

What you will be doing in this role?

As Quality Manager in the UK, you will be responsible for driving, maintaining and developing the subsidiary’s quality management incl. ISO9001 certification and ISO17025 accreditation. Ellab is aligning the quality management globally which includes implementation of global processes and establishment of one global multisite ISO9001 certification. It will be your responsibility to drive the transformation in the UK working closely with the local team.

Your responsibilities will include:

• Manage, evaluate and improve the quality processes in the UK

• Adopt and implement global quality processes

• Establish/ensure sufficient documented processes, procedures and instructions

• Manage nonconformities, complaints and change control cases

• Preparation and coordination of management review

• Handle quality agreements and questionnaires from customers

• Conduct internal audits and host audits from external stakeholders

• Liaise with external suppliers and customers when required

• Conduct internal quality training

• Collecting sustainability data to headquarter

• Participation in regular global quality meetings

Skills and experience you will bring to Ellab

We are looking for a service minded colleague with a passion for improving quality processes with a keep it simple mindset. You have excellent collaboration skills and are self-driven, proactive, positive with a can-do attitude. You are a strong and natural communicator verbal as well as written and your work approach is structured and systematic. Occasional travel to our office in Ireland will be required for training purposes and to integrate with the HSQ Team in Ireland.

Furthermore, we expect you to have:

• Relevant science or technical degree

• Minimum 2-3 years of relevant experience

• Profound knowhow of ISO9001 and ISO17025

• Knowledge of GMP and quality requirements in pharmaceutical industries

• Preferable trained auditor

• Hands-on experience with quality management incl. audits, NCs, customer complaints etc.

• Good technical understanding

• Ability to drive initiatives in a matrix organisation

What we offer

• Opportunity to work in a global, dynamic and fast-paced environment

• Opportunity to influence your own tasks/responsibilities and develop your career in a supportive environment, making a real impact on a growing international company

• You’ll be joining a team highly focused on execution and optimisation, while also recognising the importance of work-life balance.

If you find this opportunity exciting, apply today!

Seniority level

• Seniority level

  Mid-Senior level

Employment type

• Employment type

  Full-time

Job function

• Job function

  Other

• Industries

  Pharmaceutical Manufacturing

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