Quality Co-Ordinator/Supervisor (Permanent) in Waterlooville
Quality Co-Ordinator/Supervisor (Permanent)

Quality Co-Ordinator/Supervisor (Permanent) in Waterlooville

Waterlooville Full-Time 30000 - 40000 £ / year (est.) No home office possible
Advanced Resource Managers

At a Glance

  • Tasks: Coordinate and improve quality systems in a dynamic manufacturing environment.
  • Company: Exciting Cosmetics Contract Manufacturer experiencing significant growth.
  • Benefits: Permanent role with a 35-hour work week and great work-life balance.
  • Other info: Opportunity for continuous learning and career development in a luxury office setting.
  • Why this job: Join a culture of quality and compliance while making a real impact.
  • Qualifications: Experience in quality roles within regulated industries like cosmetics or pharmaceuticals.

The predicted salary is between 30000 - 40000 £ per year.

Are you an experienced Quality Coordinator with a background working within a regulated manufacturing environment such as Cosmetics, Medical Devices, Pharmaceuticals or similar? We are partnered with an extraordinary Cosmetics Contract Manufacturer who are currently going through a huge growth phase! This role is based just outside of Portsmouth in their luxury offices and is being hired for on a permanent basis, with full time hours being classed as 35 hours a week, a real employer of work life balance!

The successful candidate will support the Head of Quality, working across both Quality Control and Quality Assurance. You will be responsible for the coordination, administration, and follow-up of quality systems and processes, ensuring the effective operation of the Quality Management System and ongoing compliance with GMP and relevant standards such as ISO 22716.

  • Maintaining, updating, and improving quality processes.
  • Document control activities including SOP creation, formatting, review cycles, version control, and archiving.
  • Track and manage change controls, deviations, non-conformances, CAPAs, complaints, and investigations.
  • Maintain quality logs, trackers, and dashboards to provide clear visibility of quality performance.
  • Coordinate sample retention, testing records, and QC documentation in line with GMP requirements.
  • Support batch record review activities and follow ups.
  • Support the planning, preparation, and follow-up of internal and external audits.
  • Support new product introductions by coordinating quality documentation and ensuring readiness against quality and regulatory requirements.
  • Support the implementation of standardised ways of working and GMP across the site.
  • Assist in monitoring quality KPIs and metrics.
  • Support training administration for quality systems, GMP, and SOPs, including tracking completion and effectiveness.
  • Champion a culture of quality, compliance, and continuous improvement throughout the business.

Experience in a quality-related role (QA, QC, or Quality Systems) within a regulated manufacturing environment such as Cosmetics, Medical Devices, Pharmaceuticals, or similar. Working knowledge of GMP and quality standards such as ISO 22716 is preferred. Proactive, hands-on approach with a willingness to learn and develop within the Quality function.

Quality Co-Ordinator/Supervisor (Permanent) in Waterlooville employer: Advanced Resource Managers

Join a dynamic and rapidly growing Cosmetics Contract Manufacturer located just outside Portsmouth, where you will thrive in a supportive work environment that prioritises work-life balance with a 35-hour week. As a Quality Co-Ordinator/Supervisor, you will have the opportunity to contribute to meaningful quality improvements while benefiting from a culture that champions continuous learning and professional development. With luxury offices and a commitment to excellence, this company is dedicated to fostering a collaborative atmosphere that empowers employees to excel in their roles.
Advanced Resource Managers

Contact Detail:

Advanced Resource Managers Recruiting Team

StudySmarter Expert Advice 🤫

We think this is how you could land Quality Co-Ordinator/Supervisor (Permanent) in Waterlooville

✨Tip Number 1

Network like a pro! Reach out to your connections in the cosmetics or pharmaceuticals industry. Attend events, join relevant groups on LinkedIn, and don’t be shy about asking for introductions. You never know who might have the inside scoop on job openings!

✨Tip Number 2

Prepare for interviews by brushing up on your knowledge of GMP and ISO standards. Make sure you can discuss how you've applied these in past roles. We want you to show off your expertise and passion for quality management!

✨Tip Number 3

Don’t just apply and wait! Follow up on your applications after a week or so. A quick email expressing your continued interest can set you apart from other candidates. It shows you're proactive and really keen on the role!

✨Tip Number 4

Check out our website for the latest job openings and apply directly through us. We’re all about making the application process smooth and easy for you. Plus, it gives you a better chance of getting noticed!

We think you need these skills to ace Quality Co-Ordinator/Supervisor (Permanent) in Waterlooville

Quality Management System
GMP Compliance
ISO 22716
Document Control
SOP Creation
Change Control Management
Non-Conformance Management
CAPA Management
Quality Performance Tracking
Internal and External Audits
New Product Introduction Coordination
Quality KPIs Monitoring
Training Administration for Quality Systems
Continuous Improvement

Some tips for your application 🫡

Tailor Your CV: Make sure your CV is tailored to the Quality Coordinator role. Highlight your experience in regulated environments like Cosmetics or Pharmaceuticals, and don’t forget to mention any relevant quality standards you’re familiar with, such as GMP or ISO 22716.

Craft a Compelling Cover Letter: Your cover letter is your chance to shine! Use it to explain why you’re passionate about quality management and how your proactive approach aligns with our culture of continuous improvement. Keep it concise but impactful!

Showcase Relevant Experience: In your application, be sure to showcase your hands-on experience in quality systems, document control, and compliance. Mention specific projects or achievements that demonstrate your ability to maintain and improve quality processes.

Apply Through Our Website: We encourage you to apply through our website for a smoother application process. It’s the best way for us to receive your application and ensures you don’t miss out on any important updates from our team!

How to prepare for a job interview at Advanced Resource Managers

✨Know Your Quality Standards

Make sure you brush up on your knowledge of GMP and ISO 22716 before the interview. Being able to discuss these standards confidently will show that you understand the regulatory environment and can contribute effectively to the role.

✨Showcase Your Experience

Prepare specific examples from your past roles where you've successfully managed quality systems or processes. Highlight any achievements in improving quality metrics or compliance, as this will demonstrate your hands-on experience and proactive approach.

✨Be Ready for Scenario Questions

Expect questions that ask how you would handle specific quality-related scenarios, such as deviations or non-conformances. Practise articulating your thought process and decision-making skills, as this will showcase your problem-solving abilities.

✨Emphasise Continuous Improvement

Discuss your commitment to fostering a culture of quality and continuous improvement. Share any initiatives you've led or participated in that aimed at enhancing quality processes, as this aligns perfectly with the company's goals.

Quality Co-Ordinator/Supervisor (Permanent) in Waterlooville
Advanced Resource Managers
Location: Waterlooville

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