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- Tasks: Ensure top-notch quality standards in a dynamic lab environment and lead exciting quality improvement projects.
- Company: Join ALS, a global leader in scientific testing dedicated to building a healthier future.
- Benefits: Enjoy 25+ days of annual leave, enhanced sick pay, and a supportive learning environment.
- Why this job: Make a real impact on health and safety while developing your skills in a fast-paced setting.
- Qualifications: A scientific degree and experience in regulated environments are essential.
- Other info: Be part of a diverse team that values inclusion and personal growth.
The predicted salary is between 36000 - 60000 £ per year.
At ALS, we encourage you to dream big. When you join us, you’ll be part of a global team harnessing the power of scientific testing and data-driven insights to build a healthier future.
Hours Per Week: 40
Days Per Week: Monday to Friday (09:00 - 17:30)
Contract: Full Time and Permanent
Hiring Manager: Holly Beresford
Closing Date: Monday 26th January 2026
The Role
We are looking for a driven Site Quality Officer to help maintain and continuously improve site quality standards within a regulated laboratory environment. Working closely with the Pharmaceutical Compliance Manager and laboratory teams, you will ensure compliance with ISO 17025, UKAS, GMP and internal quality systems, playing a key role in audits, investigations and quality improvement initiatives.
The Day to Day
- Support and oversee the site Quality Management System (QMS).
- Co‑ordinate equipment calibration, servicing and mapping to schedule.
- Maintain, review and issue SOPs, ensuring staff training is up to date.
- Manage quality investigations, CAPAs and eQMS events to agreed timelines.
- Support data integrity, change control and risk assessment activities.
- Review validation, method transfer and technical project documentation.
- Conduct internal audits and support client and regulatory inspections.
- Co‑ordinate proficiency testing and internal quality control programmes.
- Provide practical quality advice to site staff and promote best practice.
- Champion health, safety and environmental compliance on site.
The Essentials
- Scientific degree or equivalent in Science, Pharmaceutical Sciences or Quality Management.
- Experience working within a regulated pharmaceutical or laboratory environment.
- Strong understanding of QMS, ISO 17025, UKAS and GMP.
- Confident Microsoft Office user with strong documentation skills.
- Excellent attention to detail and ability to manage competing priorities.
- Clear communicator with the confidence to challenge constructively.
- Proactive, organised and comfortable working in a fast‑paced environment.
Our Benefits Include
- Annual Leave commencing at 25 days (rising to 30) plus 8 public holidays (pro rata for part time)
- Ability to buy annual leave.
- Enhanced Company Sick Pay Scheme
- Salary Progression Scheme based on technical and behavioural competencies.
- ‘Celebrating Success’ Recognition Awards
- Perkbox membership providing access to discount vouchers and wellness hub.
- Learning/study support
- Group Personal Pension Plan
- Car Parking on‑site
Working at ALS
The ALS team is a diverse and dedicated community united by our passion to make a difference in the world. Our values are important to us, and shape how we work, how we treat each other and how we recognise excellence. At ALS, you’ll be supported to develop new skills and reach your full potential. We invest in our people with programmes and opportunities that help you build a diverse career with us. We want everyone to have a safe, flexible and rewarding career that makes a positive impact on our people, the planet and our communities.
Everyone Matters
ALS is proud to be an equal opportunity employer and is committed to fostering an inclusive work environment where the strengths and perspectives of each employee are both recognised and valued. ALS also welcomes applications from people with all levels of ability. Reasonable adjustments to support candidates throughout the recruitment process are available upon request.
Eligibility
To be eligible to work at ALS you must be a Citizen or Permanent Resident of the country you are applying for, or either hold or be able to obtain, a valid working visa.
How To Apply
Please apply online and provide a resume & cover letter that best demonstrate your motivation and ability to meet the requirements of this role.
Site Quality Officer in Ely employer: Als
Contact Detail:
Als Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Site Quality Officer in Ely
✨Tip Number 1
Network like a pro! Reach out to current or former employees at ALS on LinkedIn. A friendly chat can give you insider info about the company culture and maybe even a referral!
✨Tip Number 2
Prepare for the interview by brushing up on your knowledge of ISO 17025, UKAS, and GMP. We want to see that you’re not just familiar with these standards but can also discuss how you've applied them in past roles.
✨Tip Number 3
Show off your problem-solving skills! Think of examples where you’ve tackled quality issues or improved processes. We love candidates who can demonstrate their proactive approach to challenges.
✨Tip Number 4
Don’t forget to apply through our website! It’s the best way to ensure your application gets seen by the right people. Plus, it shows you’re serious about joining our team at ALS.
We think you need these skills to ace Site Quality Officer in Ely
Some tips for your application 🫡
Show Your Passion: When writing your cover letter, let your enthusiasm for the Site Quality Officer role shine through. We want to see how excited you are about maintaining and improving quality standards in a regulated environment!
Tailor Your Resume: Make sure your CV highlights relevant experience in quality management and compliance with ISO 17025 and GMP. We love seeing candidates who can connect their past roles to what we do at ALS.
Be Clear and Concise: In both your resume and cover letter, keep your language straightforward and to the point. We appreciate clarity, especially when it comes to your skills and experiences that relate to the role.
Apply Through Our Website: Don’t forget to submit your application through our website! It’s the best way for us to receive your materials and ensures you’re considered for the Site Quality Officer position.
How to prepare for a job interview at Als
✨Know Your Standards
Familiarise yourself with ISO 17025, UKAS, and GMP standards before the interview. Being able to discuss these frameworks confidently will show that you understand the regulatory environment and can contribute to maintaining quality standards.
✨Showcase Your Experience
Prepare specific examples from your past roles where you've successfully managed quality investigations or conducted internal audits. This will help demonstrate your hands-on experience in a regulated laboratory environment, which is crucial for the Site Quality Officer role.
✨Communicate Clearly
Practice articulating your thoughts clearly and concisely. As a Site Quality Officer, you'll need to communicate effectively with various teams, so showcasing your communication skills during the interview is essential.
✨Ask Insightful Questions
Prepare thoughtful questions about the company's quality management systems and how they handle compliance challenges. This not only shows your interest in the role but also your proactive approach to understanding the company's operations.
