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For Companies At a Glance
- Tasks: Implement and maintain Quality Management Systems for pharmaceutical operations.
- Company: Join Orbia, a global leader focused on advancing life through innovative solutions.
- Benefits: Enjoy a purpose-driven culture with opportunities for growth and development.
- Why this job: Make a real impact in healthcare while working in a diverse and inclusive environment.
- Qualifications: HNC in a science-related subject and 2+ years in a QA role required.
- Other info: Be part of a team that values every voice and fosters collaboration.
The predicted salary is between 30000 - 42000 £ per year.
You are purpose driven. Growth minded. Ready to stretch your potential. That’s the spirit of the community you will find at Orbia: where the purpose to advance life around the world drives our global team of over 23,000 every single day. From creating solutions to deliver clean water, secure food supplies and reliable information to steering material advances that power the future of green and smart cities, transportation, and healthcare, we never settle for “good enough” when there’s an opportunity to make life better. Where purpose comes to life, it changes lives. This is what we live for.
Fluor and Energy Materials, an Orbia business, is hiring a QA Officer to be based at Thornton Science Park, Cheshire, UK.
Main Purpose
To implement and maintain the Quality Management Systems for MDI Pharmaceutical operations at the Thornton site to meet the requirements of cGMP and customer and regulatory audits requirements. To prepare batch and support services documentation files for QP review and verify for the release of medical products prior to shipment.
Main Responsibilities
- Support and administer the Quality Management System to ensure compliance with appropriate QA standards are maintained.
- Manage appropriate documentation management systems for the MDI business to ensure compliance with the required standards.
- Identify improvements to Quality Management System and ensure that improvements targets are met, that system changes are implemented, and that such modifications are completed in full compliance with appropriate standards.
- Compile, review, and prepare batch and support services documentation for QP to release.
- Support customer/regulatory audits as required and provide QA representation or advice as and when required.
- Devise, deliver and (where necessary) validate appropriate training packages.
- Develop an understanding of all appropriate business QA standards and requirements, so that Business' competency as a quality supplier is maintained and improved.
Qualifications
Minimum: HNC in science related subject.
Knowledge/ Experience Required
- Working with and developing Pharmaceutical GMP and quality management systems.
- 2+ years of experience in a QA related role.
Behaviors that can help you succeed at Orbia:
- Develop yourself & Others
- Foster Collaboration & Inclusion
- Drive Results
- Provide Vision & Direction
We welcome purpose-driven dreamers, doers, and builders, recognizing that it takes difference to make a difference. If you’re ready to bring your skills, talents, and perspective to moving your career, the company, people, and the planet forward, we’d like to hear from you. We believe that every voice matters; every community deserves respect; and every challenge is an opportunity and united by empathy, we are stronger for our different perspectives. We are dedicated to building a more diverse, inclusive, and equitable workplace that supports the needs of all our employees regardless of their role, location, identity, and background.
Quality Assurance Officer employer: Orbia Fluor & Energy Materials
Contact Detail:
Orbia Fluor & Energy Materials Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Quality Assurance Officer
✨Tip Number 1
Familiarise yourself with the specific Quality Management Systems (QMS) used in the pharmaceutical industry, particularly those related to cGMP. Understanding these systems will not only help you during interviews but also demonstrate your commitment to quality assurance.
✨Tip Number 2
Network with professionals already working in QA roles within the pharmaceutical sector. Attend industry events or join relevant online forums to gain insights and potentially get referrals that could lead to job opportunities at Orbia.
✨Tip Number 3
Prepare to discuss specific examples of how you've contributed to improving quality management systems in your previous roles. Highlighting measurable outcomes can set you apart from other candidates.
✨Tip Number 4
Research Orbia's values and recent projects to align your personal goals with their mission. Showing that you understand their purpose-driven approach will resonate well during interviews and demonstrate your enthusiasm for the role.
We think you need these skills to ace Quality Assurance Officer
Some tips for your application 🫡
Understand the Role: Before applying, make sure you fully understand the responsibilities and qualifications required for the Quality Assurance Officer position. Tailor your application to highlight relevant experience in QA and knowledge of GMP.
Craft a Tailored CV: Your CV should reflect your experience in quality management systems and any specific achievements in previous QA roles. Use keywords from the job description to ensure your CV aligns with what Orbia is looking for.
Write a Compelling Cover Letter: In your cover letter, express your passion for quality assurance and how your values align with Orbia's mission. Highlight your experience in compliance and any successful projects that demonstrate your ability to improve QA processes.
Proofread Your Application: Before submitting, carefully proofread your CV and cover letter for any spelling or grammatical errors. A polished application reflects your attention to detail, which is crucial for a QA role.
How to prepare for a job interview at Orbia Fluor & Energy Materials
✨Understand the Quality Management System
Make sure you have a solid grasp of Quality Management Systems, especially in relation to cGMP. Be prepared to discuss your experience with these systems and how you've contributed to their implementation or improvement in previous roles.
✨Showcase Your Documentation Skills
Since the role involves preparing batch and support services documentation, be ready to talk about your experience with documentation management. Highlight any specific tools or processes you've used to ensure compliance and accuracy.
✨Prepare for Regulatory Audits
Familiarise yourself with the types of customer and regulatory audits that may occur in the pharmaceutical industry. Be prepared to share examples of how you've supported audits in the past and what you learned from those experiences.
✨Emphasise Collaboration and Inclusion
Orbia values collaboration and inclusion, so be sure to demonstrate how you've worked effectively in teams. Share examples of how you've fostered a collaborative environment and contributed to a diverse workplace.
