At a Glance
- Tasks: Oversee quality processes, manage audits, and drive operational excellence in a global pharma setting.
- Company: Join a leading global pharmaceutical organisation with a commitment to quality.
- Benefits: Competitive hourly rate, professional growth, and a dynamic work environment.
- Other info: Fast-paced role with opportunities for career advancement and cross-functional collaboration.
- Why this job: Make a real impact on quality standards and improve healthcare outcomes.
- Qualifications: Degree in a relevant field and 3+ years in Quality or related GxP environments.
The predicted salary is between 46600 - 62200 £ per year.
PE Global is currently recruiting for a Senior Quality Associate on behalf of a leading global pharmaceutical organisation.
Location: Bracknell
Contract duration: 12 months
Hourly rate: £22.42-£29.89 per hour
The Role
You will provide quality oversight across business processes, support audits and inspections, manage deviations and CAPAs, and collaborate cross-functionally to strengthen quality culture and operational excellence.
Key Responsibilities
- Quality Systems & Compliance
- Support the implementation and management of quality systems and regional quality plans
- Manage deviations, change controls, CAPAs, and management notifications
- Conduct root cause investigations and ensure effective corrective and preventative actions
- Review and contribute to quality procedures, templates, and controlled documentation
- Partner with business stakeholders to interpret regulatory and quality requirements
- Monitor compliance trends and proactively identify areas for improvement
- Quality Oversight
- Provide quality guidance and consultation across affiliate business functions
- Support risk assessments, quality planning, and continuous improvement initiatives
- Monitor quality actions arising from audits, inspections, and deviations
- Drive standardisation and share best practices across regional and global teams
- Audits & Inspection Readiness
- Support and coordinate internal and external audit activities
- Assist with inspection readiness and audit response management
- Ensure timely closure of audit findings and CAPA commitments
- Maintain accurate and inspection-ready documentation and training records
- Cross-Functional Partnership
- Act as a trusted quality partner for assigned business areas
- Build strong working relationships with internal stakeholders and quality networks
- Contribute to key quality and business projects as required
- Promote a risk-based and compliant approach across operations
Candidate Requirements
- Bachelor’s or Master’s degree in a scientific, healthcare, or related discipline
- Minimum 3 years’ experience in Quality, Regulatory, Clinical Development, Pharmacovigilance, or related GxP environments
- Strong understanding of quality systems within regulated industries (GMP, GCP, GVP)
- Experience managing deviations, CAPAs, change controls, and audit activities
- Excellent analytical, problem-solving, and organisational skills
- Strong written and verbal communication skills with the ability to influence stakeholders
- Ability to manage multiple priorities in a fast-paced environment
- Experience working within global or matrix organisations is advantageous
Please note our client cannot assist with any visa sponsorship and candidates must have the correct visa to live and work in UK.
Interested candidates should submit an updated CV.
Please click the link below to apply.
Senior Quality Associate in Bracknell employer: PE Global (UK)
PE Global is an exceptional employer, offering a dynamic work environment in Bracknell where quality and compliance are at the forefront of our operations. We prioritise employee growth through continuous training and development opportunities, fostering a collaborative culture that encourages innovation and excellence. Join us to be part of a leading global pharmaceutical organisation that values your contributions and supports your career aspirations.
StudySmarter Expert Advice🤫
We think this is how you could land Senior Quality Associate in Bracknell
✨Tip Number 1
Network like a pro! Reach out to your connections in the pharmaceutical industry and let them know you're on the hunt for a Senior Quality Associate role. You never know who might have the inside scoop on job openings or can put in a good word for you.
✨Tip Number 2
Prepare for interviews by brushing up on your knowledge of quality systems and compliance. Be ready to discuss your experience with CAPAs and deviations, as well as how you've contributed to audits and inspections in the past. Show them you’re the quality guru they need!
✨Tip Number 3
Don’t just apply and wait! Follow up on your applications through our website. A quick email or message can show your enthusiasm and keep you on their radar. It’s all about making that connection!
✨Tip Number 4
Stay organised and keep track of your applications and interviews. Use a spreadsheet or an app to note down details like company names, roles, and follow-up dates. This will help you manage your time and ensure you don’t miss any opportunities!
We think you need these skills to ace Senior Quality Associate in Bracknell
Some tips for your application 🫡
Tailor Your CV:Make sure your CV is tailored to the Senior Quality Associate role. Highlight your experience in quality systems, CAPAs, and audits, as these are key for us. Use specific examples that showcase your skills and achievements in these areas.
Craft a Compelling Cover Letter:Your cover letter is your chance to shine! Use it to explain why you're the perfect fit for our team. Mention your understanding of regulatory requirements and how you can contribute to our quality culture. Keep it concise but impactful!
Showcase Your Soft Skills:While technical skills are crucial, don’t forget to highlight your soft skills too! We value strong communication and problem-solving abilities. Share examples of how you've influenced stakeholders or managed multiple priorities in past roles.
Apply Through Our Website:We encourage you to apply directly through our website. It’s the best way for us to receive your application and ensures you’re considered for the role. Plus, it shows your enthusiasm for joining our team!
How to prepare for a job interview at PE Global (UK)
✨Know Your Quality Systems
Make sure you brush up on your knowledge of quality systems and compliance regulations. Be ready to discuss how you've managed deviations, CAPAs, and change controls in your previous roles. This will show that you understand the core responsibilities of a Senior Quality Associate.
✨Prepare for Scenario Questions
Expect to face scenario-based questions during the interview. Think about past experiences where you conducted root cause investigations or supported audits. Prepare specific examples that highlight your analytical and problem-solving skills, as these are crucial for the role.
✨Showcase Your Cross-Functional Collaboration
This role requires strong partnerships across various business functions. Be ready to share examples of how you've built relationships with stakeholders and contributed to quality projects. Highlight your ability to influence and communicate effectively with different teams.
✨Stay Updated on Industry Trends
Familiarise yourself with the latest trends and best practices in the pharmaceutical industry, especially regarding quality oversight and compliance. Being knowledgeable about current challenges and innovations will demonstrate your commitment to continuous improvement and operational excellence.
