At a Glance
- Tasks: Ensure quality oversight, manage audits, and drive operational excellence in a global pharmaceutical setting.
- Company: Join a leading global pharmaceutical organisation with a commitment to quality and compliance.
- Benefits: Competitive hourly rate, dynamic work environment, and opportunities for professional growth.
- Other info: Fast-paced role with opportunities to influence and improve quality standards.
- Why this job: Make a real impact on quality processes and collaborate with diverse teams.
- Qualifications: Degree in a relevant field and 3+ years in Quality or related GxP environments.
The predicted salary is between 46400 - 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: 6 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
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 people in the industry, attend events, and connect on LinkedIn. 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 researching the company and its culture. Understand their quality systems and compliance standards so you can speak their language and show you're the perfect fit for the Senior Quality Associate role.
✨Tip Number 3
Practice your answers to common interview questions, especially those related to managing deviations and CAPAs. We want you to feel confident and ready to showcase your skills when it counts!
✨Tip Number 4
Don’t forget to apply through our website! It’s the best way to ensure your application gets seen. Plus, we love seeing candidates who are proactive about their job search.
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 reflects the specific skills and experiences that match the Senior Quality Associate role. Highlight your experience with quality systems, CAPAs, and audits to show us you’re the right fit!
Craft a Compelling Cover Letter:Use your cover letter to tell us why you’re passionate about quality assurance in the pharmaceutical industry. Share specific examples of how you've contributed to quality culture and operational excellence in your previous roles.
Showcase Your Achievements:Don’t just list your responsibilities; we want to see your achievements! Quantify your successes where possible, like improvements in compliance trends or successful audit outcomes, to make your application stand out.
Apply Through Our Website:We encourage you to apply directly through our website for a smoother process. It’s the best way for us to receive your application and ensure it gets the attention it deserves!
How to prepare for a job interview at PE Global
✨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 the Senior Quality Associate position.
✨Prepare for Scenario Questions
Expect scenario-based questions that assess your problem-solving skills. Think of specific examples where you've conducted root cause investigations or contributed to quality improvements. Use the STAR method (Situation, Task, Action, Result) to structure your answers clearly.
✨Showcase Your Cross-Functional Experience
Highlight any experience you have working with different teams or departments. Discuss how you've built relationships with stakeholders and contributed to cross-functional projects. This will demonstrate your ability to act as a trusted quality partner within the organisation.
✨Be Audit-Ready
Familiarise yourself with audit processes and be prepared to discuss how you've supported internal and external audits in the past. Mention any specific instances where you ensured timely closure of audit findings or maintained inspection-ready documentation, as this is crucial for the role.
