At a Glance
- Tasks: Manage quality assurance activities and ensure compliance in a dynamic pharmaceutical environment.
- Company: Leading pharmaceutical organisation known for innovation and quality.
- Benefits: Competitive salary, contract role with potential for growth and development.
- Other info: Equal opportunities employer welcoming diverse applicants.
- Why this job: Join a team driving continuous improvement in a vital industry.
- Qualifications: Degree in a scientific field and 5-10 years of QA experience required.
The predicted salary is between 50000 - 60000 £ per year.
We are recruiting an Associate Principal QA Specialist (CQV) to join a leading pharmaceutical organisation in Berkshire on an initial 6‑month contract. The role supports GMP operations by managing quality assurance activities across validation and technical services functions, ensuring regulatory compliance in a multi‑product GMP setting and driving continuous improvement initiatives.
Responsibilities
- Provide shoulder‑to‑shoulder review, approval, and support for the management of quality records such as deviations, CAPA, change controls, and investigations to uphold GMP standards.
- Oversee daily quality assurance activities within validation and technical services, ensuring alignment with corporate requirements, standards, and regulatory guidelines including USFDA and European regulations.
- Utilise GMP knowledge to manage and escalate major and critical compliance issues via the site’s QMS processes.
- Actively identify, suggest, and contribute to continuous improvement initiatives to enhance quality systems and performance.
- Serve as the QA SME, support departmental quality councils and project meetings, offering technical guidance and strategic input.
Qualifications
- A degree or higher in a scientific discipline (e.g., pharmaceutical chemistry, quality assurance, quality management).
- 5–10 years of experience in a QA role within a GMP biotech or pharmaceutical environment, demonstrating comprehensive knowledge of validation and GMP compliance.
- Familiarity with database management, risk‑based decision making, and PQS processes.
- Strong communication and interpersonal skills, excellent problem‑solving, organisational and decision‑making abilities, with a commitment to quality and continuous improvement.
Associate Principal QA Specialist (CQV) employer: Hyper Recruitment Solutions LTD
Join a leading pharmaceutical organisation in Berkshire, where we prioritise quality and compliance in a dynamic work environment. Our culture fosters continuous improvement and professional growth, offering employees the chance to engage in meaningful projects that directly impact patient safety and product integrity. With a commitment to excellence and a supportive team atmosphere, we provide an exceptional platform for your career advancement in the pharmaceutical industry.
Contact Details:
Hyper Recruitment Solutions LTD Recruitment Team
StudySmarter Expert Advice🤫
We think this is how you could land Associate Principal QA Specialist (CQV)
✨Tip Number 1
Network like a pro! Reach out to your connections in the pharmaceutical industry, especially those who work in QA roles. A friendly chat can lead to insider info about job openings or even a referral.
✨Tip Number 2
Prepare for interviews by brushing up on your GMP knowledge and recent regulatory changes. We want you to shine when discussing how you can contribute to quality assurance activities and continuous improvement initiatives.
✨Tip Number 3
Don’t just apply anywhere; focus on companies that align with your values and career goals. Check out our website for tailored opportunities that match your skills in QA and GMP compliance.
✨Tip Number 4
Follow up after interviews! A quick thank-you email can keep you top of mind and show your enthusiasm for the role. Let them know you’re keen to bring your expertise in validation and quality systems to their team.
We think you need these skills to ace Associate Principal QA Specialist (CQV)
Some tips for your application 🫡
Tailor Your CV:Make sure your CV is tailored to the Associate Principal QA Specialist role. Highlight your experience in quality assurance, especially in GMP settings, and showcase any relevant projects or achievements that align with the job description.
Craft a Compelling Cover Letter:Your cover letter is your chance to shine! Use it to explain why you're the perfect fit for this role. Mention specific experiences that demonstrate your knowledge of GMP compliance and continuous improvement initiatives.
Showcase Your Skills:Don’t forget to highlight your strong communication and problem-solving skills in your application. These are key for the role, so provide examples of how you've used these skills in past positions to drive quality assurance efforts.
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!
How to prepare for a job interview at Hyper Recruitment Solutions LTD
✨Know Your GMP Inside Out
Make sure you brush up on your Good Manufacturing Practice (GMP) knowledge. Be ready to discuss how you've applied this in previous roles, especially in relation to quality assurance activities and compliance with USFDA and European regulations.
✨Showcase Your Problem-Solving Skills
Prepare examples of how you've tackled compliance issues or contributed to continuous improvement initiatives. Highlight specific situations where your problem-solving skills made a difference in maintaining quality standards.
✨Communicate Clearly and Confidently
Strong communication is key in this role. Practice articulating your thoughts clearly, especially when discussing technical guidance or strategic input. Remember, they want to see how you can convey complex information effectively.
✨Be Ready for Scenario-Based Questions
Expect questions that put you in hypothetical situations related to quality records, deviations, or CAPA processes. Think through your responses ahead of time, focusing on your decision-making process and the outcomes of your actions.
