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- Tasks: Ensure GMP compliance and support quality processes in a pharmaceutical setting.
- Company: Join a leading Pharmaceutical Manufacturing company in Slough with a strong reputation.
- Benefits: Enjoy a competitive pay of £43.82 per hour and potential remote work options after training.
- Why this job: Be part of a team focused on continuous improvement and regulatory compliance in a vital industry.
- Qualifications: 5–10 years of experience and a scientific degree are required.
- Other info: This is an initial 12-month contract with opportunities for mentorship and professional growth.
The predicted salary is between 80000 - 120000 £ per year.
I am working with a Pharmaceutical Manufacturing company in Slough who are looking for an Associate Principal QA Specialist to join their team on an initial 12 month contract.
• 5–10 years of experience and scientific degree
• Fully onsite during training; potential for 1–2 days WFH afterward
• 12-month contract
• £43.82 per hour
Role Purpose:
• Ensure GMP compliance in operations
• Manage and support GMP issues through QMS processes and site governance
• Act as a GMP SME, enforcing and improving quality processes
• Support senior QA leadership in continuous improvement and regulatory compliance
Key Responsibilities:
• Review, approve, and support quality records (Deviations, CAPAs, Change Controls, Investigations, OOS)
• Escalate compliance issues and ensure timely resolution
• Identify and participate in continuous improvement initiatives
• Mentor and coach teams in cGMP practices
• Maintain audit readiness and contribute to PQS process improvements
• Provide QA SME support for manufacturing, including out-of-hours support
Required Skills & Must-Haves:
• Strong decision-making, problem-solving, and quality mindset
• Excellent communication and interpersonal skills
• Strong continuous improvement focus
• QA approval experience for Deviations, CAPAs, Change Controls, and OOSs
If you are interested please apply or send your CV to
Quality Assurance Specialist employer: Cpl Life Sciences
Contact Detail:
Cpl Life Sciences Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Quality Assurance Specialist
✨Tip Number 1
Familiarize yourself with GMP compliance and quality management systems. Understanding these concepts deeply will help you demonstrate your expertise during interviews.
✨Tip Number 2
Network with professionals in the pharmaceutical industry, especially those in QA roles. Engaging with them can provide insights into the company culture and expectations.
✨Tip Number 3
Prepare to discuss specific examples of how you've handled deviations, CAPAs, and change controls in your previous roles. Real-life scenarios will showcase your problem-solving skills effectively.
✨Tip Number 4
Stay updated on the latest trends and regulations in the pharmaceutical industry. This knowledge will not only impress your interviewers but also show your commitment to continuous improvement.
We think you need these skills to ace Quality Assurance Specialist
Some tips for your application 🫡
Understand the Role: Take the time to thoroughly read the job description. Understand the key responsibilities and required skills, especially the emphasis on GMP compliance and quality processes.
Tailor Your CV: Customize your CV to highlight relevant experience in quality assurance, particularly focusing on your decision-making and problem-solving skills. Mention any specific experience with Deviations, CAPAs, Change Controls, and OOSs.
Craft a Strong Cover Letter: Write a cover letter that reflects your passion for quality assurance and your understanding of GMP practices. Use specific examples from your past experiences to demonstrate how you meet the requirements of the role.
Highlight Continuous Improvement Initiatives: In your application, emphasize any previous involvement in continuous improvement initiatives. This shows your proactive approach and aligns with the company's focus on regulatory compliance and quality enhancement.
How to prepare for a job interview at Cpl Life Sciences
✨Showcase Your Experience
With 5-10 years of experience required, be ready to discuss specific examples from your past roles that demonstrate your expertise in GMP compliance and quality assurance processes. Highlight any relevant projects or challenges you've successfully managed.
✨Demonstrate Problem-Solving Skills
Prepare to share instances where you've effectively resolved compliance issues or improved quality processes. This will showcase your strong decision-making and problem-solving abilities, which are crucial for the role.
✨Communicate Clearly
Excellent communication skills are a must-have for this position. Practice articulating your thoughts clearly and concisely, especially when discussing complex QA topics. This will help you connect with the interviewers and convey your ideas effectively.
✨Emphasize Continuous Improvement
Since the role focuses on continuous improvement initiatives, be prepared to discuss your approach to identifying areas for enhancement in QA processes. Share examples of how you've contributed to such initiatives in previous roles.
