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- Tasks: Join us as a QA Associate, ensuring compliance and quality in pharmaceutical operations.
- Company: Be part of a leading pharmaceutical company dedicated to excellence and innovation.
- Benefits: Enjoy a 9-month contract with opportunities for growth and skill development.
- Why this job: Make a real impact on product quality while collaborating with diverse teams.
- Qualifications: Strong GMP knowledge and attention to detail are essential; prior experience is a plus.
- Other info: Perfect for those passionate about quality assurance in a dynamic industry.
The predicted salary is between 30000 - 42000 £ per year.
We are currently looking for a QA Associate to join a leading pharmaceutical company on a 9 month contract.
Key Responsibilities:
- Quality & Compliance Support: Monitor and assess site operations for compliance with GMP and internal procedures, identifying and escalating non-conformances through appropriate QMS channels.
- Documentation Review: Perform detailed, real-time review of manufacturing and laboratory documentation, ensuring accuracy, completeness, and adherence to regulatory standards.
- Continuous Improvement & Audit Readiness: Contribute to a state of audit readiness by actively participating in quality system improvements and continuous improvement initiatives.
- Compliance Issue Management: Utilize in-depth GMP and QMS knowledge to manage and escalate major and critical quality issues, including deviations and CAPAs.
- Cross-Functional Collaboration: Serve as a quality liaison for key stakeholders across manufacturing, technical operations, and supply chain teams.
- Training & Best Practice Promotion: Mentor team members on cGMP principles and best documentation practices, supporting a culture of compliance and proactive quality.
Required Skills:
- Strong knowledge of GMP and pharmaceutical quality systems
- Proficient in documentation review and risk-based decision making
- High attention to detail with accurate data entry skills
- Strong communication and interpersonal skills
- Excellent organizational, planning, and time-management abilities
- IT literate (MS Office; familiarity with databases)
Preferred Experience:
- Prior experience in a GMP-regulated environment
- Working knowledge of deviations, CAPAs, and quality investigations
- Involvement in continuous improvement or pharmaceutical quality system (PQS) enhancement projects
Quality Assurance Associate employer: JR United Kingdom
Contact Detail:
JR United Kingdom Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Quality Assurance Associate
✨Tip Number 1
Familiarise yourself with GMP regulations and quality management systems. Understanding these frameworks will not only help you in interviews but also demonstrate your commitment to the role.
✨Tip Number 2
Network with professionals in the pharmaceutical industry, especially those working in quality assurance. Engaging with them can provide insights into the company culture and expectations, which can be invaluable during your application process.
✨Tip Number 3
Prepare to discuss specific examples of how you've contributed to quality improvements or compliance in previous roles. This will showcase your hands-on experience and problem-solving skills, making you a more attractive candidate.
✨Tip Number 4
Stay updated on the latest trends and challenges in the pharmaceutical industry, particularly regarding quality assurance. Being knowledgeable about current issues can help you stand out in discussions and interviews.
We think you need these skills to ace Quality Assurance Associate
Some tips for your application 🫡
Tailor Your CV: Make sure your CV highlights relevant experience in quality assurance, particularly in GMP-regulated environments. Emphasise your skills in documentation review and compliance management to align with the job requirements.
Craft a Compelling Cover Letter: Write a cover letter that showcases your understanding of GMP and QMS principles. Mention specific examples from your past experiences where you contributed to quality improvements or compliance initiatives.
Highlight Relevant Skills: In your application, clearly outline your strong communication, organisational, and time-management skills. Provide examples of how you've successfully collaborated with cross-functional teams in previous roles.
Proofread Your Application: Before submitting, thoroughly proofread your application for any errors or inconsistencies. Attention to detail is crucial in quality assurance, so ensure your application reflects this quality.
How to prepare for a job interview at JR United Kingdom
✨Know Your GMP Inside Out
Make sure you brush up on your Good Manufacturing Practice (GMP) knowledge. Be prepared to discuss how you've applied these principles in previous roles, as this will show your understanding of compliance and quality assurance.
✨Showcase Your Documentation Skills
Since the role involves detailed documentation review, be ready to provide examples of your experience with documentation processes. Highlight any specific tools or methods you've used to ensure accuracy and completeness.
✨Emphasise Continuous Improvement
Discuss any past experiences where you've contributed to quality system improvements or participated in audit readiness initiatives. This demonstrates your proactive approach to quality assurance and your commitment to ongoing development.
✨Prepare for Cross-Functional Scenarios
As the role requires collaboration with various teams, think of examples where you've successfully worked with different departments. Be ready to explain how you communicated effectively and resolved any conflicts that arose.
