Job Description

Q&RA Engineer

Location: Remote (Monthly meetings in Basingstoke)
Contract Type: Temporary (9 months)
Hourly Rate: 23.50
Hours: Full Time (40 hours per week)
Start Date: ASAP

Are you ready to make a meaningful impact in the Life Sciences industry? Join our client's dynamic team as a Q&RA Engineer and be part of a mission that aims to make the world healthier, cleaner, and safer!

In this exciting role, you will ensure quality compliance across operations while collaborating with talented professionals who share your commitment to excellence. This is your chance to contribute to groundbreaking solutions that tackle some of the world's toughest challenges!

Position Overview:
As a Q&RA Engineer, you'll be at the forefront of quality assurance, providing essential oversight through documentation reviews and process monitoring. You will work collaboratively with cross-functional teams to deliver life-changing products to customers.

What You'll Do:

• Support Compliance: Help maintain compliance with GMP/GxP, ISO standards, and regulatory requirements.
• Investigate Quality Issues: Lead root cause analysis efforts and manage change control activities.
• Conduct Audits: Support internal and external audits and regulatory inspections.
• Document Quality: Author and review SOPs, investigation reports, and other critical quality documentation.
• Analyse Data: Perform data analysis, trending, and reporting of quality metrics.
• Drive Improvements: Collaborate with teams to implement corrective and preventive actions and support continuous improvement initiatives.

Who You Are:

• Education: Bachelor's degree in Life Sciences, Engineering, Chemistry, Biology, or a related technical field with 5+ years of relevant experience (or an advanced degree with 3+ years).
• Experience: Background in regulated industries (pharmaceutical, medical device, or biotech preferred) with proficiency in quality management systems and CAPA processes.
• Skills: Strong knowledge of GMP/GxP regulations, ISO standards, and excellent technical writing abilities.
• Problem Solver: Advanced problem-solving skills with a keen attention to detail.
• Team Player: Exceptional interpersonal skills that enable collaboration across functions and levels.

Ready to Make a Difference?
If you are enthusiastic about quality assurance and ready to embark on a fulfilling journey in the Life Sciences sector, we want to hear from you!

Join our client's team and be a part of something bigger! Together, we can make a difference.

Adecco is a disability-confident employer. It is important to us that we run an inclusive and accessible recruitment process to support candidates of all backgrounds and all abilities to apply. Adecco is committed to building a supportive environment for you to explore the next steps in your career. If you require reasonable adjustments at any stage, please let us know and we will be happy to support you.

Adecco acts as an employment agency for permanent recruitment and an employment business for the supply of temporary workers. The Adecco Group UK & Ireland is an Equal Opportunities Employer.

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