Job Description

Quality Engineer

Location: Remote (Occasional in-person meetings in Basingstoke)
Contract Length: 9 months
Hourly Rate: 27.00
Working Pattern: Full Time (40 hours/week)

Are you ready to make a meaningful impact in the Life Sciences industry? Our client is seeking a dedicated Quality Engineer to join their high-performing team! This is an exciting opportunity to advance your career while contributing to solutions that make the world healthier, cleaner, and safer.

What You'll Do:
As a Quality Engineer, you will play a crucial role in ensuring quality compliance across operations. Your responsibilities will include:

• Quality Oversight: Conduct detailed documentation reviews and monitor processes to uphold the highest standards.
• Compliance Maintenance: Support and maintain compliance with GMP/GxP, ISO, and other regulatory requirements.
• Issue Investigation: Lead root cause analysis efforts to investigate quality issues effectively.
• Change Management: Manage and support change control activities while assisting in internal and external audits and inspections.
• Documentation: Author and review quality documentation such as SOPs and investigation reports.
• Data Analysis: Perform data analysis, trending, and reporting of quality metrics.
• Collaboration: Work closely with cross-functional teams to drive corrective and preventive actions.
• Continuous Improvement: Support initiatives aimed at enhancing quality systems and processes.

Who You Are:
To thrive in this role, you should possess:

• A Bachelor's degree in Life Sciences, Engineering, Chemistry, Biology, or a related technical field, with 5+ years of experience in quality assurance/control (or an advanced degree with 3+ years of relevant experience).
• Experience in regulated industries (pharmaceutical, medical device, or biotech preferred).
• Proficiency with quality management systems (MasterControl, Document Control Systems) and CAPA processes.
• Demonstrated expertise in root cause analysis, investigation techniques, and implementing corrective actions.
• Strong knowledge of GMP/GxP regulations, ISO standards (9001/13485), and quality system requirements.
• Excellent problem-solving skills and attention to detail.
• Strong verbal and written communication skills with the ability to collaborate across various functions.

How to Apply:
If you're excited about the opportunity to contribute to life-changing products and work with a talented team, we want to hear from you! Apply today to join our client's mission in making the world a better place.

Don't miss out on this chance to be a part of something meaningful. Let's make a difference together!

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.

By applying for this role your details will be submitted to Adecco. Our Candidate Privacy Information Statement explains how we will use your information - please copy and paste the following link in to your browser (url removed)