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Quality assurance analytical chemist

Dover
Cormica
Analytical chemist
Posted: 17h ago
Offer description

Quality Assurance Analytical Chemist

Ready to make a BIG difference?

Are you a Scientist or in a Quality role with a scientific background looking for a new challenge who excels in detail and enjoys working as part of a team. We're looking for a detail-orientated, self-motivated Quality Assurance Analytical Chemist to join our Quality Assurance team to support our site in Dover. This is a hands-on, office-based role, so if you are ready to join a group of analysts and QA colleagues working to a Quality Management System, read on!

At Cormica, we are not just another company. We're a leading provider of analytical research, development, and testing services for medical device and pharmaceutical manufacturers. With laboratories across the UK, US and Europe, our mission is to make a real impact by helping our clients launch their products safely and quickly, improving patients' lives around the world.

What you'll do:
* Adhere to Health and Safety Procedures and Culture, and complete assigned training to ensure colleague and visitor health and safety at all times
* Ensure compliance with the Quality Management System (QMS)
* Review, interpret, approve and manage Analytical Chemistry Laboratory test protocols and reports, engaging with teams during projects
* Check quality, consistency and accuracy of Analytical Chemistry Laboratory test data generated from projects to ensure quality and data integrity
* Participate with QA and Analytical Chemistry Laboratory colleagues to plan, develop and implement effective quality policies, procedures and forms, and engage with problem solving and decision-making activities
* Ensure documentation (SOPs, WIs, Datasheets, Logbooks, Protocols, Reports, Data Templates) comply with the Quality Management System (QMS), and external Standards and Regulations
* Drive and contribute to Continuous Improvement initiatives with QA and Laboratory teams
* Check quality, consistency and accuracy of Biocompatibility Evaluation and Clinical Evaluation protocols and reports for Consultancy Dept to ensure quality and data integrity
What's in it for you?

* Full-time role
* Competitive salary
* Attractive benefits package
* Opportunities for professional development and career progression
* A dynamic and collaborative work environment
* The chance to contribute to a company and Group that values quality and innovation
* Onsite parking
What we're looking for:

* Educated to degree standard in chemistry or related subject
* Proven experience working in an Analytical Chemistry Laboratory, generating test data, creating and checking digital protocols and test reports
* Experience working to a Quality Management System e.g. following procedures, work instructions
* Understanding of a GxP area, regulatory and accreditation systems
* Ability to manage multiple priorities effectively in fast-paced environments
* Detail-oriented, methodical, good organisation and time management skills
* Good command of English grammar, syntax, and vocabulary to read, create or edit documents e.g. technical reports, standards
* Good numerical skills
* Effective oral and written communication, and interpersonal skills
* Good Microsoft IT skills - e.g. Excel, Word, TEAMS
* Full eligibility to work in the UK
Equity, Diversity, and Inclusion: We are committed to creating a workplace that champions Equity, Diversity, and Inclusion (EDI). We welcome applications from individuals of all backgrounds, regardless of race, ethnicity, gender, sexual orientation, disability, or any other characteristic. We value experience and capability and encourage candidates with the right skills and passion to apply, even if you don't meet every qualification.

If you're looking for a role with real growth potential and a company that values diversity and inclusion, we'd love to hear from you. Apply today! #J-18808-Ljbffr

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