Contact us

Career Opportunities

Back to Careers >

GMP Facilities Coordinator (REF0525)

Seda Clinical Manufacturing Services are going through a period of expansion as we establish ourselves as a premier, science led, clinical product manufacturer. We have an exciting opportunity for a GMP Facilities Coordinator.

Reports to: Facilities Engineering Lead

Experience: You’ll have a strong sense of responsibility and reliability, working to a high standard with attention to detail.

Salary: Competitive Salary + Benefits (based on level of experience)

Posted: 13th Aug 2025

Closes: 29/08/2025

Apply

The Seda group was formed ten years ago and has undergone a rapid growth phase during this time.  The group is made up of two divisions, Seda Pharmaceutical Development Services (PDS) and Seda Clinical Manufacturing Services (CMS). Seda PDS is a well-established and highly regarded Contract Research Organisation (CRO) that provides integrated Pharmaceutical Development and Clinical Pharmacology services to enable clients to progress their novel new chemical entities through the drug development process. Seda CMS provides GMP manufacture, testing, and supply of the products we design under contract for our global client base. We aim to offer our clients the very highest level of scientific rigour aligned with expert knowledge of product manufacture and supply. For our colleagues we offer the opportunity of a rewarding career, making a real impact on the development and introduction of life changing medicines, with scope for outstanding personal growth.  We are currently recruiting for the role of GMP Facilities Coordinator in our Seda CMS division.  

As the GMP Facilities Coordinator, you will play a vital support role in ensuring the day-to-day operational readiness of the Seda Clinical Manufacturing Services (CMS) facility. While not a technical or manufacturing role, your contribution will be key to maintaining a compliant and professional GMP working environment. You will support the wider team by helping manage consumables, cleanliness, stock control, and general facility coordination. 

The role is located at our new, state-of-the-art GMP clinical manufacturing facility in Cheadle, South Manchester. 

You will have ideally have some experience of working in a pharmaceutical, healthcare, or GMP-regulated environment although this is not essential. It is essential that you carry a strong sense of responsibility, reliability, and attention to detail along with the ability to follow procedures accurately and consistently.  You will have high standards in your work and take pride in what you achieve. 

At Seda, we have a culture of development and collaboration, and we expect all of our team to have a self-development mindset coupled with the ability to work well in a team.   

Click here for a more detailed job description

Please review the job description, and if you wish to be considered for this role, upload your CV with a covering letter (as a single file) highlighting your suitability using the form below. The closing date for applications is Friday 29th August 2025 

For more information on the vacancy, please email Stuart.Smythe@sedacms.com 

Apply for this position

    Upload CV & Covering Letter Word / PDF

    All applicants who meet the Person Specification will receive a response by telephone call or email in due course. Applicant details, including CVs, are kept on our system for a period of 6 months in line with our Privacy Notice.