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 Process Technician.
Reports to:
Team Manager Experience:
You’ll be educated to at least degree level with relevant experience in a GMP environment. Salary:
Competitive Salary + Benefits (based on level of experience) 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 Process Technician in our Seda CMS division. Primary Purpose:
The primary purpose of this role is to provide hands-on execution of all production activities in the manufacture of GMP compliant, clinical oral solid dose (OSD) products. The role is located at our new, state-of-the-art GMP clinical manufacturing facility in Cheadle, South Manchester. You’ll be educated to Degree Level, or equivalent, in a relevant subject or with significant relevant experience. Ideally, you will have experience of manufacturing pharmaceutical products within a regulated facility and experience of operating manufacturing equipment in the production of pharmaceutical products. You will have excellent communication skills, both written and spoken English, and have a good level of attention to detail and ability to work to the highest quality standard. 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. Additionally, you will have the ability to prioritise and meet different deadlines in alignment with business needs. 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 Wednesday, 5th February 2025. 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
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Team Manager Experience:
You’ll be educated to at least degree level with relevant experience in a GMP environment. Salary:
Competitive Salary + Benefits (based on level of experience) 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 Process Technician in our Seda CMS division. Primary Purpose:
The primary purpose of this role is to provide hands-on execution of all production activities in the manufacture of GMP compliant, clinical oral solid dose (OSD) products. The role is located at our new, state-of-the-art GMP clinical manufacturing facility in Cheadle, South Manchester. You’ll be educated to Degree Level, or equivalent, in a relevant subject or with significant relevant experience. Ideally, you will have experience of manufacturing pharmaceutical products within a regulated facility and experience of operating manufacturing equipment in the production of pharmaceutical products. You will have excellent communication skills, both written and spoken English, and have a good level of attention to detail and ability to work to the highest quality standard. 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. Additionally, you will have the ability to prioritise and meet different deadlines in alignment with business needs. 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 Wednesday, 5th February 2025. 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.
#J-18808-Ljbffr
