Job Description

Do you have QA experience? Have you worked within a GMP, Biotech, Pharmaceutical or a CDMO environment? If so, this will be an excellent career opportunity for you.

I am currently working with a leading cell and gene therapy CDMO based in the golden triangle. This company has been founded in 2016, and since then, they have been providing their clients with a number of services such manufacturing in their GMP suites, QC testing, process development, warehouse and office spaces. This company supports clients with complex, breakthrough therapies for a globally diverse market.

This role presents an exciting prospect for an emerging talent in the field of Quality Assurance. To qualify, you should possess a BSc degree in life sciences and have prior experience working in a GMP, biotechnology, pharmaceuticals, or CDMO environment. Additionally, familiarity with regulatory bodies like the MHRA and a background in Quality Management Systems.

This is a permanent, full time position that requires your presence on-site in Cambridge. The salary offered can go up to \xc2\xa325,000, depending on your level of experience.

Key responsibilities for the QA role:

• Support the QA team to oversee risk assessments and change control processes
• Responsible for document control processes
• Participate in preparing the site for regulatory inspections and audits
• Adhere to and maintain regulatory standards

Knowledge/Skills Requirements:

• BSc within life sciences
• Experience working within a GMP, biotech, pharma or a CDMO environment
• Experience working with quality management systems
• Experience working under regulatory bodies such as MHRA

Please forward your CV to nicole.cooper@nextphaserecruitment.com or phone 01403 216216 where we I would be happy to tell you more about this exciting opportunity.

Next Phase Recruitment