Job Description

We are seeking an experienced and professional Production Manager to direct the Production Team at our GMP facility.


Company Information


Advent Bioservices is a growing Contract Development and Manufacturing Organisation (CDMO) providing GMP manufacturing of ATMPs and related products, process development and ancillary services. We support the development of complex, breakthrough therapies for a globally diverse market. We are at the forefront of revolutionary medicine in which life-threatening diseases are treated using advanced therapy medicinal products.


Job Summary


Based on-site in Sawston, the Production Manager will be responsible for the growth and development of the Production team. The Production Manager will directly line manage Team Leaders/Senior Production Scientists and will be responsible for overseeing the manufacture of cellular therapies in the aseptic suites; providing safe, effective and Good Manufacturing Practice (GMP) compliant products.


This role will work within regulatory frameworks governing the production of ATMPs, including the MHRA and the HTA and will working within the QMS framework including participation in audits, risk assessments and investigations.


Key responsibilities will include:

Oversee Production teams activities in the manufacture of clinical products ensuring that the highest quality standards of production and storage are met. Lead effective and efficient scheduling of production and resources against the operational plans. Coordinate activities with other departments including Warehouse for materials management and QC to ensure appropriate and timely sampling, testing and reporting of in-process controls and end-of- process samples. Develop policies and strategies for continuous improvement of manufacturing operations, to streamline processes and enhance staff productivity. Plan for and support the further development of Advent Bioservices manufacturing facility, including clean room expansion, team building and staff development.

You will have the following experience/qualifications:

BSc in a relevant scientific subject or equivalent Significant experience working within a licensed GMP aseptic product manufacturing environment Significant experience and knowledge of ATMP manufacturing including cell and gene therapies Experience with Clinical trial, Specials and Commercial medicinal product manufacturing Extensive experience of laboratory and team building, leadership and management Strong organisational and time management skills and the ability to prioritise and work well under pressure Excellent interpersonal skills and excellent IT skills Excellent attention to detail, adherence to SOPs and record keeping Self-motivated with strong initiative and drive

We offer an attractive base salary and benefits package.


Candidates must have eligibility to work within the UK.