site and related functions are in compliance with GxP regulations and applicable quality guidelines, including, but not limited to UK/EU/US GMP/GDP, ICH and other region specific guidance. The individual will have ownership for key quality system elements and will support and execute site quality more »
/revised within the documented revision time span Ensure that all documents are updated and mastered according to existing procedures Assist in compliance with GMP regulations Requirements: Educated to HNC/HND as minimum- degree preferred Experience in document review in a regulated (GMP) environment Excellent written and verbal communication more »
a cGMP environment Experience of supplier audits and/or vendor assurance would be beneficial Excellent organisational and time management skills Good knowledge of GMP and ISO regulations Awareness of regulatory requirements more »
site and related functions in maintaining compliance with GxP regulations and applicable quality guidelines, including, but not limited to UK/EU/US GMP/GDP, ICH and other region specific guidance. The individual will have support key quality system elements and compliance improvements, working closely with relevant stakeholders more »
shape, develop and manage your own team, drive quality, improve standards and ensure the development and cell trials are on time and adhere to GMP standards. The company has been established since 2014 with ambitious, yet achievable, plans for growth including expansion into the US market and are a company … operations Perform problem/solving trouble shooting of cell culture production Lead quality investigations/deviations Ensure quality standards are maintained in compliance with GMP standards The Person: Life Sciences discipline background T cell Therapy regulatory knowledge Passionate about making a difference within cancer treatment Cell therapy, pharmaceutical, Laboratory, production more »
shape, develop and manage your own team, drive quality, improve standards and ensure the development and cell trials are on time and adhere to GMP standards. The company has been established since 2014 with ambitious, yet achievable, plans for growth including expansion into the US market and are a company … operations Perform problem/solving trouble shooting of cell culture production Lead quality investigations/deviations Ensure quality standards are maintained in compliance with GMP standards The Person: Life Sciences discipline background T cell Therapy regulatory knowledge Passionate about making a difference within cancer treatment Cell therapy, pharmaceutical, production, t more »
