in a quality assurance role within the pharmaceutical industry. Deep understanding of Good Clinical Practice guidelines, regulations, and standards. Relevant certifications such as RQAP-GLP, RQAP-GCP are desirable. Leadership experience along with excellent communication, collaboration, and interpersonal skills. Detail-oriented with strong analytical and problem-solving abilities. Proven ability more »
City Of London, England, United Kingdom Hybrid / WFH Options
Proclinical Staffing
development and development of medical devices is a plus. Strong knowledge of Clinical Development and Research operations and regulatory landscape. Deep knowledge of GCP, GLP, GPVP, GCP for Labs and a general understanding of GMP. Expert in process development, industry standard problem-solving approaches, in alignment with Lean and Lean more »
Experience of managing a Quality management software system Experience working with database information. Experience of accreditation procedures and standards (e.g. CPA, UKAS, EFI, FDA, GLP) Disclosure and Barring Service Check This post is subject to the Rehabilitation of Offenders Act (Exceptions Order) 1975 and as such it will be necessary more »
Experience in aseptic technique and controlled environments with prevention of cross-contamination. Experience working within a Good Manufacturing Practice ( cGMP ) or GoodLaboratoryPractice ( GLP ) environment is highly advantageous but not essential. Strong interpersonal and communication skills. Touchlight Benefits Touchlight is a successful scale-up business with a record of more »
