Overview:
Join the client's Global Development Quality team to support clinical supply operations. This role involves reviewing batch records, ensuring GMP compliance, and preparing documentation for product release. You'll work with global teams and manufacturing sites to maintain quality standards across investigational medicines.
Key Duties:
* Audit data, systems, and facilities for GMP and SOP compliance
* Review and approve documentation for clinical product release
* Resolve audit findings and support corrective actions
* Collaborate across global teams with minimal supervision
Requirements:
* Experience in pharma, chemicals, or regulatory environments
* Strong grasp of cGMP and quality principles
* Excellent communication and attention to detail
* Science degree required; recent graduates welcome
About Planet Pharma:
Planet Pharma is an American parented Employment Business/Agency that provides global staffing services with its head-quarters in Chicago and our EMEA regional office located in Central London. We have invested significantly in creating a robust international platform that enables us to work compliantly in 30+ countries with a current network of 2500+ active contractors globally as well as a very strong permanent / direct hire recruitment offering.
Our specialist knowledge and close relationships with our clients and the wider industry really makes us unique in our field. Just recently we were recognised by FORBES as the 17th best professional staffing firm, and have won multiple awards from industry accredited bodies for our commitment to excellence and service delivery. We have extensive functional expertise including: Regulatory Affairs, Pharmacovigilance, QA, QC, Submissions experts, Clinical development, Quality, Biostatistics, and Medical Affairs / Writing.
We are an equal opportunities Recruitment Business and Agency. We welcome applications from all suitably qualified candidates regardless of their race, sex, disability, religion/belief, sexual orientation or age.