One of our most exciting clients (global leading life science company) are seeking a Technical Administrator to join their customer services team. The role offers a lucrative pay rate and the chance to make a key contribution to a company that is driving innovation in health and sustainability.
This is a contracted position ending in April 2025. It will require someone to start ASAP.
Key Responsibilities: Oversee the administration of Third-Party Contractors supporting laboratory equipment across the client's R&D sites. System administration ensuring work orders are updated and closed within the agreed metrics. Act as the first point of contact for Third-Party Contractors, managing their arrival and compliance with site and safety procedures. Inductions/training and safety/compliance checks for third-party contractors. Administer and manage calibration labeling and processes across the site. Skills & Qualifications: Experience with computerised maintenance management systems is highly desirable. Knowledge of EHS and GXP guidelines, with the ability to manage contractor inductions and safety procedures. For more information on this position or any similar opportunities, please apply directly to this role, or reach out on the below:
Phone: +44 20 3928 8381
Email:
LinkedIn: 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 recognized 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