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Planet Pharma is seeking a Risk Coordinator for a pharmaceutical CQV project on-site in Hillerød/Hillerod area. You will coordinate RAMS activities across multiple workstreams, review method statements, and collaborate with PTW and LOTO coordinators to ensure safe commissioning and qualification activities.
The role requires Pharmaceutical CQV experience, strong PSM knowledge, and GMP/EHS familiarity, with hands-on site presence and a commitment to driving continuous safety improvements on a
On-Site in Hillerod
As Risk Coordinator, you'll act as the daily coordinator and task manager for Risk Assessments and Method Statements (RAMS) across a large-scale Commissioning, Qualification and Validation (CQV) project. You'll be a visible, hands‑on presence on site — facilitating risk assessments, reviewing method statements, and working closely with Electrical, Mechanical LOTO, and Permit to Work (PTW) Coordinators to ensure safe execution of commissioning and qualification activities.
Risk Assessment Facilitation Process Safety Management Control of Work Governance Permit to Work Systems (incl. LOTO) Hazard Identification & Mitigation Safety Leadership & Communication
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.