(Contractor) Regulatory Affairs Technical Writer

(Contractor) Regulatory Affairs Technical Writer Date: May 8, 2026 Location: St. Louis, MO, United States, 63146 About Curium Curium is the world’s largest nuclear medicine company with more than a century of industry experience. We develop, manufacture and distribute world-class radiopharmaceutical products to help patients around the globe. Our proven heritage combined with a pioneering approach are the hallmarks to deliver innovation, excellence and unparalleled service. With manufacturing facilities across Europe and the United States, Curium delivers SPECT, PET and therapeutic radiopharmaceutical solutions for life‑threatening diseases to over 14 million patients annually. The name ‘Curium’ honors the legacy of pioneering radioactive researchers Marie and Pierre Curie, after whom the radioactive element curium was named and emphasizes our focus on nuclear medicine. The tagline ‘Life Forward’ represents our commitment to securing a brighter future for all those we serve: An enhanced quality of care for our patients. A trusted partner to our customers. A supportive employer to our valued team. Summary of Position The (Contractor) Regulatory Affairs Technical Writer will facilitate success of key regulatory projects by coordinating regulatory activities, deliverables, and submission content across Regulatory Affairs Staff and cross functional teams. In this capacity, the individual will work to improve organization and tracking of internal department projects and deliverables that drive success against the project timeline and FDA approval. Under general supervision, this position will also facilitate success of key company projects by supporting department Director and Managers in tracking project action items, milestones, and deliverables across functional areas. Effective communication with the international department as well as across multiple languages is essential to this position. Additional responsibilities will include facilitating regulatory data flow. Work Schedule: Mon - Friday 8am - 4:30pm Essential Functions Must maintain operational compliance with US and international regulatory agencies and guidelines (i.e. FDA, DEA, EU, HC, TGA, RIC/S, ISO, USP, NRC, cGMP, etc.) Manage project submissions as assigned by Director Regulatory Affairs including department work process. Manage key projects, planning, timing, and execution for submission, approval, and launch. Maintain project database for tracking individual and department project deliverables. Manage incoming requests through logging, assigning, tracking, working with RA staff to manage complexity and difficulty, and maintain department metrics. Maintain database and tracking of key department deliverables Facilitate use of regulatory electronic submission software to allow more efficient compilation process. Collaborate with RA staff assigned to projects in order to prospectively mitigate RA resource conflicts. Manage multiple, sometimes conflicting priorities. Maintain and track deliverables Share expertise with peers. Other duties as assigned or requested by Director Regulatory Affairs. Apply expertise to cross functional departments and provide proper leadership. Establish and review Global RA priorities as they relate to department and company goals and objectives. Requirements Bachelor’s Degree in technical discipline, pharmaceutical industry, or related life science preferred. Project Management Experience - Certification Preferred 3 or more years Regulatory Affairs support of submission content, compilation, or publishing 3 or more years Project Management experience in Pharmaceutical or Health related industry Ability to facilitate decision making specific content expertise may reside with team members Experience in Project set‑up/initiation, executions, and completion within established timeframes Building Effective work streams and work process Team Member and Team Leader experience on cross functional teams. Strong evidence and mastery of being a “Team Contributor” Experience with regulations associated with Investigational, New Chemical Entity, and Generic drug applications preferred. Experience with International Cross Functional Teams Attention to detail and overall drug application quality and internal consistency. Excellent written and oral communications skills. Strong interpersonal, and negotiation skills, conflict management, priority setting, strategic agility, building effective teams, managing vision and purpose. Proficiency in computer skills (MS Office Project, Access, Excel, Document Management Systems) Working Conditions This position will work in typical office conditions with extensive time using computer equipment. Must possess good hand‑eye coordination; close attention to detail required. Willingness to work in a team‑based environment.Willingness to travel to and work in manufacturing facilities. May be required to sit or stand for long periods of 8+ hours a day while performing duties. Willingness to complete safety training within allotted timeframes. The position deals with many deadlines. Due to the short turnaround time of deadlines and limited time, overtime is sometimes required. Disclaimer The above statements are intended to describe the general nature and level of work being performed by employees assigned to this classification. They are not intended to be construed as an exhaustive list of all responsibilities, duties and skills required of employees assigned to this position. Equal Opportunity Employer Curium is an equal opportunity employer and believes everyone deserves respect, dignity and equality. All applicants will be considered for employment without attention to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran or disability status. #J-18808-Ljbffr Curium Pharma