Curium

Redefining the experience of cancer through our trusted legacy in nuclear medicine

Pharmaceutical Manufacturing

Nuclear Medicine, PET Imaging, Molecular Imaging, cGMP Manufacturing , Contract Manufacturing, and SPECT Imaging

Headquarters

Paris, France

Founded

2017

Curium is the global leader in nuclear medicine, providing life-changing diagnostics and treatment to patients all over the world. We develop, manufacture and distribute world-class radiopharmaceutical products with a renewed focus on cancer, exploring untapped potential for new innovation. We build on remarkable foundations and a legacy of providing reliable and consistent nuclear solutions to tens of thousands of patients every day. Our proven heritage combined with a pioneering approach are the hallmarks from which we provide life-changing diagnostics and therapeutics. Our people are the root of the incredible impact they have. We strive to make the impossible possible and to be an organization that will change the face of medicine. Our diverse group of industry experts is unified under one strong and singular focus – to develop, manufacture and supply revolutionary diagnostic and therapeutic radiopharmaceuticals to our customers around the globe with unrivaled reliability and superior service.

Video - The Curium Way

The Opportunity

Manufacturing Technical Writer

St Louis, MO

Overview Responsibilities Qualifications

Overview

The Technical Writer will work in a dynamic organization in the Cold Products Focus Factory. This role has the responsibility for supporting projects and maintenance of business action items related to Curium’s business strategy in the space of sterile drug manufacturing including reactor and cyclotron derived new products.
Responsibilities

•Utilize technical writing strategies to ensure content of documentation is clear, concise, and complete.
•Author and revise technical documentation including facility and equipment SOPs, batch records, specifications, and training documents.
•Author and manage change controls as necessary to implement new procedures as well as revisions to documentation and SOPs to facilitate launch of new products.
•Participate in process and equipment testing to learn systems being documented.
•Complete deviations, CAPAs, change controls, document revisions and training activities to meet quality system requirements and timelines.
•Coordinate with New Product Development and New Product Initiatives for product/process documentation requirements.
Qualifications

• Bachelor Degree or equivalent work experience required.
• 3+ years of related professional experience preferred.
• Must be able to communicate clearly in English and have solid communication skills including grammar and composition.
• Demonstrated understanding of GMP / cGMP regulations.
• Skill in communication, written and verbal with the ability to interact with cross-functional teams.
• Proven time management skills and a strong attention to detail.
• Proven ability to manage and coordinate multiple projects in a fast-paced, highly professional environment.
• Ability to work well with others and independently.
• Able to read, understand and follow work instructions in a safe, accurate and timely manner.
• Proficiency in computer skills and experience with Microsoft Word, PowerPoint, and Excel.