(Contractor) Senior Regulatory Affairs Specialist
- Compensation
- Not disclosed
- Location
- Not listed
- Work setup
- Not specified
- Seniority
- Senior
- Employment
- Contract
- Experience
- Not specified
- Category
- Legal
- Posted
Must have
- Bachelor Degree in scientific discipline required or equivalent work experience.
- 5 or more years of Regulatory experience or related field. RAC certification preferred.
- Cross functional interaction experience, coordinating activities, driving projects and initiatives to completion, and working to align communications with other departments is required.
- Project leadership or supervisory experience is preferred.
- Strong organizational skills, strong attention to detail, ability to problem solve and to work well with others and cross-functionally.
- Excellent written and oral communication skills.
- Use of software system to manage change controls.
- Strong background using Microsoft Office tools and Adobe Acrobat.
- Travel Time Required - up to 10% (May vary depending on region/site).
Full description
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 Senior Regulatory Affairs Specialist's responsibilities encompass the support of US FDA applications (NDAs, ANDAs, DMFs) and support of Regulatory activities including but not limited to:
- Plan/author/compile/submit statutory reports in eCTD format for marketed products per FDA requirements
- Review, assess CMC regulatory impact and provide regulatory strategy for post-approval changes proposed at the manufacturing site
- Where appropriate, act as the CMC regulatory lead to cross-functional teams and other personnel on health authority requirements and preparation of information/technical data needed for support of post-approval changes
- Author/compile/submit post-approval change supplements
- Author/review updates to marketed product labeling
- Maintain regulatory knowledge of current guidelines and regulations
- Maintain current regulatory databases and produce various reports as needed
- Utilize and support electronic document management system
- Provides mentorship for entry-level and intermediate-level regulatory associates
Essential Functions
- Authoring, organization, and preparation of electronic (eCTD) regulatory filings; also includes peer review of filings.
- Understand, identify potential regulatory risks and recommend strategies based on current FDA/health authority requirements.
- Manage multiple priorities.
- Attend necessary trainings and seminars to keep abreast of new and/or changes in the Regulatory profession.
- Process, interpret and provide recommendations for complex, unusual issues.