(Contractor) Senior Regulatory Affairs Specialist

Curium Pharma; St. Louis (MO); On-site; USD 80,000 - 100,000; Full time

Job summary

Curium Pharma in St. Louis, MO, is seeking a Senior Regulatory Affairs Specialist. This role involves supporting US FDA applications and coordinating regulatory activities to ensure compliance with health authorities.

The ideal candidate should possess a Bachelor's degree in a scientific discipline and have over 5 years of regulatory experience. Strong attention to detail and excellent communication skills are essential. Opportunity to work in a dynamic environment.

Qualifications

• 5+ years of Regulatory experience or related field.
• Project leadership or supervisory experience preferred.
• Use of software system to manage change controls.

Responsibilities

• Support US FDA applications (NDAs, ANDAs, DMFs).
• Plan and compile statutory reports in eCTD format.
• Review and assess regulatory impact for CMC changes.

Skills

Regulatory experience

Attention to detail

Excellent communication skills

Problem-solving

Organizational skills

Education

Bachelor Degree in scientific discipline or equivalent work experience

Tools

Microsoft Office

Adobe Acrobat

Job description

(Contractor) Senior Regulatory Affairs Specialist

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 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/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.
• 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.
• Critically review documentation for regulatory submissions and provide input for necessary revisions.
• Must maintain operational compliance with US and international regulatory agencies and guidelines (i.e. FDA, EU, HC, TGA, PIC/S, ISO, USP, NRC, cGMP, etc.).

Requirements

• 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).

Working Conditions:

• Standard office environment.
• Willingness to work in a team‑based environment.
• May be required to sit or stand for long periods of 8+ hours a day while performing duties.
• The position deals with many deadlines. Due to the short turnaround time of deadlines and limited time, overtime, weekend work and holiday work 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.