Regulatory Affairs Specialist

We pride ourselves on a high-trust, high-accountability environment where we lift each other up. When you join Singota, you are a part of a team that respects, supports, and values its people. We celebrate wins together, brainstorm solutions together, and genuinely enjoy the work we do. The result? A team that’s not just efficient, but also passionate, dedicated, and fun to work with.

General Description

The Regulatory Affairs Specialist assists in the support and execution of regulatory affairs and compliance programs at Singota. This role will be responsible for supporting day-to-day regulatory operations including providing regulatory guidance and support to Singota’s diverse client base. The Regulatory Affairs Specialist will support the organization by providing CMC regulatory support, preparing and managing regulatory documentation, and coordinating with internal and external technical teams and stakeholders to ensure compliance with applicable regulatory standards and guidance. The role also includes supporting the implementation and maintenance of procedures to verify that the regulatory program remains effective and efficient. This is a remote position; however, routine onsite presence will be required as needed to support audit activities and other business requirements.

1. Conduct ongoing regulatory surveillance to proactively identify and address upcoming regulatory changes and collaborate with relevant departments to identify and implement necessary changes.

2. Assist in the management of Singota licensing, certifications, and registrations, including but not limited to domestic and foreign agencies, regulatory bodies, and government agencies.

3. Assist in commercial/controlled substance license evaluations of Singota’s supply chain partners to ensure compliance with Drug Supply Chain Security Act (DSCSA) requirements.

4. Support internal compliance with applicable regulatory requirements (e.g., FDA, MHRA, EMA, ICH, etc.)

5. Collaborate with internal departments in addressing regulatory topics and provide guidance as needed.

6. Assist with impact assessments for manufacturing, analytical, facility, and supplier change notifications.

7. Interface with clients during routine project meetings to provide regulatory guidance and support.

8. Coordinate information requests between Client(s) and internal technical functions.

9. Provide support during client and regulatory audits of Singota, ensuring regulatory and quality standards are met.

10. Provide support in preparation of client regulatory submission documentation, as applicable, including but not limited to Investigational New Drug Applications (INDs), New Drug Applications (NDAs), Biologics License Applications (BLAs) in accordance with regulatory requirements.

11. Provide support in preparation and submission of facility Drug Master File (DMF), as well as annual product review(s) (APRs), and annual reporting requirements.

12. Author and review site procedures and specifications to verify adherence to applicable regulations.

13. Design and deliver training sessions and refresher courses to communicate regulatory changes to key stakeholders across the organization.

14. Assist with compilation, formatting, and quality verification of regulatory submissions to ensure accuracy and completeness.

15. Assist in the development and management of audit responses, working collaboratively across functions and ensuring accurate documentation and management of all audit records.

16. Participate in the preparation, evaluation, and modification of client Quality Agreements

17. Provide primary ownership of deviations, CAPAs and change controls as needed.

18. Comply with quality and safety management systems including requirements for documentation, training, system use, SOPs, processes, and procedures.

19. Contribute to the assessment of business opportunities by evaluating potential projects from a regulatory standpoint as part of a cross-functional team.

20. General support required of a company where everyone is expected to perform multiple tasks both inside and outside their department to meet the needs of the business.