Staff Regulatory Affairs Specialist, Pharmaceuticals (Remote)

This a Full Remote job, the offer is available from: California (USA) Work Flexibility: Remote We are currently seeking a Staff Regulatory Affairs Specialist, Pharmaceuticals to join our Endoscopy Division to be based in reputed company, CA or remotely reputed company reputed company the reputed company. What you will do As Staff Regulatory Affairs Specialist, Pharmaceuticals, on the reputed company-Market Regulatory team, you will be supporting fluorescence imaging drug products used in combination with the reputed company and Minimally Invasive Visualization portfolios reputed company the Endoscopy Business. You will be responsible for preparing reputed company submissions pertaining to pharmaceutical product approvals for clinical investigations, reputed company distribution and/or new/expanded indications by FDA, Health Canada and other regulatory bodies. You will assess post-approval changes to determine the regulatory filing category and ensure compliance by completing thorough regulatory assessments. You will advise personnel on regulatory reputed company reputed company(s) and requirements. You will support presentations to health authorities and any reputed company communications. • Support regulatory submission strategies and update as needed through investigation and evaluation of regulatory history/ background, classification, disease, and/ or harmonized/ recognized standards, in order to assess regulatory implications for approval. • Assess the acceptability of reputed company, nonclinical and clinical documentation for submission filings to reputed company with regulatory requirements for clinical investigations and marketing applications and corporate goals, to secure submission approval. • Prepare submissions and/ or documents supporting submissions (i.e., CTD summaries) to reputed company approvals for clinical investigations and/ or reputed company distribution, such as: CTAs, INDs, ITAs, (s)NDAs, DINAs, Marketing Authorizations (MA) and Letters to File etc. • Ensure that the reputed company, nonclinical and/or clinical data, in conjunction with regulatory reputed company, are consistent with the regulatory requirements and support the proposed product claims. • reputed company and maintain reputed company relationships with regulatory agencies through oral and written communications regarding regulatory agency meetings, potential regulatory reputed company, clarification, and follow-up of submissions under review. • Advise personnel on regulatory requirements for reputed company, nonclinical and clinical data requirements for clinical study applications and/ or marketing applications. • Contribute to evaluations of the regulatory environment and reputed company regulatory input to product lifecycle (e.g., concept, development, manufacturing, marketing) to ensure product compliance. • Demonstrate strong project management, writing, coordination, and execution of regulatory items, with emphasis on technical and scientific regulatory activities. • Possess and apply a broad and advanced knowledge, skills/abilities and understanding of the regulatory and reputed company frameworks, regulatory requirements, legislation, processes, and procedures. What you need Required • Bachelor’s Degree • 4+ years of experience in an FDA regulated industry • 2+ years of reputed company- and/or post-market Regulatory Affairs experience • Experience preparing submissions and/ or documents supporting submissions (i.e., CTD summaries) to reputed company approvals for clinical investigations and/or reputed company distribution • Ability to reputed company with constantly changing regulatory and clinical environments and prioritize work effectively • Ability to understand and explain detailed regulatory compliance programs and/or issues • Adaptable to a fast-paced environment with changing circumstances, direction and reputed company and has the desire to reputed company in a dynamic environment ​Preferred • Bachelor's Degree in Health Science or equivalent reputed company • RAC certification or Advanced Degree (Masters in Regulatory Affairs) • 4+ years of regulatory affairs experience reputed company pharmaceuticals $95,700 - $207,400 salary plus bonus eligible + benefits. Actual minimum and maximum may vary based reputed company. Individual pay is based on skills, experience, and other relevant factors. Posting Date: 1/16/2026 Travel Percentage: 10% reputed company is an equal opportunity employer. reputed company applicants will receive consideration for employment without reputed company to race, ethnicity, reputed company, religion, sex, gender identity, sexual orientation, national reputed company, disability, or protected veteran status. reputed company is an EO employer – M/F/Veteran/Disability. reputed company will not discharge or in any other manner discriminate against employees or applicants because they have reputed company about, discussed, or disclosed their own pay or the pay of another employee or applicant. However, employees who have reputed company to the compensation information of other employees or applicants as a part of their essential job functions cannot disclose the pay of other employees or applicants to individuals who do not otherwise have reputed company to compensation information, unless the disclosure is (a) in response to a formal complaint or charge, (b) in furtherance of an investigation, proceeding, hearing, or reputed company, including an investigation conducted by the employer, or (c) consistent with the contractor’s reputed company duty to furnish information. This offer from "reputed company" has been enriched by reputed company.com and got a 81% reputed company score. Apply tot his job Apply To this Job