CMC Regulatory Consultant
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Apply Now Application ends in 2d 9h 13min
Job Detail
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Offered Salary 0
Job Description
Salamandra’s Chemistry, Manufacturing, and Controls (CMC) Regulatory Consultant will support our CMC practice area. This person will be responsible for leveraging their scientific and regulatory CMC expertise to support clients through the various phases of drug development while working closely with a multi-disciplinary development team to ensure solutions are comprehensive and tailored to each client’s unique needs.
Specific responsibilities of this position include, but are not limited to:
- Writing, as primary author, or critically reviewing CMC portions of relevant regulatory documents (INDs, NDAs, BLAs, MAAs, meeting briefing packages, IBs, annual reports, etc.) and other documents supporting strategic development (e.g., gap analyses, development plants).
- Advising clients on and providing interpretation of relevant regulatory requirements (e.g., FDA, Health Canada, EMA, etc.) to support the development of drugs and biologics and providing regulatory input for CMC development activities.
- Providing support and advice to clients on drug substance and drug product quality expectations as relevant to the stage of development and eventual commercial presentation, including researching, gathering, and integrating data to identify strategic resolutions to issues identified during drug development.
- Reviewing and assessing source documentation, methods, processes, facilities, raw materials from laboratories, contract manufacturing organization (CMO) partners, and any other companies to ensure they align with regulatory requirements.
- Collaborating and working cross-functionally with the nonclinical and clinical practice areas across the organization.
- Serving as subject matter expert regarding CMC related matters on behalf of clients including: responding to questions from regulators; providing scientific and regulatory advice while participating in teleconferences and face-to-face meetings; providing oral or written responses to questions; and other duties as assigned.
- Managing project progression by communicating with teammates, project managers and clients regarding technical issues, timelines, deliverables, etc.; elevating issues to project managers as needed.
- Providing training and mentorship to internal staff, clients, and external vendors as needed.
- Upholding and adhering to Salamandra’s quality standards; supporting/participating in, as needed, Quality System-related activities.
- Supporting efforts to identify new business opportunities and demonstrating the ability to grow client relationships and increase the department’s resources, contributing to the company’s overall growth and market presence.
- Supporting business development activities, such as drafting and/or researching information for scopes of work, proposals, or similar engagements, as needed.
Success Factors
Successful performance in this role is predicated on the ability to:
- Communicate effectively, orally and in writing, in a clear, succinct, and organized manner that is appropriate for the audience.
- Write clear and concise summaries and interpretations for reports and regulatory documents.
- Think quickly and creatively in fast-paced, high-pressure situations and provide thoughtful, measured responses appropriate for the audience.
- Demonstrate flexibility in response to new information, changing conditions, unexpected obstacles, or client needs.
- Analyze information, use sound judgment, and research precedents to generate and evaluate alternative approaches, draw logical conclusions or inferences, and make recommendations.
- Be thorough and conscientious when performing work to ensure the information is complete, accurate, and of the highest possible quality prior to submitting for peer review, quality assurance checks, and client delivery.
- Anticipate client needs and develop strategies and/or recommendations to address them.
- Work both independently as well as collaboratively across all levels of the organization in a fast-paced, matrixed leadership environment to achieve common goals and positive results.
- Manage workload and priorities to meet internal deadlines and ensure the timely preparation and finalization of client deliverables.
- Acumen in building client relationships and supporting strategic business development activities.
- Coach others on how to perform tasks and develop their capabilities within the standards of the organization using formal or informal methods.
Minimum Qualifications
- Minimum of 8 years CMC or quality-focused regulatory experience within the pharmaceutical industry; prior FDA experience and/or regulatory consulting experience strongly preferred.
- Ph.D. in chemistry, biochemistry, or closely-related discipline or an M.S. in a relevant science in combination with applicable experience.
- Expertise in CMC and Quality requirements and strategy throughout the product lifecycle, including drug development and post-approval.
- Experience with the preparation of regulatory documents (e.g., IBs, Briefing Packages, INDs, CTAs, NDAs, and MAAs) in CTD format.
- Experience with CMC strategy, data interpretation, and risk assessment.
- Knowledge of contract manufacturer function and ability to interact with CMOs/laboratories to guide programs.
- Experience interacting with the FDA on INDs, NDAs, and development programs; interaction with other regulatory authorities is a plus.
- A comprehensive understanding of CMC regulatory (e.g., FDA, ICH, EMA) requirements, guidelines, and relevant government regulations.
- Experience with device regulations, combination products and/or biologics is a plus.
- Experience supporting business development activities is a plus.
- Proficiency in Microsoft Office is required.
- Eligible to work in the U.S. without time limitations.
Apply Now
Application ends in 2d 9h 13min