MaxCyte Inc is hiring: Director, Regulatory Affairs in Rockville

Description: The Director, Regulatory Affairs will head the Regulatory function at MaxCyte. The Director, Regulatory Affairs develops and implements regulatory compliance and strategies that enable MaxCyte to meet business needs as well as safety, quality, and regulatory requirements. Utilizes knowledge of regulatory requirements and regulations to maintain current regulatory filings; interpret, plan, and communicate requirements; and maintain regulatory compliance to ensure governmental approvals are obtained.

Job Responsibilities:Researches and interprets regulations, guidance's, and precedents to support interdepartmental project teams in developing strategies, policies, and procedures that ensure regulatory compliance with global regulatory agenciesMaintains and updates existing Master Files in various countriesCreates and implements effective regulatory strategies to deliver an efficient and robust development planPartners closely with Legal, Quality, Manufacturing, Engineering, Business Development, Commercial, and other areas of the organization to ensure timely and strategic submissionsSupports projects and product teams to prioritize and identify issues that may increase regulatory risks and propose strategies to address such risks. Suggests solutions for regulatory concerns regarding country specific regulations, guidelines, and precedentsDevelops regulatory processes and procedures and implements best practicesEffectively plans, organizes, and participates in meetings with regulatory agenciesLeads and or participates in communications and meetings with various global Regulatory Authorities to ensure the review and acceptance of master file and development plans, the timely resolution of issues, and the approval of client marketing applicationsIdentifies and diminishes quality and regulatory risks in collaboration with other colleagues and stakeholdersInterfaces with consultants, auditors, regulatory advisorsAssess impact of changing regulations on submission and product development strategies and updates internal/external stakeholders in a timely mannerComplies with all applicable policies regarding health, safety, and the environmentRequirements:

BS/BA in science or engineering field with at least 8-10 years of leadership experience and at least 8 years of relevant regulatory experience within biologics drug development, ideally in cell and gene therapy. Experience in life sciences tools and enabling technologies preferredAdvanced degrees (MA/MS/Ph.D.) preferredSolid understanding of global regulatory and legal liability issues. Demonstrated knowledge of regulatory standards and processes, predominantly in FDA-regulated environmentsHands-on experience in global DMF filings and complianceProven track record of success in problem solving and developing risk-based solutionsStrong verbal and written communications skills and the ability to convey complex regulatory requirements in a straightforward and practical mannerDisplays good business acumenProven track record of success in problem solving and developing risk-based solutionsExperience working on cross-functional teams to driving change and successful implementationUnderstands relevant industry trends and regulatory developments and changesStrong written and oral communication skillsBuilds and cultivates strong relationships

Compensation details:

210000-229000 Yearly Salary

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