Senior Manager of Regulatory Affairs

Job Location
19500 S. Rancho Way, Ste. 116
Rancho Dominguez, CA 90220
Job Description

Job Description
The Senior Manager of Regulatory Affairs will provide regulatory support for DxTerity's key business functions across both domestic and international markets, including, but not limited to in-vitro diagnostic product development, clinical study support, laboratory developed tests, CLIA/CAP laboratory functions, commercialization, distribution (import/export), as well as ensuring the sustained success of marketed products. This role will lead the strategy and the preparation, review and submission of documents to FDA and other national authorities including post-market surveillance, combining knowledge of scientific, regulatory, and business issues to assure products are developed, manufactured, and distributed according to all pertinent laws and regulations.

Supervisory Responsibilities:
Supervises the Regulatory Affairs staff. May engage and supervise external consultants when needed to supplement DxTerity staff.

Essential Functions:
• Develop, coordinate and implement strategies to gain regulatory clearance for DxTerity Diagnostics' products.
• Anticipate regulatory and related obstacles and emerging issues throughout the product lifecycle.
• Oversees coordination, preparation and timely submission of regulatory documents to secure and maintain market access.
• Provides regulatory advice to other functional areas.
• Identifies perceived gaps in product development plans that may pose regulatory issues.
• Develops and maintains relationships with external vendors (logistics, import/export) and regulatory authorities to improve effectiveness in regulatory strategy execution.
• Oversees regulatory authority inspections and provides input for follow-up to inspections and audits to minimize potential for findings of noncompliance.
• Coordinates preparation of responses to queries from regulatory authorities.
• Oversees activities related to post-market surveillance and ensures compliance with product post-marketing approval requirements.
• Conducts regulatory review of complaints.
• Oversees activities related to product recall and recall communication process.
• Assures medical device reports (MDR) are reported to regulatory agencies and internal stakeholders.
• Manage processes involved with maintaining annual licenses, registrations, listings and patent information.
• Reviews and approves advertising and promotional items to ensure regulatory compliance, including online media and labeling.
• Assures QMS compliance to the QSR, 21 CFR 820, ISO 13485, and any other applicable QMS regulation.
• Other duties, as assigned.

Education and Experience:
• Bachelor's Degree is required, preferably in a technical discipline such as biology, chemistry, or engineering.
• M.S. in a technical area or M.B.A. or a Ph.D. in a technical area or law, preferred.
• 7-10 years of relevant industry experience in an FDA regulated environment with a minimum of 5 years in decision-making role.
• Certification (such as RAC from the Regulatory Affairs Professionals Society) preferred.
Experience in In Vitro Diagnostics, Nucleic Acid-based Chemistry, Molecular Genetics, Gene Expression Platform Analysis, and/or NGS Technologies are a plus.

Qualifications: To perform this job successfully, the candidate must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required.

• Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.
• Demonstrated ability to interpret and stay current with FDA, EU and other regulatory agency regulations and guidelines. International experience is desired.
• Understands the principles and requirements of promotion, advertising and labeling.
• Must demonstrate high-level of motivation to work in a fast-paced, start-up environment.
• Demonstrated ability or track record of achieving successful results in a timely manner.
• Demonstrated ability to be flexible and resourceful with excellent communication and diplomacy skills.
• Organizational, planning and detailed follow-up skills is required. Ability to utilize tasking, scheduling, and other project management tools.
• Leadership and motivational talent needed with ability to relate to both highly educated and unskilled team members.

How to Apply

Visit our LinkedIn page (link) to apply online, or email us at

About Our Organization

At DxTerity, a patient-centric genomics company located in Los Angeles, California, our team is working to bring the power of real-world genomics with From-Home RNA monitoring to improving the management of immune-mediated diseases. Currently, we have our sights set on lupus, multiple sclerosis, rheumatoid arthritis, and cancer. We believe that low-cost, from-home, immune-monitoring blood tests will help advance the treatment and care for patients living with these diseases, helping them to live life confidently. If you have a passion for healthcare, want to make a difference in transforming patient care, and have a desire to grow and excel at what you do, we want to hear from you!

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