Quest Diagnostics
Senior Specialist, Regulatory Affairs
Quest Diagnostics, San Juan Capistrano, California, United States, 92675
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Senior Specialist, Regulatory Affairs
role at
Quest Diagnostics
Pay Range:
$90,000 - $130,000 per year
Responsibilities
Provide regulatory guidance in product design, clinical studies, market authorization strategies, and labeling.
Review and edit product submissions and other communications prepared by junior department members.
Act as regulatory subject matter expert for junior department members.
Provide pre-market and post-market regulatory strategy to ensure regulatory compliance and advance commercial objectives.
Represent Regulatory on core teams providing regulatory feedback and guidance throughout the product development cycle and coordinating team inputs for submissions.
Prepare global regulatory applications, as well as internal regulatory file documentation.
Manage submissions such as US FDA Section 510(k) Notifications, Pre-market Approval (PMA) Applications and Supplements, EU IVDR, Technical Documentation, ROW submissions and global product registrations.
Independently communicate with regulatory agencies on pre-market and post-market related issues.
Document, consolidate and maintain oral and written communications with regulatory bodies like FDA, Health Canada, notified bodies, etc.
Participate in training and education seminars as appropriate to learn regulatory requirements and keep abreast of current regulatory trends.
Monitor proposed regulatory changes from the FDA and worldwide regulatory authorities and provide management with impact of changes in the Regulatory environment.
Review related regulatory publications and documents to stay informed about current regulatory actions.
Interface with industry associations to help state, federal, and international regulatory agencies develop regulations.
Provide backup to the Regulatory Affairs Director as needed.
Perform other duties as assigned. Provide technical and editorial direction to junior department members.
Qualifications
BS/MS in Biology, Immunology, Microbiology, Biochemistry, Medical Technology or related discipline required.
Must have extensive knowledge of U.S, Canadian, European and other International In vitro diagnostic regulations and standards.
At least three to five years of pre-market regulatory experience in IVD industry. Clinical research experience desired, but not required.
Demonstrated success in directly securing regulatory clearance/approvals for In vitro diagnostic products required.
Must be able to work well in team environment with individuals from diverse functional areas, as well as work independently.
Must demonstrate leadership skills without having direct authority.
Must have experience working on project/product from concept to market introduction.
Must have proven analytical capabilities, solid understanding of manufacturing and change control, and awareness of regulatory trends.
Must have experience in negotiation of technical issues with internal and external functions including health authorities.
Benefits
Medical/Prescription Drugs
Dental
Vision
Flexible Spending Accounts (FSAs)
Supplemental Health Plans
401(k) Plan – Company match dollar-for-dollar up to 5%
Employee Stock Purchase Plan (ESPP)
Supplemental Life Insurance
Dependent Life Insurance
Short- and Long-Term Disability buy-up
Blueprint for Wellness
Emotional Well-Being Resources
Educational Assistance
Paid time off / Health Time
Variable Compensation Plans
Sales Incentive Plans
Quest Diagnostics honors our service members and encourages veterans to apply.
Equal Opportunity Employer: Race/Color/Sex/Sexual Orientation/Gender Identity/Religion/National Origin/Disability/Vets or any other legally protected status.
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Senior Specialist, Regulatory Affairs
role at
Quest Diagnostics
Pay Range:
$90,000 - $130,000 per year
Responsibilities
Provide regulatory guidance in product design, clinical studies, market authorization strategies, and labeling.
Review and edit product submissions and other communications prepared by junior department members.
Act as regulatory subject matter expert for junior department members.
Provide pre-market and post-market regulatory strategy to ensure regulatory compliance and advance commercial objectives.
Represent Regulatory on core teams providing regulatory feedback and guidance throughout the product development cycle and coordinating team inputs for submissions.
Prepare global regulatory applications, as well as internal regulatory file documentation.
Manage submissions such as US FDA Section 510(k) Notifications, Pre-market Approval (PMA) Applications and Supplements, EU IVDR, Technical Documentation, ROW submissions and global product registrations.
Independently communicate with regulatory agencies on pre-market and post-market related issues.
Document, consolidate and maintain oral and written communications with regulatory bodies like FDA, Health Canada, notified bodies, etc.
Participate in training and education seminars as appropriate to learn regulatory requirements and keep abreast of current regulatory trends.
Monitor proposed regulatory changes from the FDA and worldwide regulatory authorities and provide management with impact of changes in the Regulatory environment.
Review related regulatory publications and documents to stay informed about current regulatory actions.
Interface with industry associations to help state, federal, and international regulatory agencies develop regulations.
Provide backup to the Regulatory Affairs Director as needed.
Perform other duties as assigned. Provide technical and editorial direction to junior department members.
Qualifications
BS/MS in Biology, Immunology, Microbiology, Biochemistry, Medical Technology or related discipline required.
Must have extensive knowledge of U.S, Canadian, European and other International In vitro diagnostic regulations and standards.
At least three to five years of pre-market regulatory experience in IVD industry. Clinical research experience desired, but not required.
Demonstrated success in directly securing regulatory clearance/approvals for In vitro diagnostic products required.
Must be able to work well in team environment with individuals from diverse functional areas, as well as work independently.
Must demonstrate leadership skills without having direct authority.
Must have experience working on project/product from concept to market introduction.
Must have proven analytical capabilities, solid understanding of manufacturing and change control, and awareness of regulatory trends.
Must have experience in negotiation of technical issues with internal and external functions including health authorities.
Benefits
Medical/Prescription Drugs
Dental
Vision
Flexible Spending Accounts (FSAs)
Supplemental Health Plans
401(k) Plan – Company match dollar-for-dollar up to 5%
Employee Stock Purchase Plan (ESPP)
Supplemental Life Insurance
Dependent Life Insurance
Short- and Long-Term Disability buy-up
Blueprint for Wellness
Emotional Well-Being Resources
Educational Assistance
Paid time off / Health Time
Variable Compensation Plans
Sales Incentive Plans
Quest Diagnostics honors our service members and encourages veterans to apply.
Equal Opportunity Employer: Race/Color/Sex/Sexual Orientation/Gender Identity/Religion/National Origin/Disability/Vets or any other legally protected status.
#J-18808-Ljbffr