Senior Specialist, Regulatory Affairs

Quest Diagnostics•San Juan Capistrano, CA

2d•$90,000 - $130,000

About The Position

The Sr. Specialist, Regulatory Affairs will create, evaluate and execute domestic and/or international regulatory tasks related to the following: global submissions, technical file compilation, facility registrations, special projects and strategy to drive market growth worldwide. Additionally, this individual will provide input to the Regulatory or cross-functional team on regulatory matters. Preference will be given to someone residing close to one of our Major labs in (Clifton, NJ; Pittsburgh, PA; Houston, TX; Lenexa, KS; Marlborough, MA; Dallas, TX; Wooddale, IL; Tampa, FL; Chantilly, VA; San Juan Capistrano, CA) Internal Grade: 49 No sponsorship available Pay Range: $90,000 - $130,000/ year Salary offers are based on a wide range of factors including relevant skills, training, experience, education, and, where applicable, certifications obtained. Market and organizational factors are also considered. Successful candidates may be eligible to receive annual performance bonus compensation. Benefits Information: We are proud to offer best-in-class benefits and programs to support employees and their families in living healthy, happy lives. Our pay and benefit plans have been designed to promote employee health in all respects – physical, financial, and developmental. Depending on whether it is a part-time or full-time position, some of the benefits offered may include: · 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 Quest Diagnostics honors our service members and encourages veterans to apply. While we appreciate and value our staffing partners, we do not accept unsolicited resumes from agencies. Quest will not be responsible for paying agency fees for any individual as to whom an agency has sent an unsolicited resume. Equal Opportunity Employer: Race/Color/Sex/Sexual Orientation/Gender Identity/Religion/National Origin/Disability/Vets or any other legally protected status.

Nice To Haves

Preference will be given to someone residing close to one of our Major labs in (Clifton, NJ; Pittsburgh, PA; Houston, TX; Lenexa, KS; Marlborough, MA; Dallas, TX; Wooddale, IL; Tampa, FL; Chantilly, VA; San Juan Capistrano, CA)

Responsibilities

Create, evaluate and execute domestic and/or international regulatory tasks related to the following: global submissions, technical file compilation, facility registrations, special projects and strategy to drive market growth worldwide.
Provide input to the Regulatory or cross-functional team on regulatory matters.