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Location:Audubon, PA Job Code:RAPMKB0515 Description The Regulatory Affairs Specialist assists in writing, submitting and gaining clearance for 510(k) submissions and approval for IDE/PMA submissions to the Food and Drug Administration (FDA) for class II and class III products.12/18/2016 Audubon, PA Save This Job
Company:Scientific Protein Laboratories Job Location(s):Waunakee, WI Start Date:ASAP Employment Term:Regular Employment Type:Full Time Hours per Week:40+ Work Hours (i.e. shift):days Starting Salary Range:Not Provided Required Education:Bachelor's Degree Required Experience:511/14/2016 Waunakee, WI Save This Job
Location:Audubon, PA Job Code:IRPMLB0216 Description The International Regulatory Affairs Specialist writes, submits and gains approval of product registrations and other submissions to international Regulatory agencies. This position entails development of submissions in12/18/2016 Audubon, PA Save This Job
Tracking Code 300-093 Job Description Works closely with the Senior CRA or designee and is responsible for execution of assigned clinical studies tasks in accordance with procedures and within the designated timelines. Under the direction of clinical affairs staff, responsible12/13/2016 Lexington, MA Save This Job
Tracking Code 2177 Job Description The Quality Assurance Specialist is responsible for supporting Quality Assurance operations, compliance, systems, and regulatory affairs functions. Essential Duties: An employee in this position must be able to perform the essential job11/19/2016 Grand Rapids, MI Save This Job
ALAMEDA, CAREGULATORY AFFAIRSFULL-TIME APPLY FOR THIS JOB In this role, you will work with the team that ensures that Penumbra products are approved for use in countries around the world, thereby helping to bring our life-saving technologies to patients worldwide. This position12/13/2016 Alameda, CA Save This Job
Regulatory Specialist (United States; Russia; Egypt; Turkey; UAE; Israel; Saudi Arabia) Responsibilities Ensure compliance with regulatory agency regulations and interpretations Prepare responses to regulatory agencies? questions and other correspondence Organize and maintains12/10/2016 Westborough, MA Save This Job
Posted: 9/26/2016 Category: Nuclear Job Type: - Minimum Experience: 4+ years Required Education: Bachelor (BA, BS...) Benefits: - Job Description Position Title: Employee Concerns Program Specialist The Employee Concerns Program Specialist will support the safe operation1/17/2017 New Hill, NC Save This Job
ALAMEDA, CAREGULATORY AFFAIRSFULL-TIME APPLY FOR THIS JOB As a member of our Regulatory Affairs team, you will play a key role in expediting the availability of our lifesaving products worldwide by ensuring that they meet all requirements set forth by regulatory bodies in the12/13/2016 Alameda, CA Save This Job
Senior Director, Head of Medical Affairs About Us Senior Director, Head of Medical Affairs SCOPE Exciting opportunity for a highly motivated, experienced physician with the appropriate background to build and lead the execution of the Medical Affairs strategy to support the11/20/2016 Durham, NC Save This Job
NEW YORK / NEW JERSEYCLINICAL AFFAIRSFULL-TIME APPLY FOR THIS JOB The Clinical Field Specialist is responsible for developing positive relationships with personnel at clinical study sites by providing product training and expertise, clinical protocol training, continuing11/13/2016 New York, NY Save This Job
ATLANTA, GACLINICAL AFFAIRSFULL-TIME APPLY FOR THIS JOB The Clinical Field Specialist is responsible for developing positive relationships with personnel at clinical study sites by providing product training and expertise, clinical protocol training, continuing education and11/13/2016 Atlanta, GA Save This Job
CHICAGO, ILCLINICAL AFFAIRSFULL-TIME APPLY FOR THIS JOB The Clinical Field Specialist is responsible for developing positive relationships with personnel at clinical study sites by providing product training and expertise, clinical protocol training, continuing education and11/13/2016 Chicago, IL Save This Job