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Principal Regulatory Affairs Specialist
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Principal Regulatory Affairs Specialist Are you a Regulatory Affairs Professional looking for an exciting new opportunity and a chance to be involved with life-saving Neuro technologies? At Stryker Neurovascular, the Principal Regulatory Affairs...
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From Job Vertise
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Date
2018-12-12
Company
Confidential


Location
Fremont, CA
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About the job:
Principal Regulatory Affairs Specialist Are you a Regulatory Affairs Professional looking for an exciting new opportunity and a chance to be involved with life-saving Neuro technologies? At Stryker Neurovascular, the Principal Regulatory Affairs Specialist will: Prepare complex submissions to gain approvals for clinical research, export, and commercial distribution. Coordinate and prepare document packages for regulatory submissions in one or more of the following geographic regions: United States, Europe, Japan, and Canada. Ensure that existing approvals and documentation are maintained,...
Location:
Fremont, CA
Job Type:
Full-Time
Permanent
Occupation:
Regulatory Affairs Specialists
Salary:
High Income Jobs ($80K-$99K)
Career Level/Education:
Bachelor's degree
Certifications/Licenses:
N/A
Preferred WorkKeys®
Applied Math
3
Graphic Literacy
4
Workplace Documents
4

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Regulatory Post Market Surveillance Specialist
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Company Description: Who is Intuitive Surgical? The numbers tell an amazing story. Learn more about our company. Joining Intuitive Surgical means joining a team dedicated to using technology to benefit patients by improving surgical efficacy and...
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From Job Vertise
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Date
2018-12-12
Company
Confidential


Location
Sunnyvale, CA
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About the job:
Company Description: Who is Intuitive Surgical? The numbers tell an amazing story. Learn more about our company. Joining Intuitive Surgical means joining a team dedicated to using technology to benefit patients by improving surgical efficacy and decreasing surgical invasiveness, with patient safety as our highest priority. Primary Function of Position: The Regulatory Post Market Surveillance Specialist investigates customer complaints, makes an initial reporting decision, provides failure analysis letters, and ensures completeness and consistency of complaint and related documentation. Roles...
Location:
Sunnyvale, CA
Job Type:
Full-Time
Permanent
Occupation:
Regulatory Affairs Specialists
Salary:
High Income Jobs ($80K-$99K)
Career Level/Education:
Bachelor's degree
Certifications/Licenses:
N/A
Preferred WorkKeys®
Applied Math
3
Graphic Literacy
4
Workplace Documents
4

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Cell Banking Specialist
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Cell Banking Specialist Redwood City, CA Production - Engineered Cells Full-time Synthego is looking to hire a Cell Culture & Banking Specialist who would be responsible for completing and assisting with daily tasks associated with cell-related...
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From Job Vertise
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Date
2018-12-12
Company
Confidential


Location
Redwood City, CA
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About the job:
Cell Banking Specialist Redwood City, CA Production - Engineered Cells Full-time Synthego is looking to hire a Cell Culture & Banking Specialist who would be responsible for completing and assisting with daily tasks associated with cell-related functions. Primary duties include producing various types of cells, and manufacturing final product for commercial distribution. Requirements include following, creating and updating SOPs as needed, performing daily tasks in a clean room / cGMP environment, and troubleshooting of manufacturing challenges. Follows established company rules, regulations...
Location:
Redwood City, CA
Job Type:
Full-Time
Permanent
Occupation:
Regulatory Affairs Specialists
Salary:
High Income Jobs ($80K-$99K)
Career Level/Education:
Bachelor's degree
Certifications/Licenses:
N/A
Preferred WorkKeys®
Applied Math
3
Graphic Literacy
4
Workplace Documents
4

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Evergreen Requisition - Regulatory Affairs Analyst
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Evergreen Requisition - Regulatory Affairs Analyst California, San Jose * An Evergreen Requisition is an advertisement for positions that Olympus hires for throughout the year. It is a way for Olympus to build a database of qualified, interested...
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From Job Vertise
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Date
2018-12-12
Company
Confidential


Location
San Jose, CA
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About the job:
Evergreen Requisition - Regulatory Affairs Analyst California, San Jose * An Evergreen Requisition is an advertisement for positions that Olympus hires for throughout the year. It is a way for Olympus to build a database of qualified, interested individuals for a particular job function so that when there is a need to fill that type of role, the hiring process will be faster. By applying to an Evergreen Requisition, you are expressing your interest for a particular job function within the Olympus family of companies. In addition to submitting your resume to an Evergreen Requisition, we...
Location:
San Jose, CA
Job Type:
Full-Time
Permanent
Occupation:
Regulatory Affairs Specialists
Salary:
High Income Jobs ($80K-$99K)
Career Level/Education:
Bachelor's degree
Certifications/Licenses:
N/A
Preferred WorkKeys®
Applied Math
3
Graphic Literacy
4
Workplace Documents
4

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Quality Assurance Specialist (Clinical)
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Quality Assurance Specialist (Clinical) Are you looking for unlimited opportunities to develop and succeed?With work that challenges and makes a difference, within a flexible and supportive environment, we can help our customers achieve their...
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From Job Vertise
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Date
2018-12-12
Company
Confidential


Location
Boston, MA
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About the job:
Quality Assurance Specialist (Clinical) Are you looking for unlimited opportunities to develop and succeed?With work that challenges and makes a difference, within a flexible and supportive environment, we can help our customers achieve their dreams and aspirations. Job Description Performs auditing of benefit eligibility decisions and coordinates appeal presentations to Appeal Committee. Audit timelines of intake review and onsite ordering. Audit timeliness of completion of onsite and POC by ECC. Audit timeliness of review of onsite and POC by internal care manager for new arising claims....
Location:
Boston, MA
Job Type:
Full-Time
Permanent
Occupation:
Regulatory Affairs Specialists
Salary:
High Income Jobs ($80K-$99K)
Career Level/Education:
Bachelor's degree
Certifications/Licenses:
N/A
Preferred WorkKeys®
Applied Math
4
Graphic Literacy
5
Workplace Documents
4

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Postmarket Surveillance Analyst
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Description: Initiates and manages the complaint file, maintains accurate entry of complaints in the database, communicates to field representatives regarding information needed specific to product complaints (e.G. physicians, hospital personnel,...
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From Retirement Jobs
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Date
2018-12-12
Company
EXPERIS
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Location
Minnetonka, MN
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About the job:
Description: Initiates and manages the complaint file, maintains accurate entry of complaints in the database, communicates to field representatives regarding information needed specific to product complaints (e.G. physicians, hospital personnel, sales representatives, international offices), independently assesses the complaint to determine if a medical device report needs to be filed with various global regulatory agencies (e.g. FDA, ECA) and submits reports within required timeframe, diligent of any unusual trends in product complaints and communicates them with mgmt., complies with US FDA...
Location:
Minnetonka, MN
Job Type:
Full-Time
Contract
Occupation:
Regulatory Affairs Specialists
Salary:
High Income Jobs ($80K-$99K)
Career Level/Education:
High school diploma or equivalent
Certifications/Licenses:
N/A
Preferred WorkKeys®
Applied Math
3
Graphic Literacy
4
Workplace Documents
4

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Regulatory Affairs Specialist (Home-Based) - Novella Clinical
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Join us on our exciting journey! IQVIA™ is The Human Data Science Company™, focused on using data and science to help healthcare clients find better solutions for their patients. Formed through the merger of IMS Health and Quintiles, IQVIA offers a...
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From Retirement Jobs
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Date
2018-12-12
Company
IQVIA
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Location
Morrisville, NC
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About the job:
Join us on our exciting journey! IQVIA™ is The Human Data Science Company™, focused on using data and science to help healthcare clients find better solutions for their patients. Formed through the merger of IMS Health and Quintiles, IQVIA offers a broad range of solutions that harness advances in healthcare information, technology, analytics and human ingenuity to drive healthcare forward. BASIC FUNCTIONS: To provide regulatory and quality support to select clinical research projects involving investigational or marketed drugs, devices, biologics, or new medical procedures. To provide...
Location:
Morrisville, NC
Job Type:
Full-Time
Permanent
Occupation:
Regulatory Affairs Specialists
Salary:
High Income Jobs ($80K-$99K)
Career Level/Education:
Bachelor's degree
Certifications/Licenses:
ISO Standards
Preferred WorkKeys®
Applied Math
3
Graphic Literacy
4
Workplace Documents
4

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Senior Regulatory Affairs Specialist
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Seeking a Regulatory Affairs Specialist 2 responsible for international regulatory activities associated with Notified Body in EU, and other international regulatory agencies. This position requires a person with commitment to excellence, and...
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From Monster
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Date
2018-12-11
Company
Randstad
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Location
Marlborough, MA
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About the job:
Seeking a Regulatory Affairs Specialist 2 responsible for international regulatory activities associated with Notified Body in EU, and other international regulatory agencies. This position requires a person with commitment to excellence, and ability to work in a fast-paced, technically skilled, team setting. Responsibilities: Essential Duties and Responsibilities The incumbent may be asked to perform other function-related activities in addition to the below mentioned responsibilities as reasonably required by business needs. ??? Demonstrated ability to coordinate complex projects. ???...
Location:
Marlborough, MA
Job Type:
Full-Time
Permanent
Temporary
Occupation:
Regulatory Affairs Specialists
Salary:
High Income Jobs ($80K-$99K)
Career Level/Education:
Bachelor's degree
Certifications/Licenses:
Medical Device Directive Certification
Preferred WorkKeys®
Applied Math
3
Graphic Literacy
4
Workplace Documents
4

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Senior Analyst, CMC Technical Writing
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Allergan plc (NYSE: AGN) is a bold, global pharmaceutical company and a leader in a new industry model - Growth Pharma. Allergan is focused on developing, manufacturing and commercializing branded pharmaceutical, device, biologic, surgical and...
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From CareerBuilder
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Date
2018-12-11
Company
Allergan
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Location
Madison, NJ
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About the job:
Allergan plc (NYSE: AGN) is a bold, global pharmaceutical company and a leader in a new industry model - Growth Pharma. Allergan is focused on developing, manufacturing and commercializing branded pharmaceutical, device, biologic, surgical and regenerative medicine products for patients around the world. Allergan markets a portfolio of leading brands and best-in-class products for the central nervous system, eye care, medical aesthetics and dermatology, gastroenterology, women's health, urology and anti-infective therapeutic categories. With commercial operations in approximately 100...
Location:
Madison, NJ
Job Type:
Full-Time
Permanent
Occupation:
Regulatory Affairs Specialists
Salary:
High Income Jobs ($80K-$99K)
Career Level/Education:
Bachelor's degree
Certifications/Licenses:
Certified Management Consultant
Preferred WorkKeys®
Applied Math
3
Graphic Literacy
4
Workplace Documents
5

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Regulatory affairs Specialist II
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Description Overall Purpose As Regulatory Affairs Specialist II, you will prepare global regulatory submissions and communicate regulatory strategies to product development teams. You will also be responsible for development, maintenance, and...
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From LocalJobNetwork
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Date
2018-12-11
Company
MicroPort Orthopedics, Inc.
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Location
Arlington, TN
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About the job:
Description Overall Purpose As Regulatory Affairs Specialist II, you will prepare global regulatory submissions and communicate regulatory strategies to product development teams. You will also be responsible for development, maintenance, and review of submissions, documentation, labeling, and procedures. Skills Requirements - Ability to work independently and/or with guidance from management to perform job functions - Ability to read, analyze, and interpret regulations, technical standards, guidance documents, test reports, clinical and medical terminology, technical product information, and...
Location:
Arlington, TN
Job Type:
Full-Time
Permanent
Occupation:
Regulatory Affairs Specialists
Salary:
Upper Middle Income Jobs ($50K-$79K)
Career Level/Education:
Bachelor's degree
Certifications/Licenses:
N/A
Preferred WorkKeys®
Applied Math
3
Graphic Literacy
4
Workplace Documents
4

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Senior Biodefense Regulated Quality Review Specialist
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Senior Biodefense Regulated Quality Review Specialist Location MD - Ft. Detrick, USAMRIID Job Code 5084 # of openings 1 The Alaka`ina Foundation Family of Companies (FOCs) is comprised of industry-recognized government service firms designated as...
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From LocalJobNetwork
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Date
2018-12-11
Company
Laulima Government Solutions
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Location
Maryland
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About the job:
Senior Biodefense Regulated Quality Review Specialist Location MD - Ft. Detrick, USAMRIID Job Code 5084 # of openings 1 The Alaka`ina Foundation Family of Companies (FOCs) is comprised of industry-recognized government service firms designated as Native Hawaiian Organization (NHO)-owned and 8(a) certified businesses. The Family of Companies (FOCs) includes Ke`aki Technologies, Laulima Government Solutions, Kupono Government Services, and Kapili Services. The Alaka`ina Foundation activities under the 501(c)3 principally benefit the youth of Hawaii through charitable efforts which includes...
Location:
Maryland
Job Type:
Full-Time
Permanent
Occupation:
Regulatory Affairs Specialists
Salary:
High Income Jobs ($80K-$99K)
Career Level/Education:
Associate's degree
Certifications/Licenses:
Continuing Education
Preferred WorkKeys®
Applied Math
4
Graphic Literacy
5
Workplace Documents
5

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Regulatory Compliance - Document Specialist
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COMPANY DESCRIPTION At Beyond Meat, we started with simple questions. Why do you need an animal to create meat? Why can’t you build meat directly from plants? It turns out you can. So we did. We make plant-based meats that allow families to eat...
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From Careers in Food
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Date
2018-12-11
Company
Beyond Meat
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Location
Columbia, MO
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About the job:
COMPANY DESCRIPTION At Beyond Meat, we started with simple questions. Why do you need an animal to create meat? Why can’t you build meat directly from plants? It turns out you can. So we did. We make plant-based meats that allow families to eat more, not less, of the traditional dishes they love while feeling great about the health, sustainability, and animal welfare benefits of plant protein. Our goal is to bring exciting change to the plate—and Beyond. OVERVIEW The Regulatory Compliance Document Specialist’s primary role/ position is to assist with maintaining critical information for the...
Location:
Columbia, MO
Job Type:
Full-Time
Permanent
Occupation:
Regulatory Affairs Specialists
Salary:
Upper Middle Income Jobs ($50K-$79K)
Career Level/Education:
Bachelor's degree
Certifications/Licenses:
Safe Quality Food
Preferred WorkKeys®
Applied Math
3
Graphic Literacy
4
Workplace Documents
4

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Regulatory Affairs Manager/ Specialist- Medical Device
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Employvision is looking to hire an intelligent sharp skilled senior Regulatory Affairs Advisory- Medical Device for one of A Fortune 500 Company. Role: Regulatory Affairs Advisory Role- Medical Device Location: Cambridge, MA Full Time Opportunity...
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From Monster
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Date
2018-12-11
Company
EmployVision, Inc
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Location
Cambridge, MA
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About the job:
Employvision is looking to hire an intelligent sharp skilled senior Regulatory Affairs Advisory- Medical Device for one of A Fortune 500 Company. Role: Regulatory Affairs Advisory Role- Medical Device Location: Cambridge, MA Full Time Opportunity Excellent Base Salary, Full Benefits & Perks Package, etc. Core Duties & Responsibilities: Prepare regulatory assessments and plans for new products and design changes. Prepare or direct the preparation of regulatory submissions for product approval/clearance, including 510(k) premarket notifications. Participate in interactions with regulatory...
Location:
Cambridge, MA
Job Type:
Full-Time
Permanent
Occupation:
Regulatory Affairs Specialists
Salary:
High Income Jobs ($80K-$99K)
Career Level/Education:
Bachelor's degree
Certifications/Licenses:
Medical Device Directive Certification
Regulatory Affairs Certification
Preferred WorkKeys®
Applied Math
3
Graphic Literacy
4
Workplace Documents
4

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Principal Regulatory Affairs Specialist
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Job Summary Reporting to the Director of Regulatory Affairs, the Principal Regulatory Affairs Specialist monitors and analyzes issues in various phases of government regulatory procedures and identifies trends important to the organization for use...
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From LocalJobNetwork
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Date
2018-12-11
Company
ProLacta BioScience
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Location
Duarte, CA
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About the job:
Job Summary Reporting to the Director of Regulatory Affairs, the Principal Regulatory Affairs Specialist monitors and analyzes issues in various phases of government regulatory procedures and identifies trends important to the organization for use by management in decision making. The Principal Specialist is also responsible for filing necessary applications and handling all government interactions pertaining to the regulation process for products requiring governmental approval in the US and International. Primary Duties and Responsibilities * Provides analysis and background material in...
Location:
Duarte, CA
Job Type:
Full-Time
Permanent
Occupation:
Regulatory Affairs Specialists
Salary:
High Income Jobs ($80K-$99K)
Career Level/Education:
Bachelor's degree
Certifications/Licenses:
N/A
Preferred WorkKeys®
Applied Math
3
Graphic Literacy
4
Workplace Documents
4

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Regulatory Affairs Associate - I
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Our client is an American biotechnology company that researches, develops and commercializes drugs. Responsibilities: Provides support in the preparation of regulatory submissions for investigational and commercial products in line with ICH...
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From Monster
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Date
2018-12-11
Company
COMPASS CONSULTING GROUP
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Location
Seattle, WA
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About the job:
Our client is an American biotechnology company that researches, develops and commercializes drugs. Responsibilities: Provides support in the preparation of regulatory submissions for investigational and commercial products in line with ICH requirements, regional requirements, and scientific and company policies and procedures. Works to develop and acquire required regulatory skills and knowledge, with guidance from immediate manager. May contribute to routine local process improvements, which have an impact on the working of the Regulatory Affairs function. Performs document filing and...
Location:
Seattle, WA
Job Type:
Full-Time
Permanent
Occupation:
Regulatory Affairs Specialists
Salary:
High Income Jobs ($80K-$99K)
Career Level/Education:
Bachelor's degree
Certifications/Licenses:
N/A
Preferred WorkKeys®
Applied Math
3
Graphic Literacy
4
Workplace Documents
4

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Technical Leader 1 - Global Regulatory Affairs
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Technical Leader 1 - Global Regulatory Affairs Job Description Job Technical Leader I Global Regulatory Affairs Location: Neenah, WI Position Purpose: Provide technical leadership in the development and implementation of regulatory strategies to...
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From Vindy.com
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Date
2018-12-11
Company
Kimberly-Clarke
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Location
Neenah, WI
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About the job:
Technical Leader 1 - Global Regulatory Affairs Job Description Job Technical Leader I Global Regulatory Affairs Location: Neenah, WI Position Purpose: Provide technical leadership in the development and implementation of regulatory strategies to support the achievement of business objectives for client K-C business units, while ensuring compliance with domestic and international medical device and consumer product regulations with a strong focus on the FDA, Health Canada and Consumer Product Safety Commission Agency for new product development. Provide regulatory training and strategic...
Location:
Neenah, WI
Job Type:
Full-Time
Permanent
Occupation:
Regulatory Affairs Specialists
Salary:
Upper Middle Income Jobs ($50K-$79K)
Career Level/Education:
Bachelor's degree
Certifications/Licenses:
FDA Quality System
Preferred WorkKeys®
Applied Math
3
Graphic Literacy
4
Workplace Documents
4

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QA Compliance Specialist
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Job Description Responsibilities: Perform batch record review Perform log book review Provide on the floor support to the operations department Perform media and buffer review Support internal audit preparations and conduct walkthrough inspections...
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From Monster
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Date
2018-12-11
Company
Apex Life Sciences
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Location
Framingham, MA
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About the job:
Job Description Responsibilities: Perform batch record review Perform log book review Provide on the floor support to the operations department Perform media and buffer review Support internal audit preparations and conduct walkthrough inspections Revise procedures and SOPs Initiate deviations upon identification of non-conformance Review CV related documentation against specifications Assemble intermediate Bulk release summary Maintain control of key log Provide off-hour support for batch record and log book assistance as needed Qualifications: Bachelor's degree or higher in a Scientific...
Location:
Framingham, MA
Job Type:
Full-Time
Permanent
Occupation:
Regulatory Affairs Specialists
Salary:
High Income Jobs ($80K-$99K)
Career Level/Education:
Bachelor's degree
Certifications/Licenses:
N/A
Preferred WorkKeys®
Applied Math
4
Graphic Literacy
5
Workplace Documents
4

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Regulatory Affairs Specialist - CMC
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Job Description Job Regulatory Affairs Specialist – CMC Position Summary A Regulatory Affairs Specialist - CMC's primary role is to serve as a regulatory liaison and expert to clients and internal functional departments. The Regulatory Affairs...
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From FinancialJobBank.com
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Date
2018-12-11
Company
Catalent Pharma Solutions
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Location
Bloomington, IN
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About the job:
Job Description Job Regulatory Affairs Specialist – CMC Position Summary A Regulatory Affairs Specialist - CMC's primary role is to serve as a regulatory liaison and expert to clients and internal functional departments. The Regulatory Affairs Specialist plays an important role in Catalent's Patient First philosophy by ensuring submissions are authored clearly and concisely without delays. This helps to facilitate the approval of drugs faster and therefore providing timely delivery of drugs to patients. The Role - Authoring, reviewing, and updating facility drug master file(s), change...
Location:
Bloomington, IN
Job Type:
Full-Time
Permanent
Occupation:
Regulatory Affairs Specialists
Salary:
Upper Middle Income Jobs ($50K-$79K)
Career Level/Education:
Bachelor's degree
Certifications/Licenses:
Certified Management Consultant
Preferred WorkKeys®
Applied Math
3
Graphic Literacy
4
Workplace Documents
4

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Senior Biodefense Regulated Quality Review Specialist
Quick view
Senior Biodefense Regulated Quality Review Specialist Location MD - Ft. Detrick, USAMRIID Job Code 5084 # of openings 1 The Alaka`ina Foundation Family of Companies (FOCs) is comprised of industry-recognized government service firms designated as...
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From LocalJobNetwork
Report this job
Date
2018-12-11
Company
Alaka'ina Foundation Family of Companies
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Location
Maryland
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About the job:
Senior Biodefense Regulated Quality Review Specialist Location MD - Ft. Detrick, USAMRIID Job Code 5084 # of openings 1 The Alaka`ina Foundation Family of Companies (FOCs) is comprised of industry-recognized government service firms designated as Native Hawaiian Organization (NHO)-owned and 8(a) certified businesses. The Family of Companies (FOCs) includes Ke`aki Technologies, Laulima Government Solutions, Kupono Government Services, and Kapili Services. The Alaka`ina Foundation activities under the 501(c)3 principally benefit the youth of Hawaii through charitable efforts which includes...
Location:
Maryland
Job Type:
Full-Time
Permanent
Occupation:
Regulatory Affairs Specialists
Salary:
High Income Jobs ($80K-$99K)
Career Level/Education:
Associate's degree
Certifications/Licenses:
Continuing Education
Preferred WorkKeys®
Applied Math
4
Graphic Literacy
5
Workplace Documents
5

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Regulatory Affairs Specialist
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Regulatory Affairs Specialist needs Corporate or government regulatory experience in US FDA and USDA food labeling Regulatory Affairs Specialist requires: - 2 years food regulation or related industry experience such as compliance, Quality...
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From Job Vertise
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Date
2018-12-11
Company
Global Channel Management, Inc.
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Location
Plano, TX
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About the job:
Regulatory Affairs Specialist needs Corporate or government regulatory experience in US FDA and USDA food labeling Regulatory Affairs Specialist requires: - 2 years food regulation or related industry experience such as compliance, Quality Assurance or Quality Control role - knowledge of Product Vision System highly preferred (Schawk Blue, SAP, Microsoft Office - Project management, communication with on-sight project management team and direct communication with vendor regulatory teams Regulatory Affairs Specialist duties: - interact with various Regulatory Category Leads, product...
Location:
Plano, TX
Job Type:
Full-Time
Permanent
Occupation:
Regulatory Affairs Specialists
Salary:
Upper Middle Income Jobs ($50K-$79K)
Career Level/Education:
Bachelor's degree
Certifications/Licenses:
N/A
Preferred WorkKeys®
Applied Math
3
Graphic Literacy
4
Workplace Documents
4

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2019 GE Healthcare QA and Regulatory Affairs Leadership Program Intern
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2019 GE Healthcare QA and Regulatory Affairs Leadership Program Intern - GE Healthcare - Leadership Programs - Posted 8/10/2018 12:54:12 PM - 3157838 - Job Function: Quality - Business Segment: Healthcare Quality Location(s): United States;...
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From Society of Women Engineers
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Date
2018-12-11
Company
General Electric
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Location
Waukesha, WI
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About the job:
2019 GE Healthcare QA and Regulatory Affairs Leadership Program Intern - GE Healthcare - Leadership Programs - Posted 8/10/2018 12:54:12 PM - 3157838 - Job Function: Quality - Business Segment: Healthcare Quality Location(s): United States; Massachusetts, Wisconsin; Waukesha Role Summary: The Quality & Regulatory Leadership Development Program is for high potential individuals seeking a career in Quality Assurance and Regulatory Affairs. QRLP consists of 3 eight-month business critical assignments within the Quality organization. Rotations may include: Quality Assurance, Regulatory Affairs,...
Location:
Waukesha, WI
Job Type:
Part-Time
Full-Time
Internship
Occupation:
Regulatory Affairs Specialists
Salary:
Upper Middle Income Jobs ($50K-$79K)
Career Level/Education:
Bachelor's degree
Certifications/Licenses:
N/A
Preferred WorkKeys®
Applied Math
5
Graphic Literacy
6
Workplace Documents
6

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Promotional Review Coordinator
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The ideal candidate for this role is someone who has a background in marketing and materials promotions within the pharmaceutical industry. - Manage the Promotional Review Committee (PRC) process and act as a liaison between the PRC, Marketing,...
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From Job Vertise
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Date
2018-12-11
Company
MaxisIT
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Location
Duluth, GA
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About the job:
The ideal candidate for this role is someone who has a background in marketing and materials promotions within the pharmaceutical industry. - Manage the Promotional Review Committee (PRC) process and act as a liaison between the PRC, Marketing, Regulatory Affairs, Legal, and other involved parties in order to facilitate rapid and accurate review of all U.S. Boehringer Animal Health advertising and promotional materials. - Supervise all promotional material projects submitted for review using eRoom, Veeva, and other software programs/platforms. - Notify PRC reviewers of new submissions and...
Location:
Duluth, GA
Job Type:
Full-Time
Permanent
Occupation:
Regulatory Affairs Specialists
Salary:
High Income Jobs ($80K-$99K)
Career Level/Education:
High school diploma or equivalent
Certifications/Licenses:
N/A
Preferred WorkKeys®
Applied Math
4
Graphic Literacy
4
Workplace Documents
4

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Reg Affairs Specialist (605571)
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Job Summary Responsible for assisting the team with regulatory filings as necessary to market Zimmer Biomet products. This position requires an intermediate understanding of medical devices and their use as well as an understanding of the...
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From Zimmer Biomet
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Date
2018-12-11
Company
Zimmer Biomet
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Location
Dover, OH
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About the job:
Job Summary Responsible for assisting the team with regulatory filings as necessary to market Zimmer Biomet products. This position requires an intermediate understanding of medical devices and their use as well as an understanding of the regulatory submission process. Principal Duties and Responsibilities • Assist with assembly, distribution, storage and tracking and retrieval of information pertinent to the regulatory process, including the regulatory submissions process. May author and publish electronic submissions. • Respond to requests from foreign government and/or distributors as...
Location:
Dover, OH
Job Type:
Part-Time
Full-Time
Permanent
Occupation:
Regulatory Affairs Specialists
Salary:
Upper Middle Income Jobs ($50K-$79K)
Career Level/Education:
Bachelor's degree
Certifications/Licenses:
Regulatory Affairs Certification
Preferred WorkKeys®
Applied Math
3
Graphic Literacy
4
Workplace Documents
4

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Product Scientific Specialist - III
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Title : Product Scientific Specialist Title : Location : North Wales PA Location : Duration : 11 / 26 / 18 to 11 / 22 / 19 Duration : Requirements : Requirements : - PharmD or PhD degree with 3 years medical review experience - Masters degree with...
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From Monster
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Date
2018-12-11
Company
System One
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Location
West Point, PA
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About the job:
Title : Product Scientific Specialist Title : Location : North Wales PA Location : Duration : 11 / 26 / 18 to 11 / 22 / 19 Duration : Requirements : Requirements : - PharmD or PhD degree with 3 years medical review experience - Masters degree with 5 years medical review experience - Experience in Medical Review and Medical Information with broad Therapeutic Area experience. - Ability to work effectively in a team environment. Responsibilities : - Therapeutic areas which will be supported by this role include, but are not limited to, Infectious Disease and Vaccines - As a member of a...
Location:
West Point, PA
Job Type:
Full-Time
Contract
Occupation:
Regulatory Affairs Specialists
Salary:
High Income Jobs ($80K-$99K)
Career Level/Education:
Bachelor's degree
Certifications/Licenses:
Doctor of Pharmacy
Preferred WorkKeys®
Applied Math
5
Graphic Literacy
6
Workplace Documents
7

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Senior Regulatory Affairs Specialist
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- BA/BS Degree in life sciences or engineering or an equivalent - 5+ years regulatory affairs working experience required - Specific experience in the planning, preparation, and submission of 510(k)s , Technical Files, and Design Dossiers -...
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From Job Vertise
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Date
2018-12-11
Company
The Rych Recruiting Agency
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Location
Cambridge, MA
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About the job:
- BA/BS Degree in life sciences or engineering or an equivalent - 5+ years regulatory affairs working experience required - Specific experience in the planning, preparation, and submission of 510(k)s , Technical Files, and Design Dossiers - Demonstrated proficiency with relevant US/International regulatory requirements for medical devices including Quality Systems standards and clinical investigations - Experience working directly with FDA, notified bodies and/or international health authorities - Ability to communicate complex ideas clearly and simply both orally and in writing -...
Location:
Cambridge, MA
Job Type:
Full-Time
Permanent
Occupation:
Regulatory Affairs Specialists
Salary:
High Income Jobs ($80K-$99K)
Career Level/Education:
Bachelor's degree
Certifications/Licenses:
N/A
Preferred WorkKeys®
Applied Math
3
Graphic Literacy
4
Workplace Documents
4

Display

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WorkKeys®

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