Regulatory Affairs Specialist Jobs in New Jersey

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60 New Jersey Regulatory Affairs Specialist jobs found on Monster.

Jobs 1 to 20 of 60
Henkel Adhesive Technologies is a worldwide leader in bonding, sealing and surface treatments - thanks to our ambitious people. We create unique value for our clients and our technologies can be found in many objects touching our lives every day. Our success is built on constant innovation and people who strive for excellence. Working at Henkel is much more than just a job. It’s a passion. Have yo...
GENEWIZ, Inc. is a leading global genomics service company. Excelling in both science and customer support, GENEWIZ is a trusted provider for DNA sequencing, gene synthesis, molecular biology, next generation sequencing, bioinformatics, and GLP regulatory services. Customers depend on GENEWIZ to achieve results in a rapid, cost-effective manner through specialized expertise and customizable, scala...
. A Contract Regulatory Affairs Specialist job opportunity located in central NJ is currently available via Adecco Engineering and Technology. You will be responsible for the submission and tracking of all regulatory documentation. The Regulatory Affairs Specialist job responsibilities include: Ensure readiness of submission documents in accordance with agency guidance Perform QA/QC for submis...
Description: We're changing the way health care works for the better. That means consulting with our members, partnering with our physicians, and delivering drugs in the most efficient and effective way. Join us and start doing your life's best work.(sm) The Manager, Regulatory Affairs has responsibility for managing strategic regulatory operations and providing expert advice on the guidelines a...
Sonar products, a division of stratus group USA. is actively searching for a regulatory pharmaceutical specialist to become part of our corporate team at our manufacturing facility in carlstadt NJ. The qualified professional will help to ensure the company's compliance with FDA/GMP regulatory requirements. Evaluate new pharmaceutical and OTC products and recommend changes to existing ones to ass...
Stryker Communictions Mahwah, NJ
Job Description/Information: Plan, organize and implement strategies and activities required to procure regulatory approval for new and revised product lines. Ensure compliance to all US, EU and SO international requirements and corporate policies and procedures regarding submissions and other requirements for market approval of medical devices/combination products. Participate in cross functional...
BASF - The Chemical Company Iselin, NJ
Regulatory Affairs Specialist Biotech Center of Expertise-San Diego, CA-1401217 We are an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability status, protected veteran status, or any other characteristic protected by law. Description · Are you a highly motivated self-starter l...
Overview: Valeant Pharmaceuticals International, Inc. is a diverse and decentralized pharmaceutical company that is committed to focusing on our key stakeholders while delivering consistently high performance. Our values provide the overall direction for our company, and provide us with the tools necessary to rise to any challenge by leveraging our collective hard work and effort along with our u...
Valeant Pharmaceuticals Bridgewater, NJ, 08807
Overview: Valeant Pharmaceuticals International, Inc. is a diverse and decentralized pharmaceutical company that is committed to focusing on our key stakeholders while delivering consistently high performance. Our values provide the overall direction for our company, and provide us with the tools necessary to rise to any challenge by leveraging our collective hard work and effort along with our u...
Position Summary: Provide immediate response to Flavor Regulatory requests for documentation and inquiries from external and internal customers. This is in accordance with US FDA/FEMA guidelines, customer specific guidelines and various international regulations. Provide guidance and interpretation of regulations as a resource to customer, staff members and other Symrise employees. This is to be ...
Becton Dickinson and Company Franklin Lakes, NJ
Description Responsibilities: Platform Representation: Representing the Regulatory Affairs function on the (specimen) Cell and Biomarker Preservation and (specimen) Acquisition Platform Teams and associated sub-teams as the Regulatory Affairs subject matter expert (SME) for FDA and CE requirements. This will include acting as a liaison between the Platform team and BD PAS Regulatory Affairs, Int...
UnitedHealth Group Inc. Basking Ridge, NJ, 07920
We're changing the way health care works for the better. That means consulting with our members, partnering with our physicians, and delivering drugs in the most efficient and effective way. Join us and start doing your life's best work.(sm) The Manager, Regulatory Affairs has responsibility for managing strategic regulatory operations and providing expert advice on the guidelines and regulations...
The Regulatory Affairs Head for Americas, covering USA, Canada and Latin America (consisting of Brazil and Hispanic zone) has full functional responsibilities, including managing and leading network of Scientific & Regulatory Affairs departments within the region, in line with the Corporate regulatory strategy and the requirements of each country and zone part of the Americas. II. Principal Accou...
A Regulatory Affairs Specialist III (known hereafter as RA professional) provides regulatory expertise specifically in biologic and sterile product requirements and is able to expertly advise client or Catalent in identifying and executing the required development and regulatory activities needed to support the biological product development. This position executes projects independently under th...
POSITION OVERVIEW: Lead and perform regulatory and compliance activities for the company’s regulated products (Multi compendia Production chemicals, cGMP products and medical device products) as directed with primary responsibility for USFDA and Secondary responsibilities for MHRA, TGA, SFDA. Provide International (outside North America) regulatory submission support. Coordinate with Internationa...
Catalent Somerset, NJ
A Regulatory Affairs Specialist III (known hereafter as RA professional) provides regulatory expertise specifically in biologic and sterile product requirements and is able to expertly advise client or Catalent in identifying and executing the required development and regulatory activities needed to support the biological product development. This position executes projects independently under th...
Sanofi-Aventis Ridgefield, NJ
Description Genzyme has pioneered the development and delivery of transformative therapies for patients affected by rare and debilitating diseases for over 30 years. We accomplish our goals through world-class research, collaboration with the global patient community, and with the compassion and commitment of our employees. With a focus on rare diseases and multiple sclerosis, we are dedicated to...
Celgene is a global biopharmaceutical company leading the way in medical innovation to help patients live longer, better lives. Our purpose as a company is to discover and develop therapies that will change the course of human health. We value our passion for patients, quest for innovation, spirit of independence and love of challenge. With a presence in more than 70 countries - and growing - we l...
Public Service Enterprise Group Hancocks Bridge, NJ
ES Compliance Specialist is responsible for providing oversight, support, and ability to perform activities of Emergency Services programs (Security and Emergency Preparedness) to ensure regulatory compliance, specifically: • Maintain oversight of regulatory issues in Emergency Services • Be familiar with existing, new and proposed regulatory requirements and understand how the Emergency Servic...
ES Compliance Specialist is responsible for providing oversight, support, and ability to perform activities of Emergency Services programs (Security and Emergency Preparedness) to ensure regulatory compliance, specifically: • Maintain oversight of regulatory issues in Emergency Services • Be familiar with existing, new and proposed regulatory requirements and understand how the Emergency Servic...

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Legal Career Tools

Regulatory Affairs Associate

Salaries

$38,760.00 - $94,500.00
Typical Salary for Regulatory Affairs Associate in New Jersey
(111 Respondents)
Source: Monster.com Careerbenchmarking Tool

Education / Training

Bachelor's
38.8%
Master's
38.8%
Associates
9%
Some College Coursework Completed
4.5%
High School
3%
Doctorate
3%
(67 Respondents)
Source: Monster.com Careerbenchmarking Tool

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