Regulatory Affairs Specialist Jobs in New Jersey

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88 New Jersey Regulatory Affairs Specialist jobs found on Monster.

Jobs 1 to 20 of 88
We are the maker, marketer and distributor of branded food products that have been American favorites for decades. Our employees located in more than 20 offices and plants across North America rally around our mission, Reinvigorating Iconic Brands. We work to transform our brands to be more profitable for our customers and more enjoyable for our consumers. At Pinnacle Foods, every employee has th...
Position Summary With modest supervision, support product registration internationally. Accountabilities * Prepare regulatory submissions to health authorities, assuring submissions meet relevant regulatory requirements. * Approve Artwork across all Value Streams for all regions, focusing initially on Europe and Middle East. * Confirm product or formula acceptability in local markets. * Represe...
JOB SUMMARY This will person will be a Regulatory liaison between product development and the regulatory agencies. This position will be responsible for regulatory submissions for new ANDAs and any changes being made to existing products. The position will also assist in labeling for new products, changes to labeling for existing prescription and OTC products. This position will also interact wit...
CyberCoders Matching Great People with Great Companies Learn more about CyberCoders Apply Regulatory Affairs Subject Matter Expert Princeton, NJ Full-Time $120,000 - $130,000 Apply Apply Regulatory Affairs Subject Matter Expert Princeton, NJ Full-Time $120,000 - $130,000 Apply Job Details We have an outstanding career opportunity for a Regulatory Affairs Subject Matter Expert (SME) t...
REGULATORY AFFAIRS SPECIALIST BA/BS in Scientific discipline required. Engineering strongly preferred RAC certification desired Ensure compliance to all internal, US, EU and other international requirements and corporate policies and procedures for market approval of medical devices/combination products. Apply scientific principles to understanding safety and efficacy on a wide range of produc...
Our client is currently seeking a Regulatory Affairs Specialist This job will have the following responsibilities: Ensure compliance to all internal, US, EU and other international requirements and corporate policies and procedures for market approval of medical devices/combination products. Apply scientific principles to understanding safety and efficacy on a wide range of products. Prepare d...
Pinnacle Foods Group, LLC Parsippany, NJ
Req ID: 17281 Location: Cherry Hill, NJ 08002 We are the maker, marketer and distributor of branded food products that have been American favorites for decades. Our employees located in more than 20 offices and plants across North America rally around our mission, Reinvigorating Iconic Brands. We work to transform our brands to be more profitable for our customers and more enjoyable for our cons...
Clinical Solutions Group, Inc. Princeton, NJ
Description: International pharmaceutical company with a notable stateside site in the greater Princeton area has an immediate need for a Regulatory Affairs CMC Specialist. Role is onsite with the potential to work from home 1 day per week after becoming established with the team. Top pay and benefits available. Positions Summary: The incumbent is responsible for assisting with CMC document pre...
POSITION SUMMARY: Under the direction of Director, Regulatory Affairs, the International Regulatory Affairs Specialist supports worldwide product registrations and regulatory activities including the following duties: Provide a wide variety of documentation related to a broad product line for submission to various worldwide health agencies; Prepare, submit and maintain specific dossiers per loca...
About the role This position provides regulatory support in regards to customs activities and the domestic and international transportation of hazardous materials . This position reports to the Director, Regulatory & Government Affairs and will interface on a regular basis with the Regulatory and Transportation staff. There will also be regular communications with Legal, Research & Development, ...
Abbott is a global healthcare company devoted to improving life through the development of products and technologies that span the breadth of healthcare. With a portfolio of leading, science-based offerings in diagnostics, medical devices, nutritionals and branded generic pharmaceuticals, Abbott serves people in more than 150 countries and employs approximately 69,000 people. Abbott is an Equal O...
Marten Transport Princeton, NJ
Description: International pharmaceutical company with a notable stateside site in the greater Princeton area has an immediate need for a Regulatory Affairs CMC Specialist. Role is onsite with the potential to work from home 1 day per week after becoming established with the team. Top pay and benefits available. Positions Summary: The incumbent is responsible for assisting with CMC document pre...
Stryker Communictions Mahwah, NJ
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 team activities from initia...
Position Summary With modest supervision, support product registration internationally. Accountabilities •Prepare regulatory submissions to health authorities, assuring submissions meet relevant regulatory requirements. •Approve Artwork across all Value Streams for all regions, focusing initially on Europe and Middle East. •Confirm product or formula acceptability in local markets. •Represen...
The Hartz Mountain Corporation Secaucus, NJ
The Hartz Mountain Corporation is the leading consumer packaged goods company in pet products. We are currently seeking a dynamic and results oriented leader to fill our Regulatory Affairs Specialist. Position Profile: The Regulatory Affairs Specialist is responsible for Pesticide and Pet food labels and registrations in the United States and Canada. This individual will work with R&D to ensure ...
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 team activities from initia...
Job Number: 14007746 Nestle Health Science Florham Park, NJ Nestlé Health Science is seeking a Regulatory Affairs Specialist in its Florham Park Headquarters. This individual will be responsible for ensuring ability to market our products; ensuring compliance and helping manage regulatory risks. Will also help develop and maintain regulatory records and documents in support of Nestlé Healthcare...
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...
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 ...
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...

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