Skip to main content
X

Get jobs by email for this search

By continuing you agree to Monster's Privacy policy, Terms of use and use of cookies.

Regulatory Affairs Specialist Jobs in Pennsylvania

15 jobs

DescriptionQfix is a dynamic privately held, rapidly growing innovator, manufacturer and marketer of advanced composite products for patient positioning in medical imaging headquartered in beautiful rolling hill country just west of Philadelphia, with sales in over 60 markets across the globe. The Regulatory Affairs Specialist provides global support for Class I and Class II medical devices; is r...
Lebanon Seaboard Corporation, a manufacturer of fertilizers, pesticides, soil amendments, bird food and grass seed is seeking to immediately fill a Regulatory AffairsSpecialist position. Job Summary: As a member of our Regulatory Affairs Department reporting to the Regulatory Affairs Manager you will be expected to : Provide subject matter expertise to assure regulatory compliance through disci...
Overview The Regulatory Affairs Specialist will support the implementation of Teva’s Submission Ready Standards (SRS) and Teva’s Authoring Core Templates (TACT) program. The incumbent is responsible for reviewing documents for compliance with established standards and documenting the results. Responsibilities 1. Review documents for compliance with established standards and record results 2. D...
Overview The Regulatory Affairs Specialist will support the implementation of Teva’s Submission Ready Standards (SRS) and Teva’s Authoring Core Templates (TACT) program. The incumbent is responsible for reviewing documents for compliance with established standards and documenting the results. Responsibilities 1. Review documents for compliance with established standards and record results 2. D...
Job Description This position will help coordinate, monitor and ensure compliance to all International, National, State and Local regulatory regulations and requirements for Surgical Specialty Solutions Precision Tools and Instruments. , • Assists and supports international registrations for distributor partners and regulatory authorities, as required regarding company’s licensing and registrat...
The Regulatory Affairs Specialist will support the implementation of Teva’s Submission Ready Standards (SRS) and Teva’s Authoring Core Templates (TACT) program. The incumbent is responsible for reviewing documents for compliance with established standards and documenting the results. 1. Review documents for compliance with established standards and record results 2. Data entry 3. Maintain worki...
Integra LifeSciences, a world leader in medical technology, is dedicated to limiting uncertainty for surgeons, so they can concentrate on providing the best patient care. Integra offers innovative solutions in orthopedic extremity surgery, neurosurgery, spine surgery, and reconstructive and general surgery. Integra's orthopedic products include devices and implants for spine, foot and ankle, hand...
This role advises the creative, application and commercial departments on the safe use and Regulatory Compliance of formulas. This includes the execution of regulatory compliance reviews, preparation of various documents supporting the regulatory compliance of these formulas, frequent direct interaction with major customers (both internal and external) and direct interaction with regulatory author...
Why join Boston Scientific Neuromodulation in California? We integrate all global operations at our worldwide headquarters in Valencia, California, close to Los Angeles, close to the beach, close to the mountains, close to the desert. All the advantages of Southern California but more affordable than many other areas nearby. Looking for onsite amenities? We have an on-campus bistro, credit union,...
Division Description Siemens is a global technology powerhouse that has stood for engineering excellence, innovation, quality, reliability and internationality for more than 165 years. As a global technology company, Siemens is rigorously leveraging the advantages that this setup provides. To tap business opportunities in both new and established markets, the Company is organized in nine Division...
Auto req ID 25801BR Position Title Regulatory Affairs Specialist I Job Description Position Summary: The position is responsible for compliance report generation and data analysis for Regulatory Affairs, Legal, EHS, and QA. This position will alternate between the 600 Campbell’s Run Business Center and 300 Industry Drive locations. Job duties: Support the management and renewal of Licenses Pe...
Position Summary: The position is responsible for compliance report generation and data analysis for Regulatory Affairs, Legal, EHS, and QA. This position will alternate between the 600 Campbell’s Run Business Center and 300 Industry Drive locations. Job duties: Support the management and renewal of Licenses & Permits (e.g. wholesale pharmaceutical, FDA medical device and TTB alcohol). Support p...
This role advises the creative, application and commercial departments on the safe use and Regulatory Compliance of formulas. This includes the execution of regulatory compliance reviews, preparation of various documents supporting the regulatory compliance of these formulas, frequent direct interaction with major customers (both internal and external) and direct interaction with regulatory author...
The Regulatory Affairs Coordinator is responsible for the management of current drug product licenses and obtaining product licenses for drugs in development for Kadmon Pharmaceuticals, LLC both domestic and international. The regulatory function of the unit is an integral part in the process of developing and introducing safe and effective health products. The regulatory unit focuses on the study...