regulatory affairs specialist Jobs in Philadelphia, Pennsylvania

Regulatory Affairs Specialist
Philadelphia, PennsylvaniaEPM Scientific Title: Regulatory Affairs Specialist Summary: A global leader in the ophthalmic medical device industry, is seeking an experienced and driven Regulatory Affairs Specialist to join their team in Pennsylvania. This position is perfect for a candidate with strong communication...Full Job Details
Product Stewardship and Regulatory Affairs Specialist
Philadelphia, PennsylvaniaKane Partners LLCExciting Opportunity: Product Stewardship & Regulatory Affairs Specialist Are you ready to take your career to the next level with a global chemical leader? Join a dynamic, diverse team where your expertise will make a real impact. As a Product Stewardship & Regulatory...Full Job Details
Senior Regulatory Affairs Specialist
Trenton, New JerseyEPM Scientific Summary: The Senior Regulatory Affairs Specialist is responsible for managing appropriate regulatory and technical information to ensure regulatory compliance and support product registrations globally. This individual must possess general knowledge of global regulatory...Full Job Details
Sr Specialist
Rahway, New JerseySoftworld Inc Job Title: Sr Specialist, Regulatory Affairs CMC Job Location: Rahway NJ 07065 Onsite Requirements: CMC experience or R & D experience preparing the reports that feed into the CMC section (a quality back ...Full Job Details
Sr Specialist
Rahway, New JerseyesrhealthcareJob Location: Rahway NJ 07065 Onsite Requirements: CMC experience or R & D experience preparing the reports that feed into the CMC section (a quality background could be transferrable) Experience authoring technical reports and regulatory submissions, experience reviewing...Full Job Details
Sr Specialist
Rahway, New JerseySoftworld, a Kelly Company Job Title: Sr Specialist, Regulatory Affairs CMC Job Location: Rahway NJ 07065 Onsite Requirements: CMC experience or R & D experience preparing the reports that feed into the CMC section (a quality background could be transferrable) Experience authoring technical reports...Full Job Details
Regulatory Affairs Manager
Somerset, New JerseyInternational Search Consultants Regulatory Affairs Manager Somerset, NJ ISC's team of Manufacturing Recruiters is partnering with a leading manufacturer to identify an experienced Regulatory Affairs Manager for their Somerset, NJ location. The Regulatory Affairs Manager will develop and monitor the...Full Job Details
Director Global Regulatory Affairs
Blue Bell, PennsylvaniaiECURE, inc. Reporting directly to the VP of Regulatory Affairs (RA), the Director of Global RA will be responsible for providing US and global regulatory leadership in support of the development, registration, and life-cycle management of our innovative gene therapy programs. The...Full Job Details
Regulatory Affairs AD
Princeton, New JerseyInnoCare Pharma Responsibilities: Formulate, lead and drive regulatory strategy for chemical and biological modalities to support clinical development in oncology and autoimmune disease areas from early development throughout product registration in the US and other countries. Lead and...Full Job Details
Director Of Regulatory Affairs
Malvern, PennsylvaniaOcugen, Inc. Job Purpose The Director of Regulatory Affairs will lead regulatory strategy, submission planning, and execution for Ocugen's biologics, cell, and gene therapy programs. This role is responsible for overseeing clinical and CMC regulatory activities, ensuring compliance with...Full Job Details
IT Solution Architect
Malvern, PennsylvaniaAccuro Business Title: IT Solution Architect - Regulatory Affairs domain Location: Malvern, PA (100% Remote Job: Need to be available EST) Job Type: 6+ months long term contract Clients Update: Resources have to be able to work with Regulatory IT and business partners on...Full Job Details
Regulatory Affairs Manager
New JerseyMAC Incorporated WE ARE LOOKING FOR A REGULATORY AFFAIRS MANAGER FOR A HIGH-SPEED MANUFACTURING COMPANY IN SOMERSET NJ starting pay $130-$135k. MUST BE LOCAL TO THE FACILITY NO RELOCATION FOR THIS ROLE. MUST HAVE: In-depth knowledge of ISO 15378:2017 standard or equivalent This is a This is...Full Job Details
Regulatory Affairs Manager
Trenton, New JerseyEPM Scientific Essential Functions: Product Registrations Interacts with internal and external customers, regulatory authorities, both domestic and international, regarding product submissions, change notifications, and where applicable inspections. Coordinates and manages the preparation...Full Job Details
Director Medical Staff Affairs
Elizabeth, New JerseyTrinitas Regional Medical CenterJob Overview: This in-person position oversees the entire process of verifying and maintaining healthcare provider credentials, ensuring compliance with state, federal, and institutional regulations by managing a team of credentialing specialists, developing policies,...Full Job Details
Senior Regulatory Clinical Science Specialist
Summit, New JerseyKelly Science, Engineering, Technology & Telecom PLEASE NOTE: Must be legally authorized to work in the United States for any employer without sponsorship. For immediate consideration, please (1) apply and (2) email your resume directly to: . Kelly Science & Clinical is seeking a Senior Regulatory Clinical Science...Full Job Details
Senior Manager
Princeton, New JerseyBarrington James We are seeking an experienced and highly motivated Senior Manager, Regulatory Affairs to support our expanding portfolio in the oncology area. This is an exciting opportunity to play a critical role in regulatory strategy and compliance for a fast-growing organization. Key...Full Job Details
Director Regulatory Affairs Strategy
Basking Ridge, New JerseyRegeneron Pharmaceuticals, Inc. The Director Regulatory Affairs will provide leadership on global regulatory activities for the assigned products. Responsibility will mainly focus on Clinical Regulatory filings and provide regulatory leadership on the project teams in this area. We are a hands-on culture...Full Job Details
Quality Assurance Compliance Specialist
Princeton, New JerseyAequor Title: Quality Operations Specialist Location: Princeton NJ Duration: 09 months with possibility of extension Shift: Mon -Fri 40 hours/week Position Summary: Responsible for assigned operational Quality Risk and Compliance (QRC) activities supporting Research and...Full Job Details
Senior Director
Basking Ridge, New JerseyDaiichi Sankyo Join a Legacy of Innovation 125 Years and Counting. Daiichi Sankyo Group is dedicated to the creation and supply of innovative pharmaceutical therapies to improve standards of care and address diversified, unmet medical needs of people globally by leveraging our world-class...Full Job Details
Director of Regulatory Affairs
Philadelphia, PennsylvaniaUniversity of Pennsylvania Director of Regulatory Affairs, Academic Affairs Office, Penn Law University Overview The University of Pennsylvania, the largest private employer in Philadelphia, is a world-renowned leader in education, research, and innovation. This historic, Ivy League school...Full Job Details
Associate Director Regulatory Affairs
Somerville, New JerseyAbbVie$137500.00 - 261000.00 a yearCompany Description AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic...Full Job Details
Quality Specialist
Princeton, New JerseyIntegrated Resources, Inc ( IRI ) Title: Quality Specialist- Clinical Operations Location: Princeton, NJ Duration:10+ months REMARK: Manager is seeing someone with STRONG soft skills in good and proactive communication, who can communicate with multiple sectors of the business to politely push them forward...Full Job Details
Associate Director
Basking Ridge, New JerseyDaiichi Sankyo Join a Legacy of Innovation 110 Years and Counting. Daiichi Sankyo Group is dedicated to the creation and supply of innovative pharmaceutical therapies to improve standards of care and address diversified, unmet medical needs of people globally by leveraging our world-class...Full Job Details
Summer Intern
Malvern, PennsylvaniaOcugen, Inc. Job Purpose Ocugen is seeking a Quality Assurance - Document Control Intern for a 12-week full-time internship for Summer 2025 within the Quality Assurance - Document Control Department located in Malvern, PA. This opportunity will provide hands-on experience in document...Full Job Details
Training Specialist
Philadelphia, PennsylvaniaPlanet Pharma Training Specialist needed. Overview: Seeking a Training Specialist I to join the Operations team manufacturing site. The lead candidate is an autologous, ready-to-infuse cell therapy, that has demonstrated distinctive efficacy in the treatment of metastatic melanoma. The...Full Job Details