Regulatory Affairs Specialist Jobs in Philadelphia, PA

Manage regulatory submissions and compliance for medical devices. Collaborate across departments to ensure adherence to standards, support audits, and maintain quality throughout clinical processes an...

Lead the charge in compliance strategy for U.S. Commercial and Market Access. Collaborate with senior leaders to guide complex compliance issues, manage risks, and support innovative business objectiv...

Shape the future of regulatory submissions by ensuring high-quality QC reviews of clinical documents. Collaborate with global teams to meet project timelines while maintaining compliance with industry...

Accelerate progress at drug development by leading bioanalytical studies, optimizing methods, interpreting data, and collaborating with teams to enhance innovative therapies for patients...

Champion quality and compliance initiatives to enhance orthopedic operations. Collaborate with cross-functional teams to deliver exceptional quality standards, ensuring regulatory adherence and contin...

Join a team that's committed to quality excellence by leading Compliance initiatives. Drive improvements and ensure regulatory standards are met in orthopedic distribution operations, collaborating wi...

Join a team that's shaping healthcare through innovative legal counsel. You'll oversee commercial contracting, guide compliance, and streamline legal operations for critical partnerships in health sys...

Lead global strategy for Notified Body engagement, ensuring compliance, managing audits, and driving certification readiness across various jurisdictions. Guide integration assessments, enhance proces...

Unlock your potential by leading compliance initiatives in electric reliability standards. Collaborate with teams to ensure adherence to NERC standards, enhancing PJM's compliance and operational exce...

Partner with us to lead North America regulatory strategies for Immunology projects. Drive submission planning, manage Health Authority interactions, and collaborate across teams to ensure compliance...

Elevate your career as a strategic regulatory leader, driving North America regulatory strategy and execution for Immunology projects while collaborating with cross-functional teams and navigating Hea...

Manage clinical studies to ensure compliance with regulations and human subject protection. Coordinate site monitoring and maintain quality standards while communicating effectively with site teams to...

Elevate your career as a Principal Scientist in CMC Regulatory Affairs, leading strategies for drug-device combination products, guiding cross-functional teams, and ensuring compliance with global reg...

Shape regulatory strategies for drug-device combination products, ensuring compliance with global standards while collaborating across teams to support development and lifecycle management in a hybrid...

Join a team that's committed to driving innovation in regulatory science for drug-device combination products, collaborating cross-functionally to develop and execute strategies for successful global...

Join a team that's committed to ensuring compliance and accountability in construction by performing detailed audits of payment applications, guiding project owners, and fostering best practices acros...

Engage in leadership within QC compliance, driving adherence to GMP guidelines and promoting a culture of quality. Oversee investigations, compliance documentation, and collaboration with cross-functi...

Help us drive product success in biopharma by managing lifecycle initiatives, collaborating cross-functionally, and supporting growth strategies to enhance profitability and customer satisfaction acro...

Drive commercial contract negotiations with a focus on growth, alignment, and risk management across global teams, enhancing client satisfaction and organizational objectives in a fast-paced, collabor...

Explore opportunities as a Clinical & Regulatory Information Management SME, supporting client delivery across VeevaRIM and Clinical initiatives. Engage with stakeholders, optimize processes, and enha...

Join a team that's dedicated to enhancing clinical trial quality through leadership, mentorship, and oversight. Engage remotely with cross-functional teams, driving high standards for patient safety a...

Shape the future of oncology therapeutics by driving global regulatory strategy and enabling fast track approvals for novel drug candidates. Collaborate cross-functionally to ensure compliance with FD...

Manage global regulatory strategies for clinical and commercial product registrations. Ensure compliance and successful market access for the PSMA franchise. Lead cross-functional collaborations and d...

Lead the charge in managing Quality Systems, ensuring compliance with cGMP and regulatory standards while overseeing QA activities, audits, and training within a pharmaceutical environment to uphold p...

Contribute to lead risk-based quality management for oncology trials across phases. Collaborate with cross-functional teams to assess risk, ensure data quality, and drive mitigation. Provide expert gu...