Senior Regulatory Affairs Specialist Jobs in Audubon, PA

Shape the future of regulatory strategy by leading cross-functional teams, driving innovative development strategies, and providing regulatory thought leadership to ensure compliance and accelerate pr...

Engineer innovative solutions in medical device quality and compliance, tackling diverse challenges throughout the product lifecycle, from development to post-market surveillance, ensuring effective r...

Lead regulatory compliance programs ensuring inspection readiness and proactive risk management across cross-functional teams. Monitor compliance health, manage data quality, and drive improvements al...

Unlock the power of regulatory insights! Lead comprehensive monitoring and analysis of regulatory developments, providing actionable intelligence to guide business strategy and decision-making across...

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

Create impactful trade compliance strategies by classifying products accurately and collaborating across teams to ensure adherence to regulatory standards globally. Leverage your analytical skills and...

Elevate the regulatory landscape by guiding strategic promotional communications for Oncology products. Shape impactful messaging while ensuring compliance and aligning with evolving regulations and F...

Unlock potential by leading global regulatory strategies in cardiovascular and metabolic programs. Collaborate with cross-functional teams to ensure timely drug approvals while managing complex projec...

Unlock potential by shaping global regulatory strategies and driving advocacy initiatives. Collaborate across teams to manage regulatory risks, assess opportunities, and provide strategic insights tha...

Accelerate regulatory strategy development for oncology products, leading global initiatives to secure IND/CTA approvals and marketing applications. Collaborate with cross-functional teams to navigate...

Unlock potential by providing strategic CMC regulatory expertise to accelerate the development and lifecycle management of drug-device combination products, ensuring compliance with global regulations...

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...

Champion compliance excellence by providing enterprise-level oversight and strategic leadership within External Manufacturing. Drive risk visibility and governance while ensuring a proactive complianc...

Lead the advancement of regulatory compliance across the External Manufacturing network by enhancing risk visibility, promoting proactive oversight, and fostering cross-functional collaboration to ens...

Lead enterprise regulatory compliance for External Manufacturing by providing oversight, risk visibility, and governance support across a global network. Collaborate with cross-functional teams to pro...

Join a team that's at the forefront of enhancing compliance oversight across external manufacturing. Take ownership of enterprise-level compliance strategies, driving proactive risk management and fos...

Lead sustainability initiatives to optimize energy operations, reducing emissions and costs. Collaborate with maintenance and utility teams to implement energy conservation measures and ensure adheren...

Join a dynamic team to lead global regulatory strategy for cutting-edge ophthalmology programs, ensuring alignment with development and commercialization goals while mentoring a high-performing regula...

Champion global regulatory strategies for ophthalmology programs, leading a team to navigate complex challenges in drug development while ensuring compliance and alignment with commercial objectives...

Play a key role in enhancing quality management systems through auditing, compliance, and documentation control, ensuring adherence to AS9100 and ISO standards across an aerospace and defense environm...

Join a team that advances global CMC content management capabilities. Lead strategy, enhance processes, and collaborate on digital solutions to modernize regulatory content operations for efficient, c...

Lead end-to-end GCP audits globally, ensuring compliance and driving improvements in clinical studies. Collaborate with stakeholders to interpret regulations and support regulatory inspections in a dy...

Lead the charge in quality assurance projects, ensuring compliance and timely delivery. Collaborate with cross-functional teams to manage risks, track progress, and drive success through effective com...