Senior Regulatory Affairs Specialist Jobs in Mahwah, NJ

Unlock potential by driving strategic revenue growth in RTSM within global CRO partnerships. As an expert, you'll support sales strategies, potential deals, and amplify Medidata's market presence thro...

Optimize safety and compliance by championing industrial hygiene and biosafety initiatives. Lead technical projects while partnering across various teams to assess risks and implement compliant soluti...

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...

Optimize regulatory CMC strategies for antibody-drug conjugates and biologics, leading cross-functional teams to meet milestones in both development and post-approval phases while ensuring compliance...

Shape compliance strategies and lead regulatory efforts in cosmetics, ensuring adherence to global standards while managing a dedicated team in a dynamic environment. Drive innovation through collabor...

Join a dynamic team to lead global CMC regulatory strategies for biologics and ADCs. Drive regulatory milestones through product development and ensure compliance with international guidelines while c...

Join a dynamic team that drives innovative device characterization and design. Leverage advanced analytical tools to improve drug delivery technologies while showcasing your expertise in cross-functio...

Champion regulatory compliance by overseeing GXP applications and ensuring effective validation processes within high-stakes global pharmaceutical environments while leading diverse teams with minimal...

Tackle operational readiness within the expansion of a sterile drug manufacturing facility, ensuring compliance, collaboration, and efficiency. Lead equipment design, system qualification, and support...

Drive GMP training compliance and qualification programs within a cutting-edge biologics facility. Collaborate with cross-functional teams to develop curricula and manage training records, ensuring pe...

Join a team that's driving compliance excellence in supply chain operations. This role blends collaboration across Contracts, Legal, and Supply Chain, focusing on government contracting and ensuring r...

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 quality assurance by leading a global team to ensure compliance and excellence in safety, regulatory, and medical affairs processes, fostering collaboration and innovative solution...

Manage reimbursement strategies supporting business goals across product areas. Collaborate with teams to guide product development, analyze landscapes, and educate stakeholders on reimbursement impac...

Manage site operations ensuring efficient flow of information, training, and documentation within clinical research trials while collaborating with multiple departments to enhance trial execution and...

Join a dynamic lab team to support the development of life-saving therapeutics. Contribute to solution preparation and collaborate with various teams in a fast-paced environment, while honing your ski...

Shape strategic initiatives as you oversee planning and operations, ensuring seamless collaboration across teams to elevate organizational performance while impacting patient outcomes globally...

Elevate your career as a strategic leader in global regulatory affairs, managing clinical and commercial drug product compliance. Collaborate cross-functionally to ensure adherence to regulations and...

Make your mark at the forefront of regulatory strategy! Lead clinical and commercial regulatory initiatives, ensuring compliance while driving successful drug product registrations and global submissi...

Partner with us to manage critical project agreements, ensuring compliance and facilitating collaboration across teams for effective contract execution and risk assessment in a dynamic biopharma envir...

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

Take ownership of regulatory compliance by analyzing and implementing aseptic processing standards across the enterprise, driving strategic engagement with Health Authorities, and ensuring operational...

Join a dynamic team to ensure compliance in aseptic processing and sterility assurance. Drive regulatory intelligence initiatives and enhance quality standards across commercial manufacturing operatio...

Oversee testing and analysis of pharmaceutical products and raw materials, ensuring compliance with regulations and standards. Collaborate on process validation and improvement while mentoring junior...

Elevate your career by leading strategic pharma partnerships, driving program delivery for innovative digital health solutions. Manage diverse workstreams and foster executive relationships to ensure...