Regulatory Affairs Specialist Jobs in Florham Park, NJ

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

Build your expertise in our intensive 2-year rotational PharmD/PhD program, gaining critical skills through hands-on projects in Global Development while collaborating across diverse functional areas...

Execute the end-to-end delivery of clearinghouse product features, collaborating with cross-functional teams to enhance client experiences and ensure regulatory compliance while maintaining a focus on...

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

Unlock your potential by overseeing site management and monitoring for clinical trials, ensuring compliance with regulations and enhancing site relationships to drive quality and timely delivery of cl...

Collaborate with clients and teams to manage projects, expectations, and delivery, ensuring high standards and strategic growth in a fast-paced medical affairs environment. Leverage experience to iden...

Discover a pivotal role in establishing enterprise data stewardship standards, leading cross-domain collaboration, and ensuring consistency in planning data definitions and accountability across funct...

Grow your career with a proactive role ensuring quality standards, leading CAPA initiatives, and driving continuous improvement in a dynamic environment. Leverage your experience to impact product qua...

Shape regulatory strategies that drive product innovation and compliance, ensuring alignment with FDA and global standards. Collaborate across teams to enhance product development and market entry in...

Join a team that's dedicated to maintaining Good Clinical Practice and human subject protection. Oversee site monitoring, ensure compliance, and support clinical studies through effective communicatio...

Lead the charge in ensuring compliance for sterile and OSD manufacturing processes by managing batch reviews, documentation, and investigations, while training staff and participating in regulatory in...

Elevate quality assurance and regulatory systems by managing daily operations, ensuring compliance, and supporting audits while collaborating on projects to enhance product quality and patient safety...

Lead the charge in regulatory advertising strategies while overseeing day-to-day activities and development for assigned products. Collaborate with cross-functional teams and ensure compliance with ev...

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...

Accelerate your career by leading negotiations for strategic contracts, aligning commercial goals with legal standards. Partner across teams to support growth, mitigate risks, and enhance customer sat...

Unlock potential by executing financial and operational audits, identifying control deficiencies, and collaborating with stakeholders to enhance internal control environments through effective audit s...

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...

Drive quality assurance in GMP operations, ensuring compliance and product integrity while collaborating with internal and external stakeholders. Contribute to clinical manufacturing excellence throug...

Help us shape the future of clinical trials by providing regulatory guidance and maintaining compliance. Collaborate within cross-functional teams to ensure successful submissions and uphold industry...

Unlock potential in regulatory affairs by steering clinical trial submissions, ensuring compliance and strategic oversight. Collaborate with project teams, advising on regulatory pathways for successf...

Champion the development of regulatory strategies for CMC in gene therapy, facilitating cross-functional collaboration and ensuring compliance while guiding innovative products through clinical to com...

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...

Unlock potential by driving insights for revenue management, guiding promotional strategies, and enhancing trade investments to elevate net sales growth. Collaborate across teams to deliver actionable...

Join a team that's driving quality compliance in clinical development. As a strategic leader, you'll oversee QMS effectiveness, risk management, and compliance initiatives, while partnering with stake...