Regulatory Affairs Specialist Jobs in Westborough, MA

Grow your career with a leadership role defining nonclinical drug safety strategies. Collaborate across functions to assess risks, promote innovative thinking, and drive decisions that impact therapeu...

Deliver innovative drug safety strategies across multiple therapeutic areas, driving cross-functional collaboration from discovery through to regulatory submissions. Lead risk assessments and shape pr...

Explore innovative solutions in formal methods and systems software. Collaborate on research projects, prototype features, and contribute to relevant tools while advancing the security landscape of so...

Transform discovery neuroscience by designing, executing, and interpreting cellular experiments to advance therapeutic approaches for neurodegenerative diseases in a collaborative lab setting...

Champion global CAPA processes by providing expertise, conducting reviews, and enhancing quality standards across diverse teams, enabling continuous improvement and compliance in a remote environment...

Elevate drug development by providing expert reproductive toxicology guidance across multidisciplinary teams, shaping safety strategies, and supporting regulatory interactions to ensure product safety...

Manage technology transfer and technical support in biopharma manufacturing. Collaborate with cross-functional teams to enhance processes and ensure compliance with cGMP standards. Drive continuous im...

Drive the operational strategy for a global clinical trial organization, leading a diverse team to enhance site management capabilities across multiple regions while ensuring alignment with broader co...

Join a team that drives compliance excellence in government accounting audits. Leverage your skills in DCAA, DCMA audit support, and financial submissions to ensure regulatory adherence and deliver in...

Take ownership of clinical trial management, ensuring quality outcomes through strategic planning, stakeholder collaboration, and adherence to regulations while navigating challenges and driving deliv...

Manage clinical trial operations efficiently. Collaborate with teams, ensure compliance, and drive quality outcomes while developing strong relationships with stakeholders to enhance trial success...

Lead the charge in developing compelling proposals for U.S. Government solicitations, ensuring compliance and quality across all phases. Collaborate with cross-functional teams to strategize and execu...

Drive the activation of global investigative sites ensuring timely, budget-friendly, and quality outcomes in clinical studies. Manage project coordination and exceed sponsor expectations while collabo...

Shape the future of clinical research by overseeing feasibility and site activation activities, ensuring timely and quality deliverables, while collaborating across teams to drive project success in a...

Drive compliance strategy by managing IL4/IL5 offerings, ensuring regulatory adherence across AWS-hosted environments. Collaborate with security teams, federal regulators, and technical stakeholders t...

Advance your career by supporting environmental permitting for energy and infrastructure projects. Collaborate with a dynamic team, utilizing your expertise in Massachusetts regulations and ecology in...

Shape impactful environmental projects by leveraging your expertise in permitting and ecology. Collaborate with teams on energy and infrastructure initiatives, navigating complex regulatory frameworks...

Drive effective contract management in a dynamic environment, overseeing all phases from negotiation to compliance. Collaborate with teams and stakeholders to ensure alignment with government standard...

Drive contract management excellence by collaborating with teams, mitigating risks, and ensuring compliance in an ever-changing government contracting landscape. Thrive in a dynamic environment while...

Lead the charge in early clinical development, guiding studies from inception to proof-of-concept through collaboration and strategy execution within a dynamic team setting...

Empower your career by leading engineering and validation projects in GMP-regulated environments, ensuring operational readiness and compliance while coordinating cross-functional teams for successful...

Shape the future of pharmaceutical development by leading process projects, optimizing formulations, and collaborating on advanced drug modalities while ensuring compliance with regulatory expectation...

Lead IT Quality and Compliance initiatives for regulated clinical systems. Collaborate with diverse teams, ensuring compliance with FDA and EU standards while driving operational efficiency and suppor...

Drive new business pursuits in the pharmaceutical services sector, fostering strategic partnerships and achieving growth objectives through proactive development and client engagement...

Join a dynamic team as you lead strategic initiatives for Medical Device regulatory compliance, driving quality systems and enabling digital transformation to support global regulatory readiness and i...