Regulatory Affairs Specialist Jobs

Pioneer quality assurance on cross-functional teams, ensuring compliance in design transfers and change management for medical devices while supporting product launches and regulatory submissions acro...

Join a team that's dedicated to enhancing quality across multiple sites, implementing the Quality Management System, and ensuring ISO 9001:2015 compliance while leading strategic audits and process im...

Unlock your potential as a key Trade Compliance expert, overseeing global compliance strategies for pharmaceutical trade. Collaborate with diverse teams to ensure regulatory adherence and streamline i...

Join a team that drives product success by providing top-tier support, technical training, and strategic marketing for LCMS products. Engage with clients and collaborate with multiple departments to e...

Optimize analytical project delivery as the key QC liaison, ensuring effective communication between clients and internal teams. Drive project planning, assessments, and coordination in a fast-paced e...

Unlock potential by leading data integrity and automation initiatives in a cutting-edge bioproduction facility, enhancing operational efficiency and regulatory compliance while collaborating with cros...

Lead the charge in managing labeling projects for GSS product portfolios. Collaborate across teams to ensure compliance, accuracy, and clarity in product labeling and documentation while enhancing pro...

Transform product labeling processes by partnering with cross-functional teams to create compliant, accurate documentation for GSS product portfolios, managing multiple projects while improving proces...

Contribute to critical labeling operations for GSS product portfolios by collaborating with cross-functional teams to ensure compliance and accuracy across all product labeling and documentation proce...

Join a dynamic cross-functional team to support labeling for medical devices, ensuring accuracy and compliance. Manage multiple projects while coordinating with quality and regulatory teams for succes...

Drive labeling activities for GSS product portfolios, ensuring compliance and accuracy through collaboration with cross-functional teams. Manage documentation projects and improve processes within the...

Advance your career by managing site activation activities while ensuring compliance with regulations and SOPs. Collaborate with cross-functional teams, enhance project workflows, and contribute to qu...

Drive site activation activities on a country level, ensuring compliance with regulations and SOPs while enhancing processes and systems. Collaborate with cross-functional teams to meet project timeli...

Join a team that's vital in driving site activation activities, ensuring compliance with regulations and procedures, and managing project timelines. Develop your expertise in clinical research while e...

Join a team that's dedicated to advancing crop physiology through hands-on research, experiment coordination, and data accuracy in a dynamic field environment. Contribute to innovative projects that s...

Collaborate with cross-functional teams to lead regulatory writing efforts, ensuring high-quality documentation throughout the drug development lifecycle, from preclinical to registration stages, to s...

Lead commercial management in CAPEX projects, ensuring contract compliance, risk mitigation, and value optimization to support growth. Collaborate across teams to manage contracts and claims effective...

Shape the future of drug substance development by leading regulatory strategies for starting materials. Collaborate cross-functionally and ensure compliance with global regulations to support late-sta...

Elevate your career by managing quality assurance in a GMP setting. Oversee supplier quality, lead audits, and ensure compliance with regulatory standards while driving continuous improvement across q...

Reimagine pharmaceutical impurity management by leading cross-functional teams. Develop risk-control strategies and ensure compliance with health regulations for nitrosamine impurities globally, while...

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...

Help us support clinical trials by managing site monitoring and ensuring compliance. Utilize your clinical knowledge to protect patient safety and maintain data integrity while thriving in a fast-pace...

Lead the high-quality monitoring of clinical trials, ensuring compliance with regulatory standards while managing site operations, training staff, and protecting participant safety in a fast-paced, dy...

Lead the charge in quality assurance by coordinating corrective actions and driving process improvements across departments to mitigate risks and enhance manufacturing operations...

Transform quality assurance processes by driving corrective actions and investigations across departments, ensuring compliance and effectiveness in a regulated manufacturing environment while preventi...