Regulatory Affairs Specialist Jobs in Atlanta, GA

Join a dynamic team to provide comprehensive regulatory support across clinical, submission, and post-approval phases for pharmaceutical products, ensuring compliance with global regulations while man...

Advance regulatory strategies for medical devices, managing submissions and ensuring compliance throughout the product lifecycle. Collaborate with project teams and regulatory bodies on 510(k)s, PMAs...

Engage with cross-functional teams to drive regulatory strategies and submissions for medical devices while ensuring compliance through the product lifecycle, including ongoing collaboration with dome...

Analyze regulatory landscapes to ensure compliance and facilitate product approvals across pharmaceutical and medical device sectors, collaborating with cross-functional teams to drive successful subm...

Empower our team as you ensure regulatory compliance and support product registration. Collaborate cross-functionally and resolve complex regulatory challenges while driving business success and safeg...

Join a dynamic team as you drive regulatory strategies and ensure compliance in post-approval activities for CMC processes. Collaborate cross-functionally, influencing clinical outcomes and advancing...

Join a team that's committed to driving innovative regulatory projects, ensuring compliance, and collaborating with cross-functional teams to secure timely submissions and approvals for products in th...

Drive success in regulatory affairs by preparing critical submissions for medical and diagnostic devices. Oversee compliance with U.S. and international regulations while collaborating with cross-func...

Empower medical device compliance by reviewing and submitting regulatory documentation. Collaborate across teams to secure timely approvals while ensuring adherence to FDA, ISO 13485, and global stand...

Join a team that's shaping the future of regulatory compliance in the food industry. Collaborate across functions to support domestic and international regulatory tasks, ensuring clarity and timelines...

Lead regulatory intelligence efforts to ensure compliance and strategic insight within the pharmaceutical landscape. Collaborate across teams to monitor global regulatory changes and support the devel...

Champion global regulatory strategies and practices, ensuring alignment across teams and enabling market access through effective registration processes. Drive consistency and efficiency while leading...

Join a team that's shaping the future of global regulatory affairs. You will lead compliance strategies for investigational products and marketing applications through effective submissions and collab...

Champion regulatory excellence by leading U.S. FDA engagement and strategy for product development, ensuring timely approvals and compliance while driving cross-functional collaboration and organizati...

Join a team that's dedicated to ensuring compliance in promotional activities for CNS treatments while navigating regulatory pathways in a fast-paced environment. Help shape communications, drive stra...

Join us in driving operational excellence in regulatory submissions and document workflows. Lead cross-functional teams to ensure compliance and quality across all submissions while optimizing process...

Empower regulatory excellence by managing promotional materials compliance across global markets, ensuring adherence to laws and internal policies, while aligning with strategic business objectives in...

Champion global regulatory strategies by leading diverse teams in navigating complex approval processes for medical devices. Drive compliance and ensure optimal product launch pathways while addressin...

Join a dynamic team to develop strategic regulatory pathways for medical devices, ensuring compliance from development to market. Leverage your experience to lead initiatives and mentor professionals...

Join a team that's shaping global regulatory strategy for rare disease therapies. In this pivotal role, you'll lead submissions and agency interactions across the US, EU, UK, and Japan, driving execut...

Lead the charge in regulatory affairs and quality systems, ensuring compliance for product lines in U.S., Canada, and EU. Oversee submissions, approvals, and inspections while collaborating with cross...

Drive regulatory strategies and oversee compliance for investigational therapies. Work cross-functionally to ensure timely regulatory filings and maintain vendor relationships, contributing to clinica...

Support quality assurance for external manufacturing operations by reviewing batch data and quality systems documentation. Collaborate with partners to ensure compliance and product release standards...

Manage regulatory submissions for medical devices, ensuring compliance with FDA and ISO standards. Collaborate with cross-functional teams to guide products through regulatory processes and secure tim...

Transform regulatory strategies in FDA Pharma and IVDR, ensuring compliance and driving product approvals. Collaborate with cross-functional teams, mentor associates, and enhance processes to support...