Fda Jobs

AbbVie's USAP Standards Team is hiring a PharmD student intern to support FDA advertising and promotion review, reporting, and process improvement initiatives during the 2026 summer program.

Quality Specialist needed to ensure regulatory compliance, manage training and LMS activities, perform QA release and audits, and support continuous improvement at a CSL Plasma collection center.

AbbVie is recruiting a Safety Deliverable Manager to drive and author PST safety deliverables, ensuring high-quality, regulatory-compliant safety summaries and aggregate reports across product lifecycles.

Foresight Diagnostics seeks a Senior Specialist, Regulatory Affairs to lead US regulatory strategy and submissions for next-generation sequencing-based IVD products while partnering cross-functionally through development and lifecycle management.

Care Access is hiring a Regulatory Operations Specialist to manage site-level IRB and regulatory activities for U.S. clinical trials in a remote, fast-paced environment.

Foresight Diagnostics is hiring a Senior Director, Information Technology to lead IT operations, security, and digital transformation for its Boulder-based, regulated diagnostics organization.

Lead and manage medical device clinical trials for PROCEPT BioRobotics, overseeing site selection, monitoring, regulatory compliance, and data quality with significant domestic travel.

Experienced maintenance planner needed to lead CMMS-driven scheduling, optimize preventive maintenance, and coordinate cross-functional resources at a regulated medical device manufacturing site in Roseville, CA.

Experienced advanced energy engineering leader needed to drive ultrasonic and RF device design and integration for Intuitive's robotic surgical systems.

Gilead is hiring an Associate Director of Device Engineering to lead engineering teams in the development and regulatory execution of parenteral combination products.

Experienced clinical research professional wanted to manage TI oncology trials at OHSU's Knight Cancer Institute, supporting regulatory, patient-facing, and data operations for transplant and cell therapy studies.

Lead the computational development and validation of NGS- and epigenomics-based liquid biopsy diagnostics at an early-stage company driving a novel blood-based platform.

Experienced QA and regulatory leader needed to build and run quality systems and compliance strategies for EVERSANA’s regulated healthcare services in Memphis.

Intuitive is hiring a Director of Multiport I&A Product Engineering to lead engineering teams in designing, validating, and commercializing scalable robotic instruments for minimally invasive surgery.

ORIC Pharmaceuticals seeks a Regulatory Affairs Manager to drive timely, compliant regulatory submissions and support clinical oncology programs from its San Diego office.

Support Stryker’s Regulatory Affairs team in Bloomington this summer by assisting with regulatory data collection, submission preparation, and documentation process improvements.

Lead a small systems analysis team at a leading surgical robotics company to develop control, haptics, and performance algorithms that define system feel and clinical behavior.

QRC Group seeks a Specialist Tech Engineering in Juncos to support equipment optimization and maintenance compliance for regulated pharmaceutical/medical device environments.

Represent Stratpharma as a 1099 territory sales contractor focused on expanding adoption of wound care and dermatology products within VA hospitals and affiliated clinics.

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Hims & Hers is hiring a Quality Validation Specialist to lead commissioning, qualification, and calibration programs for a sterile cGMP manufacturing site and drive regulatory compliance and continuous improvement.

Experienced food quality professional needed to lead Quality Systems, regulatory audits and SQF management at Campbell's Napoleon, OH manufacturing site.

Stratpharma is hiring 1099 independent sales contractors to drive VA hospital and affiliated-clinic adoption of its FDA-cleared wound care and scar management products across Colorado and other priority U.S. markets.

Experienced contracts attorney needed to manage and negotiate clinical and research agreements for Sobi’s R&D organization, providing pragmatic legal support to Clinical Operations and cross-functional teams.

Plexus is hiring a Design Assurance Engineer intern in Neenah, WI to assist with medical device compliance, verification testing, and risk management activities for new product development.

QRC Group seeks an experienced Quality Systems Specialist to manage and improve quality systems, support investigations, and ensure compliance with GMP, FDA 21 CFR Part 11 and data integrity requirements.

Experienced clinical monitor sought by Novartis to lead site monitoring for Phase I–IV trials in a remote, travel-heavy role ensuring data quality, regulatory compliance, and strong site relationships.

Provide strategic regulatory leadership for U.S. advertising, promotion, and medical materials for high-priority products at Novartis' East Hanover site.

ActiGraph is hiring a Senior Compliance Specialist to lead QMS and regulatory compliance activities across product development, post-market surveillance, and audits for their medical-grade wearable solutions.

Experienced document control professional needed to own DMS maintenance, ensure regulatory-compliant records, and support audits for a remote, regulated-healthcare-focused company.

Westfalia Fruit seeks an experienced Regional Operations Manager to oversee East Coast fresh produce, ripening, and copacker operations across multiple facilities.

Lead and operationalize country-level study start-up activities for Novartis’ GDD portfolio, ensuring timelines, quality and regulatory compliance across a remote U.S.-based team.

Lead strategic regulatory labeling activities for AbbVie’s US/EU products, coordinating cross-functional teams to ensure compliant, consistent and optimized product labeling.

Saputo Dairy USA seeks an experienced Sr. Packaging Specialist to lead packaging strategy, compliance, and cross-functional execution across its manufacturing network.

PROCEPT BioRobotics is looking for a Senior NPI Manufacturing Engineer to lead design-for-excellence, process validation, and manufacturing transfer for new electromechanical medical devices.

Senior marketing leader to define portfolio strategy and lead commercialization and go-to-market execution for therapy selection and MRD/ctDNA products within Exact Sciences' Precision Oncology commercial organization.

Care Access is hiring an experienced Senior Region Manager for Florida to lead site operations, staff development, quality and growth across multiple clinical research sites.

Guardant Health is hiring a Senior Regulatory Affairs Manager to lead U.S. regulatory strategy and submissions for Oncology IVD/CDx products, guiding products from development through post-market compliance.

NeuroLogica seeks a Logistics & Inventory Manager in Danvers, MA to lead warehouse operations, inventory control, and logistics for our medical imaging manufacturing and service organization.

Clinical Research Associate needed to manage and monitor early-phase medical device and imaging trials, ensuring regulatory compliance and high-quality clinical data collection across domestic and international sites.

Zoetis seeks a Senior Tooling Engineer to lead tooling design, maintenance, and optimization for high-volume injection molding in a regulated manufacturing environment near Ontario, CA.

Lead engineering, capital projects, and process optimization at a cutting-edge aseptic beverage facility as the Head of Operations Engineering, ensuring compliance, efficiency, and team development.

DeepHealth seeks a hands-on QA/RA Project Manager to drive quality, regulatory readiness, and cross-functional delivery for medical device software and digital health products in a fully remote role.

Lead and scale Tovala’s food safety and quality assurance programs across manufacturing, supply chain, and product development to ensure regulatory compliance and exceptional product quality.

Senior leader accountable for end-to-end Supply Chain Center performance, safety, and leadership development at a leading global pizza company.

Lead verification for cloud-connected medical devices and mobile health applications as a Senior Verification Engineer/Lead based in Pleasanton, CA with IBA InfoTech.

Serve as an experienced regulatory leader providing CMC strategy, hands-on submission support, and Health Authority engagement to advance drug, biologic, and device programs for Allucent clients.

Lead day-to-day inventory control and audits at Lineage's Wilmington redistribution warehouse to ensure accurate stock records, efficient slotting, and compliance with food-safety regulations.

Orchard Therapeutics seeks an experienced VP of Clinical Development to lead global clinical science, design and execute clinical strategies, and represent clinical development in regulatory and cross-functional engagements for its gene therapy programs.

UChicago Medicine seeks a Facility Operations Lead Technologist to manage environmental monitoring, equipment validation, and facility compliance for the Advanced Cellular Therapeutics facility in Hyde Park.

Dental Insurance

Disability Insurance

Vision Insurance

Equity

Paid Time-Off

Medical Insurance

Mental Health Resources

Paid Holidays

Company Retreats

Lead the Gilbert mail-order pharmacy as Pharmacy Operations Manager to drive safe, compliant, and efficient prescription fulfillment while developing and scaling a high-performing pharmacy team.