Regulatory Affairs Jobs in USA

The Associate Director Clinical QA is responsible for developing and implementing a strategy for proactive quality oversight of clinical development programs within their responsibility.This role will ensure that R&D remains in compliance with the corporate policies and applicable worldwide regulati...

The Associate Director Clinical QA is responsible for developing and implementing a strategy for proactive quality oversight of clinical development programs within their responsibility.This role will ensure that R&D remains in compliance with the corporate policies and applicable worldwide regulati...

We are seeking a Medical Director. This position will report to the Senior Medical Director of Pharmacovigilance and will be located in the Waltham office.The Medical Director is responsible for global pharmacovigilance (PV) for marketed and/or investigational products including review and analysis...

OverviewThis is a REMOTE position. The Regulatory Affairs Specialist 2 responsibilities are narrowly focused to a specific country and/or region in which the Specialist has proficient language skills (reading/writing/speaking). This position requires the ability to speak read and write in business l...

OverviewThis is a REMOTE position. The Regulatory Affairs Specialist 2 responsibilities are narrowly focused to a specific country and/or region in which the Specialist has proficient language skills (reading/writing/speaking). This position requires the ability to speak read and write in business l...

DescriptionIf youre reading this on your way from 5am spin class to festival fast-pass youreCELSIUSan everyday hustler with the essential energy toaim high live fit and go the extra mile wherever your goals take you.Joyful by design sunny by nature and unapologetically bold. If your bestie has you s...

DescriptionIfyourereading this on your way from 5am spin class to festival fast-passyoureCELSIUS an everyday hustler with the essential energy to aimhigh andgo the extra mile wherever your goals take you.Joyful by design sunny by nature and unapologetically bold. If your bestie has you saved in thei...

Simtra BioPharma Solutions (Simtra) is a world-class Contract Development Manufacturing Organization partnering with pharmaceutical and biotech companies to bring their sterile injectable products to market. With facilities in Bloomington Indiana US and Halle/Westfalen Germany we offer a wide range...

Remitee is scaling its cross-border payments platform across key markets in LATAM/USA/EU. We are looking for a Head of Regulatory Affairs (Regional) with strong hands-on experience leading regulatory filings licensing applications implementation and ongoing maintenance for payment-related licenses (...

Position: Quality Control Medical Writing Location: Hybrid in San Francisco CA (4-5 days in office Mon-Sat) Duration: Fulltime Year of Experience - 3 Scope of Role Helping design AI systems that write regulatory documents. Deconstructing authoring/review/QC heuristics for engineers. Evaluatin...

Job Title: Drug Safety Analyst Location: Los Angeles CA 90032 Schedule: 8:00 AM to 4:30 PM Expected Start Date 03/23/2026 End Date 03/26/2027 Job Description Provides operational support for global pharmacovigilance activities for investigational and marketed products. Ensures pharmacovigilance...

Job:Software Engineer Medical Device Product Development Location: Newark DE (Hybrid) Experience: 7 years Industry Preference: Medical Devices / Regulated Healthcare Products / Embedded or Product Software Role Summary: We are seeking a Software Engineer with strong product developmen...

Job Title: Product Safety Specialist Location (On-site Remote or Hybrid): South Portland ME (onsite) Contract Duration: Contract until 12/31/2026 Working hours: 8:00AM - 5:00PM Total hours: 40 Description: This position is Non-Exempt. Hours over 40 will be paid at Time and a Half. Responsible...

Job Title : Complaint Analyst / Post-Market Quality AnalystLocation : 100% RemoteLong Term ContractExperience: 7 years preferredMultiple Openings Role Summary:We are seeking a Complaint Analyst to support Post-Market Quality activities by investigating product complaints evaluating potential adverse...

The Senior Director Development Sciences Licensing & Acquisitions leads a specialized team responsible for evaluating external pipeline opportunities overseeing due diligence activities and guiding Chemical Manufacturing and Controls (CMC) strategies for licensing and acquisitions across multiple th...

The Senior Scientist I will implement and execute novel scientific research and development independently develop optimize new methods and techniques to generate reliable and reproducible data in a timely manner and demonstrate broad versatile technical expertise. They will support early phase devel...

At PGE our work involves dreaming about planning for and realizing a smarter cleaner more enduring Oregon neighborhood. Its core to our DNA and we havent stopped since we started in 1888. We energize lives strengthen communities and drive advancements in energy that promote social economic and envir...

Roles & Responsibilities1. Implementation and continuous improvement of the Medical Device Quality2. Management Systems and associated CE requirements in order to meet customer3. and regulatory requirements 4. Preparation implementation and Maintenance of Manual policies work instructions as per ISO...

Role OverviewThe successful Process Engineering candidate will play a key technical team leader role in the R&D Process Engineering function. In addition to a strong background in fundamentals of chemical engineering the ideal candidate will have demonstrated experience in the biologics peptides ADC...

Brightspeed is looking for an outgoing high-energy self-starting professional who can convey complex business and regulatory strategies information and ideas to a wide variety of internal and external this role you will be responsible for developing building and maintaining business relationships w...