FDA Regulations Jobs in USA

Job Title: 503A StaffPharmacist Reports to: General Manager and Pharmacist in Charge(PIC)FLSA Status: ExemptHours: 8:00 AM - 5:00 PMSalary: $135000 to $145000 doeABOUT FARMAKEIO CUSTOM COMPOUNDINGBe Part of the Team Thats Transforming HealthcareAt FarmaKeio were reshaping the idea of healthcare. We...

About Care AccessCare Access is working to make the future of health better for all.With hundreds of research locations mobile clinics and clinicians across the globe we bring world-class research and health services directly to communities that often face barriers to care.We are dedicated to ensuri...

McKesson is an impact-driven Fortune 10 company that touches virtually every aspect of healthcare. We are known for delivering insights products and services that make quality care more accessible and affordable. Here we focus on the health happiness and well-being of you and those we serve we care...

We anticipate the application window for this opening will close on - 7 Jul 2026At Medtronic you can begin a life-long career of exploration and innovation while helping champion healthcare access and equity for all. Youll lead with purpose breaking down barriers to innovation in a more connected co...

Position Job Title: Senior Principal Risk Based Quality Management Data Monitor Location: Research Triangle Park NC (preferred not mandatory)About This RoleAs a Senior Principal Risk Based Quality Management Data Monitor you will be a key contributor to the creation of Biogens in-house RBQM strategy...

Working with UsChallenging. Meaningful. Life-changing. Those arent words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here uniquely interesting work happens every day in every department. From optimizing a production line to the latest breakthrou...

Position Summary: The Senior Clinical Research Coordinator is responsible for overseeing the day-to-day conduct of clinical research studies while ensuring compliance with sponsor institutional and regulatory requirements. This role provides leadership mentorship and operational oversight to rese...

Job Description: Sr Lab System Support Engineer Rahway NJ - onsite 06-12 Months contract W2 ONLY Job Description/ Responsibilities Job Summary Sr Lab System Support Engineer plays a key role in supporting laboratory operations by ensuring the smooth functioning of lab systems analytical...

Job Title: Medical Writer/Clinical - II (Associate) Location (On-site Remote or Hybrid): Florham Park NJ (Remote) Contract Duration: Contract until 7/23/2027 Work Hours: 8AM - 5PM Job Description & Requirements Senior Medical Writer Education Minimum Requirements: Bachelor of Science Degree in...

The Manufacturing QA Technician will work in a high performing and fast-paced pharmaceutical finishing operation and performs sampling and visual inspection of both finished and in-process materials per the appropriate operating procedures and electronic batch record. Uses sophisticated programs (su...

We are seeking a Quality Systems Specialist to support and maintain our Quality Management System (QMS) with a strong focus on supplier quality regulatory compliance quality documentation and controlled substance processes within a regulated healthcare distribution environment. This role is responsi...

Job Title: Quality Assurance Specialist (QA Specialist)Location: Santa Clara CADuration: 6 MonthsIndustry: Medical Device (Preferred)Experience: 24 YearsJob SummaryWe are looking for a Quality Assurance Specialist with 24 years of experience to support quality system activities and maintain Design H...

Job Description: Sr Lab System Support Engineer Cambridge MA - onsite 06-12 Months contract Job Description/ Responsibilities Job Summary Sr Lab System Support Engineer plays a key role in supporting laboratory operations by ensuring the smooth functioning of lab systems analytical instrumen...

Role: Sr Lab System Support Engineer Location: Spring House PA Rahway NJ Cambridge MA - onsite W2 Position Name Required GMPs and GLPs Yes GxP operations (Good x Practice) Yes Job Description/ Responsibilities Job Summary Sr Lab System Support Engineer play...

Description: Max Bill Rate: $78.70 Job Title: Validation Specialist (Contract) KNEAT Gx Industry: Pharmaceutical & Medical Devices Contract Type: Contract (On site / Hybrid as required) Duration: Contract basis (length defined by project needs) Role Overview The Validation Specialist (Contrac...

Description: Max BR: BR Job Title: Validation Specialist (Contract) KNEAT Gx Industry: Pharmaceutical & Medical Devices Contract Type: Contract (On site / Hybrid as required) Duration: Contract basis (length defined by project needs) Role Overview The Validation Specialist (Contract) will su...

For further inquiries about this opportunity please contact one of our Talent Specialists Remy at or Sri at Title: Senior Validation Specialist - 2 Openings Location: On-site at Marion NC Duration: 12 Months with possibilities of extension. Only W2 candidates are eligible for this position....

We are seeking a motivated Scientist to join our CMC Quality Control team supporting daily analytical testing. This role will focus on preparing buffers and media maintaining cell cultures managing lab inventory logging and shipping samples and performing analytical testing. The position collaborate...

BUILD OUR FUTURE TOGETHER:As an Associate Director Field Medical Affairs (Medical Science Liaison) you will engage in the exchange of our scientific data and medical information with KOLs HCPs researchers pharmacists and population-based decision makers. You will demonstrate a thorough understanding...

Department:SOM KC Pediatrics (PEDS)-----Behavioral PediatricsPosition Title:Senior Clinical Research Coordinator - PediatricsJob Family Group: Professional StaffJob Description Summary:The Senior Clinical Research Coordinator (SCRC) in the Department of Pediatrics manages clinical research studies b...