FDA Regulations Jobs in USA

This is a remote position.Summary:The Clinical and Medical Affairs Administrator is a key role supporting the Clinical and Medical Affairs department focusing on contract execution budget oversight and operational support. This position ensures smooth coordination between Legal Fin More...

Job SummaryWe are looking for a Lead Associate Quality Assurance for Middleburgh plant (On Site) to provide support for all Quality Assurance activities. The incumbent will work closely with the Site Quality Head to ensure all aspects of the site operations are conducted using cGMP me More...

The Quality Management System (QMS) Specialist will be responsible for developing implementing maintaining and improving the companys Quality Management System (QMS). This role ensures that the QMS is compliant with ISO 13485 ISO 9001 21 CFR 820 and 21 CFR 58. The QMS Specialist will More...

The Quality Management System (QMS) Specialist will be responsible for developing implementing maintaining and improving the companys Quality Management System (QMS). This role ensures that the QMS is compliant with ISO 13485 ISO 9001 21 CFR 820 and 21 CFR 58. The QMS Specialist will More...

JOB PURPOSE AND REPORTING STRUCTURE Under the supervision of the Quality Assurance Manager the Quality Assurance (QA) Lead is responsible for ensuring that the manufacturing of food products occurs in a safe manner in compliance with federal regulations (FDA/USDA) state laws current S More...

About the job Korpack is looking for a Quality Assurance and SQF Practitioner to join its team. If you have a passion for quality and thrive in a dynamic Get S*%t Done (GSD) environment Korpack invites you to join our fastgrowing organization! The Quality Assurance and SQF Practiti More...

Job Title: Manufacturing Technician 3rd Shift Work location: San Antonio TX Job Type: C2C/Fulltime/W2 Job Description: At Globus Medical we move with a sense of urgency to deliver innovations that improve the quality of life of patients with musculoskeletal disorders. Our More...

Role: Engineering Sr Engr R&D Location: Irvine CA 92614 (Onsite Role) Duration: 11 Months of contract to begin with possible extension Job Description: Summary: Applies knowledge of R&D engineering principles and methods to ensure compliance with regulatory requirements and syst More...

For further inquiries regarding the following opportunity please contact our Talent Specialist: Infant at Title: R&D Portfolio Manager Location: San Diego CA Duration: 9 Months (with possible extension) Remote Workplace: Your location will be a home office; you are not require More...

Responsibilities: Provide leadership and be accountable for meeting approved scope schedule and cost plans Ensure project is delivered in a manner compliant with project planning documents procedures and guidelines defined by the PMO Plan monitor and control More...

This is a remote position.PSC Biotech provides the life sciences with essential services to ensure that health care products are developed manufactured and distributed to the highest standards in compliance with all applicable regulatory requirements.Our goal is to skyrocket our cl More...

As the Regulatory Affairs Intern you will be joining a strong technical service environment. In this role you will have an opportunity to work alongside experienced professionals as you provide support to the Service Center ensuring maintenance and organization of regulatory More...

Regulatory Affairs ConsultantLocation: Hybrid (Dallas TX Preferred)Yrs of Exp: 3 yrs Overview: We are seeking a highly skilled and detailoriented Regulatory Consultant to join our dynamic team in the medical device sector. This role will provide expert guidance on navigating complex More...

As the Regulatory Affairs Intern you will be joining a strong technical service environment. In this role you will have an opportunity to work alongside experienced professionals as you provide support to the Service Center ensuring maintenance and organization of regulatory More...

As the Regulatory Affairs Intern you will be joining a strong technical service environment. In this role you will have an opportunity to work alongside experienced professionals as you provide support to the Service Center ensuring maintenance and organization of regulatory More...

Job Description: We are inviting applications for the role of Senior Manager Regulatory affairs. Responsibilities: Develop global regulatory strategy for lifesaving therapeutic products in development and through life cycle management considering all relevant guidance commercial ne More...

As the Regulatory Affairs Intern you will be joining a strong technical service environment. In this role you will have an opportunity to work alongside experienced professionals as you provide support to the Service Center ensuring maintenance and organization of regulatory More...

Job Title : Regulatory Support Location : Basking Ridge NJ Remote Option: Yes. But the candidate should be available to attend customer meetings twice in a month Mandatory skills: experience in pharmaceutical environment. Experience in regulatory environment i More...

SummaryThe Clinical Operations Director is responsible for overseeing the tactical implementation of the clinical development plan for autoimmune studies. This includes managing timelines budgets resources and clinical staff to ensure efficient and highquality execution of clinical tr More...

Job Title: Polarion Senior Solution Architect Location: Massachusetts MA (Onsite) Duration/Term: Long Term Contract Key Responsibilities: Design: Lead the design and implementation of Polarion ALM solutions tailored to the Medical Devices industry. Collaboration: Collaborate with More...