Regulatory Affairs Jobs in USA

Job Title: Sr CNC MFG Engineer Location: Warsaw IN Job Description: JD as below Role: Validate CNC equipment and related processes used to manufacture medical devices. Focus: Ensure IQ/OQ/PQ calibration traceability and compliance with GMP/ISO standards in a regulated MedTech environment. Aim...

Job: Sr CNC MFG Engineer Location: Warsaw IN Experience: 4.5-8 Years Duration: Long term contract Skill (Primary): Technical Skills (ERS)-Machining & Manufacturing Process Planni-Manufacturing Process Planning Required Skills Manufacturing Process CAM programming GD&T product design and developme...

Job ID: MI-151269 Hybrid/Local Developer (5 pages resume/15) with JAVA Rhino JavaScript SQL Server AD HOC Crystal reports SSRS SVN GIT Accela Automation/GIS/design/code review/testing/Data Migration Tool and Angular React experience Location: Lansing MI (DTMB) Duration: 12 Months Position: 1 P...

JOb:Lansing MI - IT - DTMB - Agency Services - LARA - Programmer Analyst 6 - Accela JOB ID: 151269 Location : Top Skills & Years of Experience Required: 3-5 years experience with each of the following: - Java Script - Accela - SQL - .NET Clear and concise communication skills required. P...

Principal Medical Writer Publications Client has an exciting opportunity for a Principal Medical Writer at an award-winning best-in-class in-house agency at a major pharma company. Join our newly established MCS Medical Communications Team-a dynamic start-up focused on redefining how scientific s...

Title: Programmer Analyst 6 - Accela Location: Lansing MI (Hybrid Locals Only) Duration: 12 Months Job Description As a Senior Application Developer the employee performs a complete range of information system analyst assignments including but not limited to designing developing testing and imple...

The ME&C Associate Director is a global program management expert responsible for managing major global programs and projects across disciplines and multiple manufacturing locations. They organize and lead high-performing cross-functional teams in the planning and execution of device and combination...

Job SummaryProvide a variety of administrative tasks in support of the overall operation of the Office of Research Regulatory Affairs under the direction of the Research Regulatory ManagerRequired QualificationsEducation: High School diploma or GED required. Bachelors Degree Preferred and/ or any co...

Job SummaryAs a member of the nursing team with Corewell Health providing top-notch patient care is paramount. Youll be responsible for the care of our patients according to their individual plans unit routines and hospital policies. Under the direction of a Registered Nurse youll be a vital part of...

At Alcon we are driven by the meaningful work we do to help people see brilliantly. We innovate boldly champion progress and act with speed as the global leader in eye care. Here youll be recognized for your commitment and contributions and see your career like never before. Together we go above and...

Who We AreABOUT ENOVISEnovis Corporation (NYSE: ENOV) is an innovation-driven medical technology growth company dedicated to developing clinically differentiated solutions that generate measurably better patient outcomes and transform workflows. Powered by a culture of continuous improvement global...

At Alcon we are driven by the meaningful work we do to help people see brilliantly. We innovate boldly champion progress and act with speed as the global leader in eye care. Here youll be recognized for your commitment and contributions and see your career like never before. Together we go above and...

Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies spans the spectrum of healthcare with leading businesses and products in diagnostics medical devices nutritionals and branded generic medicines. Our 114000 collea...

Title: Regulatory Affairs Manager Remote USC or GC Description: The Manager supports Global Reg Teams in the development and execution of global nonclinical / clinical regulatory strategies through a programs lifecycle. The Manager leads the execution of delegated activities including prepa...

Hi Candidates Ive a below position if youre qualified with the position then share resumes to Job title: Accela Programmer Analyst (Developer) Client: State of Michigan Inteview type: 2 rounds(Webcam and In-person) Location: Lansing MI Work mode: Hybrid position Note: Candidate must att...

Job Description As a Senior Application Developer the employee performs a complete range of information system analyst assignments including but not limited to designing developing testing and implementing computer systems and applications for Department of Licensing and Regulatory Affairs (LARA). T...

Client: State of MI Posting title: Lansing MI - IT - DTMB - Agency Services - LARA - Programmer Analyst 6 - Accela Posting ID: 151269 Job Title: Programmer Analyst 6 Department: DTMB Agency: LARA Division: Agency Services Work Location: 611 W Ottawa Lansing MI 48933 Projected Start Date: 12/15/2025...

Job Title: Accela Developer (Hybrid) Location: Lansing MI Duration: 12 months Pay Rate: $90/hr on C2C / 1099 all inclusive (OR) $80/hr on W2 Interview Process: 1st round interviews will be held via MS Teams. 2nr round interviews may be held in person so candidates must...

Oversee and direct all CMC regulatory strategies in compliance with global regulatory requirements for the development of ORICs products.Provide CMC regulatory support for new and ongoing clinical trials e.g. manage/prepare CMC document packages in support of INDs CTAs and amendments to global regul...

JOB # What Youll Do Licensing Management: Manage and maintain state licenses for lending and loan servicing. Prepare submit and track licensing applications renewals annual reports and registrations. Act as a primary liaison with regulatory agencies on licensing and examination matters. Comp...