Regulatory Assistant

Education & Qualifications Required : Bachelor’s degree in Life Sciences, Pharmacy, Biomedical Engineering, or related field. Preferred : Master’s degree in a scientific discipline (Pharma, Biology, Microbiology, Chemistry). Experience Internship or ~1 year of experience in regulatory affairs in medical devices/pharma Fresh graduates with strong academic...

Education & QualificationsRequired: Bachelor’s degree in Life Sciences, Pharmacy, Biomedical Engineering, or related field.Preferred: Master’s degree in a scientific discipline (Pharma, Biology, Microbiology, Chemistry).ExperienceInternship or ~1 year of experience in regulatory affairs in medical devices/pharmaFresh graduates with strong academic...

Education & QualificationsRequired: Bachelor’s degree in Life Sciences, Pharmacy, Biomedical Engineering, or related field.Preferred: Master’s degree in a scientific discipline (Pharma, Biology, Microbiology, Chemistry).ExperienceInternship or ~1 year of experience in regulatory affairs in medical devices/pharmaFresh graduates with strong academic...

Gentell is one of the largest vertically integrated wound care companies in the world. Based in Yardley, PA and with offices, distribution centers and manufacturing plants around the world, our purpose is to make a positive difference in the quality of life for the injured, the chronically ill and those near the end of life.Our success is a result of the...

Purpose of the JobThis is a Subject Matter expertise profile which requires a detail-oriented and experienced Regulatory Reporting professional to join our team. The ideal candidate will have a strong background in banking, possess relevant regulatory knowledge Candidate will be responsible for preparing, reviewing, and submitting timely and accurate...

Role Objective Key objective of this role is to prepare, review, and maintain regulatory documents in compliance with international standards and country-specific requirements. The role ensures timely preparation and updating of Technical Master Files, supports product registrations, manages post-market surveillance activities, and contributes to audit...

The Regulatory Documents Assistant will establish and maintain the Sponsor electronic or paper Trial Master File (TMF) throughout the life of the trial and will perform record review of essential documents for accuracy and quality according to ICH-GCP. The Regulatory Documents Assistant is also responsible for the set-up of the Investigator's Study File...

The Regulatory Documents Assistant will establish and maintain the Sponsor electronic or paper Trial Master File (TMF) throughout the life of the trial, and will perform record review of essential documents for accuracy and quality according to ICH-GCP. The Regulatory Documents Assistant is also responsible for the set-up of the Investigator’s Study File...

The Regulatory Documents Assistant will establish and maintain the Sponsor electronic or paper Trial Master File (TMF) throughout the life of the trial and will perform record review of essential documents for accuracy and quality according to ICH-GCP. The Regulatory Documents Assistant is also responsible for the set-up of the Investigator’s Study File...

Job Overview The position of Trainee Regulatory Coordinator is a non-managerial role focused on assisting the department with submissions, data analysis, and communication tasks. This is an ideal entry-level position for recent graduates looking for a challenging and rewarding opportunity. Qualifications and Skills We are looking for male candidates only,...