Regulatory Affairs Pharmaceutical Jobs

Meet - , CA, United States

They are looking for a Regulatory Affairs contractor for 10 hrs a week, who will be responsible for aiding and working in a fast pace...

from: linkedin.com - 7 days ago

24 Seven Talent - New York, NY, United States

candidate will have pharmaceutical marketing experience and familiarity with MLR submissions. Regulatory Affairs Manager Responsibilities: Assist in filling in knowledge gaps on FDA regulations

from: linkedin.com - 17 days ago

Kelly Science, Engineering, Technology & Telecom - Irvine, CA, United States

Regulatory Affairs Specialist (hybrid) Kelly Science and Clinical FSP is currently seeking a medical device Regulatory Affairs Specialist II for a long-term engagement in Irvine, CA

from: linkedin.com - Yesterday

Stratacuity: Proven Scientific Placement - Boston, MA, United States

or medical discipline and possess at least 5 years of experience in Regulatory Affairs within the pharmaceutical, biotechnology, CRO, or related industry. Additional Skills, licenses, or certifications

from: linkedin.com - 4 days ago

AMISEQ - Weston, FL, United States

and related experience. Full-time work experience related to pharmaceutical industry, supply chain management (distribution), regulatory affairs or equivalent education and experience. Excellent communication

from: linkedin.com (+2 sources) - 4 days ago

Thor Companies - , NJ, United States

Title: Regulatory Affairs Associate Location: New Jersey (ONSITE) Job Type: 12-Month Contract Start Date: ASAP Reputable pharmaceutical client is seeking a Regulatory Affairs Associate to join

from: linkedin.com - 7 days ago

Atlas Search - , CA, United States

We are currently partnered with a fast growing pharmaceutical company that is seeking a VP/Senior Director, Regulatory Affairs & Quality Assurance. This is a great opportunity to become part

from: linkedin.com - 4 days ago

Proclinical Staffing - Palo Alto, CA, United States (+1 location)

level of technical competence of regulatory systems (e.g., Veeva RIM and StartingPoint templates). Strong communication and collaboration skills. Experience in regulatory affairs within the pharmaceutical

from: linkedin.com (+1 source) - 5 days ago

Bayside Solutions - Santa Clara, CA, United States (+2 locations)

related field is preferred. 15+ years of pharmaceutical/biotech drug development experience with 5+ years of experience in global CMC regulatory affairs with working experience and content knowledge in CMC

from: linkedin.com - 4 days ago

Validation Associates LLC - , VA, United States

degree in Chemical/Biomedical Engineering, Pharmaceutical/ Regulatory Affairs /Biotechnology. Good positive attitude and ability to learn fast. Willing to relocate nationwide in the US for client projects

from: linkedin.com - 7 days ago