Pharmaceutical Regulatory Affairs Jobs in South Plainfield, NJ

Katalyst Healthcares & Life Sciences - South Plainfield, New Jersey

and relevant regulatory affairs experience in pharmaceutical, vaccine, or biological products; or related fields Knowledge and hands on experience on Animal Health CMC Marketing authorization experience. Proven

from: resume-library.com - 2 days ago

Breckenridge Pharmaceutical, Inc. - Berkeley Heights, NJ, United States

regulatory affairs operations. Knowledge of eCTD publishing systems and standards, EDMS technology and related publishing tools. Working knowledge of US FDA (OGD/CDER) e-submission requirements. Strong written

from: linkedin.com - 3 days ago

Aequor - Bridgewater, NJ, United States

experience in R&D, including at least 5 years of relevant Regulatory Affairs experience (regionally and/or global).

from: linkedin.com (+1 source) - 9 days ago

Cronus Pharma - New Brunswick,New Jersey

Overview Pharmaceutical company looking for an experienced Quality Assurance and Regulatory Affairs Associate. Ideal candidates should have experience within QA and/or Regulatory Affairs department $50000-60000 k per Yearly

from: sulekha.com - 6 days ago

Leaman Life Sciences - Newark, NJ, United States

regulatory implications for business decisions. Team Leadership: Provide leadership, mentorship, and development opportunities for the regulatory affairs team, fostering a culture of excellence, innovation

from: linkedin.com - 14 days ago

Ajulia Executive Search - Princeton, NJ, United States

Manager Global Regulatory Affairs Princeton, New Jersey EU GMP requirements Must have Global Regulatory Affairs experience in the pharmaceutical or biotechnology industry. Are you looking to make

from: linkedin.com - 12 days ago

Lupin Pharmaceuticals Inc. - Somerset, New Jersey

years’ experience in the pharmaceutical industry with 3‐5 of those years in regulatory affairs preferred Prior experience of participating in managing, designing and implementing REMS systems (highly

from: resume-library.com - 13 days ago

US Tech Solutions - New York, NY, United States

launches (medical affairs, commercial/marketing, market access, clinical development, regulatory, etc.). Minimum 5+ years of full-time pharmaceutical industry or consulting experience in HEOR required

from: linkedin.com - 8 days ago

GForce Life Sciences - Princeton, NJ, United States

experience processing AE/SAE reports, generating narratives, queries, working within safety databases, and experience with regulatory submissions **Relevant experience includes experience in the pharmaceutical

from: linkedin.com - 19 days ago

Johnson and Johnson - Raritan, NJ

: Employer will accept a Bachelor's degree in Regulatory Affairs, Pharmaceutical Sciences, or related field and 10 years of progressive, post-baccalaureate experience in the job offered or in a Director

from: Johnson and Johnson - 6 days ago