Latest Pharmaceutical Regulatory Affairs jobs (page 2)

154 Pharmaceutical Regulatory Affairs Jobs - page 2

Regulatory Affairs Specialist Project Lead I (Scientific) Sanofi - Bridgewater, NJ, United States /biotechnology experience in R&D , including at least 5 years of relevant Regulatory Affairs experience (regionally and/or global). Please contact me if you are interested. Thank you. Please fill below details 2 days ago
USA-Regulatory Affairs Specialist Project Lead I (Scientific) Mindlance - Bridgewater, New Jersey years of relevant Regulatory Affairs experience (regionally and/or global), in early development. EEO: “Mindlance is an Equal Opportunity Employer and does not discriminate in employment on the basis 4 days ago
Regulatory Manager Mindlance - Bridgewater, NJ, United States of relevant Regulatory Affairs experience (regionally and/or global), in early development. 2 days ago
Senior Analytical Chemist Simply Biotech - Aliso Viejo, CA, United States , finished product method development, quantitative and qualitative analysis, and improvement of analytical methodologies. Act as R&D liaison to Regulatory Affairs responsible for defining and supplying 2 days ago
Senior Manager, CMC Facilities Regulatory Affairs GSK - Cambridge, MA validations Preferred Qualifications: MS or PhD. In Life Sciences or related field. Pharmaceutical development or regulatory affairs experience with biologics and vaccines preferred. Experience in providing 2 days ago
Vice President Government Affairs Ajulia Executive Search - Houston, TX, United States and outsourcing facilities, along with familiarity with the pharmaceutical supply chain and its regulatory environment. Strong knowledge of legislative and regulatory processes with the ability to guide public 2 days ago
Sr. Director of Regulatory Affairs - Oncology Mantell Associates - Boston, MA, United States sciences or a related field Minimum of 6 years of regulatory affairs experience in the biopharmaceutical industry, with a focus on rare diseases/oncology and orphan drug development Proven track record 2 days ago
USA-Regulatory Affairs Specialist Project Lead I (Scientific) The Fountain Group LLC - Bridgewater, New Jersey and strategy in collaboration with GRT (Global Regulatory Team) and is accountable for the communication of the key outcomes to senior management. Experience: • At least 8-10 years of relevant pharmaceutical 2 days ago
Site Quality Manager Kerry Search Partners - , FL, United States , pharmaceutical new product or medical device introductions Knowledge of project-based manufacturing processes including capital electromechanical equipment Regulatory Affairs Experience and/or RAPS Certification 6 days ago
Quality Specialist II 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 9 days ago

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