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Pharmaceutical / medical / healthcare product brand marketing or other commercial leadership experience, including prior experience with US Consumer and/or HCP Marketing (specifically to infusion biologics a plus.
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We're working with a leading pharmaceutical company to source a (Senior) Director - ADME, Large Molecules & Biologics. We're partnered with a global pharmaceutical company, who have a leading pipeline in multiple therapeutic areas & 'blockbuster' potential launches imminent.
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Knowledge of fundamental principles of pharmaceutical science essential for the development of injectable dosage forms of small molecule, protein and peptide therapeutics. Ph. D. with 0-2 years of experience or MS with 2-4 years of experience with degree in Pharmaceutics, Biochemistry, Chemistry, Pharmaceutical Chemistry, Molecular Biology, Bioengineering, Chemical Engineering or related disciplines.
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Ph. D. preferred in Chemistry, Biochemistry, Bioengineering, or Pharmaceutical Sciences with a minimum of 5-8+ years in design and development of nanoparticle-based drug delivery systems or complex biologics.
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Education: Minimum Bachelor's degree required with focus in the area of chemistry, biology or related science Licenses/ Certifications: Regulatory Affairs Certification (RAC Drugs) preferred Experience: At least 5 years’ pharmaceutical or biologics CMC submissions experience with FDA required.
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Minimum of fifteen (15) years of pharmaceutical experience with ten (10) years of regulatory affairs experience including two to three (2-3) years in Commercial Regulatory experience working with biologics, preferably Cell therapy products.
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5+ years of Specialty Sales experience in Pharmaceutical, Biopharmaceutical, Biologics or Medical Device sales experience. Lundbeck is a global pharmaceutical company specialized in brain diseases.
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Reporting to the Vice-President of Manufacturing Operations and Supply Chain, the Sr. Director, Pharmaceutical Sciences will be responsible for leadership of the Pharmaceutical Science and Analytical Development teams and will have ownership of R&D operational support for early and mid-phase programs including formulation development, process development and analytical development, management of CMOs, process tech transfer and scale up.
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Minimum 12 years Pharmaceutical/Biotech industry in engineering, technology and/or manufacturing in biologics or vaccines, with minimum 8 years in Process Engineering in Sterile DP space.
$164,800 - $259,400 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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The AstraZeneca’s US BioPharma Respiratory and Immunology (R&I) Team holds a unique position in respiratory disease, including asthma, chronic obstructive pulmonary disease (COPD) and idiopathic pulmonary fibrosis (IPF), with a range of differentiated potential medicines in development by using novel combinations, biologics and devices.
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Catalent Biologics is a fast-growing business within Catalent Pharma Solutions focused on providing innovative technologies and solutions to help more and better biologic treatments get to patients.
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0-2+ years cGMP experience in biologics, pharmaceutical and/or vaccine manufacturing operations, including experience in cell culture, recovery, purification, bulk formulation and/or fill finish.
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Principal Scientist Level: Ph. D. with 5+ years of experience or MS with 6-9 years of experience with degree in Pharmaceutics, Biochemistry, Chemistry, Pharmaceutical Chemistry, Molecular Biology, Bioengineering, Chemical Engineering or related disciplines.
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Degree in mechanical, chemical, or pharmaceutical engineering, chemistry, materials science, or a related engineering or pharmaceutical science field. It is also advantageous if the candidate has cursory knowledge of regulatory guidance such as for biologics, cell and gene therapy, aseptic processing, validation, cGMP, and combination products.
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6+ years cGMP experience in biologics, pharmaceutical and/or vaccine manufacturing operations, including experience in cell culture, recovery, purification, and bulk formulation. 6+ years cGMP experience in biologics, pharmaceutical and/or vaccine manufacturing operations, including experience in cell culture, recovery, purification, and bulk formulation.
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