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Director of Pharmaceutical Research and Development

Company: Kelly Services
Location: Clifton
Posted on: April 9, 2021

Job Description:

Director of Pharmaceutical Research and DevelopmentPOSITION SUMMARY:------ Our client is currently seeking an accomplished--Director level Scientist manage and--lead the--pharmaceutical product--development--group--at--center for biomedical research CBR----in New York City, developing--innovative sexual and reproductive health--(SRH)--products.--This position is part of a major expansion at CBR and the consolidation of--CBR's--HIV/AIDS and Reproductive Health--pharmaceutical--development teams.--The--new Director--will:--

  • Establish and oversee his/her own--pharmaceutical--development lab at CBR.--
  • Lead--CBR's--combined--pharmaceutical development--team--(currently three labs and 11 staff).--
  • Develop and execute a strategic plan to double the size of the group within the next five years.--
  • Work with colleagues to develop new strategic initiatives--and alliances--that will--guide--CBR's--product development activities--for the next 10 to 15 years.--RESPONSIBILITIES:------
  • Lead--CBR's consolidated--pharmaceutical--development team--of three laboratories.--
  • Work in partnership with cross disciplinary project team members to select--drug substances--and drug delivery systems--suitable for formulation development.--
  • Write--grant--applications and participate--in--other fund-raising activities.--
  • Work closely with Global Supply organizations involved with the design of dosage forms and development of manufacturing processes of drug product.--
  • Design,--conduct and/or oversee in vitro experiments to evaluate drug products using principles of quality by design and understanding of drug product manufacturing processes.--
  • Provide technical guidance for regulatory submissions for products--
  • Propose and execute strategies to resolve quality investigations of drug products.--
  • Mentor other scientists--
  • Maintain an awareness of and contribute to current scientific literature--through publishing in high-impact peer-review journals; actively apply--new concepts as appropriate.--
  • Lead and/or support departmental initiatives such as new technology development and continuous improvement projects.--
  • Represent the client at scientific conferences.--
  • Co-chair CBR's Jeiven/CBR Fellowship program--QUALIFICATIONS:------
  • Ph.D. in pharmaceutics, chemical engineering or chemistry, with--a--minimum of 15--years of--relevant--experience in academia or pharmaceutical industry
  • Experience in developing oral, topical, implantable, or injectable formulations; application of principles of engineering and physical chemistry in designing and characterizing formulations.--
  • STRONG FORUMLATION EXPERIENCE
  • Experience generating and interpreting experimental data; solving problems combining data with mathematical modeling of underlying phenomenon desired.----
  • Experience collaborating with pre-clinical colleagues in product development.
  • Knowledge of Good Manufacturing Practices (GMP).
  • Experience in providing support for regulatory submissions (e.g. Investigational New Drug Applications, New Drug Applications).
  • Excellent organizational skills with strong attention to detail, efficiency, forward-planning, and follow-through.--
  • Ability to prioritize and manage multiple projects and activities while meeting tight deadlines--
  • Proven ability to think critically,--proactive in problem-solving and able to independently manage timelines and priorities.--
  • Excellent interpersonal skills--and commitment to diversity:--demonstrated ability to effectively engage with a broad range of colleagues and partners at multiple levels, and--strong written and oral communication skills.--
  • Self-motivated; flexible and adaptable; creative; and hard-working with demonstrated ability to work both independently and as part of multi-disciplinary teams.--
  • Strong supervisory--skills;--ability to delegate work.--
  • Track record of scientific innovation and publication.--
  • Successful fundraising experience, grant writing and other fundraising experience.--#TJP2021_SPECWhy Kelly--?Kelly Science & Clinical is your connection to premier scientific and clinical companies looking to hire talented people just like you. Every day, we match science professionals with dream jobs that fit their skills and interests-it's the way we think job searching should be. Nearly 100 percent of our science recruiters have a professional background/education in science, so we know a thing or two about the science market and how to get you noticed.About Kelly--At Kelly, we're always thinking about what's next and advising job seekers on new ways of working to reach their full potential. In fact, we're a leading advocate for temporary/nontraditional workstyles, because we believe they allow flexibility and tremendous growth opportunities that enable a better way to work and live. Connecting great people with great companies is what we do best, and our employment opportunities span a wide variety of workstyles, skill levels, and industries around the world. Kelly is an equal opportunity employer committed to employing a diverse workforce, including, but not limited to, minorities, females, individuals with disabilities, protected veterans, sexual orientation, gender identity. Equal Employment Opportunity is The Law.]]

Keywords: Kelly Services, Clifton , Director of Pharmaceutical Research and Development, Executive , Clifton, New Jersey

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