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A Division
of
GMP
Publications
& FDA.COM
"The GxP Family of
Quality Business"




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"We stand on a higher pillar of excellence!"
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Title |
Location |
Type |
Rate |
Apply |
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Scientist II |
West
Chester PA |
Perm/Full |
$80,000 - $100,000 |
Submit |
Scientist II
Overview:
The Scientist II will perform research and/or
development activities in collaboration with
others for R&D projects and programs related to
bacterially derived cellulose. Principal
responsibility to developing functional and
design specifications of future applications for
bacterially derived cellulose. Additional
responsibility for determining manufacturing
methodology to meet the performance
characteristics related to these new
specifications.
Responsibilities:
• Perform research and/or development activities
in support of bacterially derived cellulose
projects and programs.
• Provide detailed data, results, analyses, and
summary reports to project and program teams
• Conduct critical analysis of data and results
and recommend paths forward based on analysis
• Participate in cross-disciplinary project and
program teams
• Understand and act on departmental, program,
and project objectives
• Assist in defining departmental objectives and
participate in defining project & program
objectives
• Conduct experiments and provide results and
analyses in a timeline driven process
• Independently design and execute experiments
• Provide guidance and mentor more junior staff
• Participate in proof of principle testing to
evaluate new technologies
• Develop an in-depth knowledge of intellectual
property in area of expertise and participate in
the development of company's intellectual
property
• Contribute to peer-reviewed publications and
to internal technical publications and
presentations
• Consider regulatory issues in decision making
• Develop in-depth knowledge of relevant
scientific technologies
• Demonstrate technical proficiency, scientific
creativity, and independent thought
• Participate in the evaluation of new
technologies developed externally
• Work with external partners including
researchers, clinicians, and other companies
• Work with internal partners in the global
organization including business units and
researchers
• Travel requirements 5%-10%
• Know and follow all laws and policies that
apply to one's job, and maintain the highest
levels of professionalism, ethics and compliance
at all times.
• Diligently participate in our compliance
program-related activities as denoted by your
supervisor or our Chief Compliance Officer.
Qualifications:
• PhD in biological, chemical, biomedical
engineering or related discipline. Would also
consider MS in biological or chemical sciences,
biomedical engineering or related discipline
with exceptional experience and capabilities.
• Minimum of 2-5 years experience in a
biomaterials research/development environment
and strong knowledge of biological sciences.
• Experience with biological approaches to
medical devices and orthopedics or wound
healing.
• Strong experience in conducting laboratory
experiments
• Familiarity with polymer-based medical devices
a plus.
• Familiarity with microbiology and production
of natural products from microbial sources a
plus.
• Familiarity with preclinical animal models to
evaluate medical devices a plus.
• Familiarity with Medical device product
development, including regulatory considerations
a plus.
• Skilled in Microsoft Power Point, Word, Excel,
and standard experimental analysis software
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