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Nektar Therapeutics

    Nektar Therapeutics is a clinical-stage biopharmaceutical company developing a pipeline of drug candidates that utilize its PEGylation and polymer conjugate technology platforms, which are designed to improve the benefits of drugs for patients. Its product pipeline consists of drug candidates across a number of therapeutic areas, including oncology, pain, anti-infectives, anti-viral and immunology. Nektar's research and development activities involve small molecule drugs, peptides and oth... Read More

Address      455 Mission Bay Boulevard South San Francisco, CA 94158
Website      www.nektar.com/
Holding      No Holding Details

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Analytical Services

Responsible for conducting routine and non-routine analysis of raw materials, in progress and finished formulations according to standard operating procedures. Compiles data for documentation of test procedures and prepares reports. Calibrates and maintains lab equipment. May develop testing methods. Reviews data obtained for compliance to specifications and reports abnormalities. Revises and updates standard operating procedures as needed. May perform special projects on analytical and instrument problem solving. Applies knowledge of good manufacturing practices and good laboratory practices on a daily basis.

<span title=""><label for="com.peopleclick.cp.formdata.JPM_WORKENVIRONMENT">Responsibilities</label>
Works on extremely complex problems where analysis of situations or data requires an evaluation of intangible variables. Exercises independent judgment in developing methods, techniques and evaluation criteria for obtaining results. Acts independently to determine methods and procedures on new assignments. Provides data analysis, troubleshooting and problem solving. Provides training to junior analysts. Supports QC release and stability testing. Performs various analyses, such as HPLC, UV-Vis spectroscopy, particle size determination and moisture analysis. Maintains accurate and well-organized laboratory records and worksheets. Assists with other projects as assigned. May supervise the activities of other junior Quality Analysts.

<span title=""><label for="com.peopleclick.cp.formdata.JPM_DESCRIPTION">Requirements</label>
A minimum of a Bachelors degree in a scientific discipline is required. Equivalent experience may be accepted. A minimum of 8 years related experience is required. A minimum of 5 years experience in the pharmaceutical industry working in a GMP environment is required. Previous supervisory experience is a plus. Must have a demonstrated working knowledge of scientific principles. Practical experience in HPLC, UV/Vis spectroscopy and/or moisture analysis is required. Experience in data analysis, troubleshooting and problem-solving skills is a must. Knowledge of FDA regulations and cGMPs for drugs and/or device are required. Aerosol and pulmonary delivery experience a plus. Experience in data analysis, troubleshooting and problem-solving skills is required. Good oral and written communication skills are required. Good computer and documentation skills are required. Must be well organized and willing to work as part of a team.

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Full Time

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