Scientist- Large Molecule, Caliper GMP
Pharmaceutical Product Development, Inc. - Wayne, PA

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Scientist- Large Molecule, Caliper GMP - 110589
              Job Category Biopharmaceuticals
              Primary Location North America-United States-Pennsylvania-Wayne

              Description
              The Scientist position has the same purpose and objective of the Associate Scientist position but differs in the level of expertise and supervision required. A Scientist is expected to possess a more thorough understanding of laboratory procedures and can reliably conduct more complex analysis.

              Ideal candidate will have 2-plus years of cGMP and Large Molecule experience (SDS-PAGE, Western Blotting, ELISA, HPLC). Caliper or similar technology experience required.

              Qualifications
              Education and Experience:
              • B.S./B.A. in Chemistry or related field with of 2 years experience in analytical testing laboratory.
              • Associates degree in laboratory science with 6 years of hands on laboratory experience.
              • Non-degreed with 8 years of hands on Pharmaceutical laboratory experience.

              • Or equivalent years experience in lieu of education.

              • Large Molecule GMP experience required.

              • Caliper or Similar Technology experience.

              Knowledge, Skills and Abilities:
              • Manual dexterity.
              • Communicate effectively and follow detailed written and verbal instruction.
              • Cooperate with coworkers within an organized team environment or work alone with supervision.
              • Manage time effectively to complete assignments in expected time frame.
              • Maintain a laboratory notebook and complete all documentation with clear and accurate language and according to the SOP.
              • Proficient in the use of analytical instrumentation, skills in separation science techniques in a GMP environment are desired.
              • Proficient in sample extraction procedures.
              • Ability to plan, schedule and carry out work for successful project completion.
              • Proficient in the operation of the computer and data acquisition programs.
              • Positive attitude and ability to work well with others.
              • Ability to write protocols and reports with minimum supervision
              • PPD is an Equal Opportunity Employer

              Job Posting

              About this company
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              PPD is a leading global contract research organization providing drug discovery, development, lifecycle management and laboratory services....