artechinformationsystemllc •

Scientist II

Swiftwater, PA, us Contract

Work collaboratively in a GMP lab environment, maintain instrumentation in proper operating and calibrated condition.

Follow all laboratory method, instrumentation, and safety requirements.

Participate in analytical assay development and validation activities for HPLC and UPLC based methods.

This will typically be done in a team setting but will require independent lab work, scientific assessment of progress, and recommendations for next steps.

Author GMP documents including method instructions, development reports, method validation protocols and validation reports as per site requirements.

Be able to provide training, guidance, and/or support for both new and experienced staff in matters related to areas of experience, knowledge, and/or expertise.


Skills:

Experience with analytical method development and validation.

Experience utilizing Microsoft Word, Excel, and Outlook

Experience writing and revising documents (e.g. testing methods, protocols, reports)

Experience performing testing in a GMP setting

Experience in method development and validation-related activities

Broad experience working hands-on with HPLC instrumentation and detection methods, and other general analytical methods including colorimetric assays

Experience with Waters Empower and/or Dionex Chromeleon chromatography software.

Proficiency in utilizing documentation system to author protocols and reports

Experience participating in teams and collaborative work environments.

Good communication skills (verbal and written), math skills, general computer skills


BS in Science (e.g. Chemistry, Biochemistry, Analytical Chemistry) with 4+ total years of experience working in a related industry

Best Regards,

Akriti Gupta

(973) 967-3409

Morristown, NJ 07960



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