Other
Scientist II
Artech Information System LLC
SmartRecruiters
- Location
- Swiftwater, PA, United States, United States
- Type
- Contract
- Salary
- Salary not specified
- Posted
- 17 Feb 2016
Artech is the 10th Largest IT Staffing Company in the US, according to Staffing Industry Analysts' 2012 annual report. Artech provides technical expertise to fill gaps in clients' immediate skill-sets availability, deliver emerging technology skill-sets, refresh existing skill base, allow for flexibility in project planning and execution phases, and provide budgeting/financial flexibility by offering contingent labor as a variable cost. 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
Artech is the 10th Largest IT Staffing Company in the US, according to Staffing Industry Analysts' 2012 annual report. Artech provides technical expertise to fill gaps in clients' immediate skill-sets availability, deliver emerging technology skill-sets, refresh existing skill base, allow for flexibility in project planning and execution phases, and provide budgeting/financial flexibility by offering contingent labor as a variable cost. 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