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Ryan C. Rosetti
19811 E Deschutes Avenue, Liberty Lake, WA 99016
Qualifications
• 7 years experience in the QC lab, 5+ years experience in RM group – trained on/understanding of a
majority of raw material tests
• Completed laboratory investigations for unexpected/out-of-specification results – performed analyst
interviews, root cause analysis, human error reduction, correction and preventative actions
• Contact person for manufacturing related investigations – performs testing and able to gauge RM
groups’ ability to provide necessary information for completing investigations
• Validation and/or verifications performed per ICH Q2(R1) and USP <1225> guidelines for a variety of
instruments and procedures including but not limited to: HPLC, GC, FT-IR, NIR, automated and
manual titrations, wet bench
• Filled in for supervisor during materinity leave: Led RM group meetings, kept group informed of
priorities, communicated with manager and other departments as RM group liaison, led QC internal
audit – all while performing normal RM scientist job functions
• Proactive in determining priorities for RM testing and projects – checking production schedule,
SAP/warehouse stock and assessing group availability to complete tasks on time
• Have worked on several high priority projects that have required coordinating with other groups and
departments and scheduling activities for other RM group members
• 2+ years experience on QC lab safety committee – understanding of current lab safety policies and
performed training for new hires specifically on handling hazardous waste and MSDS/SDS
• Active in facility cost-savings functions – manages chemical donation program
• Developed training programs for new RM group hires
• Technical expertise with laboratory equipment – have communicated directly with equipment
vendors/technicians and interpreted information in order to comply with necessary
procedures/specifications (UPLC – Amino Acid Analysis, NIR – identification testing)
• Effective communication with other groups within the lab and throughout the facility – active in CMPR
meetings, served as QC representative on project teams, provided information/test results to project
managers, communicated with QA investigators and tech services representatives
• Trained RM group members on several complicated RM procedures including HPLC, GC, Residual
Solvents, automated titrations
• Point person in the group for developing validation/verification protocols
• Understanding and experience of tasks of other groups including in-process testing, stability testing and
specific tests owned by other groups
Education
B.S. Biochemistry, Western Washington University (WWU) 09/03 to 06/07
Clarkston High School, Clarkston, WA 08/99 to 06/03
Relevant Experience
Scientist IV / Lead Scientist, Raw Materials 05/12 to ------
Scientist I/II/III, Raw Materials 07/09 to 05/12
MTV Scientist, 3rd
Shift, JHS 02/08 to 07/09
Testing of facility water, Nitrogen, diluents, overflow MTV assays, particulates,
Stoppers, stability testing, gave SVP pass-down safety talks
Undergraduate Biochemistry Research, WWU 09/05 to 06/06
Performed wet chemistry, maintained plant cell culture, extracted nucleic acids, ran
electrophoresis gels, reviewed and interpreted technical data, presented technical data.
Employment History
• Scientist I/II/III/IV, Lead Scientist, JHS, Spokane, WA 02/08 to -------
• Pharmaceutical Manufacturing Tech., JHS, Spokane, WA 08/07 to 02/08
• Research Intern, Boise VA Medical Center, Boise, ID 06/05 to 09/05
• Photo Center Specialist, Walmart, Lewiston, ID 06/03 to 12/04
• Lawn Care Provider, Sunset Heights, Clarkston, WA 05/01 to 10/02
• Courtesy Clerk, Albertsons, Clarkston, WA 07/00 to 10/00

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Ryan Rosetti Scientist V resume_1

  • 1. Ryan C. Rosetti 19811 E Deschutes Avenue, Liberty Lake, WA 99016 Qualifications • 7 years experience in the QC lab, 5+ years experience in RM group – trained on/understanding of a majority of raw material tests • Completed laboratory investigations for unexpected/out-of-specification results – performed analyst interviews, root cause analysis, human error reduction, correction and preventative actions • Contact person for manufacturing related investigations – performs testing and able to gauge RM groups’ ability to provide necessary information for completing investigations • Validation and/or verifications performed per ICH Q2(R1) and USP <1225> guidelines for a variety of instruments and procedures including but not limited to: HPLC, GC, FT-IR, NIR, automated and manual titrations, wet bench • Filled in for supervisor during materinity leave: Led RM group meetings, kept group informed of priorities, communicated with manager and other departments as RM group liaison, led QC internal audit – all while performing normal RM scientist job functions • Proactive in determining priorities for RM testing and projects – checking production schedule, SAP/warehouse stock and assessing group availability to complete tasks on time • Have worked on several high priority projects that have required coordinating with other groups and departments and scheduling activities for other RM group members • 2+ years experience on QC lab safety committee – understanding of current lab safety policies and performed training for new hires specifically on handling hazardous waste and MSDS/SDS • Active in facility cost-savings functions – manages chemical donation program • Developed training programs for new RM group hires • Technical expertise with laboratory equipment – have communicated directly with equipment vendors/technicians and interpreted information in order to comply with necessary procedures/specifications (UPLC – Amino Acid Analysis, NIR – identification testing) • Effective communication with other groups within the lab and throughout the facility – active in CMPR meetings, served as QC representative on project teams, provided information/test results to project managers, communicated with QA investigators and tech services representatives • Trained RM group members on several complicated RM procedures including HPLC, GC, Residual Solvents, automated titrations • Point person in the group for developing validation/verification protocols • Understanding and experience of tasks of other groups including in-process testing, stability testing and specific tests owned by other groups Education B.S. Biochemistry, Western Washington University (WWU) 09/03 to 06/07 Clarkston High School, Clarkston, WA 08/99 to 06/03 Relevant Experience Scientist IV / Lead Scientist, Raw Materials 05/12 to ------ Scientist I/II/III, Raw Materials 07/09 to 05/12 MTV Scientist, 3rd Shift, JHS 02/08 to 07/09 Testing of facility water, Nitrogen, diluents, overflow MTV assays, particulates, Stoppers, stability testing, gave SVP pass-down safety talks Undergraduate Biochemistry Research, WWU 09/05 to 06/06 Performed wet chemistry, maintained plant cell culture, extracted nucleic acids, ran electrophoresis gels, reviewed and interpreted technical data, presented technical data. Employment History • Scientist I/II/III/IV, Lead Scientist, JHS, Spokane, WA 02/08 to ------- • Pharmaceutical Manufacturing Tech., JHS, Spokane, WA 08/07 to 02/08 • Research Intern, Boise VA Medical Center, Boise, ID 06/05 to 09/05 • Photo Center Specialist, Walmart, Lewiston, ID 06/03 to 12/04 • Lawn Care Provider, Sunset Heights, Clarkston, WA 05/01 to 10/02
  • 2. • Courtesy Clerk, Albertsons, Clarkston, WA 07/00 to 10/00