rony joseph

consultant

Country

united states

City

budd lake

Industry

pharmaceuticals

Skill

change control, gmp, sop, 21 cfr part 11, pharmaceutical industry, fda, validation, v&v, gxp, lims, capa, aseptic processing, glp, protocol, management, biotechnology, computer system validation, quality assurance, quality system, analytical chemistry, hplc, regulatory affairs, business process improvement, technology transfer, quality control, software documentation, chromatography, vaccines, standard operating procedure, windows server, hematology, biopharmaceuticals, cleaning validation, regulatory requirements, pharmaceutics, regulatory submissions, laboratory, quality auditing, clinical development, formulation, clinical trials, gcp, lifesciences, pharmacovigilance, gas chromatography, trackwise, purification, calibration, cro, uv/vis

Experience

manager lab operations qc chemistry and biochemistry

pfizer

2001-1 - 2006-1 · 5 yrs 1 mo

team leader lab operations

pfizer

1996-1 - 2001-1 · 5 yrs 1 mo

senior analytical chemist

pfizer

1995-1 - 1996-1 · 1 yr 1 mo

senior analytical chemist

biocraft laboratories

1992-1 - 1995-1 · 3 yrs 1 mo

manager technical services, biotechnology

pfizer

2006-1 - 2012-12 · 7 yrs

scientist and metrologist

teva pharmaceuticals

2013-1 - 2015-9 · 2 yrs 9 mos

consultant

validant

2015-10 - Present · 11 yrs

Validant provides quality, manufacturing, engineering, and regulatory compliance expertise to biotechnology, pharmaceutical and medical device companies. We tailor our services to each client's unique needs by drawing on a broad portfolio that includes strategic consulting, program leadership, on-demand expertise, managed solutions and execution.