Job Description Help for Job Description. Opens a new window. USpharma LTD seeks Senior Quality Control Chemist w/Masters in Industrial Pharm, Sci or rltd & 2 yrs of exp in pharmaceutical qlty contrl functs & Analyt R D acts. Demonstrate expertise in analyt methods dvlpmt, verifiy, validate, & method transfer include forced degradation studies & drug excipient compatibility studies, dissolution test (apparatus I-V), stability studies, & clean verif. Lead & doc investigations for OOS, OOT, deviations, & CAPA using structured root cause analy methods, include DMAIC. Provide qlty & tech supp for regulatory submissions & regulatory inspections in compliance w/ FDA, DEA, & cGMP guidelines. Prepare & present coml product qlty reps in Site QC meetings. Ensure the integrity, accuracy, & completeness of laboratory data in accordance w/ ALCOA principles & current good mfg Practices (cGMP).
Work loc:
Miami Lakes, FL. Mail resumes to 13900, NW 57th CT, Miami Lakes, FL-33014 (OR) e-mail: jasiel.piloto@uspharmaltd.com