Daniel Hill Email & Phone Number

Ferndale, Mi, Us

Responsible for oversight/direction of processes realted to incoming raw material sampling, raw material testing, pre-mix and blend testing, finished product dosage form testing, marketed stability product testing and administration, AR&D testing and EHS program.

Analyze systems and suggest/coordinate improvements in1. QC Chemistry Lab (Stability, RM, FG, AR&D)2. QC Lab Admin (RM and Component Sampling)Set up continuous improvement program for above departments.

[formerly ALPHARMA USPD INC. / A.L. PHARMA / BARRE-NATIONAL INC. / NASKA PHARMACAL CO., INC.]Lincolnton, NCResponsible for analyzing systems and suggesting improvements within the Quality Affairs department, including the marketed product stability system; assisting QA Specialists in the performance of their duties; and coordinating the inventorying and shipment of controlled drug substances to a reverse distributor for destruction. Led investigations into non-conformances dealing with the marketed product stability system; wrote investigational report for approval by senior management; audited data for the marketed product stability program; collected, organized and presented monthly facility metrics to site management; and reviewed and approved Master Manufacturing Records and Packaging Records.

[formerly ALPHARMA USPD INC. / A.L. PHARMA / BARRE-NATIONAL INC. / NASKA PHARMACAL CO., INC.]Lincolnton, NCCoordination of quality improvement efforts across the site in response to FDA observations across the US business unit; set up teams, attended department meetings, interacted with every department regarding goals, brainstorming, actions plans, implementation and measurement. Reported progress to site management.

[formerly ALPHARMA USPD INC. / A.L. PHARMA / BARRE-NATIONAL INC. / NASKA PHARMACAL CO., INC.]Lincolnton, NC Oversight of batch record review, real-time auditing/inspections of manufacturing, labeling, document control, batch review and release and exception/deviation/non-conformance system.

[formerly NASKA PHARMACAL CO., INC.]Lincolnton, NCCoordinated chemical testing and approved all drug product raw material, in-process material, finished product and stability sample analytical data; provided direction to Methods Development team; evaluated and purchased all laboratory equipment; interacted with drug product stability program manager.

[formerly NASKA PHARMACAL CO., INC.]Lincolnton, NCSupervised and coordinated all quality operations, including document control, chemistry, microbiology, labeling, stability, technical services and site compliance. Assisted Regulatory Affairs in ANDA submissions. Reviewed and approved all departmental SOPs and process validation protocols.

Lincolnton, NCSupervised twenty (20) employees in Raw Material, Finished Product and Stability testing. Assisted in and Methods Development strategy.

Hauppauge, NYSupervised eight (8) employees in Raw Materials, Finished Product, and Stability testing.

Springfield Gardens, NYFinished product and stability testing of solid dose pharmaceuticals per USP. Extensive working knowledge of HPLC, GC, UV, IR.

New Rochelle, NYTaught all levels of HS mathematics, science, and computer programming.

M.S., Organic Chemistry

B.S., Chemistry