Daniel Hill Email and Phone Number
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Quality Control/Assurance professional with experience in solid-, liquid-, and semisolid- (including suppository) dose pharmaceutical operations, including ANDA submissions. Thirty-two-plus years of supervisory experience; solid knowledge of cGMPs; first-hand experience with FDA inspections; knowledge in chemical, microbiological, and operational quality functions; ability to adapt to new situations/learn quickly; and ability to lead as well as be a member of a team within the organization.Specialties: Annual Product Reviews, Auditing, Technical writing, CDS Management, Metrics, Chemistry, Laboratory Management, Quality Operations Management, cGMPs (210/211)
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Vice PresidentFerndale Laboratories, Inc. Sep 2018 - PresentFerndale, Mi, Us -
Director, Technical Compliance ManagementWest-Ward Pharmaceuticals Feb 2017 - Aug 2018
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Director, Quality Control LaboratoriesWest-Ward Pharmaceuticals Oct 2011 - Jan 2017Responsible 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.
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Director, Quality Control Compliance ImprovementWest-Ward Pharmaceuticals Jun 2011 - Sep 2011Analyze 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.
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Quality Affairs Project ManagerActavis Mid Atlantic Llc 2008 - 2011[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.
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Quality Improvement Project ManagerActavis Mid Atlantic Llc 2006 - 2008[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.
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Quality Operations ManagerActavis Mid Atlantic Llc 2000 - 2005[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.
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Qc Laboratory ManagerAlpharma Uspd Inc. / A.L. Pharma / Barre-National Inc. 1996 - 2000[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.
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Director Of QualityBarre-National Inc. 1992 - 1996[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.
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Quality Control Laboratory ManagerNaska Pharmacal Co., Inc. 1990 - 1992Lincolnton, NCSupervised twenty (20) employees in Raw Material, Finished Product and Stability testing. Assisted in and Methods Development strategy.
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Quality Control Chemistry Team LeaderNaska Pharmacal Co., Inc. 1988 - 1990Hauppauge, NYSupervised eight (8) employees in Raw Materials, Finished Product, and Stability testing.
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ChemistVitarine Pharmaceuticals 1987 - 1988Springfield Gardens, NYFinished product and stability testing of solid dose pharmaceuticals per USP. Extensive working knowledge of HPLC, GC, UV, IR.
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TeacherSalesian High School 1982 - 1987New Rochelle, NYTaught all levels of HS mathematics, science, and computer programming.
Daniel Hill Skills
Daniel Hill Education Details
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St. John'S UniversityOrganic Chemistry -
Manhattan UniversityChemistry
Frequently Asked Questions about Daniel Hill
What company does Daniel Hill work for?
Daniel Hill works for Ferndale Laboratories, Inc.
What is Daniel Hill's role at the current company?
Daniel Hill's current role is Vice President of Quality Control at Ferndale Laboratories, Inc..
What is Daniel Hill's email address?
Daniel Hill's email address is dm****@****ine.net
What is Daniel Hill's direct phone number?
Daniel Hill's direct phone number is +173254*****
What schools did Daniel Hill attend?
Daniel Hill attended St. John's University, Manhattan University.
What skills is Daniel Hill known for?
Daniel Hill has skills like Gmp, Quality Assurance, Hplc, Regulatory Affairs, Chemistry, Validation, Pharmaceutical Industry, Fda, V&v, Capa, Laboratory, Auditing.
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