al****@ab****.com & 3531435****

Alice Davis

Experienced Quality Assurance/Quality Control Specialist with a demonstrated history of working in the pharmaceuticals industry. Strong operations professional... | Ireland

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Alice Davis’s Emails al****@ab****.com

Alice Davis’s Phone Numbers 3531435****

Social Media

Alice Davis’s Location Ireland

Alice Davis’s Expertise Experienced Quality Assurance/Quality Control Specialist with a demonstrated history of working in the pharmaceuticals industry. Strong operations professional skilled in U.S. Food and Drug Administration (FDA), HPRA Inspections, Regulatory requirements and GMP. Currently responsible for all QC Incoming Inspection and release of packaging, manufacturing and components for the Biologics and Paharamceutical Sites. I am also responsible for Supplier Qualification Management activities at the site, including but not limited to Vendor Qualification, Approved Supplier Listing, Vendor Performance Review and Associated Sampling Plans. I am also responsible for the annual review of Defect Sets, review and approval of Defects sets and the lifecycle and management of Defect sets. These Defect sets are used as part of Qualification and Requalification of Operators and QC for Visual Inspection. I work closely with the Business Units on the setting up of these processes and procedures.

Alice Davis’s Current Industry Allergan

Alice Davis’s Prior Industry
Allergan Pharmaceuticals | Allergan

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Work Experience

Allergan

Senior Qc Manager Allergan Pharmaceuticals Westport Ireland

Sun Jan 01 2017 00:00:00 GMT+0000 (Coordinated Universal Time) — Present

Allergan

Qa Professional Supporting Botox Manufacturing

Sun Nov 01 2015 00:00:00 GMT+0000 (Coordinated Universal Time) — Sun Jan 01 2017 00:00:00 GMT+0000 (Coordinated Universal Time)

Allergan

Qc Team Lead

Sun Feb 01 2015 00:00:00 GMT+0000 (Coordinated Universal Time) — Sun Nov 01 2015 00:00:00 GMT+0000 (Coordinated Universal Time)

Allergan Pharmaceuticals

Quality Officer Gpdc

Sat Feb 01 2014 00:00:00 GMT+0000 (Coordinated Universal Time) — Sun Feb 01 2015 00:00:00 GMT+0000 (Coordinated Universal Time)

Allergan Pharmaceuticals

Qa Compliance Coordinator

Wed Sep 01 2010 00:00:00 GMT+0000 (Coordinated Universal Time) — Sat Feb 01 2014 00:00:00 GMT+0000 (Coordinated Universal Time)

Allergan Pharmaceuticals

Lab Compliance Coordinator

Fri Feb 01 2008 00:00:00 GMT+0000 (Coordinated Universal Time) — Wed Sep 01 2010 00:00:00 GMT+0000 (Coordinated Universal Time)

Allergan Pharmaceuticals

Laboratory Information Management System (Lims) Software Validation Technician

Thu Feb 01 2007 00:00:00 GMT+0000 (Coordinated Universal Time) — Fri Feb 01 2008 00:00:00 GMT+0000 (Coordinated Universal Time)

Allergan Pharmaceuticals

Microbiology Quality Control Technician & Senior Technician On The Batch Release Team

Fri Nov 01 2002 00:00:00 GMT+0000 (Coordinated Universal Time) — Thu Feb 01 2007 00:00:00 GMT+0000 (Coordinated Universal Time)

Skills

Languages

Alice Davis Email Addresses

al****@ab****.com Work Email

al****@ab****.com Personal Email

al****@al****.com Personal Email

Alice Davis Phone Number

3531435**** Phone number

FAQ About Alice Davis

Alice Davis is located at
Ireland

Alice Davis is a
Experienced Quality Assurance/Quality Control Specialist with a demonstrated history of working in the pharmaceuticals industry. Strong operations professional skilled in U.S. Food and Drug Administration (FDA), HPRA Inspections, Regulatory requirements and GMP. Currently responsible for all QC Incoming Inspection and release of packaging, manufacturing and components for the Biologics and Paharamceutical Sites. I am also responsible for Supplier Qualification Management activities at the site, including but not limited to Vendor Qualification, Approved Supplier Listing, Vendor Performance Review and Associated Sampling Plans. I am also responsible for the annual review of Defect Sets, review and approval of Defects sets and the lifecycle and management of Defect sets. These Defect sets are used as part of Qualification and Requalification of Operators and QC for Visual Inspection. I work closely with the Business Units on the setting up of these processes and procedures. Allergan

Alice Davis currently works in the
Allergan

Alice Davis specializes in
Experienced Quality Assurance/Quality Control Specialist with a demonstrated history of working in the pharmaceuticals industry. Strong operations professional skilled in U.S. Food and Drug Administration (FDA), HPRA Inspections, Regulatory requirements and GMP. Currently responsible for all QC Incoming Inspection and release of packaging, manufacturing and components for the Biologics and Paharamceutical Sites. I am also responsible for Supplier Qualification Management activities at the site, including but not limited to Vendor Qualification, Approved Supplier Listing, Vendor Performance Review and Associated Sampling Plans. I am also responsible for the annual review of Defect Sets, review and approval of Defects sets and the lifecycle and management of Defect sets. These Defect sets are used as part of Qualification and Requalification of Operators and QC for Visual Inspection. I work closely with the Business Units on the setting up of these processes and procedures.

Alice Davis speaks the following languages:
No languages available.

Alice Davis has prior experience in the following industries:
Allergan , Allergan , Allergan Pharmaceuticals , Allergan Pharmaceuticals , Allergan Pharmaceuticals , Allergan Pharmaceuticals , Allergan Pharmaceuticals

Alice Davis has the following professional experience:
Allergan , Allergan , Allergan , Allergan Pharmaceuticals , Allergan Pharmaceuticals , Allergan Pharmaceuticals , Allergan Pharmaceuticals , Allergan Pharmaceuticals .