Carlos Bonilla is a eficient professional, working in Gsk on the position of Program Manager from 2018. Carlos gained professional experience in more than 13 positions at various companies. Carlos Bonilla went to the Broward College and got education there from 2004 to 2006. Hollywood, Florida is the city, where this expert was lastly known to settle. The professional's contacts can be easily accessed through SoftwareOfficial by request.
Name variants:
Carlos Bonilla
Last updated Jul 05, 2024
Contact Information
Last Update
Jul 6, 2022
Email
ca**@hotmail.com
Location
Hollywood, FL
Company
Gsk
Workplace
Program Manager
Work History
Remmediation Engineer and Team Lead
New York, NY
Responsible for technical writing of Batch Records, SOPs and other documents in support of the site remediation effort.
Jul 2017 — Jan 2018
Batch Assessment Consultant
Conducted retrospective review of product Batch Records, Laboratory data and Deviations. The review was detailed in an Assessment Report including disposition recommendations for each batch.
Jan 2017 — Jun 2017
Quality Systems Project Lead
Currently leading the site deployment of FreeWeigh system for packaging operations; and managing the implementation of Navigation software updates to interface with CERPS for processing ship...
Apr 2015 — Dec 2016
Document Control Sme Consultant
325 Paramount Dr, Raynham, MA 02767
Successfully deployed incremental enhancements to the Change Control and Document Control systems as an integral part of their Quality Systems remediation efforts.
Sep 1, 2013 — Apr 2015
Batch Record Review Sme and Team Lead
475 Sansome St SUITE 570, San Francisco, CA 94111
Consultant: Batch Record Review SME and Team Lead for Patheon's manufacturing plant of soft gelatin capsules at Mexico City, Mexico. Team lead for a cross-functional team who evaluated Quali...
Jan 2013 — Jul 2013
Manager, Quality Assurance
609-2 Cantiague Rock Rd, Westbury, NY 11590
Managed Document Control, Change Control, Annual Product Reviews, Deviation Investigations, CAPA, Materials Disposition, Internal Audits, Customer and Regulatory Inspections, GMP Training, a...
Sep 2011 — Mar 2013
Associate Director, Quality Services
Managed the Document Control, Technical Writing and Change Management departments composed of 18 full time employees (FTE). Ensured compliant and timely implementation of proposed changes to...
May 2008 — Jun 2011
Manager, Change Control
Managed the Technical Writing and Change Management teams composed of nine FTE. Ensured compliant and successful implementation of proposed changes to controlled documentation, validated sys...
Aug 2007 — May 2008
Senior Quality Assurance Specialist
Investigated process / system deviations. Identified root cause and trends in conjunction with subject matter experts to determine appropriate corrective and preventive actions (CAPA). Gener...
Apr 2004 — Aug 2007
Supervisor, Qa In-Process
Supervised 1st and 2nd shift staff composed of 17 QA in-process inspectors. Ensured manufacturing and packaging rooms and equipments were inspected and released according to SOPs and cGMP. S...
2003 — 2004
Supervisor, Qa Materials Disposition
Supervised daily activities of the QA Materials Disposition group composed of 10 QA auditors and 1 administrative assistant. Scheduled workload for all auditors in a fast paced environment b...
2002 — 2003
Quality Assurance Auditor
Audited manufacturing batch records, QC testing results, and Process Validation / Evaluation protocols and reports.
2001 — 2002
Education
2004 — 2006
Occupations
Executive
Program Director
Team Leader
Engineer
Operations Manager
Skills
Capa
Gmp
Fda
Change Control
Validation
Quality System
Quality Assurance
Sop
Pharmaceutical Industry
V&V
21 Cfr Part 11
Deviations
Cleaning Validation
Document Management
Glp
Regulatory Affairs
Quality Auditing
Regulatory Requirements
Root Cause Analysis
Lean Manufacturing
Manufacturing
Pharmaceutics
Software Documentation
Computer System Validation
Technology Transfer
Gxp
Medical Devices
Technical Writing
Trackwise
Biopharmaceuticals
Microsoft Office
Operational Excellence
Lims
Internal Audit
Sop Development
Team Leadership
Key Performance Indicators
Iso 13485
Performance Management
Fmea
Aseptic Processing
Regulatory Submissions
Manufacturing Operations Management
Jde Enterprise One
Qumas
Livelink
Solid Oral Dosage Forms
Oracle Agile Plm
Oracle E Business Suite
Deviations Investigation
FAQs about Carlos Bonilla
What's the main profession of Carlos Bonilla?
The expert is a Program Manager.
What jobs is Carlos a professional at?
Carlos Bonilla is a professional such jobs as Executive and Program Director.
Where does Carlos Bonilla currently live?
Hollywood, Florida is the place where Carlos Bonilla currently lives
Does the professional have the email address?
ca**@hotmail.com is Carlos Bonilla's email address.
How many companies did Carlos Bonilla work at?
The professional worked at 13 jobs.
What education does Carlos Bonilla have?
Carlos studied at the Broward College from 2004 to 2006.
What languages does Carlos Bonilla speak?
Carlos Bonilla speaks English and Spanish.
What is the industry that Carlos Bonilla is connected to?
This person works in Pharmaceuticals industry.