Jessica Gillis

Validation Engineer Iii

Jessica Gillis is a qualified professional, who works in Organogenesis Inc main office of which is in 463. on the position of Validation Engineer Iii since 2020. Jessica has earned professional experience in more than 16 positions at various companies. Jessica Gillis went to the Norwich University and received education there from 1997 to 2001. Nashua, New Hampshire is the city, where the professional was lastly known to be located. Their phone and email are accessed through this website on demand.
Name variants:
Jess Gillis, Jessie Gillis
Last updated May 25, 2024

Contact Information

Last Update
Jul 8, 2022
Email
je**@gmail.com, jg**@angiodynamics.com
Location
Nashua, NH
Company
Organogenesis Inc.

Workplace

Validation Engineer Iii

Work History

Validation Engineer Iii

150 Dan Rd, Canton, MA 02021
from Feb 2020

Contract Qa Validation Engineer Ii

from Oct 2019

Validation Specialist Ii

1001 Pawtucket Blvd west, Lowell, MA 01854
Responsible for executing all phases of validation qualification protocols at customer locations. Provide Growth Direct System operational training in a way that meets or exceeds customer ex...
from Mar 2018

Senior Quality and Capa Engineer Consultant

Support facilities and calibration teams with backlog of Nonconformances, CAPAs and equipment assessments. Managed team meetings for follow-up activities on corrective and preventative actio...
Apr 2017 — Dec 2017

Quality Manager

13161 west Glendale Ave, Butler, WI 53007
Dec 2016 — Mar 2017

Senior Validation Engineer

1 Amgen Center Dr, Thousand Oaks, CA 91320
Serve as a consultant for Validation deliverables during plant outage and quality control test method transfer. Responsible for qualification and validation of laboratory equipment and manuf...
Aug 2016 — Oct 2016

Senior Design Assurance Engineer

14 Plaza Dr, Latham, NY
Dec 2015 — Aug 2016

Senior Design Quality Engineer

Support product development teams throughout the development process. Evaluate verification and validation protocols and reports to ensure compliance to external standards and internal stand...
Dec 2014 — Nov 2015

Quality Manager

12 Murphy Dr, Nashua, NH 03062
Jul 2013 — Dec 2014

Biocompatibility Engineer

920 Winter St, Waltham, MA 02451
Apr 2013 — Jul 2013

Corporate Quality Validation Engineer Ii

50 Binney St, Cambridge, MA 02142
Oct 2011 — Apr 2013

Contract Validation

121 Seaport Blvd, Boston, MA 02210
Responsible for qualification and validation of laboratory equipment and manufacturing equipment for the startup of a new facility. Executed Factory Acceptance Test protocols, Commissioning ...
Sep 2007 — Nov 2007

Contract Microbiologist

3501 Tricenter Blvd SUITE C, Durham, NC 27713
Responsible for qualification, routine maintenance, validation, and calibration of laboratory equipment. Performed steam sterilization, single medical device and reusable device testing incl...
Jan 2007 — Sep 2007

Quality Assurance Associate

170 Locke Dr, Marlborough, MA 01752
Responsible for the control of batch records, SOP’s, technical reports, protocols, stability reports, etc. Conducted training programs, data and Batch Record reviews, and analysis. Assured t...
2005 — 2006

Qc Microbiologist

5 Warehouse Ln, Elmsford, NY 10523
Responsible for sampling water from various points within the production area. Tested samples for E. coli, pseudomonas, yeast, and mold. Performed standard method agar plating for growth cou...
2004 — 2005

Research and Development Assistant

3 Highwood Dr, Tewksbury, MA 01876
Reported directly to the director of Medical Development and Research and liason between clinical sites. Collected clinical data, compile documentation, review medical records, review and pr...
Mar 2001 — Mar 2004

Occupations

Scientist
Biotechnology Professional
Engineer
Biologist
Biological Scientist

Skills

Gmp
Validation
Capa
Fda
Quality System
21 Cfr Part 11
V&V
Sop
Quality Assurance
Trackwise
Biopharmaceuticals
Biotechnology
Quality Control
Pharmaceutical Industry
Microsoft Office
Microsoft Excel
Quality Auditing
Aseptic Technique
Process Engineering
Equipment Qualification
Computer System Validation
Root Cause Analysis
Medical Devices
Change Control
Glp
Kaye Validator
Kaye Val Probes
Mesa Labs Datatraces
Qualification Development
R&D
Lives Dataloggers
Iso 13485
Calibration
Documentation
Technology Transfer
Autoclave
Hvac
Process Control
Process Verification
Commissioning
Development Design
Microbiology
Inoculation
Problem Solving
Manufacturing
Iso
Aseptic Processing
Lims
Login