Quality Control Maintenance

Jonaira Moore

Objective: I desire a position where there is an opportunity for career

development and growth, and a chance to contribute to society through using

my skills in sterile laboratory practices and exhibiting my dedication to

the greater good.

Summary of Expertise:

Cell Culture Environmental Nova Bioanalyzer

Clean Room Monitoring

Aseptic Technique DNA isolation Vicell

Media Prep Organization Delta VMCS

Buffer Prep Planning JD Edwards MFG

Seeding Training Based Computer

Expansion Documentation Systems

Harvesting Communication Pilot Planting

Transformations GMP Compliance

Serial Dilutions FDA Compliance

Process Improvements SOP Revisions

Employment:

2009 Twin Imaging Technology

Oceanside, Ca

Document Control Assistant

. Core responsibilities: Support the establishment,

distribution, maintenance and filing of documents received

during the course of the project

. Other Responsibilities: Scanning, indexing and archiving

various documents for converting to client files

. Any other necessary administrative support to various

activities and projects

2006-2008 Genentech, Inc Oceanside, Ca

Manufacturing Bioprocess Associate

. Core responsibilities: Being part of a world-class team

that produces innovative bio-therapeutic medicines for

patients with serious or life-threatening medical

conditions.

. Other Responsibilities: Maintaining the highest priority

in safety and GMP compliance inside a clean room

environment, cleaning, sterilizing and operating

bioreactors, centrifuges: troubleshooting equipment and

process issues; cell culture seeding, growth, expansion,

and harvesting; adhering to SOP's and clean room aseptic

techniques; reviewing and revising documentation and

reviewing calculations (e.g. tickets, logbooks, labels,

equipment readings); routine environmental monitoring of

facility and equipment: assisting in process improvements;

and operating computer systems for process control data

entry, performed QC environmental sampling and training,

and participation in staff and shift change meetings as

well as assisting with calibration scheduling and

maintenance PMs; Ordered documents and SOP revisions from

doc control

2002-2005 Invitrogen Corporation Carlsbad, Ca

Product Team Technician, Competent Cells

. Responsibilities include: Working in a team based

environment to manufacture molecular biology products;

adhering closely to SOP's involving material measurement,

equipment operation, maintenance; documentation;

maintaining inventory of products and raw materials; cell

culture media batching, seeding, expansion, harvesting,

labeling, freezing, and packaging of product; completion of

production and quality control testing of reagents,

components, and finished product in accordance with written

standards, within a challenging production schedule;

training and guidance of other team members on technique,

processes, and computer applications; completion of daily

process and other paperwork (i.e. batch records, inventory,

sterilization, kitting etc.)

Education:

1996-2000 Dillard University New Orleans, LA

Biology

. Completed coursework towards a B.S. in biology

Language: Proficient in reading, writing, and speaking Spanish

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