Summary
Overview
Work History
Education
Skills
Timeline
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Aaron Mom

Oakland,CA

Summary

Highly trained Manufacturing Associate with 7 years experiences in Medical device and Biopharmaceutical . Collaborative Medical Assembler committed to maintaining a clean and safe working environment by complying with company regulations, rules and procedures. Skilled at accurately completing medical device history records and operating various assembling devices such as catheters. Working in a cleanroom environments by follow the CGMP and following all the SOP.

Overview

9
9
years of professional experience

Work History

Manufacturing Associate III

Cepheid
09.2021 - 10.2022
  • Perform assembles of medical device covid test kits within CGMP
  • Follow cleanroom environment procedures
  • Follow all SOP’s
  • Wear proper PPE while performing in the cleanroom
  • Document all lots that’s been worked on the DHR
  • Use tools such as microscope, tweezer, and other handheld tools
  • Operate on automated machines
  • Made sure that products were produced on time and are of good quality.

Manufacturing Technician II

Formfactor
04.2020 - 09.2021
  • Performed functions associated with all prob cards manufacturing operations, including photo-lithography, thin films, plating, assembly, inspection
  • Follow all SOP’s, email any discrepancy to supervisor
  • High power microscope
  • Work in a class 1,000 cleanroom environment
  • Perform job duty in a full bunny suit

Process Technician II

Intarcia Therapeutics
09.2019 - 04.2020
  • Commercial manufacturing and operation teams, a process Technician II is responsible performing and document all work in a pharmaceutical manufacturing environment in accordance with CGMP
  • Clean and sanitize manufacturing equipment and production areas
  • Clean and autoclave parts
  • Set-up, and operate simple to moderately complex manufacturing processes, including component injection filling, spry dying, sub-assembly, and packing and aseptic operations
  • Follow all SOP's, document all work in writing
  • Periodically perform safety inspections
  • Ensure that a safe work environment is maintained at all times.

Quality Control Inspector

ALEMBIC LLC
12.2018 - 09.2019
  • Perform routine inspection under minimal supervision and technical support in prioritizing day to day inspections for production's incoming, in-process, finished goods, packing and sterilization
  • Interpret blueprints/schematics and inspect and test final products to drawings and required standard
  • Measure dimensions of products to verify conformance to specification, using measuring equipment such as rulers, calipers, gauge, optical, micrometer, vision system, Insteon (tensile testing)
  • Manage the team and work with production to improve the process and the work flow
  • Order, review and arrange calibration schedule for equipment used
  • Support R&D and manufacturing engineering through laboratory testing
  • Review documents after inspection to reduce the GMP errors to prevent nonconforming issues
  • Supervise others and provide on-the-job training.
  • Noted trends in product quality and functionality to determine problem areas and plan for improvements to processes.
  • Used hand tools, instruments, gauges and equipment to complete accurate measurements and noted results for official records.

Material Handler

TESLA INC
06.2018 - 12.2018
  • Pick/pull/parts needed for Production and Manufacturing areas
  • Perform cycles counts
  • Work closely with Inventory Control and Quality Control team ensure accuracy and timeless of assigned tasks
  • Identify discrepant materials/components both in writing and verbally to supervisor
  • Evaluate the assembly processes and equipment to look for continuous improvement opportunities
  • Protected company inventory with well-organized and secure storage areas.

Assembler

PENUMBRA INC
02.2015 - 04.2018
  • Assemble Catheter device according to federal QRS, ISO 13485 and SOP manufacturing instruction
  • Working in a cleanroom environment accordance GMP, SOP with minimal supervision
  • (GMP) Good Manufacturing Practices performing on the DHR and production line
  • Document training of personnel in device assembly, document review and date recording
  • Performed verification of manufacturing operation and line clearance for other assemblers.

Dual Rate Supervisor

GRATON RESORT CASINO
09.2013 - 11.2014
  • Monitored behavior of players while dealing cards in various games, observing individuals for possible cheating
  • Observed casino floor and blackjack table for suspicious activity
  • Performed functional game duties quickly by efficiently handling money and chips
  • Explained rules, took bets, and delivered payout to facilitate movement of games
  • Provided gambling chips and coin money in exchange for legal currency for players to join in games
  • Calmed down angry guests or patrons using skills in active listening and positive engagement
  • Communicated with supervisors and managers about suspicious or unruly behavior from patrons
  • Paying out players correctly

Education

Diploma -

Santa Rosa Jr College

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Elsie Allen High School

Skills

  • ISO 13485
  • Calipers
  • Quality Inspection
  • Blueprint Reading
  • Micrometer
  • CGMP
  • Manufacturing
  • Standard Operation Procedures
  • Continuous Quality Improvement (CQI)
  • Dimensional Measurement
  • Digital Multimeters
  • Maintaining Clean Work Areas
  • Dial Calipers
  • Aseptic filling

Timeline

Manufacturing Associate III

Cepheid
09.2021 - 10.2022

Manufacturing Technician II

Formfactor
04.2020 - 09.2021

Process Technician II

Intarcia Therapeutics
09.2019 - 04.2020

Quality Control Inspector

ALEMBIC LLC
12.2018 - 09.2019

Material Handler

TESLA INC
06.2018 - 12.2018

Assembler

PENUMBRA INC
02.2015 - 04.2018

Dual Rate Supervisor

GRATON RESORT CASINO
09.2013 - 11.2014

Diploma -

Santa Rosa Jr College

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Elsie Allen High School
Aaron Mom