Associate Quality Engineer

RedBrick Staffing

Irvine (CA)

On-site

USD 60,000 - 85,000

Full time

9 days ago

Get more replies from employers

Send a job-specific resume in minutes.

Job summary

RedBrick Staffing is seeking a technically minded QA/Regulated Documentation Assistant in Irvine, CA to support quality systems and manufacturing documentation in a fast-paced medical device environment.

You will draft and route quality records, assist CAPA investigations, and maintain controlled documents within the eQMS, ensuring compliance with ISO 13485 and FDA regulations. This role offers growth opportunities and on-site collaboration with cross-functional teams in a regulated setting.

Qualifications

  • Bachelor's degree in Engineering or a related field.
  • 1+ years of relevant industry experience.
  • Comfortable in a regulated environment (ISO 13485, 21 CFR Part 820/QMSR, 21 CFR Part 1271).
  • Self-driven and a team player with an eagerness to develop professionally.
  • Ability to help support cross-functionally.

Responsibilities

  • Draft & route NCRs from cradle to grave.
  • Support CAPA investigations.
  • Assist doc control in our eQMS: COs, periodic reviews, DMR/DHF filing.
  • Support internal audits.
  • Assist CMO process development: document technical reviews, track open items.
  • Support process validation (IQ/OQ/PQ): protocol execution, data collection, report creation.
  • Develop & maintain instructions & mfg. procedures.
  • Support incoming inspection & FPL upkeep.
  • Support DDFs.
  • Other duties as assigned.

Skills

Regulated environment experience
Team collaboration
Documentation skills

Education

Bachelor's degree in Engineering or similar

Tools

eQMS

Job description

  • Draft & route NCRs - from cradle to grave
  • Support CAPA investigations
  • Support doc control in our eQMS: COs, periodic reviews, DMR/DHF filing
  • Support internal audits
  • Support CMO process development: document technical reviews, track open items
  • Support process validation (IQ/OQ/PQ): protocol execution, data collection, report creation
  • Develop & maintain instructions & mfg. procedures
  • Support incoming inspection & FPL upkeep
  • Support DDFs
  • Other duties as assigned
Job Requirements:
  • Bachelor's degree in Engineering or similar
  • 1+ years of relevant industry experience
  • Comfortable working within a regulated environment (ISO 13485, 21 CFR Part 820/QMSR, 21 CFR Part 1271)
  • Self-driven and team player, eager to develop in your professional career
  • Ability to help support cross-functionally
Get your free, confidential resume review.
or drag and drop your file here.
Similar jobs

Similar jobs worth comparing

Quality Assurance Specialist II
Quality Assurance Specialist II

REVA Medical, Inc. • San Diego (CA)

On-site
USD 90,000 - 130,000
Sr. Quality Engineer
Sr. Quality Engineer

Katalyst CRO • Little Rock (AR)

On-site
USD 75,000 - 95,000
Quality Assurance Associate
Quality Assurance Associate

REVA Medical, Inc. • San Diego (CA)

On-site
USD 60,000 - 85,000
Quality Engineer - 205417
Quality Engineer - 205417

Medix™ • Minneapolis (MN)

On-site
USD 70,000 - 90,000
Quality Assurance Associate
Quality Assurance Associate

Spectrum Staffing Services/HRStaffers Inc. • Monroe (NJ)

On-site
USD 60,000 - 80,000
Quality Engineer
Quality Engineer

Cypress HCM • Irvine (CA)

On-site
USD 80,000 - 100,000
Sr Quality Engineer
Sr Quality Engineer

Katalyst CRO • Austin (TX)

On-site
USD 80,000 - 100,000
Quality Engineer
Quality Engineer

Innovative Health LLC • Scottsdale (AZ)

On-site
USD 75,000 - 98,000
Quality Engineer
Quality Engineer

Valid8 Financial, Inc. • Oak Creek (WI)

On-site
USD 70,000 - 95,000
Associate, Quality Engineering (ID: 1212)
Associate, Quality Engineering (ID: 1212)

Narda-MITEQ • Hauppauge (NY)

On-site
USD <1,000