Overview
Associate Quality Control Analyst Jobs in Plymouth, MN at Northrop Grumman
MUST HAVES: Validation, Change Control, Technical Writing, Process Mapping
Experience with Medical Device or Pharma is a big plus.
PURPOSE AND SCOPE:
Responsible for representing the sites quality initiatives and compliance objectives in the development of methods, procedures, validations and quality planning for the facility.
EDUCATION:
Bachelor’s Degree required, preferably in Science, Chemistry, or Biology.
EXPERIENCE AND REQUIRED SKILLS:
Minimum of 2-5 years of combined Quality Engineering, process validation required. Pharmaceutical manufacturing, medical
device manufacturing and/or laboratory (organic chemistry, analytical, and/or microbiology) experience preferred. With aMaster’s Degree no prior work experience may be necessary.
Knowledge of process validation (IQ, OQ, PQ), analytical instrumentation, FDA regulatory requirements (GLP/CMP/QSR), Risk
Management / HACCP concepts, statistical process control, and statistical problem solving. Also as applicable, strongknowledge of Health Canada GMP’s.certifications (i.e. ASQ, CQE, CMQ/OE) desired.
Professional auditing certification (ASQ, CQA, RAB, or equivalent) preferred for audit responsibilities.
FMCNA IMPAQ Associate or equivalent (i.e. Six Sigma Green Belt) qualification is preferred; professional quality science
Good verbal and written communication skills to make oral presentations and write technical reports
Job Type: Contract
Pay: $40.41 – $50.00 per hour
Schedule:
Day shift
Experience:
Validation: 5 years (Required)
Change Control: 3 years (Required)
Process Mapping: 3 years (Required)
Ability to Commute:
Oregon, OH 43616 (Required)
Work Location: In person
Show more
Title: Associate Quality Control Analyst
Company: Northrop Grumman
Location: Plymouth, MN
