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Quality Lab Technician


Dover, DE, US

Req ID:  440
Job Type: 

We are a global team of 6000 visionaries, doers, and makers. Our portfolio of over 25 brands touches lives in more than 50 countries. Together, we reimagine good mornings and endless summers, beauty and bonding, confidence and determination.


Position Summary:

Work in a cGMP laboratory performing sampling and testing of incoming raw materials and components. Work on routine and non-routine laboratory projects as directed by Quality Laboratory Management. 



  • Perform sampling and testing for raw materials, components, and special projects using a variety of measurement techniques.
  • Follow cGMP and 21CFR 820 requirements for laboratory testing and investigations.
  • Collaborate with internal and cross functional colleagues to assure inspections are completed on time
  • Manage material flow in conjunction with Planning and Scheduling.
  • Follow SOPs and test methods.
  • Maintain 5S standards in the lab.
  • Must display accuracy and attention to detail while completing inspections and documenting results with minimal errors.
  • Support laboratory supervisor in OOS investigations. Compiles data and participate in different steps of the investigation process.
  • Must be willing to work overtime as needed.
  • Work on non-routine projects as directed by the laboratory supervisor
  • Perform job duties in a compliant and safe manner
  • Adhere to testing and projects deadlines as assigned by quality laboratory management
  • Adhere to 5 S standards in the laboratory.
  • Escalate non-conformances and Out of Specification results in a timely manner and in accordance to local and corporate procedures.
  • Keep up with laboratory productivity standards.
  • Adhere to the designated work schedule.


Required Education, Skills and Experience

  • Associate degree or high school diploma, or equivalent experience.
  • Must be able to work with minimum supervision.
  • Effective verbal / written communication, interpersonal, and team-building skills.
  • Excellent organizational, problem-solving, prioritizing and follow-up skills.
  • Ability to handle multiple tasks / projects simultaneously.
  • Good computer skills. Proficiency with Microsoft Word, Excel, and Power Point.
  • Must be able to learn and work with computer software such as SAP, OGP, spreadsheets.
  • Must be willing to occasionally work OT as needed.
  • 0 to 1+ year of experience working in a cGMP laboratory


Desirable Education, Skills and Experience

  • Experience working in a FDA regulated laboratory.
  • Working knowledge of SAP.
  • Working knowledge of FDA 21 CFR part 820, 210 and 211 requirements.
  • Working knowledge of Canadian Medical Device Regulations SOR/98-282
  • Working knowledge of ISO 13485 and 14971 requirements

Edgewell is an equal opportunity employer, and we prohibit discrimination based on age, color, disability, marital or parental status, national origin, race, religion, sex, sexual orientation, gender identity, veteran status or any other legally protected status in accordance with applicable federal, state and local laws.


Nearest Major Market: Delaware
Nearest Secondary Market: Dover