Qa Jobs 2026 (Now Hiring) – Smart Auto Apply
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QA Specialist II
Lancesoft
Des Plaines, IL
Title: QA Specialist II and III Location: Des Plaines, IL 60018 Duration: 12 Months Job Description: Responsible for maintaining a strong collaborative partnership with cross-funct...
Posted 2 weeks ago
Data Center QA / QC Manager
Pkaza
Richmond, VA
Data Center QA / QC Manager - Richmond, VA Our client is an established Electrical Contracting Firm that is a leader in the Data Center / Mission Critical Facilities Market. They b...
Posted 30+ days ago
QA Lead
Sterling Foods
Azusa, CA
Quality Assurance Lead Classification: Non-Exempt Reports to: Quality Assurance Manager Summary: This position provides administrative support to the Quality Assurance Department....
Posted 30+ days ago
QA NDT Level II Inspector
Walashek
Norfolk, VA
The QA NDT Level II Inspector is responsible for first-time quality of production work as well as ensuring production personnel conform to local and government procedures and speci...
Posted 30+ days ago
QA Specialist II
LancesoftDes Plaines, IL
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Job Description
Title: QA Specialist II and IIILocation: Des Plaines, IL 60018Duration: 12 MonthsJob Description: Responsible for maintaining a strong collaborative partnership with cross-functional team members that facilitates organizational success for assuring high product quality and meeting business needs. Main Responsibilities:
- Works with a cross functional team to review qualification and validation documents which meet client and regulatory requirements.
- Supports the complete qualification and validation process to implement new manufacturing FUE and automation, process, test method validations in support of a manufacturing expansion.
- Especially in HPLC synthesis, purification and testing. Supports on-market change control projects.
- Bachelor s degree in Life Science;Engineering;or closely related discipline is required OR relevant combination of education or experience.
- At least 5 years work experience in Quality or related field experience;Has a history of completing successful projects and driving positive compliance outcomes.
- Bachelor's or master s degree in one of the following Engineering disciplines: Chemical, Electrical, Bio-medical, or Mechanical
- 5+ years of relative professional work experience in Medical Device Quality/Pharmaceutical or in a regulated industry
- Detailed knowledge of FDA, GMP, ISO 13485, and ISO 14971
- Strong technical writing skills;Polished verbal and written communication skills
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