4 qa lead jobs at 1 company in Concord, NH

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Research Development Quality Inspection Management Lead (GCP/GVP)
Billerica or Boston
$139k-$209k/yr HybridFull Time
Merck KGaA, Darmstadt, Germany
Merck KGaA, Darmstadt, GermanyFrankfurt Stock Exchange: MRK: A science and technology in healthcare, life sciences, and electronics.
8+ YOERequires 8+ years of QA or relevant experience, including 5+ years in Clinical QA, a scientific bachelor's degree, regulatory inspection experience, drug development knowledge, GxP expertise, and global travel up to 20%.
GCP, GVP, GLP, CAPA, Quality Management System, FDA, EMA, MHRA, PMDA
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Software Quality Assurance Lead Engineer
Manchester, New Hampshire, United States
OnsiteFull Time
Gentex
Gentex: Produces advanced personal protection systems for defense and emergency responders
5+ YOE2+ MgmtBachelor's degree in a relevant computing or engineering field and 5+ years of software QA/testing experience, including embedded systems; leadership, automated testing, CI/CD, and regulated-program experience preferred.
ISO 9001, AS9100, DO-178, MIL-STD-882, Git, Jenkins, GitLab CI, Visure, DOORS, Jira, TestRail, qTest, pytest, Robot Framework, Selenium, Appium, Python, Bash, JTAG, Bluetooth, Wi-Fi, Microsoft Office, iOS, Android, Windows, Mac, Linux
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Research Development Quality Inspection Management Lead (GCP/GVP) (Billerica, Massachusetts, US, 01821)
Billerica or Boston
$139k-$209k/yr HybridFull Time
Merck
MerckXETRA: MRK: A science and technology providing healthcare, life science, and electronics solutions.
8+ YOE8+ years QA experience (≥5 years in Clinical QA), Bachelor’s in a scientific field, experience with MHRA/FDA/EMA/PMDA inspections, knowledge of drug development and GCP/GLP/GVP, willingness to travel globally up to 20%.
1mo
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Research Development Quality Inspection Management Lead (GCP/GVP)
Billerica or Boston
$139k-$209k/yr HybridFull Time
Merck KGaA
Merck KGaAFrankfurt Stock Exchange: MRK: Develops pharmaceutical, life science, and electronics technologies.
8+ YOERequires 8 years of quality assurance or relevant experience, including 5 years in Clinical QA, a scientific bachelor's degree, regulatory inspection experience, and knowledge of drug development and GxP regulations.
GCP, GVP, GLP, FDA, EMA, PMDA, MHRA