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Quality Analysis1

Lowell,MA

1004 Quality Analysis1 jobs in Lowell,MA

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Quality Assurance Data Analyst

Corning - Tewksbury, MA

Corning - Tewksbury, MA

Quality Assurance Data Analyst
~ 16 min OnsiteHealth InsurancePaid Time OffRetirement Benefit
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Quality Assurance (QA) Inspector

SynQor

Salem, NH 03079

~ 29 min Onsite

  • Working knowledge of IPC-A-610 Class 2 & Class 3 standards.
  • Familiarity with IPC-A-620 and J-STD-001 inspection criteria.
  • Basic computer skills.
  • Ability to read & communicate in English
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Quality Assurance Manager II

General Atomics

Acton, MA 01720

~ 18 min Onsite

  • Typically requires a bachelor's in engineering or a related technical field as well as nine or more years of progressively complex QA experience. May substitute equivalent experience in lieu of education.
  • Must demonstrate detailed and extensive working knowledge and understanding of QA principles, concepts, theories, regulations and practices; extensive knowledge of ISO 9001:2015 and AS9100
  • Work on a self-initiated basis and in a team environment and be able to work extended hours and travel as required.
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New, Posted 16 hours ago
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Quality Manager - Manufacturing

Hoerbiger

Harvard, MA 01451

$95,000-$130,000/yr
Flexible Schedule
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Quality Specialist/Technical Writer

Teledyne

Billerica, MA 01821

~ 20 min Onsite

  • Bachelor's degree from an accredited institution
  • Proficient in Microsoft Office Suite (Word, Excel, PowerPoint)
  • Good technical writing skills
  • U.S. citizen
  • U.S. national
  • Legal permanent resident
  • Asylee
  • Refugee
  • Eligible to apply for and obtain the appropriate export control license from the U.S. Departments of State or Commerce
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New, Posted 18 hours ago
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DiversityJobs
Quality Control Engineer III (Hybrid - Boston, MA)

Energy Solutions

Boston, MA 02110

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Quality Specialist/Technical Writer

TELEDYNE FLIR DEFENSE, LLC

Billerica, MA 01821

~ 20 min Onsite

  • Bachelor's degree from an accredited institution
  • A Technical degree with a passion for technical writing preferred
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Quality Manager - Manufacturing

Proterial Cable America

Manchester, NH 03109

~ 43 min Onsite

  • Minimum 5 years related experience in a manufacturing environment.
  • Minimum 3 years management experience
  • Proficient skills working with Microsoft Office, Minitab or similar.
  • Must distinguish colors and pass a colorblind test.
  • Digital dexterity and hand/eye coordination in operation of office equipment, including PC
  • Light lifting and carrying of files, supplies, etc.
  • Ability to speak and hear customers, vendors, and other employees via phone or in person
  • Body motor skills sufficient to move from one office location to another
  • Prolonged periods of sitting at a desk and working on a computer
  • Must be able to lift to 30 pounds at times.
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QC Chemist III

LGC Group

Manchester, NH 03103

~ 43 min OnsiteFlexible ScheduleChildcare AssistanceHealth InsurancePaid Time OffRetirement Benefit

  • Bachelor's degree in Chemistry or a related scientific field, or equivalent combination of education and relevant laboratory experience.
  • Hands-on experience with multiple analytical techniques and execution of complex laboratory procedures with minimal supervision.
  • Experience with ICP, ICP-MS, GC, and LC across diverse product lines.
  • Strong knowledge of laboratory quality systems, data integrity principles, and procedural compliance.
  • Proven ability to interpret complex analytical data, troubleshoot instrumentation and methods, and apply sound technical judgment.
  • Proficiency in Microsoft Office and laboratory information/ERP systems.
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Research Development Quality Inspection Management Lead (GCP/GVP)

Merck Group

Billerica, MA 01821

RemoteHealth InsurancePaid Time OffRetirement Benefit

  • Minimum 8 years QA experience or other relevant experience with a minimum of 5 years in Clinical QA
  • Bachelor's degree with a focus on scientific subjects
  • Sound experience with Regulatory Authorities inspections by major authorities (MHRA, FDA, EMA, PMDA)
  • In depth knowledge of drug development processes and respective international regulations/guidelines
  • Broad knowledge of relevant GxP areas (GCP, GLP, GVP)
  • Travel globally up to 20%
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