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3 часа назад

Quality Control Analyst (Chemistry)

107 700 - 112 300$
Формат работы
onsite
Тип работы
fulltime
Грейд
senior
Английский
b2
Страна
US
Вакансия из списка Hirify.GlobalВакансия из Hirify Global, списка международных tech-компаний
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Описание вакансии

Текст:
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TL;DR
Quality Control Analyst (Chemistry): Conducting and documenting laboratory, OOS, and critical QC investigations in a cGMP environment with an accent on root cause analysis, CAPA identification, and regulatory compliance. Focus on applying 6M, 5 Whys, and fishbone analysis, coordinating with cross-functional teams and customers, and driving investigations through closure.

Location: Rensselaer, New York, United States. Monday–Friday, 8:00 AM–5:00 PM.

Salary: $107,700–$112,300 per year.

Company

hirify.global provides staffing and temporary assignment opportunities.

What you will do

  • Lead QC laboratory investigations from initiation through root-cause determination and closure.
  • Conduct and document OOS and other laboratory investigations in collaboration with internal and external stakeholders.
  • Complete impact assessments and provide investigation updates to Quality Assurance, cross-functional teams, and management.
  • Apply 6M, 5 Whys, and fishbone analysis to identify root causes and effective CAPAs.
  • Track investigation metrics, including analyst errors, equipment failures, and test method issues, to identify CAPA opportunities.
  • Develop investigation strategies, documentation templates, and training recommendations to improve consistency and reduce analyst errors.

Requirements

  • Bachelor’s degree in Chemistry or a related scientific discipline, plus at least six years of experience in a Quality Control laboratory environment, or an equivalent combination of education and experience.
  • Demonstrated experience with investigations, root cause analysis, investigation writing, and CAPA identification.
  • Experience conducting and documenting laboratory and OOS investigations.
  • Ability to work in accordance with cGMP requirements, SOPs, and global quality standards.
  • Ability to work independently as the primary investigator for critical laboratory-related investigations and collaborate with QC and cross-functional teams.

Culture & Benefits

  • Cross-functional collaboration with QC, Quality Assurance, customers, and other stakeholders.
  • Temporary assignments lasting 13 weeks or longer may include medical, dental, vision, and 401(k) benefits.
  • Statutory sick pay is provided where required.
  • Reasonable accommodations are available during the employment process.

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