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1 день назад

Senior Quality Assurance Analyst

54 200 - 77 100$
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
Senior Quality Assurance Analyst (QMS and regulated manufacturing): Supporting and improving the site's quality management system for a manufacturing facility with an accent on document control, investigations, audits, validation, laboratory operations, and regulatory compliance. Focus on analyzing quality metrics, implementing CAPA, maintaining data integrity, and driving continuous improvement under FDA, ISO, GDP, and cGMP requirements.

Location: Colonial Heights, Virginia, USA. Fully onsite, Monday–Friday, 7:00 AM–3:00 PM.

Salary: $54,200–$77,100 base salary per year

Company

Church & Dwight manufactures consumer products, including Trojan® Condoms and scent booster in-wash additives, with a focus on product quality, compliance, innovation, and operational impact.

What you will do

  • Administer, maintain, and continuously improve the site Quality Management System and prepare quality review reports.
  • Manage laboratory document control, training records, change control, impact assessments, and implementation tracking.
  • Analyze laboratory, product, and process data; trend quality metrics and present recommendations to Quality leadership.
  • Support non-conformance investigations, root cause analysis, deviations, CAPA, audits, inspection readiness, and compliance assessments.
  • Monitor calibration, preventive maintenance, validation, technology transfer, supplier quality, and environmental monitoring programs.
  • Support laboratory inventory and quality control testing while mentoring and training Quality Analysts and Quality Inspectors.

Requirements

  • Bachelor’s degree and at least 3 years of Quality experience in a regulated manufacturing environment.
  • Experience with Good Documentation Practices and current Good Manufacturing Practices.
  • Knowledge of laboratory terminology, equipment, testing methods, ISO standards, and FDA 21 CFR regulations.
  • Strong analytical, organizational, communication, prioritization, and attention-to-detail skills.
  • Proficiency with Microsoft Office Suite and experience with SAP and Agile systems.
  • Ability to work fully onsite in a laboratory and manufacturing environment.

Nice to have

  • Experience with QMS, document control, change control, CAPA, audits, supplier quality, validation, or environmental monitoring.
  • Experience using statistical tools for quality trend reporting.
  • Experience mentoring or training laboratory personnel.

Culture & Benefits

  • Collaborative and supportive work environment emphasizing ownership, courage, determination, and continuous improvement.
  • Work across office, laboratory, manufacturing, Quality, Engineering, and Laboratory settings.
  • Routine exposure to manufacturing operations and occasional lifting of up to 10 pounds.

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