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8 дней назад

Quality Control Lab Technician

Формат работы
onsite
Тип работы
fulltime
Грейд
middle
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 Lab Technician (Analytical Chemistry): Conducting routine and non-routine testing of raw materials, in-process materials, and finished goods with an accent on chromatographic analysis, laboratory instrumentation, and GMP-compliant quality control. Focus on troubleshooting and maintaining instruments, investigating deviations and OOS results, supporting CAPA, and executing method validation and transfer activities.

Location: On-site in Pensacola, Florida, United States

Company

Cytiva is a hirify.global operating company providing life-science, diagnostics, and biotechnology solutions that support biological research, vaccines, medicines, and cell and gene therapies.

What you will do

  • Perform routine and non-routine testing of raw materials, in-process materials, and finished goods using Karl Fischer titration, Buchi IPA extraction, GC, HPLC, IC, FTIR, wet chemistry, sample preparation, and data analysis.
  • Analyze and trend laboratory data in Microsoft Excel and prepare clear technical documentation and reports.
  • Operate, calibrate, troubleshoot, and maintain laboratory instruments while documenting and reviewing data under GMP, GLP, GDP, ISO, and applicable regulatory requirements.
  • Investigate laboratory deviations and out-of-specification results, support CAPA activities, and contribute to continuous improvement.
  • Support method validation, verification, and transfer through protocol execution, data collection, statistical analysis, and technical reporting.

Requirements

  • Bachelor’s degree in Chemistry, Biology, or a related scientific discipline.
  • 3+ years of laboratory experience, preferably in a regulated pharmaceutical, medical-device, manufacturing, food, environmental, or quality-testing environment.
  • Hands-on experience with analytical instrumentation, wet chemistry, laboratory testing, and instrument troubleshooting.
  • Strong analytical, organizational, problem-solving, communication, and independent-working skills with close attention to detail.
  • Proficiency in Microsoft Excel and Word.
  • Ability to travel up to 10%, stand for extended periods, and lift, move, or carry equipment weighing up to 50 lbs.

Nice to have

  • Working knowledge of cGMP, GLP, GDP, ISO 17025, ISO 9001, ISO 13485, or similar quality management systems.
  • Experience writing, revising, or auditing Quality Management System documentation.
  • Lean, Six Sigma, or other continuous improvement training or certification.

Culture & Benefits

  • Culture focused on belonging, learning, innovation, and continuous improvement.
  • Paid time off and medical, dental, and vision insurance for eligible employees.
  • 401(k) benefits for eligible employees.
  • Eligibility for bonus or incentive pay.

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