Назад
Company hidden
2 дня назад

Analyst Quality Control (Microbiology)

Формат работы
onsite
Тип работы
fulltime
Грейд
junior
Английский
b2
Страна
US
Вакансия из списка Hirify.GlobalВакансия из Hirify Global, списка международных tech-компаний
Для мэтча и отклика нужен Plus

Мэтч & Сопровод

Для мэтча с этой вакансией нужен Plus

Описание вакансии

Текст:
/
TL;DR
Analyst Quality Control (Microbiology): Designing environmental and water-system monitoring programs and performing microbiological analyses in a pharmaceutical quality-control laboratory with an accent on aseptic sampling, cGMP compliance, and accurate laboratory documentation. Focus on interpreting test data, maintaining qualified equipment and test methods, and investigating non-conformances with corrective actions.

Location: Onsite in Athens, Georgia, United States of America

Company

Johnson & Johnson MedTech develops healthcare and pharmaceutical solutions, including innovative medicines and medical technologies.

What you will do

  • Design and implement environmental and water-system monitoring programs.
  • Prepare and analyze samples, media, standards, and reagents using microbiological test methods and USP/FDA guidelines.
  • Operate, maintain, qualify, and calibrate laboratory equipment to ensure reliable test data.
  • Interpret results, assess their impact on manufacturing and shipping, and identify risks through data analysis.
  • Support non-conformance investigations, document findings, and recommend corrective actions.
  • Maintain SOPs, test methods, laboratory records, reports, and audit-ready practices while collaborating with manufacturing and technical operations.

Requirements

  • 0–2 years of experience or a four-year degree in microbiology or a closely related field.
  • Basic English proficiency is required for reading, writing, and understanding technical and regulatory documents.
  • Experience with aseptic techniques for sampling and testing materials.
  • Knowledge of cGMPs, FDA procedures, and safety and environmental regulations relevant to pharmaceutical or chemical manufacturing.
  • Ability to work accurately with minimal supervision, manage multiple priorities, and respond effectively in emergency or hazardous situations.
  • Availability for scheduled or emergency overtime work.

Culture & Benefits

  • Inclusive work environment focused on individual dignity, diversity, and merit.
  • Work supporting healthcare innovation and the development of medicines and treatments.
  • Compliance-focused environment covering FDA, EPA, OSHA, DEA, cGMP, quality, safety, and environmental requirements.
  • Training and professional development requirements are provided and maintained.
  • Physical laboratory work includes frequent standing, walking, fine-motor tasks, and lifting up to 25 pounds occasionally.

Будьте осторожны: если работодатель просит войти в их систему, используя iCloud/Google, прислать код/пароль, запустить код/ПО, не делайте этого - это мошенники. Обязательно жмите "Пожаловаться" или пишите в поддержку. Подробнее в гайде →