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7 дней назад

Senior Microbiologist - Virginia

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 Microbiologist (GMP Microbiology): Performing and overseeing microbiological assays, environmental monitoring, method validation, and microbial identification for pharmaceutical manufacturing with an accent on GMP compliance, laboratory documentation, and contamination control. Focus on leading investigations, deviations, corrective and preventive actions, process improvements, and technical support across multidisciplinary teams.

Location: Petersburg, Virginia, United States; onsite work in a pharmaceutical manufacturing facility

Company

hirify.global is a global healthcare company developing and manufacturing medicines for serious chronic diseases, including diabetes and obesity.

What you will do

  • Perform and oversee routine and non-routine microbiological assays on raw materials, water, in-process samples, packaging materials, and finished products.
  • Monitor air, surfaces, and water in manufacturing areas for microbial contamination.
  • Author, review, and approve test methods, SOPs, protocols, reports, specifications, and laboratory documentation.
  • Perform or oversee equipment and test-method validations while maintaining GMP, regulatory, and data-integrity compliance.
  • Isolate and identify microorganisms using culture-based, molecular biology, and automated techniques.
  • Lead or support investigations, deviations, corrective and preventive actions, process improvements, training, and multidisciplinary projects.

Requirements

  • Bachelor’s degree in microbiology or a related science field and at least six years of relevant experience; equivalent pathways include an associate degree with eight years or a high school diploma/GED with ten years of experience.
  • Strong knowledge of microbiology principles, microbial identification, culture techniques, and sterilization methods.
  • Experience with GMP regulations and quality-control procedures.
  • Proficiency in aseptic technique, microbial enumeration, molecular biology methods, and laboratory documentation.
  • Strong analytical, problem-solving, communication, collaboration, and project leadership skills.
  • Ability to work onsite in the manufacturing facility, handle equipment or supplies up to 33 pounds, work around hazardous materials, and comply with gowning and respiratory-protection requirements when applicable.

Culture & Benefits

  • Paid time off including 14 paid holidays.
  • Health, dental, and vision insurance effective from day one.
  • Guaranteed 8% 401(k) contribution with an individual company match option.
  • Paid parental and family medical leave.
  • Tuition assistance, life and disability insurance, pharmaceutical-product access, and employee referral awards.

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