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7 дней назад

EHSS Specialist III (Biopharma)

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
EHSS Specialist III (Biopharma): Implementing environmental, health, safety, and sustainability programs for a biologic contract development and manufacturing organization with an accent on regulatory compliance, incident response, environmental permits, and operational risk management. Focus on conducting audits and inspections, investigating incidents, managing hazardous waste and emergency preparedness, and coordinating safety training and engineering controls.

Location: USA - NC - Durham - National Way

Company

hirify.global supports biologic contract development and manufacturing operations.

What you will do

  • Implement and continuously improve environmental, health, safety, and sustainability programs for the site.
  • Coordinate incident response, reporting, investigations, and corrective and preventive actions for observations, near misses, injuries, and spills.
  • Manage environmental permits, regulatory reporting systems, waste activities, chemical inventories, inspections, and EHS&S records.
  • Conduct internal self-audits and support client, OSHA, EPA, DOL, and other regulatory inspections.
  • Develop and maintain EHS&S policies, procedures, manuals, training, PPE programs, emergency preparedness, and risk controls.
  • Collaborate with managers and operations teams, provide program status updates, and co-chair the EHS&S committee.

Requirements

  • Bachelor of Science in occupational health and safety or a technical discipline.
  • 5–10 years of industry experience as a safety professional, or 7–12 years of safety experience in R&D and/or manufacturing.
  • Relevant training or certification in regulated safety and environmental activities, such as RCRA hazardous waste management, DOT hazardous materials shipping, First Aid/CPR/AED, OSHA 30-Hour General Industry, or 40-Hour HAZWOPER.
  • Ability to manage EHS&S compliance, inspections, investigations, training, records, and risk mitigation.

Nice to have

  • Experience in a cGMP manufacturing environment within biotechnology, pharmaceutical, or medical device industries.
  • Knowledge of biotechnology and pharmaceutical industry operations.

Culture & Benefits

  • Full-time employment.
  • High-visibility presence across workspaces to support a practical, safe, and compliant work environment.
  • Collaboration with site management, operations, employees, clients, vendors, and regulatory authorities.

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