Bio-Pharmaceutical Manufacturing Site



  • Malawi 
  • Last Update: 18.12.2018 at 12:00

Job Type
Full Time
11 Month +
New York City, NY, US


Clinical and medical development


Job Duties
  • Assist site departments with investigating SHE-related events involving full-time (FTEs) or temporary employees , including:
  • driving investigations to determine root-cause;
  • identifying appropriate CAPAs with the goal of preventing future incidents;
  • reviewing and updating (as appropriate) the SHE event data management system (
  • performing effectiveness checks on CAPAs implemented to assess effectiveness at preventing future events.
  • Identify, assess and work with site departments to develop and implement mitigation strategies (CAPAs) for SHE risks associated with the manufacturing process including risk stemming from new or modified equipment or systems.
  • Prepare a management-level summary on a weekly basis that includes:
  • SHE-related events, investigation status, root cause determination, and CAPA development and status; and,
  • Risks assessed and mitigation strategy.
  • Meet with SHE managers routinely and prepare monthly project status reports.
About You Qualifications:  
  • Experience with manufacturing safety to include risk assessments and incident investigations experience at a biologics or pharmaceutical manufacturing facility.
  • BS in Science related field
  • Experience using Perillon and Trackwise systems
  • Certified Safety Professional (CSP) or Certified Industrial Hygienist (CIH)
  • Seven (7) years of related Safety, Health, and Environmental specialty
  • 3 years of the 7 years must be in Biopharmaceutical R&D and/or Manufacturing industry

Seniority Level

Entry level


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Employment Type


Job Functions

  • Management
  • Manufacturing

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