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EHS Manager, Biopharma Manufacturing (JP8063)

West Greenwich,, Rhode Island · Biotech/Pharmaceutical
Job Title: EHS Manager, Biopharma Manufacturing Facility (JP8063)
Location: West Greenwich, Rhode Island
Employment Type: Contract
Duration: 10 months with likely extensions
Job posting date: 6 Jan 2021
Note: Onsite Essential with night workshift, Monday to Thuesday 12am-8:30am and day shift, Friday 8am - 5pm
3 Key Consulting is hiring a EHS Manager for a consulting engagement with our direct client, a leading global bio-pharmaceutical company.
Job Summary:
  • EHS support to biotech pharmaceutical manufacturing operations per FDA regulations.
  • The EHS Manager is a member of the EHS Team that will interact frequently with internal clients, be action oriented, and be directly engaged providing on the floor safety support for operations within the facility. Responsible to implement, manage, and monitor aspects of facility safety and environmental compliance programs in the plant and manage competing priorities on a routine basis.
  • This role will partner with manufacturing staff and management to identify and address safety issues and concerns and serve as a subject matter expert across the safety and environmental compliance disciplines.
  • The role will primarily support weekday evening shifts and will require a significant presence on the manufacturing floor (cleanroom) supporting those activities.

  • Act as an EHS representative for internal manufacturing staff and management.
  • Assist in the interpretation of EHS regulations to ensure compliance with Corporate, Federal, State, and local requirements.
  • Coach staff and leadership to establish and maintain world class safety culture
  • Ensure work conducted on the floor matches current safety procedures and risk assessments.
  • Perform EHS inspections throughout the facility.
  • Perform job hazard analysis and support Industrial hygiene, ergonomic, and other safety assessments as needed.
  • Participate in emergency response activities as needed.
  • Maintain appropriate records and documentation.
  • Identify, develop and assist in implementing EHS program improvement initiatives.
  • Partner with all levels of internal client organizations.
  • Assist in Accident/Incident investigations and Root Cause Analysis.

    Basic Qualifications:
  • Master’s degree and 6 years of manufacturing safety experience OR Bachelor’s degree and 8 years of manufacturing safety experience OR Associate’s degree and 10 years of manufacturing safety experience

    Preferred Qualifications:
  • BS degree in environmental, safety, technical, scientific or engineering fields.
  • 6 + years of experience developing/supporting EHS programs within industry.
  • Possess one or more professional credentials (CIH, CSP, ASP, CHMM, EIT).
  • Previous experience working within the biotechnology/pharmaceutical sector, preferably in a cGMP environment.
  • Experience in developing and supporting a world class safety culture in a clean room manufacturing environment.
Top Must have Skill Sets:
  • (6+ years of experience)
  • OSHA compliance experience (General OSHA  1910)
  • manufacturing operations experience
  • experience developing safety culture (safety first mindset)
  • Ability to work with staff at all levels of the organization
  • great communication skills
  • computer skills (excel, word, outlook, etc.)
Employee Value Proposition:
opportunity to work for a world-class biotech manufacturing company, direct effect on the safety of the staff, in support of our company's mission to serve patients.
Red Flags:
prior safety experience
prior manufacturing safety experience
Interview Process:
We invite qualified candidates to send your resume to resumes@3keyconsulting.com. If you decide that you’re not interested in pursuing this position, please feel free to look at other positions on our website www.3keyconsulting.com. You are welcome to also share this posting with anyone you think might be interested in applying for this role.
3KC Talent Acquisition Team
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