EHS&S Specialist III
Boulder, CO - USA
Job Summary
The EHS&S Specialist assists the sites Environment Health Safety and
Sustainable Development Head for the implementation of the Environmental
Health Safety and Sustainability (EHSS) program.
Main part of the mission is to manage the environmental and sustainability part of site program and coordinates the implementation and maintenance of it with all the sites departments more specifically:
- Co-design and manages Standard Operating Procedures (SOP) which relates to
- hazardous waste and wastewater management in accordance with the operating permit regulations site objectives and biologic contract development and
- manufacturing organization
- Manages measurement and monitoring systems for all types of discharge (water waste air) and the consumption of natural resources (water energy etc.). Proposes the corresponding performance indicators and reports them into the sites EHS&S dashboard.
- Defines and manages specific equipment and materials in collaboration with the
- engineering department experts. Manages specific consumables necessary for the proper execution of the program.
- Manages contracts with service providers in these areas.
- Monitors technology and regulations in environmental field and makes proposals for improvement.
Secondary part of the mission includes participation in implementing and
maintaining global EHS&S program. By delegation of the of the EHS&S head
responsibilities this may include participation in:
- Incident response reporting and investigations risk management.
- Log Out Tag Out (LOTO) confined space entry industrial hygiene hazard communication PPE workers compensation emergency management etc.
- Coordinating with operations to identify and mitigate risks with effective engineering controls procedures and training.
MINIMUM REQUIREMENTS
Level I:
Bachelor of Science degree in an occupational health and safety related field and 1 to 5 years of industry experience as an EHS&S professional or Environmental specialist.
Level II:
Bachelor of Science degree in an occupational health and safety related field and a minimum of 3-8 years of industry experience as a safety professional or
Bachelor of Science in a technical discipline and minimum of 5-10 years experience as a safety professional in R&D and/or manufacturing.
Relevant training and/or certification in regulated safety and environmental activities such as:
- RCRA Hazardous Waste Management
- DOT hazardous materials shipping
- First Aid/CPR/AED
- 30 Hour General Industry OSHA Certification
- 40 Hour HAZWOPER certification etc.
Preferred:
- Experience in a cGMP manufacturing environment (biotech pharmaceutical or medical device industries).
- Knowledge of the operations typical to the biotechnology/pharmaceutical industry.
Salary Range:
Level I: $48400 - $66550
Level II: $75720 - $104115
Salary range provided per current averages and expectations. The salary and job title for this opening will be based on the selected candidates qualifications and experience and may be outside this range. KBI has a robust total rewards strategy which includes an annual bonus structure for all employees medical dental and vision coverage paid PTO and holidays 401K matching with 100% vesting in 60 days and employee recognition programs.
KBI Biopharma Inc. is an EEO/AA employer and actively seeks to diversify its work force. Therefore all qualified applicants regardless of race color national origin religion gender gender identity sexual orientation age disability or veteran status are strongly encouraged to apply.
I understand that neither the completion of this application nor any other part of my consideration for employment establishes any obligation for KBI Biopharma Inc. to hire me. If I am hired I understand that either KBI Biopharma Inc. or I can terminate my employment at any time and for any reason with or without cause and without prior notice. I understand that no representative of KBI Biopharma Inc. has the authority to make any assurance to the contrary.
I attest with my signature below that I have given to KBI Biopharma Inc. true and complete information on this application. No requested information has been concealed. I authorize KBI Biopharma Inc. to contact references provided for employment reference checks. If any information I have provided is untrue or if I have concealed material information I understand that this will constitute cause for the denial of employment or immediate dismissal.
Required Experience:
IC
About Company
KBI Biopharma Inc. is a global contract development and manufacturing organization (CDMO / CMO) offering Cell Line Development, Process Analytical & Formulation Development, Clinical & Commercial Manufacturing, and more.