EHS&S Specialist III

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National, MD
1-3 Years Experience
Biotech
The Role

The specialist has responsibility for the implementation of the environmental, health, safety, and sustainability (EHS&S) program. This includes leadership to maintain EHS&S compliance and continuous improvement. EHS&S supports operations of biologic contract development and manufacturing organization.
Responsibilities include: incident response, reporting and investigations; environmental permit management; and risk management. Implements all applicable EHS&S programs for the site such as: LOTO, confined space entry, industrial hygiene, hazard communication, PPE, workers compensation, emergency management, etc. Coordinates with operations to identify and mitigate risks with effective engineering controls, procedures, and training.

  • Interface with KBI staff: High visibility in all workspaces to support a positive, practical, safe and compliant work environment. Interface with Management: Communicate regularly with system owners or area managers to provide status reports, plan program activities and review EHS&S program effectiveness. Co-chair the EHS&S committee.
  • Assessments and Inspections: Coordinate and conduct regular internal self-audits and external client or regulatory inspections of systems as required by EHS&S procedures or programs.
  • EHS&S Incidents: Respond to reported Observations, Near Misses, Injuries and Spills, direct all reporting, assist employees and supervisors with investigations, preventative and corrective actions. Maintain regulatory reporting systems.
  • Regulatory Compliance: Represent KBI during OSHA, EPA, DOL or other regulatory inspections and client audits. Ensure that the staff understand requirements and operate the site in a compliant manner
  • EHS&S Procedures: Draft, review and revise EHS&S systems, including policies, procedures and manuals to ensure that EHS&S practices are consistent with the applicable regulations and promote safe and compliant behavior.

Minimum Requirements:

  • 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:

1. RCRA Hazardous Waste Management,
2. DOT hazardous materials shipping,
3. First Aid/CPR/AED,
4. 30 Hour General Industry OSHA Certification,
5. 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: 83,000 - 116,000

Salary range provided per current averages and expectations. The salary and job title for this opening will be based on the selected candidate’s 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, Sabbatical program, 401K matching with 100% vesting in 60 days and employee recognition programs.

KBI Biopharma is committed to providing a safe and healthy workplace. Any employee entering a KBI site located in the US must inform KBI Biopharma of their vaccination status and must submit their vaccination status. All vaccinated employees are required to provide proof of their COVID-19 vaccination, with a COVID-19 vaccination which has been granted FDA approval or Emergency Use Authorization.

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.

The Company
Boulder , CO
1,282 Employees
On-site Workplace
Year Founded: 1996

What We Do

KBI Biopharma is an award-winning biopharmaceutical contract services organization providing fully-integrated, accelerated drug development and biomanufacturing services to pharmaceutical and biotechnology companies globally.

With each of our 500+ client partners, we have worked closely to personalize and rapidly accelerate their drug development programs. Built upon a foundation of world-class analytical capabilities, we deliver efficient process development and clinical and commercial cGMP manufacturing services for mammalian, microbial, and cell therapy programs.

KBI is proud to be a JSR Life Sciences Company.

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