
Director, Head of EHS&S
KBI Biopharma
Summary
The Director has overall responsibility for the company's 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.
Job description
Job Summary
The Director has overall responsibility for the company's 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.
The Head of EHS&S provides leadership to establish high standards of compliance and collaboration for a robust safety and sustainability culture. The Director develops and implements strategies, processes, systems, procedures, and metrics to achieve excellent EHS&S outcomes and performance across multiple sites and locations.
Working with leaders, EHS&S team members, SMEs, and colleagues across the organization, the Head of EHS&S will align and implement appropriate governance, best practices, fill gaps, and drive maturity of the EHS&S program. The Head of EHS&S will develop and manage the budget and resources of a matrix organization. The Director must be an effective leader, mentor, and coach who thinks strategically and is effective tactically.
Responsibilities include the primary global contact for response, incident reporting and investigations, environmental permits, reporting, and risk management. Represents the functional area to clients, auditors, and regulatory agencies. This position is responsible for EHS&S metrics, reporting, compliance reviews, risk management, and ensuring compliance of applicable regulations. Oversees all applicable EHS&S programs for the company 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.
Oversees EHS&S support for multiple sites. Develops subject matter experts in several areas. Applies approaches to develop and implement strategies, technologies, or other major improvements. Directs, reviews, and approves EHS&S documents.
Job Responsibilities
- Manages EHS&S program activities and ensures EHS&S compliance
- Develops and implements changes to improve EHS&S performance
- Planning, reporting, metrics, administration activities
- Wastewater and Hazardous Waste programs
- Monitor the work of contracted EHS&S suppliers and service providers
Minimum Requirements
Knowledge, Skills, Abilities
BS degree in an environmental, health, safety, engineering, or scientific field of study plus 15 years' related experience.
Language Ability
Excellent oral, written, and interpersonal communication skills. Communicates complex issues and subject matter effectively to executive management and/or staff members. Ability to respond effectively to the most sensitive inquiries or complaints.
Reasoning Ability
Ability to manage multiple programs/projects and to work well within a team environment.
Math Ability
Problem solving and application of sound engineering or scientific skills.
Physical Demands
- Incumbents may be exposed to toxic materials, toxic gases, electrical hazards, and dangerous tools and equipment.
- Off-hours response time to system anomaly.
- Must comply with all applicable rules and regulations of the company and the Pharmaceutical / Biotech industry including FDA regulations such as cGMP, GDP, Environmental, Health and Safety regulations and company regulations such as the employee handbook.
Computer Skills
MS Office Suite (Word, Excel, Power Point), Outlook, MS Project.
Requirements
- BS degree in an environmental, health, safety, engineering, or scientific field of study
- 15 years' related experience
- Excellent oral, written, and interpersonal communication skills
- Ability to communicate complex issues to executive management and staff
- Ability to respond effectively to sensitive inquiries or complaints
- Ability to manage multiple programs/projects
- Ability to work well within a team environment
- Problem solving and application of sound engineering or scientific skills
- MS Office Suite (Word, Excel, PowerPoint), Outlook, MS Project
- Compliance with FDA regulations such as cGMP, GDP, Environmental, Health and Safety regulations
Company overview
KBI Biopharma is an award-winning global contract development and manufacturing organization (CDMO) that provides fully integrated, accelerated drug development and biologics manufacturing services to pharmaceutical and biotechnology companies worldwide. Founded in 1996 and now part of JSR Life Sciences, KBI has established itself as a next-generation CDMO specializing in complex biologics. The company serves over 500 client partners and has supported the advancement of more than 160 drug candidates from preclinical stages to market, including the manufacture of ten commercial products. KBI's comprehensive service portfolio includes cell line development, process development, analytical services, formulation development, and clinical and commercial cGMP manufacturing for both mammalian and microbial programs. With strategically located facilities across the United States and Europe, KBI leverages world-class analytical capabilities and proprietary platforms like SUREtechnology™ and PUREplatform™ to deliver personalized, accelerated solutions for biopharmaceutical development. The company is recognized for its scientific excellence, quality manufacturing, and commitment to helping clients bring innovative medicines to patients faster.