HSE Specialist

HSE Specialist

Location: Hazelwood, MO - ONSITE

Job Description:

• Provide HSE support to ensure the site maintains a safe and healthy workplace, protecting the environment and adhering to applicable legal requirements.
• Support all team members and processes at the STL site.
• Engage with the Site HSE Manager to define and accept a distinct role in developing and deploying a subset of the HSE process.
• Document, deploy, and train key HSE system users as defined by the HSE manager.
• Communicate progress milestones toward the HSE system development at the site level.
• Deploy specific HSE procedures following a subset of HSE processes reporting progress toward HSE goals (Job Safety Analyses, Risk assessments, Environmental Assessments, Incident Reporting System, HSE inspections).
• Support the accident investigation process including looking across the process.
• Actively participate in regional and global initiatives related to HSE.
• Interact with other USA sites to maintain a regional teamwork approach.
• Operate in an FDA/ISO regulated environment in the Medical Devices/Diagnostics Industry.
• Help drive process improvement initiatives for HSE.
• Support the implementation of HSE site policies.
• Compile and report HSE metrics.
• Support new equipment procurement user requirement specifications and commissioning activities.
• Support ISO 14001 / 45001 Certification Audits and associated activities.
• Perform all work in compliance with company quality procedures and standards.
• Take an active role in continuous improvement.

Requirements:

• Minimum 2 years of experience in the Health, Safety, Sustainability, and/or Environmental fields required.
• Minimum 2 years of experience within an ISO 14001 / 45001 certified organization preferred.
• Minimum 1 year of experience with continuous improvement preferred.
• Minimum 1 year of experience with CSR initiatives preferred.
• Knowledge and understanding of US compliance regulations including DOT/OSHA/EPA/NFPA preferred.

Additional Details:

• Demonstrate behaviors of being a self-starter who is organized, detailed, conscientious, and ambitious.
• Model behaviors such as being a team player with a positive attitude and approaching projects/tasks with a sense of ownership.
• Perform documentation requirements in a cGMP compliant manner in accordance with Quality Policies.
• Ability to work effectively as part of a team and autonomously as required.
• Communicate effectively within the team and interface with other site departments, verbally and written.
• Ability to understand at a high level the equipment, processes, and products.
• Ability to maintain and execute a project schedule.

Education:

• Bachelor's Degree Required