Pipeline for EHS Engineers (Construction) (EMEA)

At IPS, you’ll apply your knowledge, skills, and passion to make a difference in the lives of people, solving complex challenges related to pharmaceutical, biotech, and animal health research and manufacturing facilities.

We're currently in the process of pipelining talent for upcoming and current projects across mainland Europe.

Therefore if you are interested in positions in; the UK, Ireland, Germany, Switzerland, Norway, Spain, Italy and Denmark please apply here and let us know which locations are preferable to you.

In this role, you will assist with maintaining compliance with EHS policies and regulations for engineering services, construction projects, and validation/compliance services.

You will be based on client sites to audit and inspect project compliance, as well as assist in administrative compliance activities when needed.

Position Responsibilities

• Assists construction project teams by supporting subcontractor qualifications, safety plan development, safety plan implementation, project compliance inspections, and project EHS regulatory guidance.
• Researches regulations and assists with construction site EHS compliance.
• Performs EHS compliance audits and inspections at IPS project sites.
• Records and report audit reports and assist with the implementation of corrective actions.
• Collates weekly safety statistics and manages reporting system.
• Provides on-site EHS support for projects that require continuous oversight.
• Reviews and evaluates daily “Safe Plan of Action” developed by subcontractors.
• Plans and attends meetings as requested and supports EHS department administrative functions.
• Bachelor’s degree in safety, engineering, or a related field.
• 5-10 years of Construction Safety experience.
• Knowledge and experience with construction safety topics (such as RAMS review and approvals, Permitting, SPAs, Fall Protection, Trenching and Shoring, Crane Lifts, Steel Erection, Hot Work, Confined Space, Emergency Plans, etc.).

• Experience in pharmaceutical Design/Build/Validate processes.