Sr. HSE Specialist

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Bechtel's Manufacturing & Technology (M&T) Business Unit is designing and building an Active Pharmaceutical Ingredient (API) Manufacturing Facility located at Generation Park in Houston, TX. M&T is an exciting and growing business unit that serves customers in the semiconductor, datacenter, life sciences, and electric vehicle markets. M&T strives to exceed our customer objectives through utilizing our agility, innovative technologies, and world class talent. M&T solves the industry's toughest challenges, building both our company and the world for the future. Headquartered in Reston, Virginia, the M&T global business unit also includes colleagues working in Arizona, Ohio, Texas, India, and additional project locations around the world.

Will support the implementation of project ESH programs by performing both administrative and field tasks in accordance with industry standards and regulatory requirements. This role applies occupational safety practices to manage safety and health aspects of projects or facilities, with a primary focus on fieldwork. The position reports to the Area EHS Lead
Work requires physical ability for field inspections, including walking on construction sites in extreme heat or humidity, climbing ladders and scaffolding, working at heights or on uneven surfaces, and entering confined spaces. Must be able to wear assigned PPE (e.g., harness, life vest, gloves, etc.). #LI-AE2

* Develop a positive working relationship with the crews, field supervisors, and subcontractor representatives
* Integrate safety and health requirements into all project phases, including planning, design, procurement, construction, and commissioning and start up.
* Provide technical assistance on risk assessments, ESH plan development, and program implementation to project teams.
* Research, interpret, and apply organizational and regulatory requirements; prepare clear documentation and technical reports.
* Support work planning and conduct safety reviews to ensure compliance and best practices.
* Assist in the development and delivery of safety plans, permits and training programs.
* Participate in emergency response activities and incident investigations, including root cause analysis and corrective action tracking.
* Communicate safety requirements effectively and ensure their integration into project plans, contracts, and daily operations.
* Conduct regular field inspections, monitor ESH performance, and ensure compliance with all applicable standards.
* Apply trend analysis to focus on field oversight and interactions with crews and subcontractor
* Develop and disseminate safety communications using various media (e.g., presentations, bulletins, digital platforms).
* Collaborate with and support other ESH team members across all ESH disciplines as needed.

* A Bachelor of Science degree (or equivalent) in occupational safety, health, or a science-related discipline from an accredited university or college with 3 or more years of experience related to safety or occupational health; or an Associate's degree (or equivalent) in one of the same disciplines with 5 or more years of relevant experience; or 8 or more years of relevant safety or health experience.

* Ability to research, interpret, and apply regulatory and organizational requirements (e.g., OSHA, ISO 45001).
* Strong oral and written communication skills, including technical writing and report preparation.
* Analytical skills related to sampling, monitoring, and recordkeeping.
* Ability to conduct field inspections, program audits, and manage corrective actions through completion.
* Proficiency with computers to develop reports or presentations, manage data and reports.
* Demonstrated proficiency in utilizing digital safety management software to oversee ESH processes.
* Adaptable and able to work outdoors in a field environment under various weather conditions.
* Ability to support multiple work shifts, as needed, and a wide range of field related tasks.
* Valid driver's license

• Experience in pharmaceutical manufacturing facilities such as: Bulk API, sterile products, secondary packaging, devices, and lab projects
• 5-10 years of direct experience on large capital projects, including regulated or validated settings
• Deep understanding of cGMP regulations, and excellent interpersonal and organizational skills.
• Experience in the following areas: GMP manufacturing, LEAN, automation, construction, construction quality, CQV (commissioning, qualification, and validation), project controls, the engineering disciplines, safety, and scheduling
• Ability to lead and coordinate cross-functional teams (Owners, Architects, Engineers, QA/Validation, Contractors) in regulated contexts.
• Certifications or hands-on experience in CQV; CSV awareness; familiarity with FDA 21 CFR Part 11, EU Annex 11, and related regulatory frameworks.
• Demonstrated success delivering complex, multi-site projects in validated environments (GMP/GLP/ISO 17025) within labs, biopharma, pharmaceutical manufacturing, medical devices, healthcare, or related sectors.
• Specific experience delivering validated environments: GMP/GLP labs, ISO 14644 cleanrooms, ISO 17025 laboratories, or similar.

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