Engineering Specialist, Facilities and Critical Systems
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Your role at Baxter
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Your team
What you'll be doing
- Develop and maintain engineering standards and guidance documents for facilities, utilities, and capital projects.
- Provide technical support and subject matter expertise for pharmaceutical facility and utility systems.
- Review facility designs, engineering studies, and project plans to ensure alignment with company standards and regulatory expectations.
- Support manufacturing sites in the planning and execution of facility upgrades and improvement projects.
- Evaluate facility and utility system performance and recommend solutions to address technical issues and improve reliability.
- Monitor changes in industry practices and regulatory requirements and recommend updates to engineering standards and procedures.
- Develop and maintain project documentation standards, including SOWs, URSs, and BODs.
- Participate in project gate reviews and capital planning activities.
- Support sustainability initiatives through facility improvements, energy-efficient design practices, and carbon reduction efforts.
- Partner with manufacturing, maintenance, purchasing, and project teams to address facility and utility-related challenges.
- Provide technical guidance and mentorship to engineering teams across the organization.
- Travel domestically and internationally up to 25%.
What you'll bring
- Bachelor's degree in Mechanical Engineering or a related field.
- 15+ years of experience in pharmaceutical facility, utility, or systems engineering.
- 3+ years of experience supporting manufacturing operations.
- 8+ years of experience in an engineering leadership or senior technical engineering role.
- Experience applying cGMP requirements within a regulated manufacturing environment.
- Knowledge of facility and utility systems, including HVAC, WFI, compressed air, mechanical, electrical, plumbing, structural, and energy management systems.
- Knowledge of FDA, OSHA, 21 CFR, ISO, and applicable building and safety regulations.
- Experience supporting capital projects from concept through startup and turnover.
- Proficiency with AutoCAD, Revit, or similar engineering design tools.
- Strong communication and problem-solving skills with the ability to work across multiple functions and locations.
- Experience in facility design, construction management, or capital project execution.
- Knowledge of ISPE, ASME, NFPA, EPA, and environmental health and safety requirements applicable to pharmaceutical manufacturing.
- Experience developing engineering standards or governance programs for a global organization.
- Experience with Lean Manufacturing, Six Sigma, TPM, or other continuous improvement methodologies.
We understand compensation is an important factor as you consider the next step in your career. At Baxter, we are committed to equitable pay for all employees, and we strive to be more transparent with our pay practices. The estimated base salary for this position is $152,000 - $209,000 annually. The estimated range is meant to reflect an anticipated salary range for the position. We may pay more or less than of the anticipated range based upon market data and other factors, all of which are subject to change. Individual pay is based on upon location, skills and expertise, experience, and other relevant factors. This position may also be eligible for discretionary bonuses. For questions about this, our pay philosophy, and available benefits, please speak to the recruiter if you decide to apply and are selected for an interview.
Applicants must be authorized to work for any employer in the U.S. We are unable to sponsor or take over sponsorship of an employment visa at this time.
US Benefits at Baxter (except for Puerto Rico)
Equal Employment Opportunity
Reasonable Accommodations
Recruitment Fraud Notice
Not included in the source posting: qualifications.
Who can apply
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