Electrical Automation Engineer 2 (Fort Worth, TX)

Smith+Nephew; Fort Worth (TX); On-site; USD 80,000 - 100,000; Full time

Benefits offered by this job

401k Matching Program

Flexible Time Off

Medical, Dental, Vision

Employee Assistance Program

Discounts on fitness clubs

Job summary

A leading healthcare technology company is seeking an Automation Engineer 2 to support pharmaceutical manufacturing equipment and critical utility systems. This role involves leading automation projects, ensuring compliance with GMP standards, and generating quality documentation. The ideal candidate will have a bachelor's degree in engineering, at least 3 years of experience in a relevant biotech environment, and strong project management skills. The role also offers a hybrid work model and various employee benefits including tuition reimbursement and wellness programs.

Qualifications

• Minimum 3 years of experience in a Pharmaceutical/Biotech environment.
• EIT/PE License preferred; Lean/Six Sigma certification desired.
• Demonstrated project management of automation solutions.

Responsibilities

• Provide support for pharmaceutical manufacturing equipment.
• Function as a Subject Matter Expert in automation.
• Generate quality documentation for equipment and processes.

Skills

Automation Subject Matter Expert

Troubleshooting operations

Project Management

Analytical skills

Communication skills

Education

Bachelor's degree in engineering or related field

Tools

PLC

HMI

SCADA systems

MS Project

Job description

Life Unlimited. At Smith+Nebhew we design and manufacture technology that takes the limits off living. The Automation Engineer 2 will provide support towards pharmaceutical manufacturing equipment, critical utility systems and facility, for technical GMP requirements toward the successful installation and start-up of a new Biotherapeutic Manufacturing Area including manufacturing support of sustained operations while in a production state. This role is accountable for determining and delivering automation solutions to an approved budget and schedule commitments while meeting required GMP and Part 11 standards, thus will be required to follow an established project plan structure and lead/contribute to delivering on‑budget, on‑time, along with the capability to receive FDA and Health Canada Approvals. Job requirements for equipment will include, but not limited to: URS development, FAT execution, installation support, commissioning / validation, SOP development, Preventive Maintenance job plan development, production support, and efficiency improvement initiatives. This role will require the incumbent to lead investigator for authoring change control documentation, authoring / supporting deviations / manufacturing non‑conformances and CAPAs, and authoring risk assessments.

What will you be doing?

• Function as an Automation Subject Matter Expert (SME) to equipment or systems regarding troubleshooting operations and/or changes to improve efficiency. Required to be actively involved in daily operations when required to meet schedules or to resolve complex problems. Routinely audit the operational performance and regulatory compliance of a moderate number of equipment items or systems of significant complexity. Work with multiple departments in developing requirements and recommendations for system modifications. Guiding and mentoring junior team members on automation best practices and methodologies.
• Technical translation and execution of all validation requirements for new and/or modified manufacturing, and utilities equipment/systems, ensuring equipment and utility systems are available for GMP Manufacturing, in a state of compliance, and reliably performing to their validated function. Active participation of Factory Acceptance Testing (FAT), Commissioning of new equipment, IQ/OQ/PQ, Validation Summary Reports, Part 11 Compliance, etc, as required for Manufacturing, Utilities, and Computerized systems.
• Develop and lead one or more projects, ensuring technical alignment with the commercial and marketing strategy for the project and managing the project and project team to key milestones and targets. Drives the development and operational delivery of the project plan in accordance with Project Management best practices, Smith+Nebhew SOPs and Guidance Documents, and the product profile. Manages Project risks, budget, schedule variance, and change management for the project. Reports to executive management as appropriate. Completes capital requests and purchase orders as needed to support projects.
• Generate any associated quality documentation requirements such as SOPs, Change Controls, URS, Room Specification, Validation protocols, Job Plan instructions, Non‑Conformances, and CAPAs. Will also perform Risk Assessments and/or Gap assessments for equipment, process, method, and/or facility tech transfers.

What will you need to be successful?

Education

• Bachelor's degree required in engineering or related field

Certifications

• EIT/PE License preferred.
• Lean/Six Sigma certification highly desired.
• PMP certification a plus

Experience

• Minimum 3 years of experience in a Pharmaceutical/Biotech environment or a minimum of 1 year within the Automation Engineer 1 role with consistent performance.
• Strong working knowledge and experience of PLC’s, HMI’s, and SCADA systems.
• Demonstrated experience in Project Management of automation solutions with proven results.

Knowledge

• Working knowledge in aseptic manufacturing and fermentation processes.

Competences

• Design documentation, Equipment manual, and P&ID interpretation (in the English language)
• Adherence to Quality Systems and Good Manufacturing Practices with proper attention to detail
• Demonstrated ability to work in a professional, multi‑disciplinary, multi‑cultural team as a group leader, facilitator, or participant.
• Ability to influence team members, peers, and senior managers.
• Strong analytical and troubleshooting skills
• Ability to prioritize multiple projects along with multitasking
• Effective verbal and written communication skills
• Ability to identify opportunities to implement automated systems and optimize existing automation processes.
• Software: MS Project or Excel, Word, and PowerPoint

Physical Demands

• While performing the duties of this position, the Employee will be required to walk, stand, lift (up to 40 lbs), climb ladders/stairs, enter confined spaces, and work in high noise spaces. / Travel Requirements: Up to 10% (international and domestic)

You Unlimited.

• Inclusion and Belonging- Committed to Welcoming, Celebrating and Thriving on Inclusion and Belonging, Learn more about Employee Inclusion Groups on our website (https://www.smith-nephew.com/).
• Your Future: 401k Matching Program, 401k Plus Program, Discounted Stock Options, Tuition Reimbursement
• Work/Life Balance: Flexible Personal/Vacation Time Off, Paid Holidays, Flex Holidays, Paid Community Service Day
• Your Wellbeing: Medical, Dental, Vision, Health Savings Account (Employer Contribution of $500+ annually), Employee Assistance Program, Parental Leave, Fertility and Adoption Assistance Program
• Flexibility: Hybrid Work Model (For most professional roles)
• Training: Hands‑On, Team‑Customized, Mentorship
• Extra Perks: Discounts on fitness clubs, travel and more!

Smith+Nebhew provides equal employment opportunities to applicants and employees without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, or disability.

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