Manufacturing Engineer 2

Posted 6 Hours Ago
Be an Early Applicant
Fort Worth, TX, USA
In-Office
Junior
Healthtech • Biotech
The Role
Provides day-to-day engineering support for manufacturing operations, troubleshooting equipment and process issues, improving productivity, throughput, yield, cycle time, and cost. Leads Lean, Six Sigma, Kaizen, and continuous improvement initiatives; analyzes manufacturing data and implements corrective actions. Supports equipment selection, installation, commissioning, qualification, validation, production readiness, deviation investigations, CAPAs, documentation, and regulatory compliance. Requires collaboration across Operations, Quality, Maintenance, Supply Chain, and Engineering, with up to 10% domestic and international travel.
Summary Generated by Built In

Life Unlimited. At Smith+Nephew, we design and manufacture technology that takes the limits off living.


Are you looking for an opportunity where you can apply your engineering expertise to optimize production processes, implement innovative technologies, and make a direct impact on operational performance?


The Manufacturing Engineer 2 primarily supports manufacturing operations at the Fort Worth-Vickery site by providing technical leadership for production processes, equipment, tooling, and facility-related manufacturing systems.


This role partners closely with Operations, Quality, Maintenance, Supply Chain, Engineering, and Project Management to ensure safe, efficient, and compliant manufacturing processes.  Responsibilities include supporting production activities, troubleshooting manufacturing issues, driving continuous improvement initiatives, reducing waste, improving productivity, optimizing equipment performance, and supporting capital projects. The Manufacturing Engineer 2 is responsible for analyzing manufacturing data, identifying opportunities for process improvements, implementing corrective actions, and ensuring manufacturing processes meet quality, safety, cost, and delivery objectives. 



Responsible for evaluating existing equipment and configuring manufacturing systems to improve sustainability and develop best practices within the production process. Job requirements for this role will include but not limited to, assisting in URS development, FAT execution, installation / commissioning support, PQ / Process Validation development and execution, SOP development, production support, and efficiency improvement initiatives.


This role also supports equipment qualifications, production readiness activities, root cause investigations, change management, manufacturing documentation, and the introduction of new equipment and technologies into production.


What will you be doing?


  • Provide day-to-day engineering support for manufacturing operations.
  • Troubleshoot process and equipment issues impacting safety, quality, delivery, and cost.
  • Develop and maintain manufacturing work instructions, operating procedures, processing documentation, and standard work. Support production metrics, capacity planning, and operational excellence initiatives.
  • Lead productivity, throughput, yield, and cycle-time improvement initiatives.
  • Identify and implement waste-reduction and cost-saving opportunities.
  • Apply Lean Manufacturing, Six Sigma, and statistical analysis methodologies to improve performance.
  • Facilitate Kaizen events, Value Stream Mapping exercises, and continuous improvement projects.
  • Analyze manufacturing data and implement corrective actions based on performance trends.
  • Lead process improvement projects focused on productivity, throughput, yield, cycle-time reduction, waste elimination, and cost savings. Utilize Lean Manufacturing, Six Sigma, and statistical analysis tools to identify and implement improvements. Support Value Stream Mapping, Kaizen events, and performance improvement activities.
  • Support specification development, equipment selection, installation, commissioning, qualification, and startup activities. Participate in Factory Acceptance Testing (FAT), Site Acceptance Testing (SAT), and production validation activities as required. Assist with facility and equipment upgrades to improve manufacturing capabilities.
  • Support investigations related to manufacturing deviations, nonconformances, corrective actions, and process failures. Participate in risk assessments, root cause analysis, and implementation of corrective and preventive actions (CAPAs). Ensure manufacturing processes remain compliant with applicable quality and regulatory requirements. 
  • Develop process control metrics and identify trends to drive operational improvements and monitor process performance through data collection, statistical analysis, and KPI reporting 
  • Performs other duties as required.


What will you need to be successful?


Required Qualifications

Education

  • Bachelor’s Degree required.  Manufacturing Engineering, Mechanical Engineering, Chemical Engineering, Electrical Engineering; Advanced degree is a plus.

Experience

  • Minimum of 2 years of manufacturing engineering experience.
  • Experience in a Pharmaceutical/Biotech environment highly desired / manufacturing and/or experience supporting production operations in a regulated environment. Equipment validation experience a plus.
  • EIT/PE License a plus. 
  • Lean/Six Sigma certification highly desired

Competencies:  

  • Strong problem-solving and root cause analysis skills, experience with manufacturing processes, equipment, tooling, and production systems, knowledge of lean manufacturing, Six Sigma, and continuous improvement methodologies, strong communication and cross-functional collaboration skills,
  • Proficiency in Microsoft Office Applications, BMS/MES systems, ability to manage multiple projects and priorities in a fast-paced manufacturing environment. Exceptional reading comprehension and attention to detail. Ability to act independently to carry out tasks given by management in the time allotted. Demonstrated ability to learn new tasks and adapt to new situations.

Travel Requirements

  • Up to 10% domestic and international travel.


This position is not offering any type of visa transfer or sponsorship now or in the future.

You Unlimited.

We believe in creating the greatest good for society. Our strongest investments are in our people and the patients we serve.    

  • 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 
  • Training: Hands-On, Team-Customized, Mentorship  
  • Extra Perks: Discounts on fitness clubs, travel and more!  

#LI-ONSITE

Smith+Nephew 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.

Stay connected by joining our Talent Community.

We're more than just a company - we're a community! Follow us on LinkedIn to see how we support and empower our employees and patients every day.  

Check us out on Glassdoor for a glimpse behind the scenes and a sneak peek into You. Unlimited., life, culture, and benefits at S+N.

Explore our website and learn more about our mission, our team, and the opportunities we offer. 

 

Skills Required

  • Bachelor's degree in Manufacturing Engineering, Mechanical Engineering, Chemical Engineering, or Electrical Engineering
  • At least 2 years of manufacturing engineering experience
  • Experience supporting production operations in a regulated environment
  • Experience in a pharmaceutical or biotechnology environment
  • Equipment validation experience
  • Lean or Six Sigma certification
  • EIT or PE license
  • Knowledge of manufacturing processes, equipment, tooling, and production systems
  • Strong problem-solving and root cause analysis skills
  • Proficiency with Microsoft Office applications and BMS/MES systems
  • Strong communication and cross-functional collaboration skills

Smith & Nephew Compensation & Benefits Highlights

The following summarizes recurring compensation and benefits themes identified from responses generated by popular LLMs to common candidate questions about Smith & Nephew and has not been reviewed or approved by Smith & Nephew.

  • Healthcare Strength — Medical, dental, and vision plans are paired with a global mental‑health program for employees and families, indicating a robust core health package.
  • Retirement Support — U.S. employees have access to a 401(k) with company contributions, and share plans complement long‑term savings.
  • Leave & Time Off Breadth — Generous holiday, paid volunteering leave, and flexible work models point to broad time‑off options.

Smith & Nephew Insights

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The Company
HQ: Watford
15,318 Employees

What We Do

Smith+Nephew is a global medical technology company. We design and manufacture technology that takes the limits off living. We support healthcare professionals to return their patients to health and mobility, helping them to perform at their fullest potential. From our first employee and founder, T.J. Smith, to our team today, it’s our people who make Smith+Nephew a unique place. Yes, we love to innovate and develop exciting technologies, and we offer competitive salaries and progressive benefits. But it’s our culture - of Care, Collaboration and Courage - that really sets us apart. Through a spirit of ownership and can-do attitude, we work together to win.. We’re a company of people who care about each other, about our customers and their patients, and about our communities. Together, we fulfill our shared purpose of Life Unlimited. Please note: not all products referred to may be approved for use or available in all markets.

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