Quality Systems Specialist III (Fort Worth, TX)

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

We are looking for a Quality Systems Specialist 3 who will provide strategic leadership and expert support in maintaining and enhancing the maturity of the Quality Management System. This role drives compliance with regulatory requirements (GMP, GxP, FDA, etc.), leads internal and external audits, and acts as a liaison between the quality department and other business units to improve compliance culture.

What will you be doing?

• Lead and maintain the Quality Management System to ensure compliance with internal policies and regulatory standards including GMP, GxP and FDA requirements
• Manage key quality system processes including CAPA, Non-Conformance (NC) and change management, ensuring timely closure and continuous improvement
• Generate and analyze quality metrics to identify trends, support management reviews, and maintain visibility of QMS health
• Coordinate and lead internal audit activities, as well as assist in external audits, and support regulatory inspections, ensuring permanent readiness
• Provide quality expertise on the manufacturing floor, lead investigations, and guide root cause analyses to reduce quality events year over year
• Support manufacturing activities such as but not limited to SOP revisions, nonconformance investigational support, risk management, and post market surveillance activities. 
• Coach and mentor colleagues, facilitating the use of problem-solving methodologies and promoting a culture of continuous improvement

What will you need to be successful?

Education:

• Bachelor’s degree in science, engineering, life sciences or related field

Certifications:

•  Lean or Six Sigma Yellow or Green Belt preferred.
• Certified Quality Auditor (CQA) or Lead Auditor training (ISO 13485) highly desired

Experience:

• Minimum of 5 years of experience in a Quality Systems role within pharmaceutical, biotech or medical device industries
• Experience with GMP, FDA regulations, internal audits and quality investigations

Knowledge:

• Proficiency in MS Office tools and high attention to detail
• Deep understanding of cGMP (current Good Manufacturing Practices), and FDA guidance and regulations.
• Adherence to Quality Systems and Good Manufacturing Practices with high level of attention to detail

Competences:

• Strong problem-solving skills with the ability to coach teams and influence cross functional groups
• Ability to work collaboratively with site personnel to solve issues.
• Effective verbal and written communication skills

Other requirements:

• 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, and work in high noise spaces.
• Travel Requirements: Up to 10% (international and domestic)

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 
• Flexibility: Hybrid Work Model (For most professional roles)  
• Training: Hands-On, Team-Customized, Mentorship  
• Extra Perks: Discounts on fitness clubs, travel and more!  

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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.