QMS SUBJECT MATTER EXPERT (SME)

Yokogawa • Newnan, GA

8d • Hybrid

About The Position

Not just a job, but a career Yokogawa, award winner for ‘Best Asset Monitoring Technology’ and ‘Best Digital Twin Technology’ at the HP Awards, is a leading provider of industrial automation, test and measurement, information systems and industrial services in several industries. Our aim is to shape a better future for our planet through supporting the energy transition, (bio)technology, artificial intelligence, industrial cybersecurity, etc. We are committed to the United Nations sustainable development goals by utilizing our ability to measure and connect. About the Team Our 18,000 employees work in over 60 countries with one corporate mission, to "co-innovate tomorrow". We are looking for dynamic colleagues who share our passion for technology and care for our planet. In return, we offer you great career opportunities to grow yourself in a truly global culture where respect, value creation, collaboration, integrity, and gratitude are highly valued and exhibited in everything we do. The QMS Subject Matter Expert (SME) will play a critical role in driving Yokogawa’s OpreX Quality Management System (QMS) solution across Life Sciences, Biopharma, and Food & Beverage industries. This role combines deep domain expertise in quality and compliance with customer-facing responsibilities, including pre-sales support, solution consulting, project execution, and market development. The SME will collaborate cross-functionally with Sales, Product Development, and Delivery teams to ensure the QMS solution aligns with evolving regulatory requirements and market expectations, while actively supporting business growth.

Requirements

• Bachelor’s degree in Life Sciences, Engineering, Quality, or related discipline
• Minimum 5+ years of experience in Quality Management Systems or related roles
• Experience in customer-facing roles (consulting, pre-sales, or solution engineering)
• Strong understanding of validation, audit readiness, and compliance workflows
• Ability to translate business requirements into system configurations
• Hands-on experience with eQMS platforms (e.g., Veeva Vault QMS, MasterControl, TrackWise, ETQ Reliance, ComplianceQuest, or equivalent)
• Working knowledge of core QMS processes: Deviations/Nonconformance, CAPA, Change Control, Document Management, Training Management, Audit Management, Complaints, and Supplier Quality
• Familiarity with integration touchpoints between QMS and adjacent systems (MES, LIMS, ERP, DMS)
• A customer-oriented mindset, excellent analytical and problem-solving skills
• Excellent communication and presentation skills
• Experience working in cross-functional and global teams
• Self-motivation and the desire to work with customers
• Excellent oral and written communication skills
• Ability to work in diverse teams and cross-functionally, prioritize and multitask
• Excellent interpersonal skills and desire to work with customers
• Proficient with Windows operating systems and Microsoft Office
• Valid driver’s license and ability to travel domestically and internationally as required

Nice To Haves

• Master’s degree preferred
• Prior experience implementing eQMS solutions in Life Sciences, Biopharma, Medical Device, or Food & Beverage environments
• Certifications such as ASQ CQE, CQA, CMQ/OE, Lean Six Sigma, or RAC
• Exposure to digital transformation initiatives connecting Quality, Manufacturing, and Lab systems

Responsibilities

• Act as the Subject Matter Expert (SME) for Quality Management Systems
• Provide expert guidance on QA/QC processes, compliance frameworks, and digital quality transformation
• Maintain deep working knowledge of GxP regulations (GMP, GLP, GCP), 21 CFR Part 11, EU Annex 11, ICH Q9/Q10, ISO 9001, and ISO 13485 as applicable to regulated industries
• Support internal teams with domain knowledge, training, and best practices
• Support sales teams in identifying and qualifying QMS opportunities
• Lead customer workshops, discovery sessions, and requirements gathering
• Define User Requirement Specifications (URS) and ensure solution alignment with customer needs
• Deliver compelling product demonstrations and solution presentations
• Advise customers on Computer System Validation (CSV/CSA) approaches and risk-based validation strategies for eQMS deployments
• Provide domain expertise during solution implementation and project execution
• Work closely with delivery teams to ensure compliant and effective solution deployment
• Support validation readiness and ensure alignment with regulatory expectations
• Author and review validation deliverables (Validation Plan, IQ/OQ/PQ protocols, Traceability Matrix, Validation Summary Report) as needed to support customer go-lives
• Contribute to pipeline development and strategic account growth
• Identify new market opportunities within Life Sciences and adjacent industries
• Support development of value propositions and industry-specific use cases
• Analyze market trends, competitor offerings, and positioning of QMS vendors
• Define and articulate Yokogawa OpreX QMS differentiation
• Support creation of marketing collateral, thought leadership, and customer success stories
• Provide structured feedback to Product and Engineering teams
• Ensure the QMS platform evolves to meet customer needs and regulatory trends
• Act as the voice of the customer in product roadmap discussions

Benefits

• great career opportunities to grow yourself in a truly global culture where respect, value creation, collaboration, integrity, and gratitude are highly valued and exhibited in everything we do.

What This Job Offers

• Job Type: Full-time
• Career Level: Senior