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Equilibar, LLC

Quality Manager

Posted 6 Days Ago
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In-Office
28732, Fletcher, NC
Entry level
In-Office
28732, Fletcher, NC
Entry level
Manage and continuously improve the company’s ISO-based Quality Management System in a manufacturing environment. Lead root-cause investigations, corrective and preventive actions, nonconformance resolution, audits, risk management, supplier quality, documentation, training, and continuous improvement. Partner with Engineering, Manufacturing, Purchasing, Customer Support, suppliers, and regulated-industry customers to ensure product and process conformance. Develop quality personnel and promote a collaborative culture of ownership, problem-solving, safety, and operational excellence.
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Quality Manager – Equilibar
Location:    Fletcher, North Carolina 
Reports to:    President, Equilibar

The Position:
The Quality Manager is responsible for maintaining and continuously improving Equilibar’s Quality Management System (QMS) to ensure our products, processes, and customer solutions consistently meet internal, regulatory, and customer requirements. This position works across Engineering, Production, Customer Support, and other teams to identify quality issues, determine root causes, implement effective corrective actions, and ensure learnings are incorporated into the organization.
The Quality Manager serves as a key resource and responsibility for quality-related problem solving, documentation, audits, and continuous improvement, training, and safety. This position also supports customers with quality and compliance requirements, including customers in highly regulated industries such as biopharmaceutical manufacturing. Success in this role requires a hands-on approach, strong technical problem-solving skills, attention to detail, and the ability to work collaboratively across the organization.  Success also includes strong audit performance, conformance to applicable quality and customer requirements, accurate and useful documentation, timely follow-up on quality actions, and effective development of the quality team. Most importantly, the role helps build a culture where quality is used to solve problems, improve processes, and consistently deliver products and solutions that meet or exceed customer expectations.
This is a full-time, hybrid position based out of Fletcher, NC.  
Key Responsibilities
Quality Management System
•    Maintain and support Equilibar’s QMS and ensure established quality processes are being consistently followed and remain effective. 
•    Coordinate required quality activities, meetings, reviews, and documentation and support programs related to internal audits, verification, corrective and preventive actions, risk management, continuous improvement, training, safety, management review and environmental requirements. 
•    Work with process owners to identify gaps, follow up on required actions, and ensure quality issues are appropriately addressed.
Root Cause, Corrective Action & Continuous Improvement
•    Facilitate the investigation of quality issues and customer concerns using structured root-cause analysis and problem-solving methods. 
•    Work with Engineering, Manufacturing, Customer Support, and other teams to develop and implement corrective actions, verify their effectiveness, and identify opportunities to prevent recurrence. 
•    Review customer support cases and recurring issues to identify trends, determine when additional investigation or escalation is needed, and ensure important learnings are captured and communicated.
Audits & Quality Compliance
•    Coordinate internal and external quality audits and serve as primary contact with Equilibar’s certification and registration bodies. 
•    Maintain awareness of applicable quality standards, regulations, and industry practices and ensure required audits, documentation, training, and follow-up activities are completed. 
•    Support process owners in addressing audit observations and implementing corrective actions.  
•    Support customer quality reviews, questionnaires, audits, and requests for quality documentation, with particular attention to customers operating in regulated industries such as biopharmaceutical and pharmaceutical manufacturing. 
•    Work with customers and internal teams to understand applicable quality expectations and demonstrate conformance to required industry standards and customer-specific requirements. 
•    Coordinate responses to customer audit findings and quality concerns and ensure appropriate corrective actions and supporting documentation are completed.

Supplier Quality & Performance: 
•    Work with Purchasing, Engineering, Manufacturing, and suppliers to improve the quality and consistency of purchased components and services. 
•    Monitor supplier quality performance, investigate recurring or significant supplier issues, and coordinate corrective actions when needed. 
•    Communicate quality expectations to suppliers, follow up on nonconformances, and help ensure supplier improvements are effective and sustained.
Quality Leadership & Cross-Functional Support:
•    Lead and develop direct reports while working closely with Engineering, Manufacturing, Customer Support, Operations, and other teams to resolve quality issues and improve processes. 
•    Provide coaching and quality expertise in areas such as root-cause analysis, corrective actions, auditing, risk assessment, Lean manufacturing, and continuous improvement. 
•    Encourage ownership, collaboration, problem-solving, and ongoing professional development across the quality team and organization.
Qualifications Include: 
•    Experience leading or developing quality personnel.
•    Experience managing or administering an ISO-based Quality Management System in an engineering or manufacturing environment.
•    Experience with root-cause analysis, corrective actions, nonconformances, and continuous improvement.
•    Experience conducting or supporting internal and external quality audits.
•    Strong technical problem-solving and analytical skills.
•    Strong written and verbal communication skills.
•    Ability to work effectively with Engineering, Manufacturing, customers, suppliers, and other cross-functional teams.
•    Experience maintaining quality documentation and records.
•    Ability to organize and follow through on multiple quality activities and corrective actions simultaneously.
•    Bachelor’s degree in engineering, business, or related field; advanced degree preferred.
•    Experience with pharmaceutical, biopharmaceutical, life sciences, or other regulated-industry customers.
•    Familiarity with GMP and customer-specific quality requirements.

Personal Characteristics: 
•    Organized and detail-oriented 
•    Collaborative and approachable
•    Curious and analytical
•    Comfortable challenging existing processes
•    Strong sense of ownership and follow-through.
•    Committed to Continuous Improvement
•    Outstanding Problem Solver
•    Able to balance customer, technical, and business needs.
•    Motivated to develop and mentor others.
•    Committed to safe and responsible work practices.
•    Adaptable, able to thrive in a dynamic work environment

Why would this role be exciting for me?
•    Richards is a profitable, thriving company that’s investing for growth - career development is important for us
•    This is an opportunity to join a talented, hard-working team that’s pushing itself to be the best it can be.
•    This is an opportunity to work closely with a skilled, hard-working team dedicated to achieving excellence in product quality.
•    The opportunity to contribute to the development and implementation of effective quality control processes that enhance product reliability and customer satisfaction.
•    We give back to the community through philanthropy and community service.
Company Profile 
Richards Industrials, founded in 1961, is a manufacturer of pressure regulators, control valves, and other fluid control products, known by our customers for high-quality products, excellent customer service, and fast & reliable deliveries.  Our products are marketed under a series of distinct brands, each of which is used in unique applications that require precise technical attributes.  The company serves a range of end markets, including pharmaceuticals, food & beverage, chemicals, petrochemicals, and various industrial segments.  
The company has two locations, Cincinnati, OH, and Fletcher, NC, and a global headcount of 190. Equipped with an experienced, passionate team, our company focuses on driving profitable growth through operational excellence, opening new channels to market, and investing in new products.  
Equilibar, based in Fletcher, NC, manufactures specialized valves that enable pharmaceutical, green energy, and research organizations to solve complex fluid control challenges and bring innovative products to market.
Equilibar has four Core Values: 
•    Empowerment – Employees are our most valuable asset
•    Collaboration – Together we achieve more
•    Pioneering Spirit – Curiosity and innovation are our driving forces
•    Service Mindset – Never stop advocating for the Customer
And our purpose is to solve tomorrow’s demanding fluid control problems, today.  
Equilibar firmly supports the principle and philosophy of equal opportunity for all individuals. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, disability, or status as a protected veteran.

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