Quality Manager

Drucker Diagnostics; Philipsburg (Centre County); On-site; USD 100,000 - 140,000; Full time

Benefits offered by this job

Mission-driven work

Professional development opportunities

Collaborative team environment

Job summary

A healthcare technology company in Philipsburg is looking for a Quality Manager to oversee quality management systems and ensure compliance with regulatory standards. The ideal candidate will have a Bachelor's Degree and at least 5 years in a regulated environment like pharmaceuticals or medical devices. You will lead compliance initiatives, manage quality control activities, and enhance product reliability, playing a crucial role in safeguarding patient health. Join us to make a significant impact in healthcare.

Qualifications

• Minimum of 5 years of experience in an FDA-regulated environment.
• Experience with Quality System documentation required.
• Strong organizational and communication skills essential.

Responsibilities

• Lead Quality, Regulatory, and Compliance Strategy.
• Manage day-to-day Quality Control and Assurance activities.
• Track, analyze, and report Quality KPIs.
• Review and coordinate investigations, nonconformances, and CAPA with the team.
• Track and report Quality KPIs to support leadership decisions.

Skills

Leadership

Quality Management Systems

ISO 13485 Knowledge

Regulatory Affairs

Problem-solving

Customer Focus

Education

Bachelor’s Degree in Engineering, Chemistry, Biology, or related discipline

Tools

MS Office Suite

Document Management Systems

Adobe Acrobat

ERP Systems

Job description

Overview

Quality Manager — ON-SITE, Philipsburg, PA

At Drucker Diagnostics, we know that making people healthier starts with information. Behind every diagnostic test result is a patient waiting to learn what comes next. Our benchtop centrifuges prepare the samples that guide critical healthcare decisions, from routine bloodwork to urgent diagnoses, and support regenerative therapies like Platelet Rich Plasma treatments. When accuracy matters most, laboratories and clinics in over 80 countries trust the instruments we design and build right here in the USA. We believe that quality is more than a step in the inspection process. It is a commitment built into every process, every decision, and every product. We operate in an environment where our customers depend on us for compliance and precision that directly impact patient outcomes. The Quality and Regulatory Team plays a critical role in protecting that trust and ensuring our products meet the highest standards worldwide. If you want to make a real difference building something truly remarkable, join us.

Your Mission

As the Quality Manager, you will work closely with the Director of Quality & Regulatory and the members of the Quality & Regulatory Team, managing the company's Quality Management System. This role champions a proactive, prevention-focused quality culture, partners closely with cross-functional leaders, and ensures Drucker Diagnostics meets all applicable regulatory and customer requirements. Your work will directly advance our mission to make people safer, healthier, and more productive.

What You’ll Do – Essential Duties and Responsibilities

• Lead Quality, Regulatory, and Compliance Strategy
• Support a strong culture of compliance related to Safety, Environmental, and Quality standards
• Ensure all processes, procedures, and outputs meet ISO 13485, FDA, and internal quality standards.
• Coordinate and support ISO 13485 certification activities and all internal, customer, and regulatory audits.
• Partner with the Director of Quality & Regulatory to support regulatory strategies and ongoing compliance efforts.

• Champion Mission, Risk Management, and Ethical Leadership
• Demonstrate a strong commitment to the organization’s Mission, Vision, and Core Values.
• Support a company culture dedicated to safety, continuous improvement, employee growth, and well-being.
• Participate in and support risk management activities across all stages of design, manufacturing, and product lifecycle.
• Proactively identify regulatory, quality, and operational risks and lead mitigation strategies.

• Manage and Maintain the Quality Management System (QMS)
• Manage day-to-day Quality Control and Quality Assurance activities in alignment with established QMS requirements.
• Administer and continuously improve document control and configuration management systems.
• Review, support, and coordinate investigations, nonconformances, and CAPA in partnership with the Quality & Regulatory team.
• Support Management Review activities by preparing inputs, data analysis, and follow-up actions related to the QMS effectiveness

• Drive Continuous Improvement and Performance Metrics
• Track, analyze, and report Quality KPIs to support leadership decision-making and regulatory requirements. Support initiatives to reduce out-of-box failures, customer complaints, and quality-related losses.
• Apply quality improvement tools and methodologies to increase productivity, consistency, and customer satisfaction.
• Assist in the development and implementation of new quality standards, including manual and automated test procedures.

• Partner Across the Organization
• Collaborate with Engineering, Manufacturing, Supply Chain, and Operations to support product development, process improvements, and new product introductions.
• Support reliability engineering, failure analysis, supplier quality, quality engineering, and auditing activities.
• Participate in quality support for GMP manufacturing capabilities as required.

• Develop People and Support Team Effectiveness
• Support the development and day-to-day management of Quality & Regulatory team members.
• Assist with setting clear departmental goals aligned with organizational priorities.
• Maintain open communication through regular one-on-one and team meetings.
• Support a compliant, effective training program for all employees.

• Manage Resources and Planning
• Support departmental resource planning and budget tracking.
• Help ensure staffing, tools, and systems align with quality and regulatory needs.

• Supervisory Responsibilities
• This position may provide day-to-day work direction, coaching, and support to Quality and Regulatory team members and may participate in hiring, training, performance management, and employee development activities in accordance with company policies and applicable laws

What You’ll Bring

Required Qualifications:

• Always prioritize safety and actively demonstrate safe practices in every task. Follow all safety procedures, proactively report unsafe situations, and wear the required PPE.
• Lead by example in maintaining a safe work environment and encourage your co-workers to do the same.
• A passion for working in a fast-paced, safety-oriented, mission-driven manufacturing environment.
• Demonstrated leadership experience in a regulated quality environment.
• Strong working knowledge of ISO 13485 International Standard, CMDCAS, FDA, EU regulations/directives, and other international regulations as required.
• Proven ability to lead compliance, audits, and continuous improvement initiatives.
• Strong customer focus with the ability to work independently and follow tasks through to completion.
• Excellent organizational, prioritization, and problem-solving skills.
• Strong interpersonal skills with the ability to collaborate effectively across departments.
• Experience with Quality System documentation and good documentation practices.
• Active ASQ membership is desirable.
• Excellent written, verbal, and presentation communication skills.
• Ability to present information to all levels of employees and partners.

Desired Education and Experience:

• Bachelor’s Degree in Engineering, Chemistry, Biology, or a related technical discipline.
• Minimum of 5 years of experience in an FDA-regulated pharmaceutical, biotechnology, or medical device environment. Previous engineering experience in a medical device market preferred.
• At least 5 years of Quality Assurance experience.
• Or an equivalent combination of education and experience.
• Alternate education and experience considered based on the individual candida

Physical and Work Environment Requirements:

• Office and Manufacturing Environment with a strong focus on safety and quality.
• PPE is required in designated areas.
• Combination of sitting, standing, and moving throughout the facility during the workday
• Ability to frequently lift or move materials up to 25 pounds.

Computer Skills

• Strong computer skill required for documentation and training.
• Proficiency in MS Office Suite
• Experience with document management and ERP systems
• Adobe Acrobat required

Travel Requirements:

• Occasional local travel during the business day, mostly between facilities.

Why Join Us?

• Be part of a mission-driven company helping make people safer, healthier, and more productive.
• Know that your leadership directly impacts the safety and reliability of products used in laboratories, by healthcare providers, and by patients worldwide.
• Join a team that takes pride in craftsmanship, quality, and doing work that truly matters.
• Lead and develop high-performing teams within a collaborative environment that values continuous improvement and operational excellence.

At Drucker Diagnostics, we know that behind every great product is a great person. We would be honored to have you join our team and our vision for building something truly remarkable that will long outlast us!