Configuration Control & Change Management Specialist II

CQ Medical Careers; Avondale (PA); On-site; USD 90,000 - 120,000; Full time

Benefits offered by this job

Medical, dental, vision coverage (Day

Life insurance

Disability insurance

Telehealth

Employee Assistance Program

401(k) with immediate vesting

Generous PTO and 11 paid holidays

Job summary

CQ Medical is seeking a Configuration Control & Change Management Specialist II to manage BOMs, routings, and product configuration across manufacturing ERP systems. You will collaborate with Design, Manufacturing, Quality, and Regulatory Affairs to ensure accurate data and controlled processes.

The role emphasizes change implementation, data integrity, and cross‑functional support, with opportunities to improve processes and document controls in a regulated medical device context.

Qualifications

• Bachelor's degree or equivalent in Business, Manufacturing, Engineering, Quality, Information Management, or related discipline.
• Minimum 3 years of relevant experience.
• Strong understanding of controlled information and change implementation processes.
• Ability to independently coordinate multiple change activities.
• Experience with ERP, PLM, QMS, and document management systems is preferred.

Responsibilities

• Maintain complex product structures, bills of materials, routings, and controlled information.
• Verify accuracy, completeness, and consistency prior to implementation.
• Identify and resolve discrepancies across systems, records, and documentation.
• Support audits and reviews related to data integrity.
• Coordinate implementation of approved changes across affected systems and records.
• Monitor implementation status and follow up on outstanding actions.
• Support training of junior staff on configuration control practices.
• Develop and update work instructions and process documentation.

Skills

Change management

Data integrity

Cross-functional coordination

Problem solving

Communication

Organization

Independence

Attention to detail

Education

Bachelor's degree or equiv.

Tools

ERP

PLM

QMS

LMS

Document Mgmt

Job description

Job Details

Posting Details

• Posted on November 5, 2026

Locations

Showing 1 location Avondale, PA 19311, USA

• On-site
• Quality Assurance
• Full-Time
• Requisition #: CONFI001481

Description

CQ Medical is seeking a Configuration Control & Change Management Specialist II with hands‑on experience in manufacturing ERP systems, bills of material (BOMs), routings, and product configuration management.

The ideal candidate will have a solid understanding of how engineering and manufacturing BOMs relate to one another, how manufacturing routings, work centers, and operations should be structured, and how accurate product data supports effective manufacturing processes.

Beyond maintaining this information, we're looking for someone who can recognize gaps or inconsistencies, work collaboratively with Design and Manufacturing Engineering to resolve them, and help establish and reinforce good configuration management practices. This position also supports the broader change management process, ensuring that approved changes are accurately implemented across manufacturing systems, controlled documentation, and other affected business processes.

Essential Responsibilities

Configuration & Data Integrity

• Maintain complex product structures, bills of material, routings, and controlled information.
• Verify accuracy, completeness, and consistency of information prior to implementation.
• Identify and resolve discrepancies across systems, records, and documentation.
• Support audits and reviews related to product and process data integrity.

Change Implementation

• Coordinate implementation of approved changes across affected systems and records.
• Ensure required actions, documentation, training assignments, and supporting activities are completed.
• Monitor implementation status and follow up on outstanding actions.
• Support successful completion and closure of change records.

Information Quality & Problem Resolution

• Identify incomplete, inaccurate, or conflicting information.
• Work with stakeholders to obtain missing information and resolve issues.
• Recommend corrective actions to improve information quality and implementation effectiveness.
• Support investigation of recurring implementation or data integrity issues.

Cross‑Functional Support

• Serve as a resource regarding change implementation requirements and processes.
• Coordinate activities with Engineering, Manufacturing, Quality, Regulatory Affairs, and other business functions.
• Support training of Configuration Control & Change Management Specialist I personnel.

Process Improvement

• Identify opportunities to improve efficiency, accuracy, and effectiveness of change implementation processes.
• Assist with development of work instructions, job aids, and process documentation.
• Support implementation of process improvements and standardization efforts.

Knowledge, Skills & Abilities

Required

• Strong understanding of controlled information and change implementation processes.
• Ability to independently coordinate multiple change activities.
• Strong understanding of data integrity and information accuracy principles.
• Ability to identify, investigate, and resolve information discrepancies.
• Strong organizational, prioritization, and follow‑up skills.
• Ability to communicate effectively with stakeholders across multiple functions.
• Strong analytical and problem‑solving capabilities.
• Ability to work effectively with minimal supervision.
• Ability to balance accuracy, timeliness, and business needs.

Preferred

• Experience with ERP, PLM, QMS, LMS, and document management systems.
• Experience supporting engineering change, manufacturing change, or quality system change processes.
• Experience developing work instructions, job aids, or process documentation.
• Medical device or other regulated industry experience.

Education & Experience

Required

• Bachelor's degree or equivalent experience in Business, Manufacturing, Engineering, Quality, Information Management, or related discipline.
• Minimum 3 years of relevant experience.

Preferred

• Experience with ERP, PLM, QMS, and document management systems.
• Medical device or regulated industry experience.

Medical, Dental, and Vision coverage starts on Day One!

Free life insurance, short and long‑term disability insurance, Telehealth Appointments, and Employee Assistance Program.
Immediate vesting of 401(k) matching. Generous PTO and 11 Paid Holidays a year. And, most importantly... truly meaningful work!

Would you like to make a difference in the lives of cancer patients and their families? We design and manufacture radiation oncology medical devices to ensure more accurate, comfortable treatment for cancer patients. CQ Medical is the global market leader in patient positioning. As an innovative medical device company, we focus on discovering, developing, and distributing technology‑driven solutions to improve outcomes for radiotherapy patient positioning.

We are continuing to grow and expand our products. Join us and earn a Paycheck with a Purpose. www.cqmedical.com

Equal Opportunity Employer/Protected Veterans/Individuals with Disabilities
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