Quality Specialist
We are the people who give possibilities purpose
BD is one of the largest global medical technology companies in the world. Advancing the world of health™ is our Purpose, and it's no small feat. It takes the imagination and passion of all of us-from design and engineering to the manufacturing and marketing of our billions of MedTech products per year-to look at the impossible and find transformative solutions that turn dreams into possibilities.
Job Description
- Validation Planning & Execution
- Develop and execute validation protocols (IQ/OQ/PQ) for eDHR systems and related equipment.
- Ensure validation activities meet regulatory standards such as FDA 21 CFR Part 11 and ISO 13485.
- Conduct performance testing and document results to confirm system functionality and reliability.
•
System Compliance & Quality Assurance
- Ensure eDHR systems comply with internal quality standards and external regulations.
- Collaborate with Quality Assurance teams to align validation efforts with broader quality goals.
- Participate in audits and provide documentation to support compliance.
•
Process & Data Integrity
- Validate that eDHR systems accurately capture and store production data in real-time.
- Monitor data integrity across the manufacturing lifecycle-from raw materials to finished goods.
- Ensure traceability and error-proofing mechanisms are functioning as intended.
•
Documentation & Reporting
- Author and maintain validation documentation, including protocols, reports, and SOPs.
- Record and analyze test data to identify anomalies and ensure systems meet specifications.
- Prepare detailed reports for internal review and regulatory submissions.
•
Cross-Functional Collaboration
- Work with IT, OT, manufacturing, and quality teams to coordinate validation activities.
- Support changing control processes and ensure validated state is maintained during updates.
- Train and mentor team members on validation procedures and compliance requirements
Qualifications:
- Bachelor's degree in biomedical engineering, Quality Assurance, Engineering, or Information Technology.
- Hands-on experience with eDHR systems, MES platforms (preferably Apriso), and digital manufacturing environments.
- Experience developing and executing validation protocols (IQ/OQ/PQ) for software systems and equipment.
- Strong understanding of computer system validation (CSV) principles and risk-based validation approaches.
- Skilled in performance testing, data analysis, and reporting to confirm system reliability and compliance.
- Proven ability to ensure system compliance with internal quality standards and external regulatory requirements.
- Knowledge of data integrity, error-proofing, and traceability mechanisms in manufacturing systems.
- Proficient in authoring and maintaining validation documentation, including protocols, SOPs, and test reports.
- Ability to analyze test data, identify anomalies, and ensure systems meet defined specifications.
- Experience preparing regulatory submission documents and internal review reports.
- Cross-Functional Collaboration
- Collaboration skills to work with IT, OT, Manufacturing, and Quality teams.
- Experience supporting change control processes and maintaining validated states during system updates
Why Join Us?
Not included in the source posting: about the role, what you'll do, qualifications.
Who can apply
The employer didn't state any visa, work authorization, citizenship or clearance requirements in this posting. Confirm with the employer before applying.
Read automatically from the employer's posting text. Always confirm with the employer — requirements can change after a job is published.