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Quality Engineer

Job in Columbia, Howard County, Maryland, 21044, USA
Listing for: Cynet Systems
Full Time position
Listed on 2026-08-27
Job specializations:
  • Quality Assurance - QA/QC
    Quality Engineering, Data Analyst, Regulatory Compliance Specialist
Salary/Wage Range or Industry Benchmark: 47.1 - 52.1 USD Hourly USD 47.10 52.10 HOUR
Job Description & How to Apply Below

Job Title

Pay Range: $47.10hr - $52.1hr

Requirement/Must Have:
  • Bachelor of Science or higher;
    Master’s degree is preferred.
  • Technical specialization in change management and data integrity, systems development/validation, or data/trending.
  • Demonstrates an understanding of statistically-based sampling plans, application of analytical tools, and has a history of data driven decision-making.
  • Demonstrates excellent organizational, communication, and project management skills.
  • Ability to prioritize projects to meet organizational goals and objectives.
  • Demonstrates knowledge of the principles of data integrity.
  • Proficiency in the use of modern technology, especially electronic quality management systems, enterprise resource management systems, and the Microsoft suite of applications.
  • Ability to work independently with minimal supervision.
  • Knowledge of international standards and maintaining the currently recognized state-of-the-art.
  • GMP experience required in controlled / regulated environments.
  • Data Integrity experience is a huge plus.
Responsibilities:
  • Support business operations by maintaining critical management systems and assuring the efficacy of established process control programs, including calibration and maintenance, change management, validation, and environmental monitoring.
  • Participate on and lead cross-functional, problem-solving investigation and development teams.
  • Provide guidance on the development and implementation of new and updated Quality System procedures for ISO/QSR, such as validation documents, manufacturing procedures, product & material specifications, and SOPs.
  • Facilitate the development, implementation and monitoring of quality programs and policies to ensure compliance with applicable regional regulations, international standards, and corporate policies.
  • Maintain a thorough understanding of international standards and regional regulations including FDA QMSR (21 CFR Part 820), principles of Data Integrity and 21 CFR Part 11, ISO 13485, Regulation 2017/745 (EUMDR), and CMDR.
  • Support the launching of new or improved products/processes and facilitate the transfer of technology from development to commercialization.
  • Facilitate management of changes in device design and manufacturing procedures for commercialized devices.
  • Author, edit, and provide guidance on the development of validation protocols and reports, product & material specifications, design & development documentation, and quality investigations.
  • Investigate Quality Events using a systematic approach to determine root causes.
  • Develop objective evidence to supplement data driven decision making.
  • Support development of statistically based sampling plans for product testing, inspections, and validations.
  • Provide Statistical Analysis of data to support Quality Systems documentation such as validations, NCs, and Complaints.
  • Develop, review, and approve validation documentation for new and existing products, processes, and equipment.
  • Prepare monthly and quarterly trending data and analysis reports, including Statistical Process Control documentation.
  • Participate in FDA inspections, ISO Certification and surveillance audits, and customer audits.
  • Facilitate and maintain the change management system, completing quality impact assessments and assuring change controls are complete and on-time.
  • Perform Quality Investigations in response to quality events, implementing corrective and preventive actions.
Nice to Have:
  • XX Society for Quality (ASQ) or Regulatory Affairs Professionals (RAPS) certificates.
  • Coding/scripting proficiency and/or experience validating complex data management networks.
Skills:
  • GMP.
  • Data Integrity.
  • ISO 13485.
  • FDA QMSR (21 CFR Part 820).
  • 21 CFR Part 11.
  • EUMDR.
  • CMDR.
  • Statistical Process Control.
  • Change Management.
  • Validation.
  • Quality Management Systems (QMS).
  • Enterprise Resource Management Systems.
  • Microsoft Office Suite.
Qualification And

Education:
  • Candidates who are not certified must demonstrate technical competency by obtaining a relevant certification from an accredited organization within the first year of employment.
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