Regulatory/Quality Engineer - Galt OEM
Garland, TX 75041
About the Job
Regulatory/Quality Engineer
This position reports to the Director Of Quality/RA
Typical Duties and Responsibilities:
- Achieves product and engineering compliance by developing and executing compliance programs and completing documentation.
- Prevents compliance issues by collaborating with engineering planning and design teams, reviewing design data, and developing compliance policies.
- Identifies and resolves product and engineering design issues by identifying short-term and long-range issues.
- Researches and identifies applicable regulatory and industry compliance standards and codes.
- Develops compliance plans by researching, analyzing, selecting, and applying compliance engineering concepts, approaches, techniques, and criteria.
- Adapts and modifies compliance engineering options.
- Develops and evaluates new compliance methodologies.
- Organizes compliance programs by preparing timetables, cost estimates, and required resources, including test laboratories and equipment.
- Research and contracts with, and supervises, sub-contractors.
- Determines compliance by establishing compliance test standards, conducting and witnessing tests, performing diagnostic procedures, measuring performance, analyzing and evaluating findings, and performing forensic analysis and troubleshooting of failures.
- Attains compliance by isolating and resolving compliance issues, recommending product and process changes, and initiating engineering change orders.
- Documents compliance by completing approval applications, recording test results, preparing investigative reports, preparing, and filing Declarations of Conformity, and maintaining compliance database.
- Maintains engineering team accomplishments by reviewing open issues and action items, coordinating actions, and contributing information and analysis to team meetings and reports.
- Prepares compliance reports by collecting, analyzing, and summarizing measurement data and trends.
- Updates job knowledge by tracking and understanding emerging compliance engineering practices and standards, participating in educational opportunities and professional organizations, reading professional publications, and maintaining personal networks.
- Enhances engineering and organization reputation by accepting ownership for accomplishing new requests and exploring opportunities to add value to job accomplishments.
- Implements product testing and process analysis.
- Creates and maintains post market files for each product family.
- Generates and maintains technical specifications for each product family by SKU.
- Assists in Customer and Marketing requests for documentation.
- Assists in clinical evaluations for each product.
- Ensure compliance with all regulations.
- Maintains regulatory documentation database.
- Keeps up to date with changes in regulatory legislations and guidelines.
- Perform inspections to ensure compliance with local, state and federal regulations.
- Develops and evaluates new compliance methodologies.
- Identifies and interprets relevant regulatory guidelines.
- Recommends adjudication of product complaints.
- Completes final acceptance activities. Manges the sterilization process, including validations and product sterile loads.
- Track nonconforming material. Interfaces and take lead QA role in interactions with suppliers, contractors and consultants that supply components and contract processing.
- Manages corrective action and quality improvement activities.
- Assist in the performance of quality system internal auditing. Supports management review meetings. Establishes, monitors and evaluates quality system metrics.
- Other ad-hoc duties as assigned.
- 4-year College or University Degree in Business, Quality, Engineering or related field preferred.
- 2-3 years’ experience in a Quality related role, preferably in the Medical industry.
- Ability to solve complex problems and exercise judgement based on the analysis of multiples sources of information.
- Ability to read and interpret engineering drawings and specifications.
- Ability to support and/or lead root cause analysis, disciplined problem-solving and decision-making processes.
- Analysis and critical thinking.
- Proven leadership, interpersonal skills and personal development skills.
- Experience in a variety of basic operation disciplines: Manufacturing, Quality Process/Tooling and Shop Floor Supervision.
- Proficient in Microsoft Office.
- Excellent written and verbal communication skills.
- Strong knowledge of relevant software, quality assurance methods, tools and quality manufacturing processes.
- Attention to detail.
- Ability to handle stress.
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Source : Galt OEM