Quality Assurance Engineer Jobs in Oklahoma

Job Title: Quality Engineer Company: Sterling-Hoffman Life Sciences Location: Tulsa, OK Description: Our client is a publicly traded medical device company that is focused on the development and distribution of innovative products for the dental market. They boast exceptional revenue growth, an experienced management team and clear leadership positions in their core segments. This is a unique opportunity for someone that wants to put their drive and initiative to work! Qualifications/Skills Required -------------------------------------------- 1) BS in Science, Engineering or a related discipline 2) ASQ certification as CQA, CQE or CRE 3) 5 – 10 years of experience as a Quality Engineer in the medical device or comparable regulated industry 4) Working knowledge of product development life cycle from feasibility through product retirement including design verification and validation, product release, configuration management, risk management, reliability testing and post market surveillance 5) Working knowledge of GMP, quality systems, regulatory requirements, design validation principles and manufacturing methods in Medical Device regulated environment 6) General knowledge of FDA 21 CFR 820 Quality System Regulation, ISO 13485 2003, Medical Device Directive 93/42/EEC, ISO 14971 2007 7) Knowledge of policies and procedures involved in managing an organization’s risk exposures 8) Strong project management skills 9) Strong mathematical, statistical and mechanical aptitude skills 10) Effective communication skills through reading, writing and verbal media 11) Strong computer skills – Microsoft Office suite 12) Ability to multi-task and work without direct supervision 13) Ability to analyze, estimate and evaluate Qualifications/Skills Required -------------------------------------------- 1) Follow quality assurance and product development guidelines and procedures 2) Ensure that developed and marketed products comply with quality, regulatory, and engineering requirements 3) Provide quality engineering support to the Product Development Team 4) Work closely with RD, Marketing and Operations to develop and implement appropriate risk management, qualification, verification and validation plans 5) Review and approve documents that support product development activities, including design input/output, verification, validation, traceability analysis, risk analysis, packaging protocols and reports 6) Participate in design, phase and stage gate reviews to support assigned development projects as well as ensure all generated documentation is complete 7) Provide guidance in the early selection and assessment of suppliers 8) Lead problem-solving efforts to identify and resolve new and recurring quality issues 9) Ensure development and production of safe and effective medical devices 10) Prepare and review qualification and validation test plans, reports for assigned projects, including, if required, reliability assessment 11) Ensure the resolution of issues raised by testing 12) Develop, implement, manage and track effectiveness of corrective action plans and compliance improvement initiatives 13) Ensure accurate project schedules are maintained and communicated to both internal and external management 14) Perform statistical analysis of data and writes technical reports

Job Title: Process Quality Engineer Company: CPKelco, a Huber Company Location: Okmulgee, OK Description: Job ID: 247Position Description: CP Kelco, a J. M. Huber company and a leading global producer of specialty ingredients used in food, pharmaceutical and consumer products has an immediate opening for a Process Quality Engineer in our Okmulgee (Tulsa area) OK plant/facilityThe Process Quality Engineer will lead the initiative of continuous process improvement. This role is designed to integrate quality into the production operation by providing and analyzing production data that leads to process improvements. The Process Quality Engineer is responsible for defining process conditions, analyzing data to ensure optimum production, troubleshooting process problems and recommending solutions. Incumbent interprets information from various sources and recommends courses of action designed to address problem areas. Manages and direct statistical process control activities to achieve and sustain product stability. Leads cross-functional team efforts to improve products and processes. Participates as requested in special assignments such as new method and techniques development, cost studies, and providing expertise to other areas of the plant in trouble shooting problems. Responsible for Safety and Environmental compliance and assures that Quality Management system requirements, including GMP’s and GLP’s, are established and maintained.• Must interpret information from various sources and recommend courses of action designed to address problem areas.• Reviews data for trends or deviations from the norm and provides feedback to other areas of the plant.• Participates as requested in special assignments such as new method and technique development, test method validation, process capability studies, and providing expertise to other teams of the plant in trouble shooting production/testing problems. May assign specific portions of problems to various staff members.• Actively participates on manufacturing site management teams to drive continuous Quality improvement, sharing best practices and innovative solutions with other manufacturing locations.• Reviews and helps to improve site quality systems, ensuring proactive continuous improvement. Identifies and analyzes opportunities for quality improvement using six sigma tools and methodologies.• Provides imaginative, thorough and practicable solutions to a wide variety of difficult quality-related problems.Position Requirements:• The incumbent entering this position will possess a B.S. degree in a scientific discipline or chemical engineering with two to five years qualifying experience. Certified Black Belt Preferred.• The ideal candidate will possess strong initiative, have excellent team building skills, and have the ability to work in a self-directed environment.• Strong knowledge of manufacturing processes and relevant statistical techniques (Six Sigma, Statistical Process Control (SPC).• Demonstrated ability in the use and application of SPC/DOE/FMEA and other problem solving methodologies• Must demonstrate the capability to conduct independent studies, to creatively solve problems, and to provide leadership and direction to other personnel.Responsible for Safety and Environmental compliance, auditing the Quality Management system, and supporting GMP requirements for the plant.J. M Huber and CP Kelco are built on a tradition of strong customer relationships, high ethical standards and technology leadership and provide employees with strong compensation and benefits plans and a culture of innovation, tradition and respect for people.An Equal Employment Opportunity Employer M/F/D/V.

Job Title: Sr Quality Engineer (2009317) Company: Not Specified Location: Oklahoma City, OK Description: 2009317 Job Description Responsible for the management of quality control and engineering programs for designated manufacturing and development activities.  Supports new product development and implementation of an overall quality plan, including inspection, test, and audit procedures. Required Skills Must have thorough knowledge of statistics and familiarity with inspection/reliability plans.  Supervisory experience and CQE preferred. Required Experience B.S. Engineering plus 3 - 5 years engineering experience. Job Location Oklahoma City, OK, US. Position Type Full-Time/Regular