Quality Engineer I
Inovio Pharmaceuticals
About INOVIOINOVIO is a biotechnology company focused on developing and commercializing DNA medicines to help treat and protect people from HPV-related diseases, cancer, and infectious diseases. INOVIO’s technology optimizes the design and delivery of innovative DNA medicines that teach the body to manufacture its own disease-fighting tools. For more information, visit . Job SummaryThe Quality Engineer I supports the implementation and maintenance of FDA and ISO 13485:2016 compliant Quality Systems within an electro-mechanical medical device manufacturing environment, including Class 7/8 Cleanroom operations for manufacturing sterilized/disposable products. This role assists in managing the environmental monitoring system, including documenting alerts, supporting required responses and preparing trending data and reports for management. The Quality Engineer I also supports activities related to sterilization release records, investigations and resolution of non-conformances, environmental monitoring excursions, equipment calibrations and preventive maintenance, and action items associated with corrective actions. Essential job functions and dutiesManage the QMS environmental monitoring system, including response and documentation of alert notifications (e.g., Vaisala).Provide quality engineering support and guidance for cleanroom environmental operations to ensure compliance with applicable requirements. Document, manage, and drive investigations and resolutions related to environmental monitoring excursions.Assist with equipment management activities, including calibration and preventive maintenance coordination.Prepare and report environmental excursion data and trending analyses to management to support process improvements.Collaborate with other departments as needed to assist with investigations and continuous improvement activities. Assist with documentation associated with product sterilization activities.Support additional Quality Assurance/Quality Control projects and tasks as assigned. Minimum requirementsBachelor’s degree in engineering or a related field preferred, or equivalent combinations of education and experience. 1 -2 years of experience in medical device, biotech, or regulated industry.Ability to present verbal and written information, trends, and investigation results to cross-functional teams and management. Proficiency in Microsoft Word, Excel and Outlook, Visio, PowerPoint software applications.Capable of preparing technical reports, business correspondence, etc.Ability to understand engineering drawings, specifications, diagrams, schedules, and written instructions. Proven ability to plan, prioritize, and complete technical assignments with limited supervision. Able to perform varied tasks consistently and maintain clear communication across teams. Familiarity with statistical controls and data analysis tools is a plus. DisclaimerINOVIO Pharmaceuticals, Inc. is an Equal Employment Opportunity Employer, including but not limited to veterans and individuals with disabilities. We prohibit discrimination of any kind. In keeping with our policy, we recruit, hire, train, and promote the most qualified individuals for all job titles, and we provide equal opportunities to all employees and applicants for employment.A current US work authorization is required. The above statements are intended to describe the general nature and level of work being performed by people assigned to this job. They are not to be construed as an exhaustive list of all responsibilities, duties, and skills required of personnel so classified. All personnel may be required to perform duties outside of their normal responsibilities from time to time, as needed. INOVIO offers an attractive benefits package and is an equal opportunity employer. Important notice to employment businesses/agenciesINOVIO does not accept referrals from employment agencies unless written authorization from the INOVIO Human Resources department has been provided. In the absence of written authorization, any actions undertaken by employment agencies shall be deemed to have been performed without our consent and therefore INOVIO will not be liable for any fees arising from employment agency referrals in respect to current or future position vacancies at INOVIO.
$102.38k - $153.56k
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$91.8k - $137.6k
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$122k - $184k
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...Description Leidos Defense is seeking a Quality Engineer at our San Diego CA. office to join our team in the Quality Assurance Department Program which provides quality assurance, control, inspection and technical installation support for PEO IWS5 NAVSEA SONAR SQQ...Contract workLocal areaImmediate startWorldwide$70.3k - $85k
...bonuses may be awarded semi‑annually based upon your achievement of performance goals and targets. About This Job The Sr. Commercial Quality Control AI Automation Associate is a member of the Commercial Quality Control (CQC) program, dedicated to building and operating...Work at officeLocal area$75k - $95k
...Candidates should have a strong foundation in quality assurance and quality management. Candidates from engineering or applied science backgrounds are welcome to apply, provided they can demonstrate a foundational, working level understanding of electronics and electronic...Work experience placement- The Quality Engineer Level 4 - Risk Management is a senior, highly experienced individual contributor responsible for leading complex risk management activities across the medical device and/or in-vitro diagnostic product lifecycle. The role provides technical leadership...
- The Quality Engineer Level 3 - Risk Management is an experienced individual contributor within Regulatory and Quality for Diagnostics. This role is responsible for performing and maintaining product and process risk management activities for medical device and/or in-vitro...
$95.38k - $160.85k
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$83.4k - $125.2k
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...portfolio. Our mission is to provide objective evidence of software quality, reliability, and mission readiness by building scalable... ...Loop (VIL) environments. As a Senior Software Test & Automation Engineer, you will design and develop automated test infrastructure, execute...Full timeTemporary workPart timeWorldwide- Veteran Categories Disabled veteran: A veteran who served on active duty in the U.S. military and is entitled to disability compensation (or who but for the receipt of military retired pay would be entitled to disability compensation) under laws administered by the ...
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$110k - $125k
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The Digital Product Engineering organization powers digital experiences and engagement to enhance the lives of millions of people every... ...analysis. Act as a bridge between Product Engineering and ResMed Quality/Regulatory teams and bring knowledge on the latest safety-...Full timeTemporary workWork experience placementLocal areaFlexible hours
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