Quality Engineer II (Temporary/Contractor)

INOVIO PHARMACEUTICALS INC; San Diego (CA); On-site; USD 63,000 - 73,000; Full time

Job summary

INOVIO Pharmaceuticals, Inc. seeks a Temporary/Contractor Quality Engineer II to provide hands-on quality engineering and systems support for product development and pilot manufacturing.

You will create and revise quality records, review data for accuracy, and track action items across cross-functional teams. The role emphasizes adherence to FDA QMSR, ISO 13485:2016, and ISO 14971:2019 requirements, with responsibilities spanning documentation, change control, CAPA, and quality metrics to ensure

Qualifications

• Bachelor's degree or higher in a relevant technical field.
• Experience with regulated environments and medical devices or combination products.
• Knowledge of quality system requirements and regulatory expectations.
• Experience authoring or revising SOPs and quality records.
• Experience with CAPA, change control, nonconformance, and document control.

Responsibilities

• Support day-to-day quality engineering and quality systems operations.
• Prepare, review, and revise quality system documents for accuracy and compliance.
• Review records for completeness and data integrity.
• Collect and trend quality metrics for management reporting.
• Assist with calibration and preventive maintenance activities for equipment.
• Support equipment qualification and validation activities (IQ/OQ/PQ).
• Identify documentation gaps and escalate quality issues as needed.
• Collaborate with cross-functional teams to obtain necessary technical information.
• Assist investigations, CAPAs, and process improvement tasks.

Skills

Quality engineering

Quality systems

SOPs

CAPA

Regulatory compliance

FDA QMSR / 21 CFR Part 820

ISO 13485:2016

ISO 14971:2019

Document control

Change control

Cross-functional collaboration

Electrical/electromechanical devices

Quality documentation

Data analysis

Education

Bachelor’s degree in Engineering, Life Sciences, Quality, or related

Tools

MasterControl

BMRAM

Minitab

JMP

eQMS platforms

Job description

If you are unable to complete this application due to a disability, contact this employer to ask for an accommodation or an alternative application process.

Quality Engineer II (Temporary/Contractor)

Contractor - 3rd Party Mesa Ridge, San Diego, CA, US

2 days ago Requisition ID: 1046

Salary Range: $45.67 To $52.88 Hourly

About INOVIO

INOVIO 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, visitwww.inovio.com .

Job summary

The Temporary Quality Engineer II provides hands-on quality engineering, and quality systems support for product development and pilot manufacturing activities. This position supports a variety of assigned quality projects, including document creation and updates, record review, and follow-up on action items.

This role will assist with implementation and maintenance of quality processes related to process changes, documentation updates, quality metrics, management review support, and general quality system compliance activities. The temporary Quality Engineer II will work cross-functionally with Engineering, Manufacturing, Quality Control, and other functions to help ensure that quality records are complete, accurate, timely, and compliant.

This role requires strong attention to detail, solid organizational skills, technical capability, and the ability to work effectively in a fast-paced environment with shifting priorities. This position requires flexibility and willingness to support both technical and routine quality tasks as needed. Experience in regulated environments and the ability to analyze information, communicate clearly, and work effectively with engineers and operations teams is important.

This role supports activities within a quality system aligned with applicable medical devices and combination product quality requirements, including FDA QMSR, ISO 13485:2016, ISO 14971:2019, and applicable constituent-part quality requirements under 21 CFR Part 4.

Essential job functions and duties

• Support day-to-day activities related to quality engineering and quality systems operations.
• Support preparation, review, and revision of quality system documents (SOPs, work instructions, forms, and quality records) to ensure accuracy, clarity, and compliance.
• Review completed records for completeness, accuracy, data integrity, and adherence to applicable procedures and regulatory expectations.
• Support collection, compilation, and trending of quality metrics and other data for management reporting, process monitoring, and quality improvement activities.
• Support manufacturing related activities such as calibration and preventive maintenance programs for manufacturing, laboratory, inspection, and quality equipment.
• Support equipment qualification and validation activities, including IQ/OQ/PQ documentation as assigned.
• Help identify documentation gaps, incomplete or overdue records, and other quality system issues requiring escalation or corrective action.
• Work closely with engineers and other cross-functional team members to obtain technical information required to complete quality records, investigations, and documentation accurately.
• Support investigations, CAPAs, and process improvement activities as assigned.
• Maintain organized files and records within paper-based and/or electronic quality systems.
• Perform other duties as required to support Quality Assurance and quality systems operations in fast-paced environment.
• Bachelor’s degree in Engineering, Life Sciences, Quality, or a related technical discipline.
• Minimum 2-5 years of quality engineering or quality systems experience in a regulated medical device, combination product, biotechnology, or similarly regulated environment.
• Working knowledge of quality system requirements applicable to medical devices and/or combination products, including FDA QMSR / 21 CFR Part 820, ISO 13485:2016, ISO 14971:2019 and applicable elements of 21 CFR Part 4.
• Experience authoring or revising SOPs, work instructions, forms, templates, validation-related documents, or other controlled quality system documentation.
• Experience with change control, document control, nonconformance, CAPA, or other core quality system processes.
• Experience with equipment qualification and computerized systems.
• Experience working cross-functionally with engineering teams and reviewing technical documentation such as drawings, specifications, design documents, test methods, validation documents, and risk management records.
• Ability to manage multiple assignments and deliver high-quality work within timelines in a dynamic environment.
• Proficiency in Microsoft Office applications, especially Excel, Word, PowerPoint, and Outlook.
• Preferred experience with electromechanical devices, software-controlled devices, manufacturing process changes, design changes, or validation change impacts.
• Preferred experience with eQMS platforms such as MasterControl or similar systems.
• Preferred Experience using electronic calibration, maintenance, and asset management systems, preferably Blue Mountain Regulatory Asset Manager (BMRAM).
• Preferred experience using statistical analysis software such as Minitab, JMP, or comparable tools
• Preferred experience supporting combination products, including constituent-part quality system considerations.
• Preferred ability to work independently with limited supervision while exercising sound judgment in identifying and escalating compliance or quality risks.
• Six Sigma Green Belt, Certified Quality Engineer (CQE), Certified Quality Auditor (CQA), or other relevant quality certification preferred.

Disclaimer

INOVIO 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/agencies

INOVIO 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.