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, visit www.inovio.com.

Job summary
The temporary Quality Control (QC) Technician performs a wide variety of duties including, but not limited to, receiving & inspecting raw materials, Supply Chain Quality activities, supporting the Returned Goods Authorization (RGA) process, performing Device History Record (DHR) reviews, and supporting Quality System compliance to all applicable standards and regulations. The temporary QC Technician is knowledgeable in the application and performance of mechanical and visual evaluations utilizing all facility inspection and test equipment and will be assigned various auditing, investigation and testing tasks to meet departmental and facility goals. The position is responsible for processing of NCMRs through the QC area including initiating NCMRs, assigning NCMR numbers, evaluating/reviewing need for MRB review, closure/review of completed NCMRs, and data entry into the NCMR database.

Essential job functions and duties

• Perform Receiving and Inspection functions for incoming raw materials and finished purchased goods.
• Support the Returned Goods Authorization (RGA) process as needed to maintain continuous flow and increase inventory accuracy.
• Perform visual and mechanical inspection of product and components per procedure, specification or drawings using measuring equipment (i.e. caliper, micrometer, tape, height gauge, etc.)
• Perform work-in-process and inventory transactions to ensure systems and physical product movement.
• Assist in the resolution of Non-Conforming materials and product related issues.
• Perform documentation reviews of Device History records, inspection and test results.
• Support activities of the Corrective Action Board (CAB) as necessary.
• Inspect Work in Progress (WIP) and finished goods items.
• Provide administrative / technical support to the Functional Area Leader of Device Quality in the performance of investigations on reported product failures, adverse events or field complaints in accordance with FDA, MDD, CMDR, and ISO 9000 requirements.
• Update and create Standard Operating Procedures for Quality System related activities.
• Perform other related tasks as assigned.

• Associate's degree (AA) or equivalent from two year college or an equivalent combination of education and experience.
• 3-5 years of Quality Control experience in the medical device or pharmaceutical / biotech industry, with working knowledge of FDA and ISO regulations.
• ASQ CQT certification a plus.
• Strong organizational, project management and communication skills and the ability to perform varied tasks in a disciplined, consistent manner.
• Ability to work under minimum supervision and in a team environment.
• Ability to read, analyze, and interpret technical procedures and regulations.
• Ability to work with mathematical problems such as adding, subtracting, multiplying, dividing, decimals and math conversions. Ability to apply concepts such as fractions, percentages, ratios, and proportions to practical situations.
• Ability to solve practical problems and deal with a variety of concrete variables in situations where only limited standardization exists.
• Ability to lift heavy items (35 lbs.).

The hourly range for this role is $22.14 to $26.74. Individual pay decisions ultimately depend on various factors including, but not limited to, relevant experience, knowledge, skills, education, geography, internal equity and alignment with external market data.

Disclaimer

INOVIO Pharmaceuticals, Inc. is committed to a policy of equal employment opportunity. In keeping with our policy, INOVIO will recruit, hire, train and promote into all job titles the most qualified individuals, without regard to race, color, creed, gender, gender identity and expression, religion, marital status, registered domestic partner status, age, national origin or ancestry, military or veteran status, physical or mental disability, medical condition including genetic characteristics, sexual orientation, or any other consideration made unlawful by federal, state, or local laws.

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.