Quality Control Inspector Jobs

Hello, Good day! This is Harsha from Intellectt Inc. One of our clients in the medical device industry is currently seeking a Quality Control Inspector in Princeton, NJ - 8540. If you are interested, please send your updated CV to [email protected], or you can reach me at +1 732-276-1830.

Role: Quality Control Inspector

Location: Princeton, NJ - 8540

Duration: 12 Months on W2

Essential Duties And Responsibilities

• Maintain accurate and current inspection and/or testing records such as nit not limited to Material Certifications, Inspection/Test Results and reports, Certificates of Conformance, Rejection reports/tags, as required by applicable procedure and/or specification.
• Perform first article, incoming/receiving, and in-process inspections of materials or parts; determine acceptance or rejection after inspection and/or testing of materials, parts, and/or equipment.
• May also perform other related duties, responsibilities, and special projects as assigned.
• Read and interpret sampling pan as per the American national standard institute (ANSI),
• Assist in the review and disposition of non-conforming material and customer returned material, including rework, scrap, and return to vendor.
• Responsible for the maintenance of appropriate conditions of all quarantine locations.
• Maintain the QC inspection areas in an orderly fashion conducive to carrying out safe and efficient inspections and procedures.
• Inspection requirements include training and working in classified clean rooms as necessary to perform in process inspections.
• Promote and participate in continuous improvement initiatives.
• Assist in training new associates according to the Quality System Regulations and company SOPs as applicable.
• Coordinate and inform other departments of inspection and/or testing status in support of production and project goals and initiatives.
• Identify and implement opportunities for continuous improvement, including document revisions in order to maintain accurate SOPs.
• Perform line clearances and quality reviews in manufacturing, labeling, or other assigned areas during manufacturing activities.
• Perform inspection by using a variety of inspection measuring and test equipment to determine acceptance or rejection of material or parts.
• Provide quality support to various departments as needed, e.g. engineering, product development, etc.)
• Interpret and work within the guideline of drawings, specifications, charts, procedures, and other data to determine acceptance or rejection of materials.
• Maintain records of inspection and all testing performed on the appropriate test records.

Desired Minimum Qualifications

• Attention to detail, strong time management are essential
• Ability to integrate quality objectives across multiple functions
• Strong organizational skills, self-directed, strong problem solving and interpersonal skills.
• High School diploma (or GED) and some college level courses
• Must have strong written and verbal communication skills.
• 2-7 years of relevant GMP/GLP experience specific to incoming, line clearance, in-process, and finished goods inspections in pharmaceutical or medical device industry.
• QA experience in the medical device industry preferred.
• Ability to work effectively in a cross functional environment
• Working knowledge of ISO 13485, 21CFR820 FDA QSR, and cGMP.
• Ability to define problems, collect data, establish facts and draw valid conclusions
• Must be able to work independently with minimal supervision.
• Knowledge of CAPA, Validations, Change Control, preferred.
• Knowledgeable in Microsoft Office Suite (Word, Excel, PowerPoint, Outlook) preferred.