Quality Control Inspector II, Weekend

Integra LifeSciences Corporation; Plainsboro Township (NJ); On-site; USD 50,000 - 90,000; Full time

Job summary

An established industry player is seeking a dedicated Quality Control Inspector II to play a pivotal role in ensuring product safety and compliance in the medical device sector. This position involves inspecting raw materials and finished products, maintaining detailed records, and collaborating with cross-functional teams to enhance quality standards. The ideal candidate will have a strong background in GMP/GLP practices and effective communication skills. Join a team that values innovation and quality, making a tangible impact on patient care and healthcare outcomes. This is a fantastic opportunity for those looking to advance their careers in a dynamic environment focused on excellence.

Qualifications

• 3-7 years of relevant GMP/GLP experience in inspections.
• Strong written and verbal communication skills are essential.

Responsibilities

• Inspect raw materials and finished products for defects.
• Maintain detailed records of inspections and test results.
• Ensure compliance with industry regulations like FDA and ISO.

Skills

GMP/GLP experience

Communication Skills

Organizational Skills

Problem Solving

Attention to Detail

Time Management

Education

Associate degree in science

Tools

Microsoft Office Suite

Job description

Changing lives. Building Careers.

Joining us is a chance to do important work that creates change and shapes the future of healthcare. Thinking differently is what we do best. To us, change equals opportunity. Every day, our colleagues are challenging what’s possible and making headway to innovate new treatment pathways to advance patient outcomes and set new standards of care.

A Quality Control (QC) Inspector II plays a critical role in ensuring that products meet the required safety, performance, and regulatory standards before they reach the market. Their responsibilities typically include:

1. Inspection and Testing: QC Inspectors examine raw materials, in-process components, and finished products for defects, inconsistencies, or non-compliance with established specifications. They perform visual, mechanical, and sometimes functional tests to ensure products meet regulatory requirements (such as FDA or ISO standards).
2. Documentation and Reporting: They maintain detailed records of inspections, test results, and any deviations from quality standards. They document any non-conformities, assist with root cause analysis, and work with engineering or production teams to address issues.
3. Regulatory Compliance: Ensure that all processes and products comply with industry regulations, such as FDA's Good Manufacturing Practices (GMP) or ISO 9001, ISO 13485 standards. They may be involved in preparing for audits and assisting with the implementation of corrective and preventive actions (CAPA).
4. Collaboration with Teams: They work closely with production, engineering, and design teams to resolve quality issues and contribute to continuous improvement initiatives, such as process optimizations or design changes to enhance product quality.
5. Training and Support: They may provide training to production staff on quality standards and best practices, and occasionally, they might also assist in the development of standard operating procedures (SOPs) for inspection processes.

QC Inspectors in medical device companies play a crucial role in maintaining product integrity and ensuring that devices are safe and effective for patient use.

This role will be on the Weekend Shifts Friday, Saturday and Sunday - 1st Shift (12 hours per shift)

To perform this job successfully, an individual must be able to perform each essential duty satisfactorily.

• Perform inspection by using a variety of inspection measuring and test equipment to determine acceptance or rejection of material or parts.
• 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.
• Interpret and work within the guideline of drawings, specifications, charts, procedures, and other data to determine acceptance or rejection of materials.
• Read and interpret sampling plans as per the American National Standards Institute (ANSI).
• Assist in the review and disposition of non-conforming material and customer returned material, including rework, scrap, and return to vendor.
• Maintain accurate and current inspection and/or testing records such as Material Certifications, Inspection/Test Results and reports, Certificates of Conformance, Rejection reports/tags, as required by applicable procedure and/or specification.
• Coordinate and inform other departments of inspection and/or testing status in support of production and project goals and initiatives.
• Promote and participate in continuous improvement initiatives.
• 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.
• Maintain records of inspection and all testing performed on the appropriate test records.
• Perform line clearances and quality reviews in manufacturing, labeling, or other assigned areas during manufacturing activities.
• Identify and implement opportunities for continuous improvement, including document revisions in order to maintain accurate SOPs.
• Provide quality support to various departments as needed, e.g. engineering, product development, etc.
• Assist in training new associates according to the Quality System Regulations and company SOPs as applicable.
• May also perform other related duties, responsibilities, and special projects as assigned.

The requirements listed below are representative of the knowledge, skill, and/or ability required for this position.

• Associate degree in science is preferred.
• 3-7 years of relevant GMP/GLP experience specific to incoming, line clearance, in-process, and finished goods inspections in the pharmaceutical or medical device industry.
• QA experience in the medical device industry preferred.
• Must have strong written and verbal communication skills.
• Strong organizational skills, self-directed, strong problem solving and interpersonal skills.
• Knowledge of CAPA, Validations, Change Control, preferred.
• Working knowledge of ISO 13485, 21CFR820 FDA QSR, and cGMP.
• Knowledgeable in Microsoft Office Suite (Word, Excel, PowerPoint, Outlook) preferred.
• Ability to define problems, collect data, establish facts and draw valid conclusions.
• Ability to work effectively in a cross-functional environment.
• Ability to integrate quality objectives across multiple functions.
• Attention to detail, strong time management are essential.
• Must be able to work independently with minimal supervision.

Integra LifeSciences is an equal opportunity employer, and is committed to providing equal employment opportunities to all qualified applicants and employees regardless of race, marital status, color, religion, sex, age, national origin, sexual orientation, physical or mental disability, or protected veteran status.

This site is governed solely by applicable U.S. laws and governmental regulations. If you'd like more information on your rights under the law, please see the following notices:

EEO Is the Law | EOE including Disability/Protected Veterans

Integra LifeSciences is committed to providing qualified applicants and employees who are disabled veterans or individuals with disabilities with needed reasonable accommodations in accordance with the ADA. If you have difficulty using our online system due to a disability and need an accommodation, please email us at [e-mail] or call us at 855-936-2666.

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