Quality Control Inspector Review and Release
About The Position
Nova Biomedical: One Global Brand. One Vision. Together under one name. Advanced Instruments and Nova Biomedical are now united under one brand, Nova Biomedical , marking a major milestone in our journey to deliver greater value to our customers. By combining our strengths, we're accelerating innovation, supporting critical workflows, and delivering world-class service across the biopharmaceutical and clinical markets. About the company At Nova Biomedical, were not just building instruments, were powering breakthroughs that improve lives. Our smart, science-driven solutions are trusted in over 100 countries to speed drug development and enhance patient care. Our integration brings together more than 70 years of scientific excellence with Novas cutting-edge innovation, forming a powerhouse of precision, purpose, and possibility. With FDA-registered, ISO-certified manufacturing, more than 125 FDA approvals, and industry-trusted diagnostics, were setting new standards in quality and reliability. Nova Biomedical is proud to be a global leader in osmolality testing and biotechnology and in vitro diagnostic (IVD) instrumentation, dedicated to advancing patient care and scientific discovery with a legacy that continues to shape the future of life sciences. With headquarters in Norwood and Waltham, Massachusetts, and a global team of nearly 2,000 employees, were building a collaborative, empowered culture grounded in shared values: Customer Centricity, Ingenuity, Ownership & Accountability, Collaboration, and Integrity . Working at Nova Biomedical means joining a mission-driven organization where your contributions matter. Whether you're in engineering, science, manufacturing, or support, youll be part of a team that values innovation, invests in your growth, and is committed to making a real-world impact on global health. Explore whats next with us at novabiomedical.com or aicompanies.com About the role this role is responsible for the completion of the work assigned to your and will contribute to the overall success of the Quality Control (QC) Department. Under limited supervision and following established procedures and guidelines, this position supplies assistance and support to the manufacturing operations (consumables or Reagent department areas) and R&D groups. You will be self-motivated and responsible for performing the Real Time Inspection of the Reagent Department filling and packaging, review of Device History Records (DHR), the inspection of labels / final products, the performance of line clearances, and possibly the processing of Non-Conforming Materials in support of Manufacturings schedule. You will be highly experienced in the inspection of consumables and fluid manufacturing products. You will electronically transact product to Finished Goods and will generate and maintain certification for all released products. You will be familiar with retrieving various DHRs per established procedures. You will train other Review & Release Inspectors. If you are passionate about quality and want to be part of a team that is shaping the future of life sciences, wed love to hear from you, apply today!
Requirements
- Read, Write, Speak and understand English
- Familiar with Good Documentation Practices (GDP)
- Proficient in Word, Excel, Access and PowerPoint
- Understanding of data trending techniques
- Attention to detail
- Ability to multi-task
- Math skills and able to use calculator
- Basic to advanced computer knowledge and use
- Able to follow written protocols or procedures in the execution of daily assigned work and working in a Quality System Regulated (QSR) FDA regulated industry.
- High school diploma, or equivalent, with a concentration in the sciences with 5+ years of applicable experience.
- Associates Degree with a concentration in the sciences with 3 plus years experience as a QC Inspector.
- Undergraduate Degree with a concentration on the sciences with 1 plus years experience as a QC Inspector.
- Ability to pay attention to detail
- Ability to multi-task
- Math skills and able to use a calculator
- Basic to advanced computer knowledge and use
- Able to follow written protocols or procedures in the execution of daily assigned work and working in a Quality System Regulated (QSR) FDA regulated industry.
Responsibilities
- Understanding of QSR, GMP, GDP requirements as it relates to assigned responsibilities
- Read and understand APs, TPs, OIs, OPs, drawings, MVs, ECOs, test data and any other documentation in the DHR for the area.
- Correctly scan and file DHRs and product related information, as needed.
- Perform data entry, as needed
- Final approval of test results and the DHR for product to be released to Finished Goods.
- Perform inspection of documentation revision.
- Will perform visual and/or mechanical inspections on all completed consumable and Reagent Department products
- Will assist in the processing of non-conforming materials.
- Will generate and maintain certification for reagent products and all consumables for customer use
- Will perform Real Time Inspections in both the Reagent Department and consumables
- Will perform or verify area inspections.
- Communicate to QC group staff and supervisor information to maximize quality and productivity.
- Attend meetings when required.
Benefits
- Flexible Medical, Dental, & Vision Coverage
- Competitive 401k company match
- Bonus Program, Generous PTO and paid holidays
- Generous Tuition reimbursement
- Professional development, engagement and events
- Company marketplace for lunch and snacks in our Norwood, MA and Billerica, MA offices
- Company subsidized cafeteria in our Waltham, MA office
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What This Job Offers
Job Type
Full-time
Career Level
Entry Level
Education Level
High school or GED
