QC Inspector, Level II Review and Release - Second Shift

ZipRecruiter; Waltham (MA); On-site; USD 50,000 - 75,000; Full time

Job summary

A leading company in biotechnology is seeking a QC Inspector Level II for its Waltham facility. The role includes overseeing quality assurance processes, conducting inspections, and ensuring compliance with regulatory standards. Candidates should possess a strong attention to detail and a background in science, with fluency in English essential.

Benefits

Blue Cross Blue Shield medical coverage

Tuition reimbursement

Matching 401K plan

Subsidized cafeteria

Innovative scholarship program for employees' children

Qualifications

• Minimum 1 year QC inspector experience.
• Ability to follow protocols in a regulated industry.
• Basic to advanced computer skills required.

Responsibilities

• Oversee daily QC operations ensuring product quality.
• Perform inspections and approve test results.
• Train interns and junior QC inspectors.

Skills

Attention to detail

Good Documentation Practices

Computer skills

Fluency in English

Education

High school diploma with science focus

Associate's degree with science concentration

Tools

Word

Excel

Access

PowerPoint

Job description

Job Description

Nova Biomedical is hiring a QC Inspector Level II for our Review and Release team at our Waltham, MA facility. This is a second shift position, from 3:00 pm to 11:30 pm. The QC Inspector will partner with the Quality Control Supervisor to oversee the daily operations of the assigned Quality Control group, ensuring the quality of all products manufactured or received by Nova Biomedical.

Essential Responsibilities and Accountabilities include:

• Read and understand APs, TPs, OIs, OPs, drawings, MVs, ECOs, test data, and other documentation in the DHR for the area.
• Complete all assigned work in a compliant manner, documenting work according to Nova and Quality Control policies and procedures.
• Scan and file DHRs and related product information correctly.
• Detect and report discrepancies to appropriate personnel.
• Perform data entry accurately.
• Provide final approval of test results and DHRs for product release to Finished Goods.
• Perform electronic transactions for completed reagent products and consumables as required.
• Inspect documentation revisions and perform label and pallet inspections for Reagent Department products.
• Conduct visual and mechanical inspections on consumables and Reagent Department products.
• Review and inspect at labor standards.
• Collaborate with engineering and manufacturing personnel regarding quality issues.
• Manage DHR retrieval processes.
• Generate and maintain certifications for reagents and consumables for customer use.
• Train interns, Level I, and Level II QC inspectors.
• Communicate daily work priorities across shifts.

Qualifications:

• Fluent in reading, writing, speaking, and understanding English.
• Knowledge of Good Documentation Practices (GDP).
• Proficient in Word, Excel, Access, and PowerPoint.
• Strong attention to detail.
• Basic to advanced computer skills.
• Ability to follow written protocols and procedures in a regulated industry (QSR, FDA).

Education/Experience:

• High school diploma or equivalent with a science focus plus at least 1 year of QC inspector experience.
• Associate's degree with a science concentration is preferred.

At Nova Biomedical, we uphold core values of mutual respect, honesty, and integrity. Our workplace fosters a family-like environment, with one-third of employees having over 10 years of service.

Benefits include Blue Cross Blue Shield medical coverage, tuition reimbursement, a matching 401K plan, a subsidized cafeteria, and an innovative scholarship program for employees' children.