MedTech Quality Inspector I - Inspections & ISO Compliance

Biopharma Careers

Danvers (MA)

On-site

USD 39,000 - 62,000

Full time

5 days ago
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Benefits offered by this job

Paid vacation
Sick time
Holiday pay
Parental Leave
Volunteer Leave

Job summary

Johnson & Johnson in Danvers, MA, seeks a Quality Inspector I to perform basic inspections and sort incoming materials. You will support the Operations group and document results precisely.

Responsibilities include visual and dimensional inspections, data entry, and maintaining test records under SOPs. Qualifications include a high school diploma and up to 1 year of manufacturing or medical device experience.

Qualifications

  • High School graduate or equivalent required.
  • 1 year or less in a manufacturing environment – Medical device experience a plus.
  • Ability to use inspection gauges and microscopes
  • Attention to detail with ability to follow SOPs and inspection procedures
  • Basic math knowledge
  • Verbal and written communication skills
  • Continuous improvement mindset
  • Ability to execute tasks under general supervision
  • Computer literacy; MS Word and Excel

Responsibilities

  • Perform inspections of purchased parts according to defined criteria using standard measurements
  • Visual inspection on large lots size under a microscope
  • Accurately document inspection and test results
  • Maintain controlled document files and test records timely and accurately
  • Data entry into associated data systems

Skills

Agility
Compliance
Detail-Oriented
Customer Centricity
Documentation
Quality Control
Quality Standards
Process Adherence

Education

High School Diploma

Job description

Johnson & Johnson in Danvers, MA, seeks a Quality Inspector I to perform basic inspections and sort incoming materials. You will support the Operations group and document results precisely.

Responsibilities include visual and dimensional inspections, data entry, and maintaining test records under SOPs. Qualifications include a high school diploma and up to 1 year of manufacturing or medical device experience.

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