Receiving Inspector 2

Hologic, Inc.; Newark (DE); On-site; USD 45,000 - 68,000; Full time

Job summary

Hologic, Inc. in Newark, DE is seeking a Quality Inspector to perform incoming inspections for a medical device manufacturing environment. You will interpret drawings and GD&T, verify documentation, and record results in GDP-compliant records.

You will use calipers, micrometers, and Excel; familiarity with GMP/GDP and ERP systems is a plus. A high school diploma or GED is required, with 1–2 years of relevant experience in a regulated setting.

Qualifications

• Reading and following written procedures with accuracy.
• Experience using standard QC tools and measurement devices.
• Experience in a regulated manufacturing environment is preferred.
• Familiarity with GMP and GDP practices is beneficial.

Responsibilities

• Perform incoming inspection activities per approved procedures and inspection plans.
• Interpret drawings, GD&T, material specs, and manufacturing requirements.
• Verify dimensional, visual, labeling, and documentation requirements.
• Record inspection results and complete quality records in GDP.
• Review supplier CoCs, test reports, and inspection records.
• Identify non-conforming materials and support nonconformance events.
• Maintain compliance with QMS and regulatory requirements.
• Utilize Excel to complete inspection records and communicate discrepancies.

Skills

Microsoft Office Suite

Reading procedures

Communication skills

Attention to detail

Quality control tools

Reading schematics/blueprints

GMP/GDP knowledge

Independent / team work

Education

High School diploma or GED

Associate Degree (preferred)

ASQ Certified Quality Inspector (beneficial)

Tools

Oracle ERP

Agile PLM

Job description

Essential Duties and Responsibilities:

• Perform incoming inspection activities in accordance with approved procedures, specifications, drawings, and inspection plans.
• Interpret engineering drawings, geometric dimensions and tolerances (GD&T), material specifications, and manufacturing requirements.
• Verify dimensional, visual, labeling, and documentation requirements for incoming materials and components.
• Utilize precision measuring equipment including but not limited to calipers, micrometers, height gauges, optical comparators, and pin gauges.
• Accurately record inspection results and complete the required quality records in accordance with Good Documentation Practices (GDP)
• Review supplier documentation including Certificates of Conformance (CoC), test reports, and inspection records.
• Identify and segregate non-conforming materials.
• Initiate and support nonconformance events (NCEs) when required.
• Support nonconformance investigations when required.Maintain compliance with Quality Management System (QMS) and regulatory requirements.
• Utilize Microsoft Excel to complete inspection records.
• Communicate with internal customers to resolve inspection discrepancies.
• Ensure daily inspection priorities are met.
• Perform first article inspections.
• Complete all training requirements in a timely manner.
• Ability to adhere to standardized production schedule and work overtime to support production needs as necessary.
• Act as an advocate for compliance, data integrity, and continuous improvement.

Qualifications:

Education

• Highschool diploma or equivalent required.
• Preferred Minimum Non-Technical Degree: High School (H.S./GED) or Associate Degree

Experience

• Preferred Minimum Non-Technical Degree: 1-2 Years
• Preferred 1-2 years’ experience in medical device manufacturing or other highly regulated manufacturing industry.
• Experience with Oracle ERP or Agile Product Lifecycle Management System is beneficial.
• ASQ Certified Quality Inspector is beneficial.

Skills

• Strong understanding and working knowledge of Microsoft Office programs including Excel, Work, SharePoint and OneDrive.
• Ability to read, understand, and follow all written procedures.
• Strong effective communication skills, both written and verbal
• Ability to work both independently and as a member of a team.
• Excellent attention to detail and documentation practices.
• Ability to use quality control tools such as calipers, micrometers, scales, gauges, microscopes, etc.
• Advanced ability to read and interpret basic schematics, blueprints, part lists and other technical data.
• Understanding of Good Manufacturing Practices (GMP) and Good Documentation Practices (GDP).
• Familiarity with GMP (Good Manufacturing Practices) and GDP (Good Documentation Practices) is beneficial.

The annualized base salary range for this role is $45,400 - $68,100 and is bonus eligible. Final compensation packages will ultimately depend on factors including relevant experience, skillset, knowledge, education, business needs and market demand.

Why join Hologic?

We are committed to making Hologic the destination for top talent. For you to succeed, we want to enable you with the tools and knowledge required and so we provide comprehensive training when you join as well as continued development and training throughout your career.

Agency and Third-Party Recruiter Notice

Agencies that submit a resume to Hologic must have a current executed Hologic Agency Agreement executed by a member of the Human Resource Department. In addition, Agencies may only submit candidates to positions for which they have been invited to do so by a Hologic Recruiter. All resumes must be sent to the Hologic Recruiter under these terms or they will not be considered.

Hologic, Inc. is proud to be an Equal Opportunity Employer inclusive of disability and veterans.

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