Quality Control Inspector 3

Hologic•Newark, DE

About The Position

Are you detail-oriented and passionate about delivering high-quality products? At Hologic, we are seeking a Quality Control Inspector to ensure our products meet the highest standards of quality and compliance. In this role, you’ll perform inspections, testing, and sampling procedures for manufacturing processes, packaging lines, and incoming materials. You’ll play a key part in maintaining compliance with safety standards, supporting investigations, and driving continuous improvement initiatives. If you have a keen eye for detail, a commitment to excellence, and a desire to work in a collaborative environment, we’d love to hear from you!

Requirements

Familiarity with Good Manufacturing Practices (GMP) and Good Documentation Practices (GDP).
Basic understanding of quality control tools, including measuring tapes, calipers, micrometers, scales, gauges, and microscopes.
Knowledge of process auditing, documentation, and record-keeping.
Ability to read and interpret basic schematics and blueprints.
Proficient in Microsoft Office applications, including Excel, Word, SharePoint, and OneDrive.
Strong verbal and written communication skills for accurate documentation and collaboration.
High attention to detail and focus on quality assurance processes.
Ability to follow written procedures and maintain accurate, organized records.
Capable of working both independently and collaboratively as part of a team.
Analytical mindset for supporting non-conformance investigations and identifying process improvements.
Safety-conscious, maintaining a safe work environment and promptly addressing hazards.
Proactive and dependable, with a strong sense of accountability for quality and timelines.
Collaborative and team-oriented, fostering positive working relationships.
Adaptable and eager to contribute to continuous improvement initiatives like Kaizen events.
Reliable and punctual, with a commitment to maintaining attendance and meeting deadlines.
2-4 years of experience in quality assurance or manufacturing roles, preferably in an FDA-regulated medical device environment.
High School Diploma (H.S./GED) required

Nice To Haves

Awareness of FDA-regulated environments and medical device quality standards (preferred).
Hands-on experience with quality control tools and techniques is beneficial.
Familiarity with clean rooms, controlled environments, and production processes is a plus.
Experience with Oracle ERRP or Agile Lifecycle Management System is beneficial
an Associate Degree is a plus.