Manufacturing Quality Inspector

DanaherFajardo, PR
Onsite

About The Position

At Cytiva, one of Danaher’s operating companies, our work saves lives—and we’re all united by a shared commitment to innovate for tangible impact. You’ll thrive in a culture of belonging where you and your unique viewpoint matter. And by harnessing Danaher’s system of continuous improvement, you help turn ideas into impact – innovating at the speed of life. Working at Cytiva means being at the forefront of providing new solutions to transform human health. Our incredible customers undertake life-saving activities ranging from fundamental biological research to developing innovative vaccines, new medicines, and cell and gene therapies. At Cytiva you will be able to continuously improve yourself and us – working on challenges that truly matter with people that care for each other, our customers, and their patients. Take your next step to an altogether life-changing career. Learn about the Danaher Business System which makes everything possible.

Requirements

  • Associate Degree or bachelor’s degree in sciences, Engineering, Business Administration, technical school certificate, or equivalent experience.
  • Two (2) to four (4) years of work-related significant clerical and/or secretarial functions in Documentation, Manufacturing Environment preferred or Two years of work as Quality Inspector in Fajardo Facility.
  • Good oral and written communication skills (English and Spanish).

Nice To Haves

  • Preferred experience with lot file review and product release.
  • Documentation Revision, Manufacturing Environment, Computer oriented, knowledge in Enterprise Resource Planning (ERP), Electronic Document Management (EDM), MS applications (Excel, Word, PowerPoint), SAP and Documentation (QA) System, as Veeva System.

Responsibilities

  • Responsible to conduct process, material and or product inspection to verify if met specification requirements before and after manufacturing process for final Release.
  • Prepares and submits reports of non-conformances, block Non-Conformance products in ERP System and maintain Inventory Control in Hold Area.
  • Perform verification of random sampling of final product and related documentation package to confirm compliance and release for shipment.

Benefits

  • paid time off
  • medical/dental/vision insurance
  • 401(k)

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What This Job Offers

Job Type

Full-time

Career Level

Mid Level

Education Level

Associate degree

Number of Employees

5,001-10,000 employees

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