Inspector I

Medtronic • Juncos, PR

5d

About The Position

At Medtronic you can begin a life-long career of exploration and innovation, while helping champion healthcare access and equity for all. You’ll lead with purpose, breaking down barriers to innovation in a more connected, compassionate world. A Day in the Life This position is an exciting opportunity to work with Medtronic's Diabetes business. Medtronic has announced its intention to separate the Diabetes division to promote future growth and innovation within the business and reallocate investments and resources across Medtronic, subject to applicable information and consultation requirements. This separation provides our team with a bold opportunity to unleash our potential, enabling us to operate with greater speed and agility. As a separate entity, we anticipate leveraging increased investments to drive meaningful innovation and enhance our impact on patient care. Responsible to perform product, process, and documentation audits to determine the extent of compliance and effectiveness of operations to documented policies, procedures, specifications, and regulatory requirements.  Also, performs inspection and tests in conformance to Drawings, Standard Inspection Procedures, and other applicable specifications.  Prepares required inspection reports, defect reports and other related inspection duties as required and in accordance with GMP’s regulations and Standards. Responsibilities may include the following and other duties may be assigned. 2nd Shift: Tuesday to Saturday Uses predetermined methods, operations, setups and prescribed specifications to inspect visually in-process and completed products such as electronic units and subsystems, precision electromechanical assemblies or mechanical units, subassemblies, structural flaws, internal defects, and missing welds. Uses various measuring devices and testing equipment. Accepts, rejects, or reworks defective or malfunctioning units or systems. Works from blueprints, diagrams, dial indicators, preset micrometers, scales, fixtures, customer specifications, drawing or inspection instructions and checklists. May monitor and verify quality in accordance with statistical process or other control procedures. Performs line clearances after each lot to ensure all materials from the previous lot have been removed.

Requirements

• Requires 0 years of experience.

Nice To Haves

• Previous experience in medical device manufacturing or regulated industry
• Familiarity with GMP, ISO 13485, and FDA regulations
• Strong analytical and problem-solving skills
• Experience with inspection tools (calipers, micrometers, etc.) and visual inspection methods
• Proficiency with documentation systems and basic computer skills (MS Office, SAP, etc.)
• Excellent communication and teamwork abilities
• Attention to detail and commitment to continuous improvement

Responsibilities

• Responsible to perform product, process, and documentation audits to determine the extent of compliance and effectiveness of operations to documented policies, procedures, specifications, and regulatory requirements.
• Performs inspection and tests in conformance to Drawings, Standard Inspection Procedures, and other applicable specifications.
• Prepares required inspection reports, defect reports and other related inspection duties as required and in accordance with GMP’s regulations and Standards.
• Uses predetermined methods, operations, setups and prescribed specifications to inspect visually in-process and completed products such as electronic units and subsystems, precision electromechanical assemblies or mechanical units, subassemblies, structural flaws, internal defects, and missing welds.
• Uses various measuring devices and testing equipment.
• Accepts, rejects, or reworks defective or malfunctioning units or systems.
• Works from blueprints, diagrams, dial indicators, preset micrometers, scales, fixtures, customer specifications, drawing or inspection instructions and checklists.
• May monitor and verify quality in accordance with statistical process or other control procedures.
• Performs line clearances after each lot to ensure all materials from the previous lot have been removed.

Benefits

• Medtronic offers a competitive Salary and flexible Benefits Package
• We offer a wide range of benefits, resources, and competitive compensation plans designed to support you at every career and life stage.
• This position is eligible for a short-term incentive called the Operations Incentive Plan (OIP).

What This Job Offers

• Job Type: Full-time
• Career Level: Entry Level
• Education Level: No Education Listed
• Number of Employees: 5,001-10,000 employees