Senior Quality Inspector

Stryker Corporation; Plainfield (IN); On-site; USD 32,000 - 43,000; Full time

Job summary

Stryker Corporation seeks a Senior Quality Inspector for our US Central Distribution Center, focusing on inspecting and dispositioning product returns. The role involves reviewing packaging, checking finished goods against drawings, and following regulatory procedures.

You will use ERP systems, including SAP, and work independently with minimal supervision. 1+ years in a regulated medical device environment and strong communication skills are preferred. Travel about 10%.

Qualifications

• 1+ years in medical device or other regulated industry experience preferred.
• Prior experience with quality control and/or inspection.
• ERP systems experience (SAP) preferred.
• Independent worker with minimal supervision.
• Strong interpersonal skills, both written and verbal.

Responsibilities

• Perform formal review of product packaging and labelling to ensure they meet company and regulatory standards.
• Work from engineering drawings, prints and guidance documents to perform accurate checks on finished goods.
• Follow and explain detailed instructions and regulatory procedures and policies.
• Use electronic data entry systems and ERP platforms accurately and efficiently.
• Prioritise work effectively across competing demands.
• Apply understanding of Quality discipline procedures to daily tasks.

Skills

Quality inspection

Regulated industry experience

SAP

Independent worker

Communication skills

Tools

SAP ERP

Job description

Work Flexibility: Onsite

Why Join Stryker?

Stryker is one of the world's leading medical technology companies and is consistently ranked as one of the best places to work globally.

• Our total rewards package includes bonuses, healthcare, insurance benefits, retirement programmes, wellness programmes, and service and performance awards.

Position Summary

The Senior Quality Inspector role sits within Stryker's US Central Distribution Center, supporting reverse logistics. This individual contributor role is responsible for inspecting and dispositioning product returns coming through the center.

What You'll Do

• Perform formal review of product packaging and associated labelling to ensure they meet company and regulatory standards.
• Work from engineering drawings, prints and associated guidance documents to perform accurate checks and assessments of finished goods.
• Follow and explain detailed instructions and job-related procedures, including regulatory procedures and policies.
• Use electronic data entry systems and associated ERP platforms accurately and efficiently.
• Prioritise work effectively and efficiently across competing demands.
• Apply understanding and knowledge of Quality discipline procedures and concepts to daily tasks.

What You'll Need

• 1+ years in medical device or other regulated industry experience preferred.
• Prior experience with quality control and/or inspection.
• ERP systems experience (SAP) preferred.
• This is an individual contributor role requiring the use of professional judgement, with an expectation to work independently with minimal supervision.
• Strong interpersonal skills, both written and verbal.

$26.60

Travel Percentage: 10%

Equal Opportunity Statement

Stryker Corporation is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, ethnicity, color, religion, sex, gender identity, sexual orientation, national origin, disability, or protected veteran status. Stryker is an EO employer - M/F/Veteran/Disability. Stryker Corporation will not discharge or in any other manner discriminate against employees or applicants because they have inquired about, discussed, or disclosed their own pay or the pay of another employee or applicant. However, employees who have access to the compensation information of other employees or applicants as a part of their essential job functions cannot disclose the pay of other employees or applicants to individuals who do not otherwise have access to compensation information, unless the disclosure is (a) in response to a formal complaint or charge, (b) in furtherance of an investigation, proceeding, hearing, or action, including an investigation conducted by the employer, or (c) consistent with the contractor’s legal duty to furnish information.

Stryker is one of the world's leading medical technology companies and, together with its customers, is driven to make healthcare better.

We offer innovative products and services in Orthopaedics, Medical and Surgical, and Neurotechnology and Spine that help improve patient and hospital outcomes.

We are proud to be named one of the world's best workplaces!

For more information, visit: www.stryker.com

Work Flexibility

• Remote - Role allows you to work the majority to 100% of time from an alternate workplace. These roles could have travel expectations, and you must work within the country of the job requisition location.
• Field-based - You can expect to regularly work a majority to 100% of time at customer facilities and has a set territory or expectation to travel within a set boundary. Almost all sales roles would likely be qualified as field-based.
• Onsite - Role is 100% located at a Stryker facility. Some ad hoc flexibility may be available depending on role, level, and job requirements. Manufacturing roles and any role that requires physical presence at the office would qualify under this category.
• Hybrid - You can expect to regularly work in both an alternate workplace and a Stryker facility. Roles that are partially remote or co-located would qualify as hybrid, and the expectation to be onsite would be defined and agreed upon by your manager/supervisor.