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SCstryker.com logo

stryker.com

Alajuela

Staff Quality Management Systems Specialist (Onsite).

ON-SITE
Work Flexibility: Onsite As a Quality Management Systems Specialist, you will support the administration and continuous improvement of document and change control processes within a regulated medical device environment. You will coordinate controlled documentation, quality records, and change activities while partnering with cross-functional teams to maintain compliance with Quality Management System requirements. What you will do •Coordinate document and change control activities, including the release, revision, implementation, and maintenance of controlled documents in electronic systems. •Review quality records for compliance with Good Documentation Practices (GDP), established procedures, and Quality Management System requirements. •Review change orders and supporting documentation to verify compliance with document and change control procedures. •Track documentation reviews, approvals, implementation activities, and closure to support timely completion of document changes. •Verify completion of change-control activities, including material disposition and required training, before closure. •Maintain controlled documents and records according to established retention, integrity, accessibility, and record-management requirements. •Collaborate with cross-functional partners to create and revise procedures, resolve documentation discrepancies, and communicate technical information accurately. •Guide Document Control team members and monitor metrics to identify opportunities for continuous improvement. What you will need Required •Associate degree from an accredited college or university, or equivalent relevant experience. •Minimum 5 years of experience in Document Control, Quality Systems, or a combination of both. •Intermediate to advanced English proficiency, including the ability to read, understand, and communicate technical information. •Professional experience using Microsoft Office 365. Preferred •Bachelor’s degree in Science, Engineering, Biochemistry, Biotechnology, Biology, Biomedical Engineering, or a related field. •Experience supporting document control, change control, or Quality Management Systems within the medical device or another regulated industry. Travel Percentage: 10% 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.
Pay
Not stated
Where
Alajuela · Grecia Evolution Free Zone Building 2 · Costa Rica
Work
On-site
Type
Not stated
Posted
6 Nov, 2026
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