Quality Specialist II

Quality Specialist II

At Zimmer Biomet, we believe in pushing the boundaries of innovation and driving our mission forward. As a global medical technology leader for nearly 100 years, a patient's mobility is enhanced by a Zimmer Biomet product or technology every 8 seconds.

As a Zimmer Biomet team member, you will share in our commitment to providing mobility and renewed life to people around the world. To support our talented team, we focus on development opportunities, robust employee resource groups (ERGs), a flexible working environment, location specific competitive total rewards, wellness incentives and a culture of recognition and performance awards. We are committed to creating an environment where every team member feels inspired, invested, cared for, valued, and have a strong sense of belonging.

What You Can Expect

Paragon 28 (P28), a Zimmer Biomet Company is hiring a Quality Specialist II. Quality Specialist II is responsible for managing and maintaining the accuracy, completeness, and accessibility of quality assurance documentation and records. This position ensures that all documentation meets regulatory requirements and industry standards and supports the organization's quality management system. The specialist works closely with cross-functional teams to develop and implement documentation control procedures and systems. This position is hybrid and will be expected onsite at our Englewood, Colorado location at least 3 days a week.

Essential Responsibilities and Duties

Develop, implement, and maintain documentation control procedures and systems to ensure compliance with regulatory requirements and industry standards.

Manage the creation, revision, and approval process for quality & engineering change documentation, including policies, procedures, and forms.

Ensure the accuracy, completeness, and accessibility of quality records and documentation.

Conduct periodic reviews of documentation to identify areas for improvement and ensure ongoing compliance.

Provide training and support to cross-functional teams on documentation control procedures and systems.

Collaborate with cross-functional teams to develop and implement quality improvement initiatives related to documentation control.

Generate reports on documentation control metrics, audit findings, and improvement initiatives for management review.

Maintain knowledge of industry trends and best practices in documentation control and quality management systems.

Qualifications

Bachelor's degree in a related field, such as quality management, engineering, or business administration or another quality field.

Minimum of 3-5 years of experience in documentation control or quality assurance.

Strong knowledge of regulatory requirements and industry standards related to documentation control.

Experience with electronic document management systems.

Excellent written and verbal communication skills.

Strong attention to detail and ability to manage multiple projects simultaneously.

Ability to work independently and as part of a team.

Work Environment

This job operates in a professional office environment. This role routinely uses standard office equipment such as computers, phones and copy machines.

Physical Demands

The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job.

While performing the duties of this job, the employee is regularly required to communicate with individuals internal and external to the organization. The employee frequently is required to move about the facility. The employee may be required to lift up to 15 lbs. by themselves.

Position Type / Expected Hours of Work This is a full-time position with typical business hours and is eligible for a hybrid schedule of work from home / office OR This role requires full time onsite presence.

Travel Expectations

Up to 10% travel possible

Compensation Data

Hourly Rate : $25-30.00 USD

Physical Requirements