QMS Documentation and Training Analyst at Bioventus LLC in Memphis, Tennessee

Job Description:

Are you ready to work for a more active world?

At Bioventus, our business depends on developing our people. We invest in you and challenge you to be the best. We value our colleagues for their different perspectives and individual contributions, and our leaders listen. Our success rests on working together to achieve shared goals and rewards. Join a diverse team of global colleagues driven to help patients resume and enjoy active lives.

Maintain completeness and accuracy associated with the tactical and strategic processes of record and file management within Documentation Control Center in accordance with FDA 21 CFR 820 and ISO 13485.
What you will be doing:

• Maintains the Document Control processes and procedures.


• Verifies documents for compliance with state, federal and international regulatory requirements.


• Utilizes critical industry standards and formats within the Document Control system.


• Generates and/or incorporates changes to released documentation. Verifies drafting checks.


• Prepares, edits, files, assembles documentation such as reports or technical documents, records, or correspondence.


• Maintains tracking and back-up systems for Training and Document Control systems.


• Works with individual departments to ensure training requirements are met. Responsible for file maintenance and record keeping.


• Supports the implementation and maintenance of eQMS.


• Responsible for global system administration tasks.


• Able to react to change productively and to perform other essential tasks assigned.


• Holds oneself and others accountable to conduct business in a manner compliant with Bioventus' Code of Compliance and Ethics, policies and procedures and internal controls applicable to their role.


• Other duties as assigned.

What you will bring to the table:

• Associate degree or equivalent experience and four years related experience.


• Experience in a regulated medical device environment is preferred.


• Experience with or quality system compliance software is desirable.


• Ability to read and interpret documents such as safety rules, operating and maintenance instructions, and procedure manuals.


• Ability to calculate figures and amounts such as proportions and percentages.


• Ability to interpret a variety of instructions furnished in written, oral, diagram, or a schedule form.


• Proficient with Microsoft Office tools.


• Proficient in record management for product release systems, file management of production and distribution of multimedia and organizational relationships.


• Proficient in Microsoft Office Suite and databases.

Apply now! Hit the "Apply" button to send us your resume and cover letter.

Bioventus is committed to fostering an inclusive and diverse community of employees with a strong sense of belonging. We believe we are bettered by all forms of diversity and take pride in working with top talent from every walk of life. In the spirit of inclusivity, qualified applicants will be considered without regard to age, ethnicity, disability, gender, veteran status, gender expression, gender identity, nationality, race, religion or sexual orientation. All individuals, regardless of personal characteristics, are encouraged to apply.