Document Control Coordinator
Job Description
Job Summary
Medline has an immediate opening for a Document Control Coordinator at our Mankato, MN location. This is a full-time, onsite role with a Monday through Friday schedule. This person will responsible for maintaining and overseeing the revision control of product and raw material documents. This role will also be responsible for coordinating the daily/weekly/monthly workflow and reviewing documentation for the department.Job Description
Responsibilities:
Ensure that corporate documents are properly maintained, updated, and filed correctly.
Initiate and circulate document changes for review and update.
Assist in ensuring that all three year reviews are completed for all procedures.
Coordinate and ensure training is completed on new/revised documents. Maintain and update monthly training reports and update training groups as needed.
Log training in Reliance for non-email training groups.
Address issues and concerns and keep the department on track to assure procedures and standards are in compliance.
Conduct laboratory work to fabricate and/or evaluate sample prototypes.
Assist the Product Development Manager in monitoring product and raw material electronic files.
Minimum Job Requirements
Education
High School Diploma or equivalent
Work Experience
At least 1 years of experience in Quality or Regulatory Affairs.
Knowledge / Skills / Abilities
Intermediate skill level with SAP.
Intermediate skill level in Microsoft Excel and Microsoft Office.
Working knowledge of regulations regarding document control and GDP.
Medline Industries, LP, and its subsidiaries, offer a competitive total rewards package, continuing education & training, and tremendous potential with a growing worldwide organization.
The anticipated salary range for this position:
$18.25 - $25.50 HourlyThe actual salary will vary based on applicant’s location, education, experience, skills, and abilities. Medline will not pay less than the applicable minimum wage or salary threshold.
Our benefit package includes health insurance, life and disability, 401(k) contributions, paid time off, etc., for employees working 30 or more hours per week on average. For a more comprehensive list of our benefits please click here. For roles where employees work less than 30 hours per week, benefits include 401(k) contributions as well as access to the Employee Assistance Program, Employee Resource Groups and the Employee Service Corp.
We’re dedicated to creating a Medline where everyone feels they belong and can grow their career. We strive to do this by seeking diversity in all forms, acting inclusively, and ensuring that people have tools and resources to perform at their best. Explore our Belonging page here.
Medline Industries, LP is an equal opportunity employer. Medline evaluates qualified individuals without regard to race, color, religion, gender, gender identity or expression, sexual orientation, national origin, age, disability, neurodivergence, protected veteran status, marital or family status, caregiver responsibilities, genetic information, or any other characteristic protected by applicable federal, state, or local laws.
Job Summary
Medline has an immediate opening for a Document Control Coordinator at our Mankato, MN location. This is a full-time, onsite role with a Monday through Friday schedule. This person will responsible for maintaining and overseeing the revision control of product and raw material documents. This role will also be responsible for coordinating the daily/weekly/monthly workflow and reviewing documentation for the department.Job Description
Responsibilities:
Ensure that corporate documents are properly maintained, updated, and filed correctly.
Initiate and circulate document changes for review and update.
Assist in ensuring that all three year reviews are completed for all procedures.
Coordinate and ensure training is completed on new/revised documents. Maintain and update monthly training reports and update training groups as needed.
Log training in Reliance for non-email training groups.
Address issues and concerns and keep the department on track to assure procedures and standards are in compliance.
Conduct laboratory work to fabricate and/or evaluate sample prototypes.
Assist the Product Development Manager in monitoring product and raw material electronic files.
Minimum Job Requirements
Education
High School Diploma or equivalent
Work Experience
At least 1 years of experience in Quality or Regulatory Affairs.
Knowledge / Skills / Abilities
Intermediate skill level with SAP.
Intermediate skill level in Microsoft Excel and Microsoft Office.
Working knowledge of regulations regarding document control and GDP.
Medline Industries, LP, and its subsidiaries, offer a competitive total rewards package, continuing education & training, and tremendous potential with a growing worldwide organization.
The anticipated salary range for this position:
$18.25 - $25.50 HourlyThe actual salary will vary based on applicant’s location, education, experience, skills, and abilities. Medline will not pay less than the applicable minimum wage or salary threshold.
Our benefit package includes health insurance, life and disability, 401(k) contributions, paid time off, etc., for employees working 30 or more hours per week on average. For a more comprehensive list of our benefits please click here. For roles where employees work less than 30 hours per week, benefits include 401(k) contributions as well as access to the Employee Assistance Program, Employee Resource Groups and the Employee Service Corp.
We’re dedicated to creating a Medline where everyone feels they belong and can grow their career. We strive to do this by seeking diversity in all forms, acting inclusively, and ensuring that people have tools and resources to perform at their best. Explore our Belonging page here.
Medline Industries, LP is an equal opportunity employer. Medline evaluates qualified individuals without regard to race, color, religion, gender, gender identity or expression, sexual orientation, national origin, age, disability, neurodivergence, protected veteran status, marital or family status, caregiver responsibilities, genetic information, or any other characteristic protected by applicable federal, state, or local laws.
About Medline Industries
Medline is the largest provider of medical-surgical products and supply chain solutions serving all points of care. Through its unique offering of world-class products, supply chain resilience and clinical practice expertise, Medline delivers improved clinical, financial and operational outcomes. Headquartered in Northfield, Illinois, the company employs 43,000 people worldwide and operates in over 100 countries and territories.
It has always been Medline's intention and purpose to create a great place to work for everyone. We believe tapping into the richness of our employees' diversity allows us to find innovative solutions for our customers, who themselves represent a diverse group both in the U.S. and around the world. The Belonging and Engagement team at Medline is dedicated to fostering an inclusive and supportive workplace culture. We focus on creating opportunities for employees to feel seen, supported, and connected through initiatives like Employee Resource Groups (ERGs), cultural awareness events, new hire engagement, and leadership training.
Every hour of every day, healthcare professionals rely on Medline to help them do their job. Our agile and resilient global team is determined to get our customers exactly what they need, at the right time, every time. If you're a self-starter, eager to grow your career within a high-performing environment, this is the place for you. Together, we make healthcare run better.
For more on all things Belonging at Medline Industries, check out our home page here.
Medline Industries would like you to finish the application on their website.