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Quality & Regulatory Compliance Intern Job in Mentor, Ohio US
Monster
 
 
 
 

Job Summary

Company
STERIS CORPORATION
Location
Mentor, OH
Job Type
Per Diem
Employee
Years of Experience
Less than 1 Year
Job Reference Code
51556445

Quality & Regulatory Compliance Intern

About the Job

Job Title:             Quality & Regulatory Compliance Intern                                           
           
       
   
                                                Req ID:             23007                   
           
       
   
                                                Job Category:             Intern                   
           
       
   
                                                Country/Region:             US                   
           
       
   
                                                State:             OH                   
           
       
   
                                                City:             MENTOR                   
           
       
   
                                                Zip:             44060                   
           
       
   
                   
   
                                                Description:                            
At STERIS, we help our Customers create a healthier and safer world by providing innovative healthcare and life science product and service solutions around the globe.
Position Summary:


The STERIS Quality & Regulatory Compliance team is seeking an intern. Ideally, the indivdual could start working part-time as soon as possible, full-time in the summer, and potentially continue in the fall - but we are open to Summer only applicants as well. This role will provide a foundation for applying what has been learned in the classroom environment to practical hands-on application in a corporate environment. The Quality & Regulatory Compliance Intern will have exposure to domestic and international regulations and standards, business processes to ensure adherence to applicable regulations and standards, and collaboration with STERIS corporate domestic and international staff, Customers, Notified Bodies, and U.S and foreign government agencies.

What you will do:


Develop knowledge with the following regulations and standards
21 CFR Part 820 – Medical Device Quality System Regulations (QSR)
21 CFR Part 803 – Medical Device Reporting
21 CFR Part 806 – Medical Device Corrections and Removals
21 CFR Part 211 – Current Good Manufacturing Practice for Finished Pharmaceuticals (cGMP)
21 CFR Part 11 – Electronic Records, Electronic Signatures
ISO 13485:2016 Medical devices – Quality management systems
ISO 9001:2015 Quality management systems – Requirements
EN ISO 11135-1:2007 – Sterilization of healthcare products – Ethylene Oxide
EN ISO 11137-1:2006 – Sterilization of healthcare products – Radiation
ISO/IEC 17025:2017 General requirements for the competence of testing and calibration laboratories
EU Medical Device Regulation

Responsible for assembling product and Customer data concerning product corrections, removals, and field upgrades, tracking of Customer notifications and Field Service repairs, and maintenance of correction documentation
Support execution of the supplier quality program, including, qualifications and/or audits, routine monitoring, assessment meetings, action requests and as necessary, issue resolution.
Provide support to the Quality & Regulatory Compliance team with investigation and resolution to audit findings
Track corrective action activities for external audit observations and obtain and review objective evidence as actions are completed in accordance with prescribed commitments.
 Perform data analysis/trending as requested.

What you will need to be successful:


Currently enrolled in college with a major in Science, Engineering, Regulatory, Internal Audit, or general business core concentration.
Minimum GPA of 3.0
Bilingual skills are a plus, but not required.
Proficient PC skills, including Microsoft Office applications.
Self-starter that is highly organized.
Strong interpersonal skills – ability to work closely with people at all levels within the organization and facilitate the implementation of corrective action; able to work effectively and professionally with external people including Customers and government officials.
Ability to exercise judgment regarding which approaches are acceptable for meeting compliance requirements and to timely recognize and communicate significant compliance issues for resolution to Quality & Regulatory Compliance management.
Strong oral and written communication skills.
Ability to balance multiple high priority responsibilities on-time and effectively.
Ability to perform assigned tasks in a highly complex environment.

Offering you in return:


An opportunity to gain corporate experience in compliance at a large global healthcare company to supplement your education.

STERIS is a $3B, publicly traded (NYSE: STE) organization with approximately 12,000 associates worldwide and operates in more than 100 countries.

If you need assistance completing the application process, please call 1 (440) 392.7047. This contact information is for accommodation inquiries only and cannot be used to check application status.

STERIS is an Equal Opportunity Employer.  We are committed to equal employment opportunity and the use of affirmative action programs to ensure that persons are recruited, hired, trained, transferred and promoted in all job groups regardless of race, color, religion, age, disability, national origin, citizenship status, military or veteran status, sex (including pregnancy, childbirth and related medical conditions), sexual orientation, gender identity, genetic information, and any other category protected by federal, state or local law.  We are not only committed to this policy by our status as a federal government contractor, but also we are strongly bound by the principle of equal employment opportunity.

The full affirmative action program, absent the data metrics required by * 60-741.44(k), shall be available to all employees and applicants for employment for inspection upon request. The program may be obtained at your location's HR Office during normal business hours.
                                   
           
       
   

               
Nearest Major Market: Cleveland
Nearest Secondary Market: Akron                                   
Job Segment:                     Intern, Medical, Quality Manager, Engineer, Quality, Entry Level, Healthcare, Engineering                                       
                               

STERIS Corporation is an Equal Employment Opportunity (EEO) employer and welcomes all qualified applicants. Applicants will receive fair and impartial consideration without regard to race, sex, color, religion, national origin, age, disability, veteran status, genetic data, or religion or other legally protected status.
 

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