Lavori attuali relativi a Regulatory Affairs Intern - Pomezia - Tn Italy
-
Regulatory Affairs Intern
4 mesi fa
Pomezia, Italia STERIS A tempo pienoJob Title: Regulatory Affairs Intern Job Category: Regulatory Affairs 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 We are looking for a Regulatory Affairs Intern to join our team base...
-
Regulatory Affairs Intern
5 mesi fa
Pomezia, Italia Steris Canada Corporation A tempo pienoSelect how often (in days) to receive an alert: 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 We are looking for a Regulatory Affairs Intern to join our team base in Pomezia (Roma). The mission of the STERIS...
-
Regulatory Affairs Intern
5 mesi fa
Pomezia, Italia STERIS A tempo pienoAt 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 We are looking for a Regulatory Affairs Intern to join our team base in Pomezia (Roma). The mission of the STERIS Regulatory Affairs function is to implement...
-
Regulatory Affairs Specialist
1 mese fa
Pomezia, Lazio, Italia STERIS A tempo pienoRegulatory Affairs InternSTERIS is seeking a highly motivated and detail-oriented Regulatory Affairs Intern to join our team in Pomezia, Italy. As a Regulatory Affairs Intern, you will play a critical role in supporting the implementation of efficient and effective processes to obtain and maintain clearance to market STERIS products globally.Key...
-
Regulatory Affairs Specialist
1 mese fa
Pomezia, Lazio, Italia STERIS A tempo pienoJob Title: Regulatory Affairs InternJob Category: Regulatory AffairsDescription:STERIS is a leading provider of innovative healthcare and life science solutions. We are seeking a highly motivated and detail-oriented Regulatory Affairs Intern to join our team in Pomezia, Italy.Job Summary:The Regulatory Affairs Intern will support the implementation of...
-
Regulatory Affairs Specialist
4 settimane fa
Pomezia, Lazio, Italia STERIS A tempo pienoJob Title: Regulatory Affairs InternJob Category: Regulatory AffairsDescription:STERIS is a leading provider of innovative healthcare and life science solutions. We are seeking a highly motivated and detail-oriented Regulatory Affairs Intern to join our team in Pomezia, Italy.Job Summary:The Regulatory Affairs Intern will support the implementation of...
-
Regulatory Affairs Specialist
3 settimane fa
Pomezia, Lazio, Italia STERIS A tempo pienoJob Title: Regulatory Affairs InternSTERIS is seeking a highly motivated and detail-oriented Regulatory Affairs Intern to join our team in Pomezia, Italy. As a Regulatory Affairs Intern, you will play a critical role in supporting the development and implementation of regulatory strategies for our medical device products.Key Responsibilities:Support the...
-
Regulatory Affairs Specialist
2 settimane fa
Pomezia, Lazio, Italia STERIS A tempo pienoJob Title: Regulatory Affairs SpecialistDescription:STERIS is seeking a highly motivated and detail-oriented Regulatory Affairs Specialist to join our team in Pomezia, Italy. As a key member of our Regulatory Affairs team, you will be responsible for ensuring compliance with regulatory requirements for medical devices in the European market.Key...
-
Regulatory Affairs Specialist
2 mesi fa
Pomezia, Lazio, Italia STERIS A tempo pienoJob Title: Regulatory Affairs SpecialistJob Category: Regulatory AffairsWe are seeking a highly motivated and detail-oriented Regulatory Affairs Specialist to join our team at STERIS. As a key member of our Regulatory Affairs function, you will play a critical role in ensuring the compliance of our medical devices with regulatory requirements in the European...
-
Regulatory Affairs Specialist
6 giorni fa
Pomezia, Lazio, Italia Steris Canada Corporation A tempo pienoAbout the Role:We are seeking a highly motivated Regulatory Affairs Intern to join our team at Steris Canada Corporation.Job Summary:The Regulatory Affairs Intern will assist in the preparation, monitoring, and maintenance of documents for submissions to regulatory agencies, including the National Health Authority (NHA). The successful candidate will have a...
-
Regulatory Affairs Specialist
1 settimana fa
Pomezia, Lazio, Italia STERIS A tempo pienoAt STERIS, we strive to create a healthier and safer world by providing innovative healthcare and life science solutions.Position OverviewWe are seeking a highly organized and detail-oriented Regulatory Affairs Intern to support our team in Pomezia, Italy.The Regulatory Affairs function at STERIS is responsible for implementing efficient processes to obtain...
-
Regulatory Affairs Specialist
3 mesi fa
Pomezia, Italia Steris Canada Corporation A tempo pienoJob Title: Regulatory Affairs SpecialistAt 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 SummaryWe are looking for a Regulatory Affairs Specialist to join our Regulatory Team based in Pomezia (Rome). The mission of the STERIS...
-
Regulatory Affairs Specialist
1 settimana fa
Pomezia, Lazio, Italia STERIS A tempo pienoJob Title: Regulatory Affairs SpecialistDescription:STERIS is seeking a highly motivated and detail-oriented Regulatory Affairs Specialist to support the implementation of efficient and effective processes to obtain and maintain clearance to market STERIS products.Key Responsibilities:Develop a working knowledge of market and regulations associated with...
-
Regulatory Affairs Specialist
2 settimane fa
Pomezia, Lazio, Italia STERIS A tempo pienoAt STERIS, we strive to create a healthier and safer world by providing innovative healthcare and life science solutions.Position OverviewWe are seeking a highly organized and detail-oriented Regulatory Affairs Intern to support our team in Pomezia, Italy.The Regulatory Affairs function at STERIS is responsible for implementing efficient processes to obtain...
-
Regulatory Affairs Specialist
3 mesi fa
Pomezia, Italia Steris Canada Corporation A tempo pienoJob Title: Regulatory Affairs Specialist 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 We are looking for a Regulatory Affairs Specialist to join our Regulatory Team based in Pomezia (Rome). The mission of the STERIS...
-
Regulatory Affairs Specialist
6 giorni fa
Pomezia, Italia Steris Ims A tempo pienoAt 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 We are looking for a Regulatory Affairs Specialist to join our Regulatory Team based in Pomezia (Rome). The mission of the STERIS Regulatory Affairs function is to implement...
-
Regulatory Affairs Specialist
6 giorni fa
Pomezia, Italia Steris Ims A tempo pienoAt 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 We are looking for a Regulatory Affairs Specialist to join our Regulatory Team based in Pomezia (Rome). The mission of the STERIS Regulatory Affairs function is to implement...
-
Regulatory Affairs Specialist
4 settimane fa
Pomezia, Lazio, Italia STERIS A tempo pienoRegulatory Affairs InternAt STERIS, we strive to create a healthier and safer world by providing innovative healthcare and life science solutions. We are seeking a highly motivated and detail-oriented Regulatory Affairs Intern to join our team in Pomezia, Italy.Key Responsibilities:Support the implementation of efficient and effective processes to obtain and...
-
Regulatory Affairs Specialist
2 settimane fa
Pomezia, Lazio, Italia STERIS A tempo pienoRegulatory Affairs Intern**Job Summary**STERIS is seeking a highly motivated and detail-oriented Regulatory Affairs Intern to support the implementation of efficient and effective processes to obtain and maintain clearance to market STERIS products in support of STERIS's global business plans. The successful candidate will develop a working knowledge of the...
-
Regulatory Affairs Specialist
3 settimane fa
Pomezia (RM), Italia STERIS Canada Corporation A tempo pienoJob Title: Regulatory Affairs Specialist 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 We are looking for a Regulatory Affairs Specialist to join our Regulatory Team based in Pomezia (Rome). The mission of the STERIS...
Regulatory Affairs Intern
2 mesi fa
col-wideJob 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
We are looking for a Regulatory Affairs Intern to join our team base in Pomezia (Roma).
The mission of the STERIS Regulatory Affairs function is to implement efficient and effective processes to initially obtain and then maintain clearance to market STERIS products in support of STERIS's global business plans. This includes determining submission to NB for the CE marking and in some cases of registration and/or submission requirements in the International markets, working with STERIS International Registration staff to identify requirements in other targeted markets, and working with product acquisition or development teams to ensure these requirements are met.
The Regulatory Affairs Intern will develop a working knowledge of the following market and the regulations and standards associated:
Europe/Middle East/Africa (EMEA) ???European Union: Medical Device Directive 93/42/EC as amended by 2007/47/EC EU MDR Regulation 2017/745
Key International Standards: ISO 13485: Medical devices – Quality management systems ISO 9001: Quality management systems ISO 14971 Application of Risk Management to Medical Devices
The Regulatory Affairs Intern will have responsibility to support the duties of the functional areas described below, as assigned, under the guidance and direction of his/her manager and other senior Regulatory Affairs staff.
General Duties
Responsible for maintaining understanding of and compliance with all current active Corporate Procedures applicable to his/her job functions
Maintain conduct in accordance with the principles of the STERIS Code of Business Conduct and comply with all Company policies
Protect company confidential information by properly storing, retrieving, and disseminating such information only to those authorized
Conduct daily activities of assigned job responsibilities and projects as assigned
Support a safe, clean and secure working environment through adherence to applicable procedures, rules and regulations
Assist in the updating and maintenance of essential requirements and GSPR checklists and technical files for products sold into the EU market. Assist to complete change control documentation for regulatory related product changes
Support in the execution of regulatory affairs and compliance activities for company product lines in both the Italian and international markets in which the Company conducts business
Registration and technical Duties
Support in the preparation, monitoring and maintenance of documents for any submissions to NB and shared drive folders, and databases in an accurate, complete and timely manner to ensure prompt and accurate access to company regulatory information
Assist in the preparation, compilation, and submission of regulatory documents for the registration of current and new products in some markets
Assist in Monitoring and maintenance of regulatory documents to keep the CE marking
Support local commercial and tender offices with RA documentation/information
Interact with Regulatory Affairs personnel at regulatory agencies, including NB, consultants, contract manufacturers, and distributors to ensure requirements are understood and submissions are complete and accurate to avoid any potential delays in approval
Education Degree
High School Diploma or GEDBachelor's Degree in Engineering General or Biology
Specific Work Requirements
Excellent PC skills, including Microsoft Office applications
Italian mother tongue and English fluent are mandatory
Competencies
Strong interpersonal skills – ability to work closely with people at all levels within the STERIS organization and facilitate the implementation of corrective action; able to work effectively and professionally with external people including Customers and government officials
Self-starter that is highly organized
Strong oral and written communication skills.
Additional Information
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, sex, sexual orientation, gender identity, genetic information, and any other category protected by state or local law.
STERIS is a leading global provider of products and services that support patient care with an emphasis on infection prevention. WE HELP OUR CUSTOMERS CREATE A HEALTHIER AND SAFER WORLD by providing innovative healthcare, life sciences and dental products and services. STERIS is a $5 billion, publicly traded (NYSE: STE) company with approximately 17,000 associates and Customers in more than 100 countries.
STERIS strives to be an Equal Opportunity Employer.
