HCL Technologies Opportunities For Regulatory Affairs MDR – Email Resume

HCL Technologies Released Job Openings On 20/05/2022.HCL Technologies is a next-generation global technology company that helps enterprises reimagine their businesses for the digital age. Our technology products and services are built on four decades of innovation, with a world-renowned management philosophy, a strong culture of invention and risk-taking, and a relentless focus on customer relationships. HCL also takes pride in its many diversity, social responsibility, sustainability, and education initiatives. Through its worldwide network of R&D facilities and co-innovation labs, global delivery capabilities, and over 187,000+ Ideapreneurs’ across 50 countries, HCL delivers holistic services across industry verticals to leading enterprises, including 250 of the Fortune 500 and 650 of the Global 2000.Eligibility Criteria / Educational Qualification, Official Notification, Apply Online Form Link & Other Relevant Details for HCL Technologies Recruitment 2021 are provided below. Interested and eligible candidates can  submit application along with resume. 

Vacancy Details:

HCL Technologies Recruiting Any Graduate Candidates with 03-08+ Years Experience For Regulatory Affairs MDR Position.Complete Details for the Regulatory Affairs MDR as follows.

Important Details :

• Location :Chennai
• No of Vacancies:NA
• Details of Salary: NA
• Opening date for online Application: 20/05/2022
• Mode of application :WALKIN
  
• How To Apply: If Interested, kindly share your updated resume to krajitha.gowd@hcl.com

Related Job : Sanofi Walk-In Interviews On 22nd May 2022 

For more Latest pharma jobs https://pharmajobscooin.wordpress.com/

Job Description/Skills Required

• To manage the teams in implementing products’ regulatory standards & compliances for multiple accounts/clients clients/products requirements and review the same as per the target markets’ product/ government laws
• To participate in product standards and regulations compliance internal audits/reviews of the assigned product and make necessary modifications as required; and, also participate in accredited external Compliance test audits for each of the identified product’s target market
• To independently identify & implement product standards and regulatory requirements (with the cross functional product development teams) in compliance to target market/country’s product compliance regulations
• To lead the product design discussions pertaining to standards compliance (pre-design and post-implementation phase of the product) with cross functional development teams to ensure that all product global standards and product regulatory compliances are incorporated and strictly adhered
• Should have thorough knowledge in Medical QARA.
• Should have knowledge about regulatory standards ISO13485
• Determine the regulatory reportability of each complaint in accordance with business procedures and regulatory / reportability guidelines
• Adhere to and ensure the compliance of all company policies, guidelines, procedures and standards
• Working knowledge of appropriate global medical device regulations, requirements, and standards

If Interested, kindly share your updated resume to krajitha.gowd@hcl.com with below details

• Total experience:
• Relevant experience in Regulatory:
• Current CTC:
• Expected CTC:
• Current Company:
• Current Designation:
• Notice Period:
• Current Location:
• Preferred Location:

Click here for Official notification and Apply