Cepheid QA Associate Vacancy
--Must See--

Cepheid QA Associate Vacancy For BSc Biology, Apply Online

Cepheid QA Associate Vacancy For BSc Biology, Apply Online. BS Biology QA Validation Professional I Vacancy. Interested and eligible applicants can check out all of the details on the same below

Hey there, looking for some assistance with the possible interview questions and answers for the role of QA Validation Professional I at Cepheid? Then check them out below

QA Validation Professional I

Location – Bangalore, Karnataka, India

Job Family – Quality & Regulatory Affairs

Job ID – R1243576

At Cepheid, we are passionate about improving health care through fast, accurate diagnostic testing. Our mission drives us, every moment of every day, as we develop scalable, groundbreaking solutions to solve the world’s most complex health challenges. Our associates are involved in every stage of molecular diagnostics, from ideation to development and delivery of testing advancements that improve patient outcomes across a range of settings. As a member of our team, you can make an immediate, measurable impact on a global scale, within an environment that fosters career growth and development.

Cepheid is proud to work alongside a community of six fellow Danaher Diagnostics companies. Together, we’re working at the pace of

change on diagnostic tools that address the world’s biggest health challenges, driven by knowing that behind every test there is a patient waiting.

Learn about the Danaher Business System which makes everything possible.

The Quality Validation Associate position that supports quality systems activities related to software validation, with a focus on design control and risk management in accordance with FDA and ISO regulations. This position contributes to the completion of milestones associated with software projects or activities using existing procedures and under direct supervision.

This position is part of the Cepheid Quality Team and will be located at Danaher India Development Center (IDC), Bengaluru, Hybrid. At Cepheid, our vision is to be the leading provider of seamlessly connected diagnostic solutions.

In this role, you will have the opportunity to:

  • Perform duties as an individual contributor and/or team member with 100% hands-on work
  • Participate in creating and updating of test protocols, the submission, execution, and review of test protocols in accordance with SOPs
  • Record, report, and verify software defects to accurately depict the software requirements
  • Participate in test design reviews and work closely with Software Engineering team toward the reporting and resolution of design issues and/or software defects
  • Participate in Validation to ensure the software meets user needs requirements of user workflows for a regulated environment
  • Provide test data to drafts of validation report, update traceability matrices and quality metrics
  • Create change orders in document control system
  • Participate in daily management using DBS tools

The essential requirements of the job include

  • BE/BS degree or equivalent work experience in Computer Science, Biology, BioMedical or related field.
  • 2+ years of software validation testing experience in a regulated environment.
  • Understanding of FDA and ISO regulations, e.g., design controls and risk management
  • Excellent interpersonal, writing and communication skills, and troubleshooting skills and passionate about testing, product quality, and customer satisfaction.
  • Experience with: Windows environments, Web application testing, and working knowledge of SQL, including the ability to run queries, and interpret results.

Cepheid, a Danaher operating company, offers a broad array of comprehensive, competitive benefit programs that add value to our lives. Whether it’s a health care program or paid time off, our programs contribute to life beyond the job. Check out our benefits at danaherbenefitsinfo.com.

Hybrid Job Posting Language:

At Cepheid we believe in designing a better, more sustainable workforce. We recognize the benefits of flexible, hybrid working arrangements for eligible roles and are committed to providing enriching careers, no matter the work arrangement. This position is eligible for a hybrid work arrangement in which you can work part of the time at the Company location identified above and part of the time remotely from your home. Additional information about this hybrid work arrangement will be provided by your interview team. Explore the flexibility and challenge that working for Cepheid can provide.

When you join us, you’ll also be joining Danaher’s global organization, where 80,000 people wake up every day determined to help our customers win. As an associate, you’ll try new things, work hard, and advance your skills with guidance from dedicated leaders, all with the support of powerful Danaher Business System tools and the stability of a tested organization.

At Danaher, we value diversity and the existence of similarities and differences, both visible and not, found in our workforce, workplace and throughout the markets we serve.  Our associates, customers and shareholders contribute unique and different perspectives as a result of these diverse attributes.

If you’ve ever wondered what’s within you, there’s no better time to find out.

APPLY ONLINE

Hey there, looking for some assistance with the possible interview questions and answers for the role of QA Validation Professional I at Cepheid? Then check them out below

  1. Can you explain your experience in software validation testing in a regulated environment?
    • Answer: In my previous role, I worked for [X] years in a regulated environment, conducting software validation testing. I followed FDA and ISO regulations, ensuring compliance with design controls and risk management processes. I have experience in creating and executing test protocols, recording and reporting software defects, and collaborating with software engineering teams to resolve design issues.
  2. How familiar are you with FDA and ISO regulations related to software validation?
    • Answer: I have a solid understanding of FDA and ISO regulations, particularly in the areas of design controls and risk management. I am well-versed in the requirements and guidelines set forth by these regulatory bodies, which ensures that software validation activities align with industry standards.
  3. Could you describe your experience with web application testing and working in Windows environments?
    • Answer: Throughout my career, I have gained extensive experience in testing web applications. I am familiar with the unique challenges associated with web-based software and have successfully executed test cases in such environments. Additionally, I have worked extensively in Windows environments, allowing me to effectively test and validate software within that framework.
  4. How proficient are you in SQL and using it for running queries and interpreting results?
    • Answer: I have a working knowledge of SQL and have utilized it for running queries and analyzing data. I am comfortable writing SQL statements to retrieve information from databases, and I can interpret query results to gain valuable insights for software validation purposes.
  5. Can you provide an example of how you contributed to ensuring software met user needs and regulatory requirements in a previous project?
    • Answer: In a previous project, I actively participated in the validation process to ensure that the software aligned with user needs and complied with regulatory requirements. I collaborated closely with the software engineering team, attending design reviews and identifying potential issues or defects. By providing valuable feedback and testing insights, I contributed to the successful validation of the software, ensuring its suitability for use in a regulated environment.

Remember, these answers should be customized based on your specific experience and achievements in the field of software validation testing.

Editor’s Note: Cepheid QA Associate Vacancy For BSc Biology, Apply Online. Cepheid QA Associate Vacancy 2023. Please make sure that you are subscribed to the Biotecnika Times Newsletter and our YouTube channel to be notified of all of the latest in the industry. Follow us on all of our social media like TwitterTelegramFacebook and Instagram.

Diluxi Arya
Diligence + Intelligence + Learned +Understanding +Xenial + Idealistic = DILUXI. Girl with the golden hands, She has worked hard and transformed BioTecNika's Alerts section with Latest Notifications and Articles with most profound insights. When we need a reliable hand at work, All eyes turn to her!