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Veeva · 전략·분석

  • 생명과학
  • 2007년 설립(해외 본사) (20년차)
  • 상장 이력

Validation Analyst - RTSM

South Korea - Seoul공식 채용 공고

이 브라우저에 저장돼요 · 최근 확인

무슨 일을 하고, 무엇을 요구하나요?

전략·분석

공고에서 경력 조건을 확인하지 못했어요. 경력 무관으로 모집한다는 뜻은 아니에요.

주요 업무
  • Participate in RTSM requirement gathering sessions with clients and RTSM team members
  • Closely collaborate with RTSM Development and Project Management teams to ensure requirements are defined in a clear, testable, and compliant format
  • Ensure requirements are adequately tested following a risk-based approach
  • Develop and maintain CSV deliverables including requirements specifications, test scripts, summary reports, and trace matrices
주요 업무 4개 더 보기
자격 요건
  • Working knowledge of software development cycle (SDLC)
  • Exceptional attention to detail
  • Good interpersonal skills and ability to communicate in English with team members and customers of varying roles and skill levels
우대 사항
  • Working knowledge of GCP Guidance such as 21 CFR Part 11, EU Annex 11
  • Veeva’s headquarters is located in the San Francisco Bay Area with offices in more than 15 countries around the world.
  • Veeva is an equal opportunity employer.
  • All qualified applicants will receive consideration for employment without regard to race, color, sex, sexual orientation, gender identity or expression, religion, national origin or ancestry, age, disability, marital status, pregnancy, protected veteran status, protected genetic information, political affiliation, or any other characteristics protected by local laws, regulations, or ordinances.

공고 원문의 문장을 그대로 옮겼어요. 근무 조건과 전형은 바뀔 수 있으니 지원 전에 원문을 확인하세요.

Veeva, 어떤 회사일까요?

  • 생명과학
  • 2007년 설립(해외 본사) (20년차)
  • 상장 이력

생명과학 분야를 중심으로 산업별 클라우드 소프트웨어를 제공하는 글로벌 기업입니다. 글로벌 모회사의 2007년 설립 이력과 서울 삼성동 한국 사무실을 확인했습니다.

Veeva 더 알아보기
포지션 소개 · 공고 전문 읽기

Veeva Systems is a mission-driven organization and pioneer in industry cloud, helping life sciences companies bring therapies to patients faster. As one of the fastest-growing SaaS companies in history, we surpassed $3B in revenue in our last fiscal year with extensive growth potential ahead.

At the heart of Veeva are our values: Do the Right Thing, Customer Success, Employee Success, and Speed. We're not just any public company – we made history in 2021 by becoming a public benefit corporation (PBC), legally bound to balancing the interests of customers, employees, society, and investors.

Join us in transforming the life sciences industry, committed to making a positive impact on its customers, employees, and communities.

The Role

We are looking for a Computer Software Validation (CSV) professional with a specialty in clinical trial software. This role would give you the opportunity to work on a leading solution in Randomization and Trial Supply Management (RTSM) software. To excel in this role, you will require strong technical writing capabilities and the ability to simplify complex topics.

As a member of the RTSM team, you will work closely with Development and Project Management teams to support customer RTSM implementations in a dynamic environment. You will use your expertise to take ownership of the validation process for assigned projects and play an important role in building and maintaining product excellence for the RTSM system.

What You’ll Do

  • Participate in RTSM requirement gathering sessions with clients and RTSM team members
  • Closely collaborate with RTSM Development and Project Management teams to ensure requirements are defined in a clear, testable, and compliant format
  • Ensure requirements are adequately tested following a risk-based approach
  • Develop and maintain CSV deliverables including requirements specifications, test scripts, summary reports, and trace matrices
  • Manage Validation testing cycles and resolution of issues and enhancement requests
  • Maintain change control documentation to ensure ongoing validation of the RTSM system
  • Provide technical expertise to RTSM team members in computer system validation, applicable regulations, and other quality system requirements
  • Support customers as needed in RTSM validation activities

Requirements

  • Working knowledge of software development cycle (SDLC)
  • Exceptional attention to detail
  • Good interpersonal skills and ability to communicate in English with team members and customers of varying roles and skill levels

Nice to Have

  • Working knowledge of GCP Guidance such as 21 CFR Part 11, EU Annex 11

#LI-Associate

Veeva’s headquarters is located in the San Francisco Bay Area with offices in more than 15 countries around the world.

Veeva is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, sex, sexual orientation, gender identity or expression, religion, national origin or ancestry, age, disability, marital status, pregnancy, protected veteran status, protected genetic information, political affiliation, or any other characteristics protected by local laws, regulations, or ordinances.

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