- Страна
- США
- Зарплата
- 175 000 $ – 215 100 $
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Associate Director IT Business Systems R&D
Отличная вакансия в инновационной биотех-компании с конкурентной зарплатой, расширенным пакетом льгот (100% оплата страховки) и возможностью работать с передовыми технологиями (AI/ML).
Сложность вакансии
Высокая сложность обусловлена необходимостью глубоких знаний в узкой нише (Veeva Vault), опыта работы в строго регулируемой среде GxP и навыков управления изменениями при миграции систем.
Анализ зарплаты
Предлагаемый диапазон $175k–$215k полностью соответствует рыночным стандартам для позиции Associate Director в Сан-Франциско, где медиана составляет около $195k. Верхняя граница выше среднего, что отражает высокие требования к экспертизе в Veeva.
Сопроводительное письмо
I am writing to express my strong interest in the Associate Director IT Business Systems R&D position at BridgeBio. With over 7 years of experience in biotech IT and a deep specialization in Veeva Vault systems, I am excited by your "moneyball for biotech" approach and the opportunity to lead GxP-compliant digital transformations. My background in migrating legacy systems to Veeva and my hands-on experience with Quality, Clinical, and RIM modules align perfectly with your current initiatives.
In my previous roles, I have successfully led cross-functional teams to optimize R&D workflows and ensure strict GxP compliance. I am particularly intrigued by BridgeBio's commitment to ethical AI integration. I have experience exploring AI/ML applications for metadata extraction and document authoring within regulated environments, and I am eager to bring this expertise to your team to accelerate innovation and operational excellence.
BridgeBio’s mission to develop life-changing medicines for rare diseases resonates with my professional values. I am confident that my technical leadership and stakeholder management skills will contribute significantly to your IT R&D roadmap. Thank you for considering my application; I look forward to the possibility of discussing how I can support your mission in San Francisco.
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Описание вакансии
Mavericks Wanted
When was the last time you achieved the impossible? If that thought feels overwhelming, you might want to pause here, but if it sparks excitement...read on
In 2015, we pioneered a “moneyball for biotech” approach, pooling projects and promising early-stage research from academia together under one financial umbrella to reduce risk and unleash innovation. This model allows science and small teams of experts to lead the way. We build bridges to groundbreaking advancements in rare disease, and develop life-changing medicines for patients with unmet needs as fast as humanly possible.
Together we define white space, push boundaries, and empower people to solve problems. If you're someone who defies convention, join us and work alongside some of the most respected minds in the industry. Together, we'll ask "why not?" and help reengineer the future of biopharma. At BridgeBio, we value curiosity and experimentation—including the ethical & thoughtful use of AI to improve clarity, speed, and quality of work.
Responsibilities
- Support, administer, maintain IT systems supporting Quality and R&D, including Veeva Vault Quality, Clinical, RIM and Safety systems.
- Lead and oversee the migration of data and processes from legacy systems to Veeva (e.g., ZenQMS to Veeva Vault Quality) to ensure seamless transition, data integrity, and GxP compliance
- Partner with business leaders to understand their requirements and continuously improve user adoption and implement new systems, integrations, and GxP compliance initiatives
- Partner with Quality, Clinical, Regulatory, and Safety leaders to support business needs, implement roadmaps, identify, recommend solutions (e.g., Artificial Intelligence (AI)) to drive business value and accelerate innovation
- Work with Managed Service providers and internal IT teams for supporting and monitoring GxP-regulated systems to ensure high-quality service delivery
- Collaborate with CSV QA and compliance functions to validate and ensure alignment with regulatory requirements (e.g., GxP, HIPAA, GDPR)
- Establish governance, documentation, and change control procedures for GxP systems to ensure sustained compliance and operational excellence.
- Drive continuous improvement across the GxP systems landscape by assessing emerging technologies (e.g., AI) and optimizing workflows that support BridgeBio’s business strategy.
Where You’ll Work
- This is a local role and will require minimum 2 days in our San Francisco office.
Who You Are
- Bachelor’s degree in information technology, Computer Science, Business Administration, or related field; advanced degree preferred
- 7+ years of progressive IT experience within biotech/pharma, including at least 5 years supporting Veeva Quality systems
- Demonstrated expertise in GxP Quality processes, including document lifecycle management, training assignment and compliance tracking, deviation, CAPA, and change control workflows, and inspection readiness. Ability to partner with Quality stakeholders to design, configure, and continuously improve Veeva Vault QualityDocs,
- QMS, and Training solutions in alignment with regulatory expectations (e.g., FDA, EMA) and company SOPs
- Hands-on experience administering and supporting Veeva Vault Quality systems including RIM, Safety and eTMF is strongly preferred
- Experience applying AI/ML and generative AI solutions within GxP environments to improve Quality operations, including use cases such as intelligent document authoring, metadata extraction, quality event trend analysis, and training effectiveness insights, with a strong focus on validation, auditability, data privacy, and integration with Veeva Vault platforms.
- Skilled in leading cross-functional collaboration across Quality, Clinical, Regulatory, and DSPV teams to ensure system alignment and process harmonization
- Experienced in vendor and Managed Service Provider oversight to ensure reliable, compliant, and high-quality system performance
- Strong communication, leadership, and stakeholder management skills with the ability to translate technical concepts into business outcomes
At BridgeBio, we strive to provide a market-competitive total rewards package, including base pay, an annual performance bonus, company equity, and generous health benefits. Below is the anticipated salary range for candidates for this role who will work in California. The final salary offered to a successful candidate will depend on several factors that may include but are not limited to the type and length of experience within the job, type, and length of experience within the industry, educational background, location of residence and performance during the interview process. BridgeBio is a multi-state employer, and this salary range may not reflect positions based in other states.
Salary
$175,000—$215,100 USD
As a global company, our comprehensive benefits may vary based on location. We have high expectations for our team members. We make sure those working hard for patients are rewarded and cared for in return.
For USA based roles:
Financial & Rewards
- Market-leading compensation
- 401(k) with employer match
- Employee Stock Purchase Program (ESPP)
- Pre-tax commuter benefits (transit and parking)
- Referral bonus for hired candidates
- Subsidized lunch and parking on in-office days
Health & Well-Being
- 100% employer-paid medical, dental, and vision premiums for you and your dependents
- Health Savings Account (HSA) with annual employer contributions, plus Flexible Spending Accounts (FSA)
- Fertility & family-forming benefits
- Expanded mental health support (therapy and coaching resources)
- Hybrid work model with flexibility
- Flexible, “take-what-you-need” paid time off and company-paid holidays
- Comprehensive paid medical and parental leave to care for yourself and your family
Skill Development & Career Paths:
- People are part of our growth and success story - from discovery to active drug trials and FDA pipelines, there are endless opportunities for skill development and internal mobility
- We provide career pathing through regular feedback, continuous education and professional development programs via LinkedIn Learning, LifeLabs, & BetterUp Coaching
- We celebrate strong performance with financial rewards, peer-to-peer recognition, and growth opportunities
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Навыки
- Machine Learning
- HIPAA
- AI
- GDPR
- eTMF
- Quality Management Systems
- GxP
- Change Control
- Veeva Vault
- Clinical Information Systems
- RIM
- CSV QA
Возможные вопросы на собеседовании
Проверка практического опыта миграции данных в критически важных системах.
Опишите ваш опыт руководства миграцией из ZenQMS или аналогичных систем в Veeva Vault. С какими основными трудностями вы столкнулись в плане целостности данных?
Оценка понимания регуляторных требований в биотехнологиях.
Как вы обеспечиваете соответствие систем требованиям GxP, HIPAA и GDPR при внедрении новых ИТ-решений?
Проверка инновационного мышления и понимания современных технологий.
Какие конкретные кейсы использования генеративного ИИ вы видите в контексте управления качеством (Quality) и R&D в биотехнологической компании?
Оценка навыков взаимодействия с бизнесом.
Как вы расставляете приоритеты в дорожной карте ИТ-систем, когда требования отделов Clinical, Regulatory и Quality вступают в конфликт?
Проверка навыков управления внешними ресурсами.
Каков ваш подход к управлению Managed Service Providers (MSP) для обеспечения высокого уровня SLA в регулируемой среде?
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- Страна
- США
- Зарплата
- 175 000 $ – 215 100 $