- Страна
- США
- Зарплата
- 215 000 $ – 235 000 $
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Director, IT Business Partner - Biopharma GXP
Отличная вакансия в перспективной биотех-компании с четкой миссией, конкурентной зарплатой и расширенным пакетом льгот, включая закрытие компании на каникулы.
Сложность вакансии
Высокая сложность обусловлена необходимостью глубоких знаний в узкоспециализированных областях: GXP, CSV и требованиях FDA, а также опытом вывода фарм-продуктов на коммерческий рынок.
Анализ зарплаты
Предлагаемый диапазон $215k–$235k полностью соответствует рыночным стандартам для позиции ИТ-директора в биофармацевтическом секторе США, особенно в хабе Кембридж/Бостон.
Сопроводительное письмо
I am writing to express my strong interest in the Director, IT Business Partner - Biopharma GXP position at Nuvalent. With over a decade of experience in pharmaceutical IT and a proven track record of leading GXP-regulated system implementations, I am confident in my ability to align your IT capabilities with the strategic objectives of your clinical and manufacturing operations as you prepare for commercial launch.
Throughout my career, I have specialized in bridging the gap between complex regulatory requirements and scalable technology solutions. My expertise in 21 CFR Part 11 compliance, Computer System Validation (CSV), and Veeva systems aligns perfectly with Nuvalent's current needs. I have successfully led cross-functional teams through the rigors of commercial scale-up, ensuring that data integrity and audit readiness remain at the forefront of all IT initiatives.
I am particularly drawn to Nuvalent’s mission of creating selective medicines for cancer patients. I am eager to bring my strategic thinking and technical leadership to your team to help drive operational excellence and support the delivery of life-changing therapies.
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Описание вакансии
The Company:With deep expertise in chemistry, Nuvalent is working to create selective medicines designed with the goal to address the needs of patients with cancer. Nuvalent is an exciting early-stage company, bringing together experienced scientists and industry veterans with a proven track record in drug discovery, oncology drug development, and company building.
The Role:
Reporting to the Vice President, Information Technology, the Director, IT Business Partner, GXP will serve as a strategic technology leader responsible for aligning IT capabilities with business objectives across all GXP-regulated departments (GMP, GLP, GCP) as the organization prepares for commercial launch. This role requires deep expertise in pharmaceutical IT systems, regulatory compliance, and the ability to translate complex business requirements into scalable technology solutions that support quality, compliance, and operational excellence.
Responsibilities:
- Partner with GXP business leaders to understand strategic objectives and translate them into comprehensive IT roadmaps that support launch readiness and sustainable operations
- Oversee selection, implementation, and validation of critical GXP systems
- Ensure all IT systems comply with FDA 21 CFR Part 11, EU Annex 11, and data integrity requirements (ALCOA+)
- Lead Computer System Validation (CSV) activities and maintain audit readiness
- Drive IT readiness for commercial launch including system scalability, disaster recovery, and capacity planning
- Build and lead team of IT professionals focused on GXP systems; manage vendor relationships
- Partner with Quality and Regulatory Affairs to support inspections and maintain compliance
- Lead project lifecycle activities such as planning, requirement gathering, design, build, testing, implementation and post-implementation support of GxP applications and related business processes.
- Develop enterprise architecture
Competencies:
- Deep understanding of GXP regulations and their application to IT systems
- Strong knowledge of pharmaceutical manufacturing, quality, and clinical operations
- Experience with GAMP 5, industry standards, and cloud technologies in regulated environments
- Exceptional stakeholder management and communication skills across all organizational levels
- Strategic thinker with strong business acumen and ability to deliver complex projects on time and budget
- Experience in leveraging Enterprise Architecture to deliver business value
Qualifications:
- Bachelor's degree in Computer Science, Information Technology, Engineering, Life Sciences, or related field required
- 10+ years of progressive IT experience in pharmaceutical, biotechnology, or regulated healthcare manufacturing environments
- 5+ years in a leadership role managing IT business partnerships, systems implementations, or GXP IT operations
- Demonstrated experience supporting commercial launch activities or significant operational scale-up in a pharmaceutical setting
- Proven track record implementing and managing multiple GXP-regulated systems, especially Veeva systems
- Hands-on experience with Computer System Validation (CSV) and regulatory compliance requirements (21 CFR Part 11, EU Annex 11, data integrity)
- Experience managing IT budgets, vendor relationships, and cross-functional projects
- PMP, ITIL, or relevant IT certifications
- Knowledge of serialization, track-and-trace, and emerging technologies (AI/ML, analytics)
Additional Information:
Nuvalent is committed to fair and equitable compensation practices, aiming to provide employees with competitive total rewards packages.
The targeted salary range below reflects what Nuvalent reasonably and in good faith expects to offer for this position at the time of posting, but the final salary determination may be within or outside this range based on various factors, including, but not limited to, experience, skills, education, and market factors. The range will be reviewed regularly and is subject to change.
Nuvalent also offers a comprehensive benefit package to support our employees at each stage of their career, financial, health, and well-being journey, including medical, dental, and vision insurance, 401(k) retirement savings plan, generous paid time off (including a summer and winter company shutdown), and much more.
Annual Salary Range
$215,000—$235,000 USD
Nuvalent provides equal employment opportunities (EEO) to all employees and applicants for employment without regard to religion, race, creed, color, sex, sexual orientation, alienage or citizenship status, national origin, age, marital status, pregnancy, disability, veteran or military status, predisposing genetic characteristics or any other characteristic protected by applicable federal, state or local law.
Nuvalent is aware that many companies are dealing with fraudulent job postings on third-party employment search sites and/or individual(s) or entities claiming to be employees of such companies. Those involved are offering fraudulent employment opportunities to applicants, often asking for sensitive personal and financial information, and using such information for criminal activities.
Please be advised that all legitimate correspondence from a Nuvalent employee will come from "@nuvalent.com" email accounts. Automated system response emails from our Greenhouse applicant tracking system come from a “no-reply@greenhouse.io” email address. There are no variations of these email addresses and Nuvalent would not request personal and/or financial information via email. Job opportunities would only be extended after a completed job application is submitted by a candidate and a thorough interview process including 1:1 and/or group interviews via phone, video conferencing and/or in-person.
If you believe you have been contacted by anyone misrepresenting themselves as an employee of Nuvalent, please contact Nuvalent at 857-357-7000. Thank you.
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Навыки
- ITIL
- Disaster Recovery
- GCP
- GMP
- Cloud Computing
- Data Integrity
- Project Management Professional
- Enterprise Architecture
- GLP
- GxP
- Veeva
- Computer System Validation
- GAMP 5
- FDA 21 CFR Part 11
Возможные вопросы на собеседовании
Роль требует глубокого понимания регуляторных норм для ИТ-систем в фарминдустрии.
Опишите ваш опыт обеспечения соответствия систем требованиям 21 CFR Part 11 и принципам ALCOA+ при внедрении облачных решений.
Важной частью работы является управление валидацией компьютерных систем.
Как вы подходите к планированию и выполнению Computer System Validation (CSV) для критически важных GXP-систем в условиях сжатых сроков перед запуском продукта?
Вакансия подразумевает работу с конкретными отраслевыми платформами.
Расскажите о вашем опыте внедрения и управления системами Veeva (например, Vault, Quality, Clinical) и их интеграции в общую архитектуру предприятия.
Позиция требует взаимодействия с топ-менеджментом и различными отделами.
Приведите пример, когда вам приходилось убеждать бизнес-лидеров в необходимости изменения ИТ-стратегии для обеспечения соответствия регуляторным требованиям.
Компания готовится к коммерческому запуску.
Какие ключевые ИТ-риски вы видите при переходе биофармацевтической компании от стадии разработки к коммерческому производству и как вы планируете их минимизировать?
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- Страна
- США
- Зарплата
- 215 000 $ – 235 000 $