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genetixbiotherapeutics
Страна
США
Зарплата
220 000 $ – 235 000 $
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DirectorГибридПолная занятость

Director, LVV Manufacturing and MS&T

Оценка ИИ

Привлекательная позиция уровня Director в инновационной сфере генной терапии с конкурентной зарплатой и расширенным пакетом льгот (unlimited PTO, equity). Четко прописанные обязанности и гибридный график делают вакансию очень качественной для топ-менеджмента.


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Сложность вакансии

ЛегкоСложно
Оценка ИИ

Высокая сложность обусловлена требованием более 12 лет опыта в биофармацевтике и глубокой экспертизы в производстве лентивирусных векторов (LVV). Роль требует совмещения стратегического руководства CDMO-сетями и глубоких технических знаний в области MS&T и GMP.

Анализ зарплаты

Медиана230 000 $
Рынок210 000 $ – 265 000 $
Оценка ИИ

Предложенная зарплата ($220k - $235k) находится в пределах рыночной нормы для позиции Директора в биотехнологическом секторе Массачусетса, хотя верхняя граница рынка для крупных компаний может достигать $260k+. Учитывая наличие опционов (equity) и неограниченного отпуска, предложение является очень конкурентоспособным.

Сопроводительное письмо

I am writing to express my strong interest in the Director, LVV Manufacturing and MS&T position at Genetix Biotherapeutics. With over 12 years of experience in biopharmaceutical manufacturing and a proven track record in leading Manufacturing Sciences & Technology (MS&T) teams, I am confident in my ability to drive process robustness and ensure a reliable commercial supply of lentiviral vectors. My background includes extensive experience managing CDMO networks and overseeing complex tech transfers, which aligns perfectly with your current strategic needs.

Throughout my career, I have successfully led cross-functional teams to achieve GMP compliance and operational excellence in the advanced therapies space. I am particularly drawn to Genetix's mission of pursuing curative gene therapies and appreciate your commitment to a culture of radical care and technical rigor. I look forward to the possibility of bringing my expertise in LVV operations and lifecycle management to your leadership team to help scale your manufacturing capabilities and support your growing pipeline.

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Присоединяйтесь к Genetix Biotherapeutics, чтобы возглавить производство инновационной генной терапии и изменить жизни пациентов!

Описание вакансии

About Genetix Biotherapeutics

At Genetix Biotherapeutics every role has meaning, every team member is respected, and every day is a chance to make a difference. When you join Genetix, you're not just landing a new role, you become part of a company that's pursuing curative gene therapies to give patients and their families more days. We are doers, thinkers and collaborators who embrace and live by our values:

Our innovation is rooted in the diversity of our teams and results are achieved through cooperation and the integration of multiple viewpoints. This is personal and we approach every challenge with radical care.

SUMMARY

The Director of LVV Manufacturing & MS&T will provide strategic and technical leadership for end-to-end lentiviral vector operations, spanning GMP Manufacturing and Manufacturing Sciences & Technology (MS&T). This role is accountable for ensuring reliable commercial supply, driving process robustness and lifecycle management, and leading cross-functional execution across Manufacturing, Quality, Supply Chain, and Regulatory functions for LVV production.

The Director will own tech transfer through commercial manufacturing, continuous improvement, and regulatory support, while serving as the PIP for manufacturing operations for the CDMO network.

This is a full-time hybrid position (3 days a week) in our Somerville – Assembly Row, Massachusetts office. This role will also require travel to manufacturing sites (10% travel).

RESPONSIBILITIES

Manufacturing Leadership

  • Provide end-to-end ownership of LVV processes, from tech transfer through commercial manufacturing and lifecycle management
  • Establish and execute manufacturing strategy to support commercial demand, pipeline growth, and long-term scalability
  • Partner with Supply Chain to ensure capacity planning, readiness, and risk mitigation
  • Ensure compliant, reliable GMP manufacturing of LVV drug substance for commercial supply
  • Oversee deviation management, CAPAs, change control, and inspection readiness initiatives

MS&T Leadership

  • Lead or support MS&T activities including process characterization, validation, comparability, and continued process verification (CPV)
  • Drive process robustness, yield improvement, and cost-of-goods reduction initiatives
  • Provide technical leadership for process deviations, investigations, and root cause analysis

Cross-Functional Collaboration

  • Act as a key technical interface with Quality, Regulatory Affairs, Process Development, Analytical, and External Manufacturing partners
  • Support regulatory filings, responses, and lifecycle submissions related to LVV manufacturing changes
  • Represent LVV manufacturing in governance forums and senior leadership discussions

Leadership & Collaboration

  • Lead the LVV manufacturing team contributing to the overall CMC and manufacturing strategy for commercial products
  • Collaborate closely with CDMO as site liaison for all Tech Transfer and Manufacturing activities
  • Establish a strong culture of accountability, continuous improvement, and technical rigor

QUALIFICATIONS

Education and Experience

  • Bachelor’s degree in Engineering, Life Sciences, or related field; advanced degree (MBA or MS) preferred
  • 12+ years of experience in manufacturing, MS&T or CMC roles in the biopharma industry, with at least 5 years in a senior leadership role
  • Deep experience managing contract manufacturing and external supply networks in LVV manufacturing
  • Strong understanding of GMP compliance, quality systems, and regulatory expectations for advanced therapies
  • Strategic thinker with strong financial acumen and a hands-on, results-driven leadership style
  • Demonstrated ability to lead cross-functional teams, manage complex projects, and influence at all levels of the organization

Skills and Competencies

  • Demonstrated ability to lead cross-functional teams, manage complex projects, and influence at all levels of the organization
  • Deep knowledge of cGMP, GDP, and regulatory requirements (FDA, EMA, ICH)
  • Exceptional leadership, communication, and cross-functional collaboration skills

Key Attributes

  • Strong demonstrated leadership across multiple functions within Technical Operations
  • Strategic thinker with hands-on operational expertise in LVV manufacturing

Compensation is based on a number of factors, including market location, and may vary depending on job-related knowledge, skills, and experience. Equity and other forms of compensation may be provided as part of a total compensation package, in addition to a full range of medical, dental, vision, 401k, and other benefits, including unlimited paid time off and parental leave.

Pay Transparency

$220,000—$235,000 USD

Genetix is proud to be an equal opportunity employer, seeking to create a welcoming and diverse environment.  All applicants will receive consideration for employment without regard to race, color, religion, gender, gender identity or expression, sexual orientation, national origin, genetics, disability, age, veteran status or any other applicable legally protected characteristics.

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Навыки

  • LVV Manufacturing
  • MS&T
  • GMP
  • CMC
  • CDMO Management
  • Tech Transfer
  • Process Validation
  • Quality Systems
  • FDA Compliance
  • EMA Compliance
  • Supply Chain Planning
  • Root Cause Analysis

Возможные вопросы на собеседовании

Проверка опыта управления внешними партнерами, что критично для данной роли.

Опишите ваш опыт управления CDMO: с какими основными трудностями вы сталкивались при трансфере технологий LVV и как их решали?

Оценка технических навыков в области обеспечения стабильности процессов.

Какие стратегии вы используете для обеспечения надежности процесса (process robustness) и снижения себестоимости (COGS) в производстве векторов?

Проверка знаний регуляторных требований для передовых методов терапии.

Как вы подходите к подготовке документации для CMC-разделов при подаче в FDA/EMA, особенно в контексте изменений в процессе производства?

Оценка лидерских качеств в кризисных ситуациях.

Расскажите о случае, когда серьезное отклонение в производстве угрожало срокам поставки. Как вы координировали работу отделов качества и производства для минимизации рисков?

Проверка навыков долгосрочного планирования.

Как вы планируете масштабирование мощностей LVV для перехода от клинических стадий к полноценному коммерческому производству?

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genetixbiotherapeutics
Страна
США
Зарплата
220 000 $ – 235 000 $