出海雷达

制药毒理学研究学者(美国-远程,美国)

Research Fellow, Pharma Toxicology (USA - Remote, US)

其他限定地区(需当地身份)
公司Bausch Health US, LLC
薪资$150,000 - $200,000/年
工作地点United States
地域资格限定地区(需当地身份)
时区要求日间重叠约 9 小时,基本正常作息
用工类型Full Time
发布时间13 天前
数据来源Himalayas
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注意地域限制:该职位明确限定在 United States 招聘。如果你是位于中国大陆的求职者,通常需要当地工作身份才能投递,或需与雇主确认是否接受独立合同(Contractor)形式合作。

Bausch + Lomb (NYSE/TSX: BLCO) 是一家全球领先的眼科健康公司,致力于保护和提升全球数百万人的视力——从出生那一刻起,贯穿生命各个阶段。我们的使命简单而有力:帮助您看得更清楚,从而生活得更好。
我们拥有超过 400 种产品的完整产品组合,全面整合,旨在满足客户在生命全周期中各种眼科健康需求。我们的知名品牌建立在 170 年历史中积累的客户深厚信任和忠诚之上。我们拥有约 13,000 名员工的全球研发、生产、销售和商业布局,在约 100 个国家设有业务,使我们能够触及全球数十亿潜在客户。我们长期参与眼科健康领域的诸多重大进展,并相信我们已做好充分准备,继续引领未来眼科健康的发展。
药理毒理研究学者将为内部和外部利益相关者提供全面的跨职能非临床专业知识,重点在于毒理学及相关科学领域,以支持药品开发和持续的产品生命周期管理。研究学者将代表部门,通过书面和口头方式清晰、专业且有效地沟通,确保所有互动中都留下强大而可信的第一印象。
职责:

  • 领导药品、非处方产品和消费品的非临床安全性评估策略。
  • 确保非临床开发计划及其执行符合整体产品开发目标、产品生命周期管理活动以及关键监管期望和里程碑。
  • 监督关键非临床数据的生成、解读和传达,以支持成功的临床开发、监管申报/注册、产品上市、持续市场支持和合规活动。
  • 为初级团队成员提供指导、辅导和培训,以支持他们的科研和职业发展。管理毒理学团队。
  • 跟踪不断变化的行业标准、监管指南和科学最佳实践,将相关更新整合到新产品开发中,并评估其对现有产品的影响。
  • 撰写、审核并批准技术文档
查看英文原文

Bausch + Lomb (NYSE/TSX: BLCO) is a leading global eye health company dedicated to protecting and enhancing the gift of sight for millions of people around the world—from the moment of birth through every phase of life. Our mission is simple, yet powerful: helping you see better, to live better.
Our comprehensive portfolio of over 400 products is fully integrated and built to serve our customers across the full spectrum of their eye health needs throughout their lives. Our iconic brand is built on the deep trust and loyalty of our customers established over our 170-year history. We have a significant global research, development, manufacturing and commercial footprint of approximately 13,000 employees and a presence in approximately 100 countries, extending our reach to billions of potential customers across the globe. We have long been associated with many of the most significant advances in eye health, and we believe we are well positioned to continue leading the advancement of eye health in the future.
The Research Fellow, Pharma Toxicology, will provide comprehensive, cross functional preclinical expertise to internal and external stakeholders, with a focus on toxicology, and related scientific disciplines that support pharmaceutical development, and ongoing lifecycle management. The Research Fellow will represent the department by delivering clear, professional, and effective communication, both written and verbal, to ensure a strong and credible first impression across all interactions.
Responsibilities:

  • Lead nonclinical safety assessments strategies for pharmaceuticals, over the counter products, and consumer goods.
  • Ensure that nonclinical development plans and their execution align with overall product development objectives, lifecycle management activities, and key regulatory expectations and milestones.
  • Oversee the generation, interpretation, and communication of essential nonclinical data to enable successful clinical development, regulatory submissions/registrations, product launch, ongoing market support, and compliance activities.
  • Provide guidance, coaching, and mentorship to junior team members to support their scientific and professional development. Manage toxicology staff.
  • Stay current with evolving industry standards, regulatory guidance, and scientific best practices, integrating relevant updates into new product development and assessing their impact on existing products.
  • Author, review, and approve technical documents and scientific reports as needed to support departmental deliverables.
  • Collaborate and interface effectively with cross functional partners—including Product Development, Clinical Development, Analytical Chemistry, Regulatory Affairs, Quality, and Compliance—to support program objectives.
  • Partner with international company sites to address nonclinical safety requirements for country specific submissions, registrations, and ongoing business needs.
  • Lead the development, implementation, and continuous improvement of departmental processes, standards, and best practices.

Requirements:

  • Ph.D. in Toxicology or related discipline
  • 12+ years of relevant Pharmaceutical industry experience.
  • Experience in ophthalmology drug development is highly desirable.
  • DABT preferred.

This position may be available in the following location(s): US - Remote
All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or veteran status.
For U.S. locations that require disclosure of compensation, the starting pay for this role is between $150,000.00 and $200,000.00. The estimated salary range reflects an anticipated range for this position. The actual base salary offered may depend on a variety of factors.
U.S. based employees may be eligible for short-term and/or long-term incentives. They may also be eligible to participate in medical, dental, vision insurance, disability and life insurance, a 401(k) plan and company match, a tuition reimbursement program (select degrees), company holidays, and well-being benefits, among others. U.S. based employees are also eligible to receive sick time, floating holidays and paid vacation.
Job Applicants should be aware of job offer scams perpetrated through the use of the Internet and social media platforms.
To learn more please read Bausch + Lomb's Job Offer Fraud Statement.
Applicants must be authorized to work for ANY employer in the U.S. We are unable to sponsor or take over sponsorship of an employment Visa at this time.
Originally posted on Himalayas

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