Research Fellow, Pharma Toxicology

Bausch + Lomb; Carson City (NV); On-site; USD 150,000 - 200,000; Full time

Benefits offered by this job

401(k) plan and company match

Medical, dental, and vision insurance

Tuition reimbursement program

Paid vacation and sick leave

Job summary

Bausch + Lomb is seeking a Research Fellow in Pharma Toxicology to provide cross-functional preclinical expertise for pharmaceutical development and lifecycle management. The role emphasizes toxicology leadership, data communication, and collaboration with multiple departments across the organization.

The candidate will mentor junior staff, stay abreast of evolving regulatory expectations, and contribute to continuous process improvements.

Qualifications

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

Responsibilities

• Lead nonclinical safety assessment strategies for pharmaceuticals, OTC products, and consumer goods.
• Ensure nonclinical development plans align with product objectives and regulatory milestones.
• Oversee generation, interpretation, and communication of nonclinical data for regulatory submissions and launches.
• Provide guidance and mentorship to junior staff; manage toxicology personnel.
• Stay current with industry standards and regulatory guidance; adapt processes accordingly.
• Author, review, and approve technical documents and scientific reports as needed.
• Collaborate with Product Development, Clinical Development, Regulatory Affairs, Quality, and Compliance.
• Coordinate with international sites for country-specific submissions.
• Lead development and improvement of departmental processes and best practices.

Skills

Toxicology

Preclinical

DABT certification

Education

PhD in Toxicology

Job description

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 worldfrom 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 partnersincluding Product Development, Clinical Development, Analytical Chemistry, Regulatory Affairs, Quality, and Complianceto 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): [[location_obj]]

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.

Our US Benefit Programs:Employee Benefits: Bausch + Lomb. (https://www.bausch.com/careers/benefits/)

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.