Global Senior Director, Pharma Toxicology

Bausch + Lomb

Madison (WI)

On-site

USD 225,000 - 300,000

Full time

5 days ago
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Benefits offered by this job

Medical insurance
Dental insurance
Vision insurance
401(k) with matching
Tuition reimbursement
Paid holidays
Sick time & vacation

Job summary

Bausch + Lomb is seeking a Senior Director of Pharma Toxicology to lead global nonclinical safety across its pharmaceutical, OTC, and consumer portfolios. You will set the nonclinical safety strategy, supervise the toxicology organization, and serve as the scientific authority for development programs and regulatory interactions with health authorities.

You will partner with R&D, Regulatory, Clinical, Quality, and Commercial leaders to enable portfolio decisions, accelerate development, and

Qualifications

  • Requires PhD in Toxicology or related field with extensive pharma nonclinical safety experience.
  • Demonstrated leadership of toxicology teams across multiple programs and lifecycle stages.
  • Experience interacting with health authorities (FDA and others) and presenting risk assessments.

Responsibilities

  • Define global nonclinical safety strategy for pharma, OTC, and consumer products.
  • Lead nonclinical safety programs from discovery to regulatory submissions and lifecycle management.
  • Oversight of GLP studies, CRO/vendor relationships, and study quality.
  • Partner with R&D, Regulatory, Clinical, and Quality to align nonclinical plans with portfolio goals.
  • Represent the company in scientific forums and external collaborations.
  • Mentor and develop a high-performing toxicology organization.

Skills

Toxicology leadership
Regulatory liaison
Strategic planning
People leadership
Budget management
GLP compliance
FDA interactions

Education

Ph.D. in Toxicology/related
DABT certification preferred

Job description

Bausch + Lomb is seeking a Senior Director of Pharma Toxicology to lead global nonclinical safety across its pharmaceutical, OTC, and consumer portfolios. You will set the nonclinical safety strategy, supervise the toxicology organization, and serve as the scientific authority for development programs and regulatory interactions with health authorities.

You will partner with R&D, Regulatory, Clinical, Quality, and Commercial leaders to enable portfolio decisions, accelerate development, and

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