Bausch & Lomb Incorporated

Research Fellow, Medical Device Toxicologist

Bausch & Lomb Incorporated$150K — $200K *
US-Anywhere
+ 2 other locationsRemote
Pharmaceuticals & Biotech
11 - 15 years of experience
Job Overview by Ladders

Qualifications

  • Ph.D. in Toxicology or related field required
  • 12+ years medical device industry experience
  • Proven experience managing a team
  • DABT certification preferred
  • Experience with ophthalmic medical devices is a plus

Responsibilities

  • Manage a team providing biocompatibility support for medical devices
  • Develop project strategies and risk assessments for medical device evaluation
  • Align nonclinical strategies with product lifecycle and regulatory milestones
  • Present essential nonclinical data for regulatory and market approval
  • Mentor and coach junior team members
  • Stay updated on medical device standards and implement changes
  • Author and review technical documents for the department
  • Coordinate cross-functionally with various departments and offices
  • Enhance department best practices and processes

Benefits

  • Medical, dental, and vision insurance
  • Disability and life insurance
  • 401(k) plan with company match
  • Tuition reimbursement program for select degrees
  • Paid holidays, sick leave, and vacation time
  • Well-being benefits
Full Job Description
The Research Fellow - Medical Device Toxicologist will provide cross functional Preclinical medical device expertise supporting internal and external stakeholders pertaining to biocompatibility and associated focus areas, for medical device development, product expansion and maintenance. The Research Fellow - Medical Device Toxicologist is responsible for professional, first-line impression of the department within and outside the company through effective interactions via written and oral communications.

Responsibilities:
  • Manage team responsible for medical device biocompatibility support
  • Responsible for project strategies, risk assessments, biocompatibility evaluation plans and reports for medical devices
  • Ensures that development and execution of nonclinical strategies are aligned with product development and life cycle management activities, and with key regulatory expectations and milestones
  • Ensures that essential nonclinical data are obtained, and effectively presented for successful clinical development, regulatory and quality compliance, market launch, and maintenance of business
  • Coaches and mentors junior staff
  • Deep understanding of medical device relevant standards staying abreast of changes to applicable industry practice and guidance documents
  • Implement new and revised standards into product development projects and/or assess impact on existing products as appropriate
  • Authors and reviews department's technical documents as needed
  • Manage interactions with other functions (e.g., Product Development, Clinical Development, Analytical Chemistry, Regulatory, Quality, Compliance)
  • Liaise with company international offices on nonclinical safety matters for country-specific submissions/registrations and maintenance of business activities
  • Development and maintenance of department best practices and processes


Requirements:
  • Ph.D. in Toxicology or related discipline
  • 12+ years of relevant Medical Device industry experience
  • Experience managing a team
  • DABT preferred
  • Ophthalmic medical device experience a plus


This position may be available in the following location(s): Remote

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.

Our Benefit Programs: Employee Benefits: Bausch + Lomb

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.

About Bausch & Lomb Incorporated

Bausch & Lomb is a leading global eye health company that specializes in the design, manufacture, and sale of a wide range of eye care products, including contact lenses, lens care products, and surgical instruments. The company has a strong presence in the United States and Europe, and is expanding its operations in Asia and Latin America. Bausch & Lomb is committed to innovation and research, and has a long history of developing new technologies and products to improve eye health.
Learn more about Bausch & Lomb Incorporated
Size
12,000 employees
Industry
Net Income
$100 million
5 Year Trend
-5%
Revenue
$5 billion
NASDAQ

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