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Supervisor, Senior Team Leader

Job in City of Rochester, Rochester, Monroe County, New York, 14602, USA
Listing for: Bausch + Lomb
Full Time position
Listed on 2026-02-03
Job specializations:
  • Manufacturing / Production
    Quality Engineering, Manufacturing Engineer, Regulatory Compliance Specialist, QA Specialist / Manager
Salary/Wage Range or Industry Benchmark: 80000 USD Yearly USD 80000.00 YEAR
Job Description & How to Apply Below
Location: City of Rochester

Overview

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 portfolio includes over 400 products and serves customers across the full spectrum of eye health needs. We have a ~170-year history, a global footprint with ~13,000 employees in ~100 countries, and a tradition of advances in eye health. We are positioned to continue leading in this field.

Responsibilities
  • Product & Process Development: Support the execution and documentation of new product and process development in alignment with regulatory, Quality System, and cGMP requirements.
  • Laboratory Operations & Compliance: Facilitate seamless transfer of new products and processes to manufacturing by ensuring required documentation, training, and lab activities are completed. Oversee daily compliance of the development lab with cGMPs, Quality System standards, and company policies.
  • Maintain laboratory controls and ensure products are manufactured per approved procedures, specifications, and documentation.
  • Team Leadership & Resource Management: Coordinate daily staffing and workflow to ensure appropriate skill coverage and effective prioritization of work. Support budget planning and monitor materials, resources, and expenditures within assigned areas. Ensure required training is completed and maintained for all lab personnel.
  • Quality & Continuous Improvement: Support quality activities such as documentation review, investigations, change controls, and CAPAs related to lab operations. Monitor key lab performance indicators and contribute to continuous improvement initiatives and operational excellence efforts.
  • Cross-Functional Collaboration: Work closely with R&D, Manufacturing, Quality, Regulatory, Clinical, and other site teams to align practices and optimize shared resources.
Qualifications
  • Bachelors degree in engineering, materials science, chemistry, polymer science, or a related technical discipline (general science) strongly preferred.
  • 5+ years of experience in a regulated product development, laboratory, or pilot manufacturing environment (medical devices, pharmaceuticals, or combination products).
  • Proven experience as a hands-on supervisor or technical lead, consistently meeting timelines, compliance expectations, and operational goals.
  • Ability to take ownership of lab operations, ensuring accurate planning and execution with minimal oversight.
  • Strong working knowledge of cGMP and ISO requirements with a history of compliant, high-quality documentation.
  • Demonstrated learning agility and ability to quickly master new processes, technologies, and regulatory requirements.
  • Strong accountability for safety, quality, and ethical standards for self and others.
  • Clear and concise communication skills suitable for regulated environments.
  • Experience in clinical or early commercialization production under tight controls and schedules.
  • Participation in deviations, investigations, change controls, and CAPAs with focus on root cause and sustainable fixes.
  • Effective cross-functional collaboration with R&D, Quality, Manufacturing, Regulatory, and Clinical teams.
  • Working knowledge of Lean concepts (5S, waste reduction, visual management) and commitment to continuous improvement and standardization.
Benefits
  • Medical, Dental, Eye Health, Disability and Life Insurance begins on your hire date
  • 401K Plan with company match and ongoing company contribution
  • Paid time off vacation (3 weeks - prorated upon hire), floating holidays and sick time
  • Employee Stock Purchase Plan with company match
  • Employee Incentive Bonus
  • Tuition Reimbursement (select degrees)
  • Ongoing performance feedback and annual compensation review

This position is available in the following location(s): [[]]

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 $80,000.00 and $. 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…

Position Requirements
10+ Years work experience
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