Research Scientist

Bausch+Lomb Companies Inc. • Rochester, NY

5d • $70,000 - $95,000 • Onsite

About The Position

Bausch + Lomb is a global eye health company focused on protecting and enhancing sight. With a diverse portfolio of over 400 products and a history spanning 170 years, the company has a significant global presence with approximately 13,000 employees in about 100 countries. Bausch + Lomb has been associated with major advancements in eye health and aims to continue leading in this field. This role involves contributing to research and development, particularly in analytical method development and laboratory operations.

Requirements

• B.S. in Chemistry, Pharmaceutical Sciences, Biochemistry, or a closely related physical or biological science from an accredited institution.
• Minimum of 3 years of relevant analytical or pharmaceutical laboratory experience (for B.S. degree holders).
• Hands-on HPLC analytical method development for cGMP use.
• Demonstrated record of semi-independent contribution.
• Analytical techniques: reversed-phase HPLC and UHPLC (isocratic and gradient); detection by UV/PDA, RI, fluorescence, and ELSD (LC-MS a plus); GC/GC-MS principles; sample preparation (extraction, dilution, filtration, SPE); dissolution, rheology, and particle size testing.
• Scientific knowledge: strong foundation in analytical chemistry and separation science; experimental design and basic statistical evaluation; pharmaceutical dosage forms and excipients; vitamin chemistry; ICH guidelines (Q1A, Q2, Q3) and USP General Chapters (e.g., <621>, <1225>, <2040>).
• Software & data systems: chromatography data systems (Empower, OpenLab, or Chromeleon); Microsoft Office, including Excel for statistical calculations.
• Attention to detail and commitment to data accuracy and integrity, with a problem-solving and analytical troubleshooting mindset.
• Strong written and verbal communication for technical reporting and cross-functional collaboration, including with external partners.
• Effective time management across concurrent projects and a collaborative, continuous-learning orientation within a multidisciplinary R&D environment.
• Ability to stand for extended periods, lift up to 25 lbs, and perform repetitive motions associated with sample preparation.
• Must be authorized to work for any employer in the U.S. and unable to sponsor or take over sponsorship of an employment Visa.

Nice To Haves

• M.S. or Ph.D. in Analytical Chemistry, Chemistry, or Pharmaceutical Sciences, with coursework in instrumental analysis, separation science, and pharmaceutical analysis.
• M.S. with a minimum of 2 years, or Ph.D with 0–2 years of relevant analytical or pharmaceutical laboratory experience.
• Method development experience with vitamins, dietary supplements, or oral solid dosage forms.
• Familiarity with USP monograph and compendial testing.
• Exposure to manufacturing processes and forensic investigation approaches.
• ELN and LIMS familiarity.

Responsibilities

• Develop, optimize, and validate HPLC, UHPLC, and GC methods for identifying and quantifying active pharmaceutical ingredients (APIs), vitamins, excipients, and related impurities in pharmaceutical and nutraceutical formulations.
• Serve as technical lead for method validation and verification activities of limited scope.
• Transfer validated methods to QC laboratories and contract testing partners, and lead method troubleshooting.
• Generate and interpret data to support specification setting for new and existing products.
• Operate and maintain analytical instrumentation including HPLC, UHPLC, GC, UV-Vis spectrophotometers, dissolution apparatus, and Karl Fischer titrators.
• Perform stability testing and physical testing methods (e.g., dissolution, rheology, particle size, content uniformity) for prototype and commercial products.
• Prepare reagents, mobile phases, standards, and sample solutions; support laboratory safety, housekeeping, inventory, and compliance audits.
• Maintain accurate, contemporaneous records in laboratory or electronic laboratory notebook (ELN) systems, consistent with ALCOA+ data integrity principles.
• Author and review analytical method procedures, validation protocols, and validation reports.
• Lead or support investigations of laboratory deviations and out-of-specification (OOS) or out-of-trend (OOT) data.
• Function in a semi-independent role as a technical driver across assigned projects, taking responsibility for technical projects of limited scope or defined parts of larger efforts.
• Deliver essential, measurable contributions such as innovative methods, technique/process improvements, resolution of technical issues, technical reports, or presentations.
• Partner with Formulation Development, Quality Control, Regulatory Affairs, Manufacturing, contract manufacturers, and CROs to support project deliverables.
• Provide guidance to junior scientists and technicians.
• Manage personal resources and laboratory time across concurrent projects, and present technical findings in team meetings and project updates.

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
• Well-being benefits

What This Job Offers

• Job Type: Full-time
• Career Level: Entry Level