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Quality Control Analyst Chemist Jobs in Rochester, NY

Chemist II

Rochester, NY · On-site

$71K - $80K/yr

... quality standards. Responsibilities: * Serve as the primary analyst supporting the internal ... with Lab Control and Compliance Team activities, as appropriate. * Communicate monthly status ...

Title: Lab Quality Analyst Duration 12 Months Location: Rochester NY Schedule: 2-week rotations ... Full understanding of quality control is expected. This position requires an individual who can ...

Senior Development Chemist Who we are? We are a French pharmaceutical industrial group, recognized ... Implements improvements to lab quality systems. Provides analytical support commercial, and ...

... quality procedures. • Perform other assigned analytical chemistry tasks and project support activities as needed. Requirements: • Bachelor's degree in Chemistry, Analytical Chemistry ...

Quality Technician

Batavia, NY · On-site

$18.50 - $24/hr

Quality Control Supervisor FLSA Status & EEO Code: Non-Exempt & Division/Department: GHM/Quality ... While performing the duties of this position, the incumbent is required to read, write, analyze ...

Quality Technician

Batavia, NY · On-site

$18.50 - $24/hr

Quality Control Supervisor FLSA Status & EEO Code: Non-Exempt & Division/Department: GHM/Quality ... While performing the duties of this position, the incumbent is required to read, write, analyze ...

Quality Technician

Batavia, NY · On-site

$18.50 - $24/hr

Quality Control Supervisor FLSA Status & EEO Code: Non-Exempt & Division/Department: GHM/Quality ... While performing the duties of this position, the incumbent is required to read, write, analyze ...

Quality Technician

Batavia, NY

$17 - $23/hr

Quality Control Supervisor FLSA Status & EEO Code: Non-Exempt & Division/Department: GHM/Quality ... While performing the duties of this position, the incumbent is required to read, write, analyze ...

Quality Technician

Batavia, NY · On-site

$17 - $23/hr

Quality Control Supervisor FLSA Status & EEO Code: Non-Exempt & Division/Department: GHM/Quality ... While performing the duties of this position, the incumbent is required to read, write, analyze ...

As part of a technical team operates the VITROS analyzers to complete assay testing experiments ... This includes Design History files, QC, equipment maintenance, and other associated testing ...

Showing results 21-40

Quality Control Analyst Chemist information

See Rochester, NY salary details

$17

$31

$44

How much do quality control analyst chemist jobs pay per hour?

As of Aug 22, 2026, the average hourly pay for quality control analyst chemist in Rochester, NY is $31.17, according to ZipRecruiter salary data. Most workers in this role earn between $25.38 and $36.06 per hour, depending on experience, location, and employer.

What does a quality control analyst chemist do?

A Quality Control Analyst Chemist is responsible for testing and analyzing materials and products to ensure they meet established quality and safety standards. They perform laboratory tests on raw materials, in-process samples, and finished products, using various analytical instruments and techniques. Their work helps to identify any deviations or defects, ensuring that only products that meet regulatory and company standards are released. In addition, they document results, maintain lab equipment, and often assist in troubleshooting quality-related issues.

What are the key skills and qualifications needed to thrive as a quality control analyst chemist?

To thrive as a Quality Control Analyst Chemist, you need a strong background in chemistry, analytical techniques, and laboratory procedures, typically supported by a bachelor's degree in chemistry or a related field. Familiarity with analytical instruments such as HPLC, GC, UV-Vis spectrophotometers, and knowledge of Good Laboratory Practice (GLP) or ISO standards is crucial. Attention to detail, problem-solving ability, and effective communication are essential soft skills for ensuring accurate results and clear reporting. These competencies are vital for maintaining product quality, regulatory compliance, and the integrity of laboratory operations.

What are some common challenges faced by quality control analyst chemists in ensuring product consistency and compliance?

Quality Control Analyst Chemists often encounter challenges such as maintaining accuracy under tight deadlines, managing large volumes of samples, and staying up-to-date with changing regulatory requirements. They must also effectively troubleshoot unexpected results and ensure all testing procedures adhere to strict protocols. Collaboration with production, R&D, and regulatory teams is essential to resolve discrepancies and support continuous improvement in product quality.

What are popular job titles related to Quality Control Analyst Chemist jobs in Rochester, NY?

For Quality Control Analyst Chemist jobs in Rochester, NY, the most frequently searched job titles are:

What job categories do people searching Quality Control Analyst Chemist jobs in Rochester, NY look for?

The top searched job categories for Quality Control Analyst Chemist jobs in Rochester, NY are:

What cities near Rochester, NY are hiring for Quality Control Analyst Chemist jobs?

Cities near Rochester, NY with the most Quality Control Analyst Chemist job openings:

Infographic showing various Quality Control Analyst Chemist job openings in Rochester, NY as of August 2026, with employment types broken down into 100% Full Time. Highlights an 100% In-person job distribution, with an average salary of $64,837 per year, or $31.2 per hour.

$71K - $80K/yr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted 3 days ago


Bausch & Lomb rating

8.6

Company rating: 8.6 out of 10

Based on 39 frontline employees who took The Breakroom Quiz

21st of 544 rated manufacturers


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 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 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.
Objective:
Perform activities required to ensure reference standards within the B+L program are evaluated, documented, maintained and controlled throughout their lifecycle in compliance with regulatory requirements and internal quality standards.
Responsibilities:
  • Serve as the primary analyst supporting the internal Reference Standards program. This includes evaluating materials proposed for use as reference standards and determining appropriate characterization methodology to meet business needs.
  • Coordinate testing of reference standard samples with laboratory analysts to ensure timely completion and reporting of results.
  • Author characterization protocols, characterization reports, and reference standard protocols.
  • Review reference standard protocols to ensure testing is accurate, compliant with current applicable pharmacopeial requirements, and that the reference standard purity assignments are scientifically justified.
  • Continuously improve existing methods and reference standards by staying current with pharmacopeial updates, business needs, and technical capabilities.
  • Identify opportunities to reduce external testing costs and improve program efficiency by insourcing testing activities when feasible.
  • Participate in Reference Standard Review Board meetings and collaborate cross-functionally to support new and existing reference standards.
  • Maintain technical knowledge and skills through participation in applicable training programs.
  • Maintain a safe and compliant work environment by adhering to company policies, procedures, and regulatory requirements.

Additional responsibilities may include:
  • Support general laboratory housekeeping activities, including reference standard inventory management, sample disposal, sample closeout and archiving.
  • Assist with Lab Control and Compliance Team activities, as appropriate.
  • Communicate monthly status updates and pending actions to relevant stakeholders.
  • Assist with reference standard distribution activities.
  • Conduct nonconformance investigations and laboratory investigations related to out of tolerance (OOT) and out of specification (OOS) results.

Qualifications:
Education:
  • Bachelor's degree (BS) in Chemistry or related scientific field preferred, with a minimum of 2 years of experience preferably in an FDA regulated industry.
  • Associate of Applied Science (AAS) degree in Chemistry or related scientific field, with a minimum of 5 years of relevant experience, preferably in pharmaceutical or medical device industry.
  • Equivalent combinations of education, specialized training, and experience may be considered.
  • Candidates with 5+ years of relevant experience in the pharmaceutical or medical device industry may be considered in lieu of related degree.

Preferred Experience/Competencies:
  • Strong analytical problem solving skills.
  • Working knowledge of cGMP requirements and data integrity principles.
  • Excellent written, verbal, and organizational skills.
  • Experience with Laboratory Information Management Systems (LIMS).
  • Ability to work effectively in cross-functional teams and manage multiple priorities.

What We Offer:
  • Comprehensive health, wellness, and retirement benefits.
  • Paid time off and programs that support work-life balance.
  • Opportunities to learn, grow, and contribute to meaningful work.

Check out our US benefits here - Employee Benefits: Bausch + Lomb
This position may be available in the following location(s): US - Rochester, NY (GEHC)
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 annual pay for this role is between $71,000.00 and $80,000.00. 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.
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.

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About Bausch & Lomb

Sourced by ZipRecruiter

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 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 nearly 170-year history. We have a significant global research, development, manufacturing and commercial footprint of approximately 12,500 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.

Industry

Medical equipment and supplies manufacturing

Company size

10,000+ Employees

Headquarters location

Bridgewater, NJ, US

Year founded

1853