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Research Development Chemist Jobs in Rochester, NY

... Chemistry, Engineering, or related) * 3-4 years of experience in an industrial biotechnology ... Ability to collaborate effectively across Sales, Marketing, and R&D * Willingness to travel 50% or ...

... through chemistry and biotechnology that enhance sustainability. We offer a broad portfolio of ... R&D centers, all committed to our customers' success. As a Controls Technician in Rochester, NY ...

... through chemistry and biotechnology that enhance sustainability. We offer a broad portfolio of ... R&D centers, all committed to our customers' success. As a Controls Technician in Rochester, NY ...

Senior DevOps Engineer

Rochester, NY · On-site

$100 - $120/hr

... chemistry and transfusion medicine. We are more than 6,000 strong and do business in over 130 ... Join our mission as our next Senior DevOps Engineer to join our R&D Instrument Platforms ...

New

Senior DevOps Engineer

Rochester, NY · Remote

$128K - $164K/yr

... chemistry and transfusion medicine. We are more than 6,000 strong and do business in over 130 ... Join our mission as our next Senior DevOps Engineer to join our R&D Instrument Platforms ...

Senior DevOps Engineer

Rochester, NY · Remote

$128K - $164K/yr

... chemistry and transfusion medicine. We are more than 6,000 strong and do business in over 130 ... Join our mission as our next Senior DevOps Engineer to join our R&D Instrument Platforms ...

Chemical Operator

Rochester, NY · On-site

$26 - $27/hr

... through chemistry and biotechnology that enhance sustainability. We offer a broad portfolio of ... R&D centers, all committed to our customers' success. At Arxada, our Chemical Operators play a ...

Chemical Operator

Rochester, NY · On-site

$26 - $27/hr

... through chemistry and biotechnology that enhance sustainability. We offer a broad portfolio of ... R&D centers, all committed to our customers' success. At Arxada, our Chemical Operators play a ...

Showing results 41-60

Research Development Chemist information

See Rochester, NY salary details

$39K

$84.2K

$153.4K

How much do research development chemist jobs pay per year?

As of Aug 23, 2026, the average yearly pay for research development chemist in Rochester, NY is $84,191.00, according to ZipRecruiter salary data. Most workers in this role earn between $52,800.00 and $108,500.00 per year, depending on experience, location, and employer.

What does a Research Development Chemist do?

A Research Development Chemist is responsible for developing and improving chemical products and processes. They design experiments, analyze results, and collaborate with other scientists to create new materials or enhance existing ones. Their work often involves problem-solving, innovation, and ensuring that products meet safety and regulatory standards. Research Development Chemists can work in various industries including pharmaceuticals, materials science, and consumer goods.

What are the key skills and qualifications needed to thrive as a Research Development Chemist?

To thrive as a Research Development Chemist, you need a solid background in chemistry, analytical techniques, and laboratory research, usually supported by a bachelor's or advanced degree in chemistry or a related field. Proficiency with analytical instrumentation (like HPLC, GC, and spectroscopy), chemical analysis software, and adherence to regulatory standards such as GLP or GMP is essential. Strong problem-solving abilities, attention to detail, and effective collaboration and communication skills help set top performers apart. These competencies ensure accurate experimentation, innovative product development, and compliance with safety and quality standards in a competitive research environment.

How does a Research Development Chemist typically collaborate with cross-functional teams during the product development process?

A Research Development Chemist frequently works alongside colleagues from engineering, manufacturing, quality assurance, and marketing to bring new chemical products from concept to market. This collaboration often involves regular meetings to discuss progress, resolve technical challenges, and ensure that formulations meet both regulatory and performance requirements. Chemists may provide technical insights, interpret test results, and adjust formulations based on feedback from these teams, making strong communication skills and adaptability essential. Such cross-functional teamwork not only accelerates innovation but also helps ensure products align with customer needs and company goals.

What is the difference between Research Development Chemist vs Quality Control Chemist?

AspectResearch Development ChemistQuality Control Chemist
Primary FocusDeveloping new products and formulationsEnsuring products meet quality standards
Work EnvironmentLaboratories, R&D departmentsManufacturing, quality labs
Required CredentialsBachelor’s or Master’s in Chemistry or related fieldBachelor’s in Chemistry or related field
Industry UsagePharmaceutical, chemical, consumer goodsPharmaceutical, chemical, manufacturing

Research Development Chemists focus on creating and improving products through experimentation, while Quality Control Chemists ensure products meet safety and quality standards. Both roles require similar educational backgrounds and are essential in the product lifecycle, but they serve different functions within the industry.

What are popular job titles related to Research Development Chemist jobs in Rochester, NY?

For Research Development Chemist jobs in Rochester, NY, the most frequently searched job titles are:

What job categories do people searching Research Development Chemist jobs in Rochester, NY look for?

The top searched job categories for Research Development Chemist jobs in Rochester, NY are:

Infographic showing various Research Development Chemist job openings in Rochester, NY as of August 2026, with employment types broken down into 96% Full Time, and 4% Part Time. Highlights an 73% In-person, 8% Hybrid, and 19% Remote job distribution, with an average salary of $84,191 per year, or $40.5 per hour.

Senior Global Procurement Lead

Ortho Clinical Diagnostics

Rochester, NY • On-site

$93K - $126K/yr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted 4 days ago


Job description

The Opportunity

QuidelOrtho unites the strengths of Quidel Corporation and Ortho Clinical Diagnostics, creating a world-leading in vitro diagnostics company with award-winning expertise in immunoassay and molecular testing, clinical chemistry and transfusion medicine. We are more than 6,000 strong and do business in over 130 countries, providing answers with fast, accurate and consistent testing where and when they are needed most - home to hospital, lab to clinic.

Our culture puts our team members first and prioritizes actions that support happiness, inspiration and engagement. We strive to build meaningful connections with each other as we believe that employee happiness and business success are linked. Join us in our mission to transform the power of diagnostics into a healthier future for all.

The Role

At QuidelOrtho, we're advancing the power of diagnostics for a healthier future for all. Join our mission as our next Senior Global Procurement Lead. This position will provide leadership, direction and focus to ensure operational excellence for the suppliers providing finished goods and direct materials within the Packaging and Finished Good Kitting commodities to the QuidelOrtho plants and distribution centers. Senior Global Procurement Lead will have responsibility for cost/quality/delivery/service including supplier controls, leading the development of the commodity strategy, contract negotiations, productivity initiatives, supplier selection and sourcing projects and overall commodity management, supporting across QuidelOrtho business units. Senior Global Procurement Lead will lead and partner with functional areas to support continuous improvement, supplier changes, new product launches and strategic business initiatives.

This position will be onsite in Rochester, NY, Carlsbad, CA San Diego, CA or Pompano Beach, FL.

The Responsibilities
  • 20% Responsible for driving supplier selection, serve as lead negotiator for complex, high value transactions including the support of due diligence activities, ensuring all aspects of commercial, operation and supply chain in contract execution, focusing on supplier quality, total cost and performance while minimizing risk exposure. Partner with supply chain and finance teams such that suppliers meet the required standards for financial health, quality management, IP protection, and risk management profiles.

  • 20% Responsible for developing the Global Commodity Strategy, Asset Lifecycle Total Cost Management strategies as applicable to the commodity.

  • 20% Execute strategic sourcing and relationship management strategies for supply partners that enable new product development to meet their technical and cost objectives while ensuring quality and driving innovation into the business. Such as generating supplier performance scorecards - OTIF, Quality, PPV participating in supplier business reviews, supplier capacity tracking e.g. shift patterns, OEE, utilization etc., work to resolve escalated supply issues. Ensuring adherence to supplier management/governance standards including assessment, classification, mitigation and adding suppliers to the Approved Supplier List.

  • 10%Develop/Foster supplier partnerships across the company. Understand business/operation issues cross functionally, communicates the consequences to QuidelOrtho Leadership and develop proposal to mitigate / resolve the challenge

  • 20% Partner with Supply Chain, R&D, Product Management and Finance to drive supplier process, quality, and compliance improvements to achieve optimal value, pricing and service performance. Identify and progress annual continuous improvement initiatives in alignment with the sourcing strategy & business needs (e.g. lowering inventory levels, increasing yields, improving supplier operations, etc.).

  • 5% Facilitate supplier change notices or material obsolescence with business partner team.

  • Perform other work-related duties as assigned

The Individual

Required:

  • Bachelor's degree in Business discipline, Operations Management, Engineering or relevant technical discipline. Professionally recognized qualification in related field

  • Experienced in developing and sustaining products in compliance with ISO standards and in an FDA regulated environment

  • 8 to 10 years Technical / Procurement Management experience in medical device and/or a regulated manufacturing environment in healthcare or high technology.

  • Proven track record of managing employees, building high-performance supply organization and ensuring delivery of high-quality products on-time and on budget

  • Previous experience in packaging commodity procurement, an advantage

  • Proficient in use of Microsoft Office, Power BI

  • 5% travel (domestic and international), depending on supply base and business needs.

  • This position is not currently eligible for visa sponsorship.

Preferred:

  • Master's degree

The Key Working Relationships

Internal Partners:

Global Procurement Leadership, Finance, Legal, Product Management, R&D, Product Engineering. To deliver supplier strategies that achieve optimal value, pricing and service performance.

External Partners:

Suppliers under management, Potential suppliers. Developing strong mutually beneficial relationships with suppliers to meet technical and cost objectives while minimizing risk exposure

The Work Environment

Traditional office workspace or remote/home (hybrid). Flexibility to manage suppliers in different time zones. Travel: Up to 5% - US and international

The Physical Demands

Typically, 40% of time in meetings; 50% of time at the desk on computer/doing paperwork/ on phone, doing analytical work and 5% travel to work related events. Walking, standing, and sitting for long periods of time are routine to accomplish tasks in this role.

Salary Transparency

The salary range for this position takes into account a wide range of factors including education, experience, knowledge, skills, geography, and abilities of the candidate, in addition to internal equity and alignment with market data. At QuidelOrtho, it is not typical for an individual to be hired at or near the top range for their role and compensation decisions are dependent on the facts and circumstances of each case. The salary range for this position is $110,000.00 - $140,000.00 and is bonus eligible. QuidelOrtho offers a comprehensive benefits package including medical, dental, vision, life, and disability insurance, along with a 401(k) plan, employee assistance program, Employee Stock Purchase Plan, paid time off (including sick time), and paid Holidays. All benefits are non-contractual, and QuidelOrtho may amend, terminate, or enhance the benefits provided, as it deems appropriate.

Equal Opportunity

QuidelOrtho believes in Equal Opportunity for all and is committed to ensuring all individuals, including individuals with disabilities, have an opportunity to apply for those positions that they are interested in and qualify for without regard to race, religion, color, national origin, citizenship, sex, sexual orientation, gender identity, age, veteran status, disability, genetic information, or any other protected characteristic. QuidelOrtho is also committed to providing reasonable accommodations to qualified individuals so that an individual can perform the duties. If you are interested in applying for an employment opportunity and require special assistance or an accommodation to apply due to a disability, please contact us at recruiting@quidelortho.com.

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