
Job Overview
Employment Type
Full-time
Compensation
Hourly
Range $24.25 - $39.00
Work Schedule
Standard Hours
Benefits
competitive base pay
Annual performance-based bonus
Annual merit-based salary increases
Comprehensive medical benefits
Paid Time Off
Employee Referral Bonus Program
Career advancement opportunities
Job Description
Thermo Fisher Scientific is a global leader in serving science, committed to making the world healthier, cleaner, and safer through innovative scientific solutions. With more than 100,000 employees worldwide, the company provides cutting-edge products and services that support advancements in biological therapeutics, vaccines, and life sciences research. The BioProduction campus located in Grand Island, New York, is a hub of scientific excellence, integrating state-of-the-art technology with a collaborative work environment. This campus supports the development and manufacturing of high-quality cell culture media, custom services, and analytical testing that are essential to biologics and vaccine production. As part of a division dedicated to premium cell culture media, buffers, and single-use solutions, Thermo Fisher Scientific offers a dynamic setting for professionals passionate about making a meaningful impact on global health.
The Quality Control (QC) Scientist I role, based at the Grand Island campus, is a full-time, first-shift position (Monday through Friday, 8:00 AM to 4:30 PM) with some schedule flexibility during training or to meet production demands. This position plays a crucial role in ensuring the quality and safety of raw materials used in the manufacture of cell culture media for life-saving biologic products. The successful candidate will work primarily in laboratory and cold room environments, applying rigorous analytical chemistry techniques in compliance with Good Laboratory Practices (GLP), current Good Manufacturing Practices (cGMP), and standard operating procedures (SOPs).
As a QC Scientist I, you will engage in performing both routine and complex qualitative and quantitative analyses using a wide range of analytical instrumentation such as FTIR, UV-Vis spectroscopy, HPLC, GC, polarimetry, moisture determination by autotitrators, and other wet chemistry methods. Your responsibilities include serving as a technical expert to support raw material release decisions and collaborating with internal teams and external partners to guarantee precise and timely laboratory results. You will also execute lot management activities, maintain documentation with Laboratory Information Management Systems (LIMS), and contribute to continuous improvement initiatives within the laboratory setting.
Safety is paramount in this role, as it involves handling hazardous and toxic materials and working in environments requiring personal protective equipment, including safety glasses, lab coats, gloves, gowns, and hearing protection. The position demands strong organizational skills, attention to detail, and the ability to manage multiple priorities independently in a fast-paced scientific environment. Opportunities for professional growth include internal mobility, method development, and participation in laboratory validations and investigations.
Thermo Fisher Scientific offers a competitive salary range estimated between $50,000 and $72,000 annually with eligibility for variable annual bonuses based on performance. The company provides comprehensive benefits, including medical, dental, and vision plans, paid time off, tuition reimbursement, retirement savings programs, and stock purchase plans. Joining Thermo Fisher means becoming part of a collaborative culture focused on scientific excellence, teamwork, and making a tangible difference in advancing therapies that save and improve lives worldwide.
The Quality Control (QC) Scientist I role, based at the Grand Island campus, is a full-time, first-shift position (Monday through Friday, 8:00 AM to 4:30 PM) with some schedule flexibility during training or to meet production demands. This position plays a crucial role in ensuring the quality and safety of raw materials used in the manufacture of cell culture media for life-saving biologic products. The successful candidate will work primarily in laboratory and cold room environments, applying rigorous analytical chemistry techniques in compliance with Good Laboratory Practices (GLP), current Good Manufacturing Practices (cGMP), and standard operating procedures (SOPs).
As a QC Scientist I, you will engage in performing both routine and complex qualitative and quantitative analyses using a wide range of analytical instrumentation such as FTIR, UV-Vis spectroscopy, HPLC, GC, polarimetry, moisture determination by autotitrators, and other wet chemistry methods. Your responsibilities include serving as a technical expert to support raw material release decisions and collaborating with internal teams and external partners to guarantee precise and timely laboratory results. You will also execute lot management activities, maintain documentation with Laboratory Information Management Systems (LIMS), and contribute to continuous improvement initiatives within the laboratory setting.
Safety is paramount in this role, as it involves handling hazardous and toxic materials and working in environments requiring personal protective equipment, including safety glasses, lab coats, gloves, gowns, and hearing protection. The position demands strong organizational skills, attention to detail, and the ability to manage multiple priorities independently in a fast-paced scientific environment. Opportunities for professional growth include internal mobility, method development, and participation in laboratory validations and investigations.
Thermo Fisher Scientific offers a competitive salary range estimated between $50,000 and $72,000 annually with eligibility for variable annual bonuses based on performance. The company provides comprehensive benefits, including medical, dental, and vision plans, paid time off, tuition reimbursement, retirement savings programs, and stock purchase plans. Joining Thermo Fisher means becoming part of a collaborative culture focused on scientific excellence, teamwork, and making a tangible difference in advancing therapies that save and improve lives worldwide.
Job Requirements
- Bachelor's degree in Chemistry, Biology, or a related scientific discipline
- Minimum of 2 years laboratory experience in a cGMP or Quality Control/Quality Assurance environment
- Experience operating and maintaining analytical instrumentation such as HPLC, GC, FTIR, UV-Vis, polarimetry, autotitrators
- Ability to work in cold room/freezer environments and with hazardous/toxic materials
- Strong organizational and multitasking skills
- Excellent communication skills
- Proficiency with laboratory information management systems and Microsoft Office applications
- Ability to lift up to 40 pounds and wear appropriate PPE including safety glasses, gloves, lab coat, gowning, and hearing protection as needed
Job Qualifications
- Bachelor's degree in Chemistry, Biology, or another scientific discipline
- 2+ years of laboratory experience in a cGMP environment or Quality Control/Quality Assurance laboratory
- Experience with laboratory instrumentation and analytical techniques such as wet chemistry, HPLC, GC, FTIR, UV-Vis, polarimetry, refractive index, moisture determination, thin layer chromatography (TLC), and autotitrators
- Strong organizational and time management skills
- Ability to work independently while managing multiple priorities in a fast-paced laboratory environment
- Excellent written and verbal communication skills
- Strong attention to detail and documentation practices
- Proficiency with Microsoft Office applications
- Experience performing method verifications and method validations in a cGMP Quality Control laboratory preferred
Job Duties
- Perform routine and complex qualitative and quantitative analyses of raw materials used in cell culture media production
- Utilize analytical techniques including FTIR, UV-Vis spectroscopy, HPLC, GC, polarimetry, moisture determination by autotitrator, and other wet chemistry methods
- Follow and maintain compliance with Good Laboratory Practices (GLP), current Good Manufacturing Practices (cGMP), Standard Operating Procedures (SOPs), and laboratory safety requirements
- Serve as a subject matter expert for testing methodologies and provide technical support for raw material release decisions
- Collaborate with internal site teams and external testing partners to ensure accurate and timely analytical results
- Execute lot management activities including sample logging, review, documentation, and tracking using LIMS and related systems
- Support laboratory method verifications, validations, and instrument qualification activities
- Lead or support investigations related to laboratory testing issues, deviations, and out-of-specification events
- Assist with updates to laboratory procedures and drive continuous improvement initiatives
- Demonstrate professionalism, sound judgment, and effective communication with internal customers, auditors, and external partners
Job Criteria
Experience
Mid Level (3-7 years)
Job Location
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