JOB DETAILS
Analytical Scientist II
CompanyNutramax Laboratories
LocationLancaster
Work ModeOn Site
PostedApril 28, 2026

About The Company
To provide safe, effective, quality products that improve the quality of life for our customers, using:
• High quality ingredients
• Researched ingredients
• Quality manufacturing standards
In addition to its national growth, Nutramax Laboratories has achieved international expansion with products available in numerous countries. Our commitment to quality, integrity and science has not and will not be compromised by our growth.
About the Role
Description
The hours for this position are Monday - Friday 8:30am - 5pm.
Summary of the Position: The Analytical Scientist II will be expected to validate, optimize and develop practical analytical methods with minimum to no supervision. Must be able to complete assigned tasks and major projects consistently with urgency and initiative.
Roles and Responsibilities:
Testing:
- Support Quality Release testing as needed, Special Request testing of finished products and raw materials and Stability samples either following Standard Operating Procedures (SOPs) and in-house test methods, compendial methods or methods still in the development phase.
- Capable of assessing testing methodologies and their application to different sample matrix including evaluation of testing results from contract laboratories to ensure agreed upon methods and testing parameters were properly followed.
Laboratory Instrumentation/Software:
- Able to perform intermediate troubleshooting of most Analytical instruments such as HPLC, GC, ICP-MS/OES and LC-MS/MS.
- Knowledge of experimental design, chemical theory and analytical instrumentation theory for HPLC, GC, ICP-MS/OES and LC-MS/MS.
- Proficient in main laboratory softwares such as Empower and Tiamo. Software such as MassHunter and MassLynx are preferred as well as other laboratory software used in the Quality Laboratory environment for chromatographic and spectroscopic methods.
Mentoring and Teamwork:
- Takes initiative to act as a mentor to others and helps others without having to be asked.
- Is flexible to changes in priorities with projects and assignments and can adapt to laboratory improvements implemented from management and/or peers.
- Has the aptitude to take the lead and provide technical support with the optimization of analytical methods used for marketed products and products in the development phase.
- Is capable of training junior chemists in the proper execution of laboratory techniques including interpretation of development and validation studies.
- Assists with training of new laboratory personnel in accordance with established laboratory SOPs and the Nutramax training program. Possesses techniques and tools to successfully train others with empirical data to support training.
Safety Requirements:
- Participates without hesitation in all safety initiatives, consistently exhibits an excellent safety record and ensures proper safety practices are followed in the laboratory.
- Responsible for producing and handling hazardous waste from point of generation to satellite storage. Hazardous waste produced is managed in accordance with RCRA and SCDHEC regulations and includes: proper containers, accumulation, labeling, marking and storage.
- Must have a Safety-First mindset and be aware of surroundings while working in the laboratory.
- Maintains a safe work environment and ensures all instruments used in testing procedures are calibrated and properly maintained.
General Responsibilities:
- The Analytical Scientist II should be capable of planning and experiment design of analytical activities in order to ensure the success of projects.
- Capable of working with outside departments such as Operations, Innovations, Marketing, Purchasing and Engineering to investigate external and internal quality and compliance related issues.
- Should be familiar and supportive of Analytical projects and Special Request testing in the laboratory.
- Effective and practical development and validation of scientifically sound analytical methods to ensure analysis and prompt release of raw materials, finished products and stability studies.
- Design and execute method transfer protocols of analytical methods oriented to the timely manner release of Quality Laboratory samples.
- Ensure competency of ISO 17025 test methods are current as needed.
- Maintain current knowledge of latest technological and scientific trends and serves as an expert resource for the Quality department.
- Perform other assigned duties as may be required in meeting company objectives.
- Communicate effectively with other departments within the organization and function within a team environment.
- Regular attendance is required.
Minimum Requirements:
- Understands urgency and initiative to drive projects/assignments to completion.
- Capable of assisting and developing analytical methods for chromatographic, spectroscopic, titrimetric and wet chemistry analyses.
- Is proficient in intermediate laboratory instrument troubleshooting.
- Intermediate understanding of most laboratory instrumentation such as FTIR, HPLC, ICP, GC, UV-Vis, LC-MS/MS, GC-MS, ICP-MS/OES and HPTLC.
- Has some basic knowledge in the characterization and elucidation of botanical compound structures by study of the compound structure, spectroscopic methods and mass spectrometry.
- Basic understanding in the selection of analytical columns for chromatographic analyses, proper techniques or technologies and the selection for proper reagents to design effective analytical methods in timely manner.
- Knowledge in effective sample preparation techniques to support high number of samples for testing such as liquid-liquid extraction, derivatization, chemical manipulation and mechanical manipulation.
- Knowledge of statistical techniques, such as data trend analysis and design of experiments is highly desirable. Proficient in reviewing and interpretation of laboratory data.
- Detailed knowledge in principles of routine laboratory operations.
- Thorough working knowledge of industry regulations, FDA and ICH guidelines; experience implementing and maintaining adherence to pharmaceutical and/or nutritional supplement GLP/GMP is strongly desired.
- Proven ability to communicate effectively and cooperatively within all levels of an organization.
- Strong communicator both verbal and written.
- Demonstrated aptitude to function in a dynamic fast-paced environment.
- Attention to detail and some process analytical skills necessary.
- Regularly required to stand and bend
- Ability to climb up and down stairs
- Regularly required to stand and bend
- Must be able to use hands and arms to lift and reach
- Ability to stand and walk for a minimum of 8 hours
- Ability to lift, pull and push a minimum of 50 pounds
- Ability to use both arms to push, pull or lift.
- Ability to bend and squat
- Requires the ability to use fractions, decimals, and commercial arithmetic as well as a basic knowledge of grammar, spelling and punctuation.
Education and Experience
- A bachelor’s degree in Chemistry with 5 years of experience in method development and validation of analytical methods for nutraceuticals and/or pharmaceutical samples in a GMP environment. If degree has concentration; Biochemistry, Inorganic, Physical or Polymer Chemistry preferred; or, a Master’s/Ph.D. degree in Chemistry with a minimum of 3 - 5 years of technical experience in a GMP environment.
- Must have prior experience of working on the bench as this position is primarily on the bench working in the laboratory.
Supervisory Responsibilities: None
Key Skills
Analytical method developmentMethod validationHPLCGCICP-MSLC-MS/MSEmpowerTiamoGMPGLPData interpretationExperimental designTroubleshootingTechnical trainingHazardous waste managementQuality control
Categories
Science & ResearchManufacturingHealthcare
Job Information
📋Core Responsibilities
The Analytical Scientist II is responsible for developing, validating, and optimizing analytical methods while supporting quality release testing and stability studies. They also provide technical mentorship to junior staff and ensure laboratory operations comply with safety and regulatory standards.
📋Job Type
full time
📊Experience Level
5-10
💼Company Size
620
📊Visa Sponsorship
No
💼Language
English
🏢Working Hours
40 hours
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