5 West Caldwell, NJ Job Details Full-time From $70,000 a year 2 hours ago Benefits Health savings account Health insurance Dental insurance 401(k) Flexible spending account Paid time off Vision insurance 401(k) matching Employee discount Professional development assistance Life insurance Referral program Retirement plan Qualifications Microsoft Word Environmental regulations Data integrity assurance Workplace health and safety waste management Instrumentation troubleshooting Chemical handling safety procedures Teamwork Laboratory inventory control Laboratory safety Microsoft Excel Quality control product testing Safety regulations Efficiency improvement High-performance liquid chromatographs Protein analysis (analytical chemistry specialty) Continuous improvement (laboratory quality control method) Equipment troubleshooting Good documentation practices (GDP) GMP Chromatography Math Bachelor's degree Data management Attention to detail Pharmaceutical analysis Materials analysis (analytical chemistry specialty) Compliance documentation Data interpretation Quality control problem-solving Food industry Full Job Description Quality Control Chemist Great opportunity to become part of the Vitaquest team! Vitaquest is an industry-leading development and commercialization partner for consumer products in nutraceutical and functional foods. With over 40 years of history, Vitaquest has the market insight, global reach and scale of operations to support emerging and existing consumer brands from the idea to the store shelf with flawless execution in every phase. Today, Vitaquest creates and produces more than 4,000 customer formulas for more than 500 brands in over 40 countries. Vitaquest's employees follow an internal communications plan to encourage productivity and engagement within the organization. This is known as Vitaquest PROUD. We believe that each employee contributes directly to the organization's growth and success. We are looking for individuals who share our innovative spirit and will take pride in being a part of our Company. The objective of the QC Chemist position is to perform analytical testing of incoming raw materials, in-process samples, stability and finished goods within the QC Laboratory.

Position:

Senior Chemist•

Quality Control Schedule:

Monday-Friday 7:00 am to 3:30 pm

Title:

QC Chemist Department:

Quality Control Reports To:

QC Lab Manager Position Purpose and Objectives

Senior Chemist
Quality Control Performs analytical testing of incoming raw materials, in-process samples, stability, and finished goods within the QC Laboratory. Essential Job Functions
Senior Chemist
Quality Control Perform routine analytical testing of incoming raw materials, in-process materials, stability samples, and finished dietary supplement products using approved specifications, methods, SOPs, and cGMP requirements.

Independently perform HPLC/UPLC or ICP-MS testing using PDA, RI, QDa, TQD, and ELSD detection, as applicable to assigned methods, including instrument setup, sample and standard preparation, system suitability assessment, data processing, integration review, and routine troubleshooting. Perform assigned testing using Protein Analyzer and Total Organic Carbon (TOC) instrumentation and established wet chemistry assay techniques in accordance with approved procedures and qualification status. Accurately and efficiently document laboratory activities, sample preparation, calculations, instrument use, observations, chromatographic processing, and analytical results in controlled records and applicable computerized systems in accordance with data integrity requirements. Compile complete analytical data packages for review and perform peer or secondary data review when trained and qualified, including review for completeness, accuracy, calculations, system suitability, integration, traceability, and scientifically supportable results. Recognize and promptly escalate out-of-specification (OOS), out-of-trend (OOT), atypical, questionable, or potentially invalid data and laboratory events; support or initiate investigations, deviations, or other quality records in accordance with established procedures. Maintain sample, reagent, solution, reference standard, column, and instrument-use traceability through accurate labeling, logbooks, controlled records, and applicable laboratory systems. Prepare, label, standardize, store, track, and maintain laboratory solutions, mobile phases, chemicals, reagents, and reference standards in accordance with approved procedures, expiration/retest requirements, and storage conditions. Facilitate installation and operational readiness of laboratory equipment, including coordination of required utilities, accessories, consumables, gases, chemicals, reagents, reference standards, and other materials needed for implementation and routine use. Plan and support routine ordering and inventory control for laboratory supplies, gases, chemicals, reagents, reference standards, chromatography columns, consumables, and other materials required to maintain uninterrupted laboratory operations. Monitor inventory levels, expiration/retest dates, storage conditions, and availability of critical materials and proactively communicate or initiate replenishment needs before testing is impacted. Support instrument readiness by maintaining required instrument logbooks and coordinating or communicating calibration, preventive maintenance, qualification, repair, and service needs in accordance with established procedures. Clean and maintain multi-use laboratory consumables and reusable equipment components, including glassware, pipettes, sample-preparation items, and chromatography-related components, in accordance with laboratory procedures and contamination-control practices. Properly segregate, label, handle, store, and dispose of chemical and solid laboratory waste in accordance with site procedures, environmental health and safety requirements, and applicable regulations. Maintain industry-standard laboratory hygiene, housekeeping, and organization practices, including clean and inspection-ready work areas, proper material storage, and adherence to applicable PPE and laboratory safety requirements. Support cGMP and inspection readiness through accurate documentation, controlled-record organization, adherence to current procedures, timely completion of training, and prompt correction or escalation of identified deficiencies. Collaborate effectively with QC colleagues, Quality Assurance, Manufacturing, Product Development, Technical Services and other cross-functional partners to facilitate daily testing execution, resolve workflow barriers, and support timely product disposition. Actively participate in laboratory continuous improvement initiatives, including improvements to workflow, organization, testing efficiency, error reduction, documentation practices, and laboratory readiness. Perform other QC laboratory responsibilities consistent with training, qualification, and business needs. Knowledge, Skills, and Abilities Required

Senior Chemist
Quality Control Demonstrated hands-on proficiency with HPLC/UPLC and chromatographic data systems, including practical experience using PDA, RI, QDa, TQD, and ELSD detection across assigned analytical methods.

Hands-on experience with Protein Analyzer, ICP-MS, TOC, and wet chemistry assay techniques, with the ability to independently execute assigned methods following training and qualification. Sound understanding of chromatographic principles, sample and standard preparation, system suitability, integration, data interpretation, routine troubleshooting, and scientifically sound analytical data review. Working knowledge of cGMP laboratory practices and dietary supplement requirements under 21 CFR Part 111, including documentation, laboratory controls, specifications, testing, and quality-related escalation expectations. Understanding of data integrity expectations, including attributable, legible, contemporaneous, original, accurate, complete, consistent, enduring, and available records. Ability to recognize OOS, OOT, atypical, questionable, or potentially invalid data and to promptly escalate and support appropriate investigation or quality-system documentation. Knowledge of laboratory reagent preparation, chemical handling, reference-standard control, sample and material traceability, inventory management, waste handling, and laboratory safety/hygiene practices. Strong organizational and prioritization skills with the ability to manage multiple testing activities while maintaining accuracy, completeness, and compliance. Excellent verbal and written communication skills and the ability to communicate technical issues clearly, respectfully, promptly, and constructively. Strong team-player mindset with demonstrated willingness to support colleagues, share technical knowledge, coordinate work, and contribute to a collaborative and accountable laboratory culture. Demonstrated initiative to facilitate daily execution, maintain laboratory readiness, identify execution barriers, and contribute to continuous improvement. Proficiency with Microsoft Word and Excel and the ability to work effectively within chromatography data systems, LIMS, and other applicable laboratory computerized systems. Competency in mathematical and scientific calculations applicable to analytical chemistry and QC testing. Supervisory Responsibility

Senior Chemist
Quality Control None.

May provide peer support, technical guidance, and training assistance based on demonstrated qualification and experience. Working Conditions Dynamic, fast-paced cGMP Quality Control laboratory environment requiring routine use of analytical instrumentation and handling of chemicals, reagents, laboratory gases, samples, glassware, and laboratory waste. Requires adherence to established PPE, chemical hygiene, waste-handling, and laboratory safety procedures. Minimum Qualifications

Senior Chemist
Quality Control Bachelor's degree in chemistry, Biochemistry, Pharmaceutical Science, Food Science, or a related physical or life science discipline; equivalent relevant education and laboratory experience may be considered.

Three (3) to five (5) years of hands-on analytical laboratory experience in Quality Control, pharmaceutical, nutraceutical, dietary supplement, food, or a closely related regulated environment is preferred. A minimum of one (1) year of directly relevant hands-on experience performing the analytical testing and operating the instrumentation described in this job description is required, including

HPLC/UPLC

with applicable detector technologies. Experience in the nutraceutical or dietary supplement industry and practical experience working under cGMP requirements of 21 CFR Part 111 is strongly preferred. Success Factors

Self-motivated, dependable, and accountable team player who takes ownership of assigned work and daily laboratory execution.
Highly organized and detail oriented, with a consistent commitment to accurate, complete, contemporaneous, and traceable documentation.
Professional and respectful communicator who raises concerns promptly, seeks clarification when needed, shares information, and supports team success.
Quality
and compliance-focused, with sound scientific judgment and a willingness to stop, question, and escalate when data or laboratory conditions do not support proceeding.
Continuous-improvement mindset with a demonstrated willingness to improve laboratory efficiency, organization, reliability, and execution.

Job Type:

Full-time Pay:

From $70,000.00 per year

Benefits:

401(k) 401(k) matching Dental insurance Employee discount Flexible spending account Health insurance Health savings account Life insurance Paid time off Professional development assistance Referral program Retirement plan Vision insurance

Education:

Bachelor's (Preferred)

Experience:

Raw Material testing: 5 years (Preferred)

Chromatography:

3 years (Preferred)

HPLC:

5 years (Preferred)

Work Location:

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