1

Associate Quality Control Analyst Jobs in New Jersey

Reporting to the Quality Control leadership team, the Quality Control Analyst is responsible for performing analytical testing of raw materials, intermediates, and finished products to ensure ...

Quality Control Analyst

Holmdel, NJ · On-site

$26.75 - $36/hr

Laboratory testing experience or strong interest in quality control laboratory activities. * Ability to perform routine analytical and sensory testing with attention to detail. * Strong problem ...

$24.25 - $32.75/hr

The Quality Control Analyst I is responsible to perform environmental monitoring (EM) of aseptic manufacturing operations in Grade A, B, C and D clean room environments and other classified areas as ...

Quality Control Analyst

Summit, NJ · On-site

$25.50 - $34.25/hr

Responsible for assisting with laboratory analysis for clinical release and routine stability testing. May conduct routine release and stability analyses of developmental compounds, prototype ...

Micro QC Analyst I

Ridgefield, NJ · On-site

$33 - $38/hr

Have previous quality control microbiology experience. * Experience in bioburden testing, membrane ... help a fellow analyst. Benefits Our Benefits Include: * Medical, Dental & Vision Insurance ...

QC Chemist

Cranbury, NJ · On-site

$36 - $40/hr

M-F 8am-5pm Pay : $36-40/hour depending upon experience Overview Seeking an experienced QC Chemist / Quality Control Analyst to support batch release, stability testing, and analytical testing in a ...

QC Chemist

Cranbury, NJ · On-site

$36 - $40/hr

M-F 8am-5pm Pay : $36-40/hour depending upon experience Overview Seeking an experienced QC Chemist / Quality Control Analyst to support batch release, stability testing, and analytical testing in a ...

QC Chemist

Cranbury, NJ · On-site

$36 - $40/hr

M-F 8am-5pm Pay : $36-40/hour depending upon experience Overview Seeking an experienced QC Chemist / Quality Control Analyst to support batch release, stability testing, and analytical testing in a ...

QC Chemist

Cranbury, NJ · On-site

$36 - $40/hr

M-F 8am-5pm Pay : $36-40/hour depending upon experience Overview Seeking an experienced QC Chemist / Quality Control Analyst to support batch release, stability testing, and analytical testing in a ...

QC Chemist

Cranbury, NJ · On-site

$36 - $40/hr

M-F 8am-5pm Pay : $36-40/hour depending upon experience Overview Seeking an experienced QC Chemist / Quality Control Analyst to support batch release, stability testing, and analytical testing in a ...

QC Chemist

Cranbury, NJ · On-site

$36 - $40/hr

M-F 8am-5pm Pay : $36-40/hour depending upon experience Overview Seeking an experienced QC Chemist / Quality Control Analyst to support batch release, stability testing, and analytical testing in a ...

next page

Showing results 1-20

Associate Quality Control Analyst information

What does an associate quality control analyst do?

An Associate Quality Control Analyst is responsible for testing and inspecting products, materials, or processes to ensure they meet established quality standards. They perform routine laboratory tests, document results, and identify any deviations from specifications. These analysts often work in industries like pharmaceuticals, manufacturing, or food production, supporting senior analysts and quality managers. Their role is crucial in maintaining product safety, consistency, and regulatory compliance.

What are the key skills and qualifications needed to thrive as an associate quality control analyst?

To thrive as an Associate Quality Control Analyst, you need a solid background in biology, chemistry, or a related scientific field, often with a relevant bachelor's degree. Familiarity with laboratory equipment, quality management systems (such as LIMS), and regulatory guidelines like GMP is typically required. Attention to detail, analytical thinking, and effective communication are crucial soft skills for identifying and resolving quality issues. These skills and qualifications ensure accuracy, compliance, and consistent product quality in laboratory and manufacturing environments.

What are some common challenges faced by associate quality control analysts during routine testing, and how can they be addressed?

Associate Quality Control Analysts often encounter challenges such as tight deadlines, managing multiple sample types, and handling complex analytical instruments. Staying organized and maintaining clear documentation helps manage workflow efficiently. Regular calibration and maintenance of laboratory equipment, along with ongoing training, are essential to minimize errors and ensure accurate results. Collaborating closely with senior analysts and cross-functional teams can also help troubleshoot unexpected issues and streamline processes.

What is the difference between Associate Quality Control Analyst vs Quality Control Technician?

AspectAssociate Quality Control AnalystQuality Control Technician
CredentialsBachelor's degree in life sciences or related field; certifications like CQE are commonHigh school diploma or associate degree; technical certifications may be preferred
Work EnvironmentLaboratories, manufacturing facilities, quality assurance departmentsManufacturing sites, laboratories, production lines
Job ResponsibilitiesData analysis, documentation, reviewing quality processes, supporting auditsPerforming tests, inspecting products, recording test results

While both roles support quality assurance, the Associate Quality Control Analyst typically focuses on data analysis and documentation, whereas the Quality Control Technician primarily conducts tests and inspections. The analyst role often requires a higher level of education and analytical skills, making it suitable for those interested in quality systems and compliance.

What are the most commonly searched types of Quality Control Analyst jobs in New Jersey?

The most popular types of Quality Control Analyst jobs in New Jersey are:

What cities in New Jersey are hiring for Associate Quality Control Analyst jobs?

Cities in New Jersey with the most Associate Quality Control Analyst job openings:

$26 - $31/hr

Full-time

Medical, Dental, Vision, Life, Retirement

Re-posted 6 days ago


Job description

Berjé Inc. is a third-generation, family-owned company with more than 70 years of excellence in the flavor and fragrance industry. Built on a foundation of innovation and resourcefulness, Berjé has grown into a trusted global supplier of high-quality aromatic ingredients. We are committed to delivering exceptional products and service while upholding the highest standards of sustainability, ethics, safety, and regulatory compliance.

Our success is driven by our people. We invest in training, professional development, and career growth, providing employees with opportunities to build meaningful and rewarding careers. Guided by our core values of integrity, accountability, leadership, legacy, diversity, and passion, we strive to make a positive impact on our customers, our communities, and the industries we serve worldwide.

Reporting to the Quality Control leadership team, the Quality Control Analyst is responsible for performing analytical testing of raw materials, intermediates, and finished products to ensure compliance with customer specifications, regulatory requirements, and company quality standards. This role also supports the development of Quality Control Technicians by providing guidance on laboratory best practices, analytical techniques, and proper instrument operation. The ideal candidate is detail-oriented, analytical, and collaborative, with the ability to manage special projects, investigate quality-related issues, and contribute to continuous improvement initiatives within the laboratory.

Key Responsibilities: 

  • Perform analytical testing of chemicals, essential oils, and fragrance compounds using Gas Chromatography (GC) and Gas Chromatography-Mass Spectrometry (GC-MS).
  • Conduct routine GC analysis of quality control samples to verify compliance with product specifications and quality standards.
  • Perform GC analysis of fragrance compounds to support product evaluation, release, and customer requirements.
  • Analyze essential oils and natural materials using GC-MS for identification, characterization, and quality verification.
  • Conduct GC-MS analysis of fragrance compounds to support quality control, investigations, and product authentication.
  • Perform laboratory-scale distillation of essential oils, natural products, and aromatic raw materials to support quality evaluation, product verification, method development, and investigative analysis.
  • Operate, monitor, and maintain laboratory distillation equipment while documenting distillation parameters, yields, and analytical observations.
  • Perform extraction, duplication, and comparative analysis of finished fragrance compounds and raw materials.
  • Conduct extraction and duplication of raw materials, ingredients, and natural products to support quality investigations, reference standards, and product development.
  • Develop, optimize, and validate GC and GC-MS analytical methods to improve identification, characterization, and testing of fragrance compounds.
  • Maintain GC-MS instrumentation by performing routine source cleaning, software updates, and spectral library maintenance to ensure optimal performance.
  • Interpret chromatographic and mass spectral data, investigate atypical results, and communicate findings to Quality Control management.
  • Maintain accurate laboratory documentation, test records, and analytical reports in accordance with company procedures and regulatory requirements.
  • Support laboratory continuous improvement initiatives, method enhancements, and special analytical projects as assigned.
  • Provide technical guidance and mentorship to Quality Control Technicians on laboratory procedures, analytical techniques, and proper instrument operation.
  • Follow all laboratory safety procedures, Good Laboratory Practices (GLP), and company quality policies to ensure a safe and compliant work environment.

Qualifications & Skills

  • Bachelor's degree in Chemistry, Chemical Engineering, Biology, Food Science, or a related scientific discipline; equivalent combination of education and relevant experience may be considered.
  • Minimum of three (3) years of Quality Control laboratory experience within the flavor and fragrance, essential oils, specialty chemicals, or related industry.
  • Demonstrated experience operating and maintaining analytical laboratory instrumentation, including Gas Chromatography (GC), Gas Chromatography-Mass Spectrometry (GC-MS), Karl Fischer titrators, and other standard laboratory equipment.
  • Experience with laboratory distillation techniques, extraction methods, and analytical method development is preferred.
  • Strong knowledge of analytical chemistry principles, laboratory best practices, Good Laboratory Practices (GLP), and quality systems.
  • Ability to read, interpret, and communicate complex technical, regulatory, and compliance requirements.
  • Proficient in Microsoft Office Suite, including Outlook, Teams, Excel, Word, and PowerPoint.
  • Experience using Laboratory Information Management Systems (LIMS) and ERP/MES platforms such as IBM iSeries, SAP, DataNinja, NetSuite, or similar enterprise systems.
  • Strong analytical, organizational, and problem-solving skills with exceptional attention to detail.
  • Excellent written, verbal, interpersonal, and teamwork skills, with the ability to collaborate effectively across departments.
  • Ability to prioritize multiple assignments, manage competing deadlines, and work independently in a fast-paced laboratory environment.
  • Experience mentoring or training laboratory personnel is preferred.
  • Ability to stand, walk, and sit for extended periods and safely perform the physical requirements of a laboratory environment.

Benefits – Medical, Dental, Vision, STD, LTD, Life, 401k w Match, Free access to Financial Planner, EAP
Compensation -$26.00 an hr. to $31.00 an hr.  and eligibility to participate in discretionary bonus programs
Â