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Quality Control Analyst Per Diem Jobs in Raritan, NJ

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

Bridgewater, NJ · On-site

$90K - $210K/yr

We are seeking an innovative, creative, and detail-oriented Quality Control Analyst to join our team in Bridgewater, New Jersey. This position will be responsible for routine and non-routine QC ...

Quality Control Analyst

Bridgewater, NJ · On-site

$90K - $210K/yr

We are seeking an innovative, creative, and detail-oriented Quality Control Analyst to join our team in Bridgewater, New Jersey. This position will be responsible for routine and non-routine QC ...

We are seeking an innovative, creative, and detail-oriented Quality Control Analyst to join our team in Bridgewater, New Jersey. This position will be responsible for routine and non-routine QC ...

QC Analyst III

Piscataway, NJ · On-site

$103K/yr

Job Type Full-time Description QC Analyst III (Piscataway, NJ): Be primarily responsible for the ... Salary: $103,000 per year. Requirements Req's Master's degree (or foreign equivalent degree) in ...

Description QC Analyst III (Piscataway, NJ): Be primarily responsible for the execution and review ... Salary: $103,000 per year. Requirements Req's Master's degree (or foreign equivalent degree) in ...

QC, Analyst I

Raritan, NJ · On-site

$24.50 - $33/hr

Legend Biotech is seeking a QC Analyst I (IPL) as part of the Quality Operations team based in Raritan, NJ . Role Overview The QC Analyst (IPL) is an exempt level position with responsibilities for ...

QC, Analyst I

Raritan, NJ · On-site

$24.50 - $33/hr

Role Overview The QC Analyst (IPL) is an exempt level position with responsibilities for performing QC testing related to the manufacturing of cell therapy products for clinical trials and commercial ...

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 ...

QC Chemist

Cranbury, NJ · On-site

$36 - $40/hr

Contract-to-Hire Schedule : 40 hrs/week Shift: M-F 8am-5pm Pay : $36-40/hour depending upon experience Overview Seeking an experienced QC Chemist / Quality Control Analyst to support batch release ...

QC Chemist

Cranbury, NJ · On-site

$36 - $40/hr

Contract-to-Hire Schedule : 40 hrs/week Shift: M-F 8am-5pm Pay : $36-40/hour depending upon experience Overview Seeking an experienced QC Chemist / Quality Control Analyst to support batch release ...

QC Chemist

Cranbury, NJ · On-site

$36 - $40/hr

Contract-to-Hire Schedule : 40 hrs/week Shift: M-F 8am-5pm Pay : $36-40/hour depending upon experience Overview Seeking an experienced QC Chemist / Quality Control Analyst to support batch release ...

QC Chemist

Cranbury, NJ · On-site

$36 - $40/hr

Contract-to-Hire Schedule : 40 hrs/week Shift: M-F 8am-5pm Pay : $36-40/hour depending upon experience Overview Seeking an experienced QC Chemist / Quality Control Analyst to support batch release ...

QC Chemist

Cranbury, NJ · On-site

$36 - $40/hr

Contract-to-Hire Schedule : 40 hrs/week Shift: M-F 8am-5pm Pay : $36-40/hour depending upon experience Overview Seeking an experienced QC Chemist / Quality Control Analyst to support batch release ...

QC Chemist

Cranbury, NJ · On-site

$36 - $40/hr

Contract-to-Hire Schedule : 40 hrs/week Shift: M-F 8am-5pm Pay : $36-40/hour depending upon experience Overview Seeking an experienced QC Chemist / Quality Control Analyst to support batch release ...

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Showing results 1-20

Quality Control Analyst Per Diem information

See Raritan, NJ salary details

$17

$28

$42

How much do quality control analyst per diem jobs pay per hour?

As of Aug 10, 2026, the average hourly pay for quality control analyst per diem in Raritan, NJ is $28.59, according to ZipRecruiter salary data. Most workers in this role earn between $23.65 and $31.73 per hour, depending on experience, location, and employer.

What is the difference between Quality Control Analyst Per Diem vs Quality Control Analyst?

AspectQuality Control Analyst Per DiemQuality Control Analyst
Work ScheduleTemporary, on-call, or daily assignmentsFull-time, permanent position
CertificationsTypically requires industry certifications (e.g., GMP, GLP)Same certifications as Per Diem role
Work EnvironmentLaboratory or manufacturing settings, often in multiple locationsConsistent workplace, often in a single facility
Employment TypePer diem, often with flexible hoursFull-time employment with benefits

Both roles require similar credentials and work in laboratory or manufacturing environments. The key difference is that Per Diem positions are temporary and flexible, while full-time roles offer stability and benefits.

What does a quality control analyst per diem do?

As a Quality Control Analyst Per Diem, you are responsible for performing laboratory tests on raw materials, in-process samples, and finished products to ensure compliance with regulatory and company standards. Your work typically includes documenting results, identifying deviations, and communicating findings to production and quality assurance teams. Since this is a per diem position, you may be called upon to support peak workloads or cover for absent staff, requiring flexibility and adaptability. Your contributions are crucial in maintaining product integrity, minimizing recalls, and ensuring customer safety. Collaboration with other departments, such as manufacturing and R&D, is common to address and resolve quality issues efficiently.

What is a quality control analyst per diem?

Quality Control Analyst Per Diem jobs are positions where professionals are responsible for testing and ensuring the quality of products, typically in industries like pharmaceuticals, food, or manufacturing, but work on an as-needed or temporary basis. 'Per diem' means 'per day,' so these analysts are usually hired to fill in for regular staff, handle increased workloads, or assist with special projects. Their primary duties include sampling, testing materials, documenting results, and ensuring compliance with regulatory standards. Per diem roles offer flexibility but may not guarantee regular hours or benefits.

How much does a quality control analyst earn?

A quality control analyst's average salary varies by location and experience but typically ranges from $45,000 to $70,000 annually. Per diem roles may offer hourly wages or daily rates, often influenced by industry, certifications, and workload demands.

What skills and qualifications are needed to thrive as a quality control analyst per diem?

To thrive as a Quality Control Analyst Per Diem, you need a solid understanding of laboratory testing, analytical techniques, and quality assurance principles, generally supported by a bachelor's degree in a scientific field. Familiarity with laboratory information management systems (LIMS), Good Manufacturing Practices (GMP), and common analytical instruments such as HPLC or GC is typically required. Strong attention to detail, problem-solving skills, and effective communication are essential soft skills in this role. These competencies ensure that products meet strict quality standards and regulatory requirements, which is vital for consumer safety and organizational compliance.
What cities near Raritan, NJ are hiring for Quality Control Analyst Per Diem jobs? Cities near Raritan, NJ with the most Quality Control Analyst Per Diem job openings:
Infographic showing various Quality Control Analyst Per Diem job openings in Raritan, NJ as of August 2026, with employment types broken down into 1% As Needed, 74% Full Time, 21% Part Time, 3% Contract, and 1% Nights. Highlights an 90% Physical, 1% Hybrid, and 9% Remote job distribution, with an average salary of $59,461 per year, or $28.6 per hour.

$26 - $31/hr

Full-time

Medical, Dental, Vision, Life, Retirement

Posted 18 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
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