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Quality Control Analyst Per Diem Jobs in Raritan, NJ

System One

QC Chemist

Cranbury, NJ · On-site

$36 - $40/hr

M-F 8am-5pm Pay : $36-$40 per hour depending upon experience Overview This is a hands-on ... Manage stability programs, sample pulls, and trending analysis * Collaborate with QA and ...

Tris Pharma

QC Analytical Chemist

Monmouth Junction, NJ · On-site

$90K/yr

Our Quality Control Department is growing and we have openings for QC Analytical Chemists at various levels requiring multiple levels of experience. Title and salary commensurate with experience.

Tris Pharma

QC Analytical Chemist

Monmouth Junction, NJ · On-site

$90K/yr

Our Quality Control Department is growing and we have openings for QC Analytical Chemists at various levels requiring multiple levels of experience. Title and salary commensurate with experience.

Cellares

Quality Control Raw Material Analyst

Bridgewater, NJ · On-site

$24.50 - $33/hr

We are seeking a detail-oriented and operationally rigorous Quality Control Raw Material Analyst to ... Execute testing per approved test methods and SOPs; record data contemporaneously in batch records ...

TeamSoft

QC Analytical Color Matcher

Wharton, NJ · On-site

$24/hr

? Quality Control Analytical Technician (2nd & 3rd Shift) ? Wharton, NJ ?$24.00 to $25.00/hour ? Direct Hire Do you have an eye for color and a passion for quality? ZING is seeking a Quality Control ...

Cellares

Manager, Quality Control

Bridgewater, NJ

$90K - $210K/yr

This individual will lead a group of QC analysts performing analytical testing of in-process and final product from cell therapy products. They will interface across different parts of the company to ...

Cellares

Manager, Quality Control

Bridgewater, NJ · On-site

$90K - $210K/yr

This individual will lead a group of QC analysts performing analytical testing of in-process and final product from cell therapy products. They will interface across different parts of the company to ...

Cellares

Manager, Quality Control

Bridgewater, NJ

$90K - $210K/yr

This individual will lead a group of QC analysts performing analytical testing of in-process and final product from cell therapy products. They will interface across different parts of the company to ...

Osmo

Technician, Quality Control

Elizabeth, NJ · On-site

$67K - $81K/yr

The Technician, Quality Control supports fragrance manufacturing operations by performing routine ... Accurately document analytical and observational results in laboratory records and quality systems ...

Network Temp Inc

Per Diem Registered Nurse

New York, NY · On-site

$70 - $75/hr

Description: Per Diem Float Pool Registered Nurse Join our dynamic healthcare team as a Per Diem Float Pool Registered Nurse, where you will have the opportunity to provide high-quality ...

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Showing results 21-40

All JobsQuality Control Analyst Per Diem JobsQuality Control Analyst Per Diem Jobs in Raritan, NJ

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:
Quality Control Analyst Per Diem jobs near you
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.

QC Chemist

System One

Cranbury, NJ • On-site

$36 - $40/hr

Contractor

Medical, Dental, Vision, Life, Retirement

Re-posted 24 days ago

Job description

Job Title: QC Chemist (cGMP / HPLC / Solid Dose) Location: Cranbury, NJ (Onsite) Type: Contract-to-Hire Schedule: 40 hrs/week Shift: M-F 8am-5pm Pay: $36-$40 per hour depending upon experience Overview This is a hands-on, laboratory-based Quality Control role supporting batch release and stability programs within a cGMP pharmaceutical manufacturing environment. We are seeking candidates with strong operational QC experience supporting solid oral dosage manufacturing (tablets / capsules) in a fast-paced, production-driven environment, coupled with hands-on experience with HPLC / UPLC analysis. Responsibilities

  • Perform batch release and stability testing for pharmaceutical products
  • Conduct assay, dissolution, impurity, and related substances testing
  • Operate, calibrate, and troubleshoot HPLC / UPLC systems
  • Maintain GMP documentation and ensure audit readiness (ALCOA)
  • Investigate OOS / OOT results and support CAPA activities
  • Manage stability programs, sample pulls, and trending analysis
  • Collaborate with QA and Manufacturing to meet production timelines

Requirements

  • 6–8+ years of pharmaceutical QC experience (cGMP REQUIRED)
  • Strong background in solid oral dosage (tablets, capsules)
  • Recent hands-on experience with HPLC / UPLC (REQUIRED)
  • Experience with assay, dissolution, impurities, and stability testing
  • Working knowledge of FDA, GMP, ICH guidelines
  • Experience with Empower, LIMS, or similar systems
  • Strong documentation, data integrity (ALCOA+), and troubleshooting skills
  • Ability to work independently and in a fast-paced manufacturing setting

Key Skills QC Chemist, Quality Control Analyst, cGMP, GMP, Pharmaceutical, Solid Dose, Solid Oral Dosage, Tablets, Capsules, HPLC, UPLC, Dissolution, Assay, Impurities, Stability Testing, Batch Release, OOS, OOT, CAPA, FDA, ICH, Empower, LIMS, Analytical Chemistry, Drug Product, Manufacturing, Validation Benefits Medical, Dental, Vision, 401(k), Life Insurance, and additional voluntary benefits System One, and its subsidiaries including Joulé and Mountain Ltd., are leaders in delivering outsourced services and workforce solutions across North America. We help clients get work done more efficiently and economically, without compromising quality. System One not only serves as a valued partner for our clients, but we offer eligible employees health and welfare benefits coverage options including medical, dental, vision, spending accounts, life insurance, voluntary plans, as well as participation in a 401(k) plan.

System One is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity, age, national origin, disability, family care or medical leave status, genetic information, veteran status, marital status, or any other characteristic protected by applicable federal, state, or local law.

#M3 Ref: #558-Scientific