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Quality Control Analyst Per Diem Jobs in Rutherford, NJ

Careers at RK Pharma Inc.

QC Chemist

Pearl River, NY · On-site

$55K - $95K/yr

Perform calibrations of all the QC analytical instruments/equipment 's as per the calibration calendar schedule or when required. * Perform Instrument/ equipment performance qualification as and when ...

Marquis Home Care

PER DIEM NURSE

New City, NY

$50 - $150/hr

Per Diem Registered Nurse (RN) Location: Rockland County, NY Pay Rate: $50 - $150 per hour (based ... Key Responsibilities: - Provide high-quality patient care in accordance with established protocols ...

Marquis Home Care

PER DIEM NURSE

New City, NY

$50 - $150/hr

Per Diem Registered Nurse (RN) Location: Rockland County, NY Pay Rate: $50 - $150 per hour (based ... Key Responsibilities: - Provide high-quality patient care in accordance with established protocols ...

Reliance Private Label Supplements

Be Seen First

QC Microbiologist

Edison, NJ · On-site

$65K - $70K/yr

Routinely report test output per week to QC Supervisor and Quality Manger. * Perform routine ... Prepare Microbiological media and performs QC analysis on prepared media, including positive ...

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 ...

TP ICAP

Risk & Control Analyst

New York, NY · On-site

Quality assurance & management of the loss event reporting in the 1st Line of Defence. * Support ... control analysis, metric reporting, scenario analysis, stress testing, etc.) * Assist Senior ...

Kelly Services

QC Lab Supervisor

Manhattan, NY

Supervise QC laboratory personnel, including chemists, analysts, and technicians. * Manage daily ... paid holidays per benefit year), and a transit spending account. In addition, employees are ...

Polaris Healthcare

PER DIEM REGISTERED NURSE

Yonkers, NY

$50 - $150/day

Per Diem Registered Nurse (RN) Location: Westchester, NY Pay Rate: $50 - $150 per hour (based on ... Key Responsibilities: - Provide high-quality patient care in accordance with established protocols ...

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

Quality Control Analyst Per Diem information

See Rutherford, NJ salary details

$17

$28

$41

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

As of Jul 15, 2026, the average hourly pay for quality control analyst per diem in Rutherford, NJ is $28.46, according to ZipRecruiter salary data. Most workers in this role earn between $23.51 and $31.63 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 are the typical responsibilities of a Quality Control Analyst Per Diem, and how do they contribute to the overall production process?

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.

Is QC analyst a good job?

A Quality Control (QC) analyst is responsible for inspecting and testing products to ensure they meet quality standards, often working in laboratory or manufacturing environments. The role typically requires attention to detail, knowledge of testing procedures, and sometimes certifications; it can offer stable employment with opportunities for advancement in quality assurance fields.

What are Quality Control Analyst Per Diem jobs?

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.

What do quality control analysts do?

Quality control analysts examine products and materials to ensure they meet specified standards and regulations. They perform tests, inspections, and documentation using tools like microscopes and testing equipment, often working in laboratory or manufacturing environments. Their work helps maintain product quality and safety throughout the production process.

How to become a QC analyst?

To become a Quality Control (QC) analyst, candidates typically need a bachelor's degree in a relevant field such as biology, chemistry, or pharmacy. Gaining experience with laboratory techniques, quality assurance processes, and familiarity with industry regulations is important, and certifications like ASQ's Certified Quality Auditor can enhance prospects. Strong attention to detail and proficiency with testing tools are also essential for success in this role.

What are the key skills and qualifications needed to thrive as a Quality Control Analyst Per Diem, and why are they important?

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.

How much do quality control analysts make in the US?

Quality Control Analysts in the US typically earn an average annual salary ranging from $45,000 to $70,000, depending on experience, industry, and location. Per diem roles may offer hourly wages or daily rates that vary based on the employer and specific job requirements.
What cities near Rutherford, NJ are hiring for Quality Control Analyst Per Diem jobs? Cities near Rutherford, NJ with the most Quality Control Analyst Per Diem job openings:
Quality Control Analyst Per Diem jobs near you
Quality Control Analytical Scientist

Quality Control Analytical Scientist

Lynkx Staffing LLC

Saddle Brook, NJ

Full-time

Re-posted 11 days ago

Job description

Quality Control Analytical ScientistAllendale, NJ Lynkx Staffing LLC specializes in placing talented professionals in the Biotechnology, Pharmaceutical and Medical Devices industries in New Jersey. The QC Analytical Scientist will be a member of the Quality Control Department. As a Senior Member of the team the QC Analytical Scientist will be involved in various QC projects and should have a deep understanding of general QC flow and the Product Cycle.
  • Support internal and external customers to ensure that proper and timely execution of all aspects of the clinical analytical method life cycle across clients.
  • Support routine GMP testing as assigned. Mentor and train team members
  • Evaluate corporate and regulatory requirements along with coordination of activities for implementation of these requirements.
  • Write the contents of Analytical Method Transfer and Validation life cycle documentation including master plans, protocols, test methods, and reports.
  • Create validation project plan i.e., timelines and resources and provides status updates to management. Utilize statistical tools for evaluation of method validation and trending data.
  • Identify, evaluate, and implement continuous business process improvements.
  • Perform troubleshooting activities with respect to methods/assays, equipment malfunctions and investigations (Deviations and OOS).
  • Provide support during laboratory investigations.
  • Train QC personnel during method transfer and validation. Provide support during equipment qualification.
  • Consistently produce elevated level of documentation accuracy and clarity according to cGMP documentation practices.
  • Ability to set deadlines and prioritize work for self, group members, and support groups involved. Ability to review/approve work performed by coworkers for accuracy and alignment with procedures.
  • Indirectly may supervise cross functional teams including product development, QA, PMP, and Manufacturing.
REQUIREMENT
  • B.S Analytical Chemistry or other scientific field or MS/Ph.D. in Analytical Chemistry or other scientific field with demonstrated experience in Quality Control laboratories for biotechnology products.
  • 8-10 years of experience in the areas of method development, validation, and transfer.
  • Direct GMP Experience.
  • Proficiency in project management skills and tools.
  • Strong background and in-depth knowledge in analytical chemistry e.g. Flow Cytometry, ELISA, HPLC, CE, PCR, etc.
  • Extensive knowledge and experience of QC assay development, transfer and validation, along with cGMPs.
  • Strong Quality orientation with attention to detail required. Analytical and problem-solving skills required.
  • Excellent communication skills, both written and verbal, with all levels of the organization, including the ability to state opinions clearly, ask questions, seek clarification, communicate facts objectively, challenge when appropriate, and pursue issues to resolution.
  • Excellent presentation skills. Ability to communicate to upper management, across departments and within the immediate QC team.
  • Ability to create and manage work plans and timelines and independently manage competing priorities with limited instruction.
  • Highly motivated individual with good interpersonal skills that have proven effective in managing relationships and negotiating solutions while maintaining a level of approachability with colleagues both internal and external.
  • Must be familiar with GMP lab environment and Aseptic techniques.
Working EnvironmentMust have the ability to work in a team-oriented environment and with clientsMust be able to work during the weekend, holidays, or overtime and as required by the companyMay be exposed to infectious diseases transmittable through human blood, tissues, or bodily fluidsMust utilize proper personal protective equipment (PPE) when handling all human specimens, gases, corrosive chemicals, and liquid nitrogenMust have the ability to work with specialized equipmentMust be able to handle the standard/moderate noise of the manufacturing facilityMay work with hazardous materials and chemicals Please note this job description is not designed to cover or contain a comprehensive listing of activities, duties, or responsibilities that are required of the employee for this job. Duties, responsibilities, and activities may change at any time with or without notice.