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Quality Control Analyst Per Diem Jobs in Raleigh, NC

Position Overview The Supervisor, QC Chemistry, first shift is responsible for day-to-day ... analysis, peptide mapping, and physical appearance per Standard Operating Procedures (SOPs) and ...

Position Overview The Supervisor, QC Chemistry, first shift is responsible for day-to-day ... analysis, peptide mapping, and physical appearance per Standard Operating Procedures (SOPs) and ...

... as per your organization's needs. Take a shot at us for your IT requirements and experience a radical change. Short Description: Sr. Software Tester; Sr. Quality Control Analyst; Sr. Quality ...

Director, Quality Control

Raleigh, NC · On-site

$120 - $150/hr

The Director QC oversees all QC functions, including analytical, microbiological, and environmental monitoring programs, and ensures alignment with the overall control strategy. This role ensures ...

The Director QC oversees all QC functions, including analytical, microbiological, and environmental monitoring programs, and ensures alignment with the overall control strategy. This role ensures ...

The Director QC oversees all QC functions, including analytical, microbiological, and environmental monitoring programs, and ensures alignment with the overall control strategy. This role ensures ...

Quality Control

Henderson, NC · On-site

$21.70 - $25.20/hr

Hourly Wage: $21.7 - $25.2 per/hour *The actual hourly rate will equal or exceed the required ... Quality Assurance, System Operator. Administration roles such as Human Resource Clerk and Office ...

Revlon is seeking a Director, Quality Control to lead Quality Control laboratory operations at the ... Oversee analytical method qualification, validation, verification, transfer, and lifecycle ...

Showing results 21-40

Quality Control Analyst Per Diem information

See Raleigh, NC salary details

$16

$27

$39

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

As of Aug 17, 2026, the average hourly pay for quality control analyst per diem in Raleigh, NC is $27.14, according to ZipRecruiter salary data. Most workers in this role earn between $22.45 and $30.14 per hour, depending on experience, location, and employer.

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.

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 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 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 most commonly searched types of Quality Control Analyst jobs in Raleigh, NC?

The most popular types of Quality Control Analyst jobs in Raleigh, NC are:

What are popular job titles related to Quality Control Analyst Per Diem jobs in Raleigh, NC?

For Quality Control Analyst Per Diem jobs in Raleigh, NC, the most frequently searched job titles are:

What job categories do people searching Quality Control Analyst Per Diem jobs in Raleigh, NC look for?

The top searched job categories for Quality Control Analyst Per Diem jobs in Raleigh, NC are:

What cities near Raleigh, NC are hiring for Quality Control Analyst Per Diem jobs?

Cities near Raleigh, NC with the most Quality Control Analyst Per Diem job openings:

Infographic showing various Quality Control Analyst Per Diem job openings in Raleigh, NC as of August 2026, with employment types broken down into 1% As Needed, 76% Full Time, 18% Part Time, 4% Contract, and 1% Nights. Highlights an 88% Physical, 3% Hybrid, and 9% Remote job distribution, with an average salary of $56,444 per year, or $27.1 per hour.

Supervisor, QC Chemistry

Fujifilm

Holly Springs, NC • On-site

Full-time

Posted 24 days ago


Fujifilm rating

8.4

Company rating: 8.4 out of 10

Based on 68 frontline employees who took The Breakroom Quiz

50th of 540 rated manufacturers


Job description

Position Overview

The Supervisor, QC Chemistry, first shift is responsible for day-to-day supervision, audit readiness, and planning activities for the Chemistry laboratory. This Supervisor will lead a team responsible for performing routine testing of QC analytical chemistry methods used in biological product manufacturing, including chromatography, spectroscopy, electrophoresis, wet chemistry, glycan analysis, peptide mapping, and physical appearance.

Company Overview

FUJIFILM Biotechnologies is building the future of bioproduction in Holly Springs, North Carolina. By end of 2025, we'll open North America's largest end-to-end CDMO biopharmaceutical manufacturing facility, offering drug substance production, fill-finish, and packaging under one roof.

We're looking for passionate, mission-driven people to help us realize this exciting vision and deliver the next vaccine, cure, or therapy. We offer a dynamic work environment and we're proud to cultivate a culture that will fuel your purpose, energy, and drive-what we call Genki. Ready to shape the future of medicine? Let's transform healthcare together!

Holly Springs, North Carolina, combines small-town warmth with proximity to Raleigh's thriving tech scene, making it the perfect blend of community and opportunity.

Fujifilm is globally headquartered in Tokyo with over 70,000 employees across four key business segments of healthcare, electronics, business innovation, and imaging. We are guided and united by our Group Purpose of "giving our world more smiles." Visit: https://www.fujifilm.com/us/en/about/region/careers

Job Description

What You'll Do

  • Provide supervision and manage scheduling of the QC Chemistry team to ensure testing timelines are achieved.
  • Ensure analytical testing of in-process, drug substance (DS), drug product (DP), and stability samples is performed according to appropriate GMP regulations.
  • Perform, review, and provide expertise in physical and chemical analytical testing methods, including chromatography (HPLC, UPLC, SEC), spectroscopy (UV, UV-Vis, ELSD), electrophoresis (GE, non-reducing and reducing CE-SDS, imaged capillary isoelectric focusing (icIEF)), wet chemistry, glycan analysis, peptide mapping, and physical appearance per Standard Operating Procedures (SOPs) and test methods.
  • Act as primary point of contact for the team and first-line escalation.
  • Lead the team to meet project deliverables.
  • Set up and maintain operations of a QC testing laboratory.
  • Review and approve SOPs, protocols, reports, change controls, TrackWise deviations, out-of-specification (OOS) and out-of-trend (OOT) investigations, and CAPAs for the QC Chemistry team, as needed.
  • Assist senior management with resource planning and budget-related tasks.
  • Gather recommendations for enhancements and gaps; collaborate with leadership to prioritize and implement solutions.
  • Liaise with Contract Laboratory Organizations (CLOs) to monitor method execution and the timely delivery of results, as needed.
  • Participate in cross-functional collaborations with other QC Departments, Manufacturing, Process Science, and Quality Assurance stakeholders to achieve customer and FUJIFILM Biotechnologies objectives.
  • Allocate and plan adequate resources for laboratory testing activities and QA support; provide technical guidance to the team.
  • Lead cross-functional teams to achieve operational readiness objectives and new product introduction goals using a risk-based, right-sized approach.
  • Lead or guide laboratory staff in investigating deviations/excursions and implementing CAPAs as needed.
  • Serve as SME in audits and inspections; prepare and guide the laboratory team to ensure audit readiness.
  • Collaborate with the LIMS team and IT department to build new method functionality that meets end-user and customer requirements.
  • Establish and maintain internal and external training goals for self and team to ensure compliance with cGMPs and regulatory requirements.
  • Provide training, coaching, and mentorship; identify areas for improvement, reduce blind spots, and create growth opportunities aligned to career objectives.
  • Perform other duties, as assigned.

Minimum Qualifications

  • Bachelor's in Chemistry, Biochemistry, Biological Sciences, or related science field with 5+ years of experience; OR,
  • Master's in Chemistry, Biochemistry, Biological Sciences, or related science field with 3+ years of experience.
  • 2+ years of team management experience.
  • Analytical laboratory experience preferably in biotechnology, Pharma, Contract Research Organization (CRO), or Contract Laboratory Organization (CLO).
  • 3+ years of experience working in a regulated GMP environment.
  • Ability to guide and influence teams in a laboratory setting.
  • Excellent oral and written communication skills.
  • Experience in large pharma/biotech operations or projects.
  • Knowledge and experience of physical and chemical analytical testing methods for biological products, including chromatography (GC, HPLC, UPLC, SEC), spectroscopy (MS, GC/MS, LCMS/MS, UV, UV-Vis, FTIR), electrophoresis (GE, non-reducing and reducing CE-SDS, imaged capillary isoelectric focusing (icIEF)), wet chemistry, glycan analysis, peptide mapping, and physical appearance.
  • Proven ability to lead teams.

Preferred Qualifications

  • Experience managing complex projects.
  • Experience with customer relationship management.
  • Prior drug substance or manufacturing experience, including process validation, transfer, commercialization, and manufacturing support and troubleshooting.
  • Experience using quality systems (e.g., deviation management system, change control, corrective and preventive action (CAPA), document management system).
  • Working knowledge of LIMS, Smartsheet, TrackWise, and/or Kneat validation software.
  • Experience and high-level familiarity/understanding of laboratory equipment, utilities qualification, environmental monitoring qualification, quality systems, automation, IT systems, and/or method validation.
  • Experience in and thorough understanding of Data Integrity and application of regulatory requirements for QC assays.

Physical Requirements:

The physical demands described here are representative of those that must be met by an employee to

successfully perform the essential functions of this job. Reasonable accommodations may be made to

enable individuals with disabilities to perform essential functions. While performing the duties of this job,

the employee is required on a regular basis to:

  • Ability to discern audible cues.
  • Ability to inspect or perform a task with 20/20 corrected vision, visual acuity, including distinguishing color.
  • Ability to stand for prolonged periods of time up to 240 minutes.
  • Ability to sit for prolonged periods of time up to 240 minutes.
  • Ability to conduct activities using repetitive motions that include wrist, hands and/or fingers.
  • Ability to conduct work that includes moving objects up to 10 pounds.
  • Ability to bend, push or pull, and reach to retrieve materials from 18" to 60" in height, and use twisting motions.
  • Will work in warm/cold environments.
  • Will work in small and/or enclosed spaces.

To all agencies: Please, no phone calls or emails to any employee of FUJIFILM about this requisition. All resumes submitted by search firms/employment agencies to any employee at FUJIFILM via-email, the internet or in any form and/or method will be deemed the sole property of FUJIFILM, unless such search firms/employment agencies were engaged by FUJIFILM for this requisition and a valid agreement with FUJIFILM is in place. In the event a candidate who was submitted outside of the FUJIFILM agency engagement process is hired, no fee or payment of any kind will be paid.

EEO Information

Fujifilm is committed to providing equal opportunities in hiring, promotion and advancement, compensation, benefits, and training regardless of nationality, age, gender, sexual orientation or gender identity, race, ethnicity, religion, political creed, ideology, national, or social origin, disability, veteran status, etc.

ADA Information

If you require reasonable accommodation in completing this application, interviewing, completing any pre-employment testing, or otherwise participating in the employee selection process, please direct your inquiries to our HR Department (FDBN_PNC@fujifilm.com).

Employment Type: OTHER

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About Fujifilm

Sourced by ZipRecruiter

With each Industry we enter, We’ve learned to Leverage and Adapt our knowledge, Expertise and rRsources to make the World a better place. When it comes to Innovating for a Healthier World and a more sustainable society, we’ll NEVER STOP. Fujifilm will contribute to the social challenges by creating new value in a wide range of business domains through innovation in Products, Services, and Technological Development. We launched our Healthcare Business with X-ray film in 1936. And now, We are developing our business in areas of prevention, diagnosis, and treatment as a Comprehensive Healthcare Company. We will never stop Innovating for a Healthier World.

Industry

Chemical manufacturing

Company size

10,000+ Employees

Headquarters location

Minato-ku, Tokyo, JP

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