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 ...
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 ...
Join a high-impact Quality Control team where you'll own the lifecycle of critical analytical instruments that keep life-changing therapies moving. As Sr. Specialist 2, QC Instrumentation, you will ...
Join a high-impact Quality Control team where you'll own the lifecycle of critical analytical instruments that keep life-changing therapies moving. As Sr. Specialist 2, QC Instrumentation, you will ...
Position Overview Join a high-impact Quality Control team where you'll own the lifecycle of critical analytical instruments that keep life-changing therapies moving. As Sr. Specialist 2, QC ...
Position Overview Join a high-impact Quality Control team where you'll own the lifecycle of critical analytical instruments that keep life-changing therapies moving. As Sr. Specialist 2, QC ...
Position Overview Join a high-impact Quality Control team where you'll own the lifecycle of critical analytical instruments that keep life-changing therapies moving. As Sr. Specialist 2, QC ...
Position Overview Join a high-impact Quality Control team where you'll own the lifecycle of critical analytical instruments that keep life-changing therapies moving. As Sr. Specialist 2, QC ...
... 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 ...
... 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 ...
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 Manager
Raleigh, NC · On-site
$85K - $120K/yr
... testing, analyze results, and manage corrective actions for non-compliant work, including ... Compensation: $85,000.00 - $120,000.00 per year We are an equal opportunity employer and all ...
Quality Control Manager
Raleigh, NC · On-site
$85K - $120K/yr
... testing, analyze results, and manage corrective actions for non-compliant work, including ... Compensation: $85,000.00 - $120,000.00 per year We are an equal opportunity employer and all ...
Director, Quality Control
Raleigh, NC · On-site
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 ...
Director, Quality Control
Raleigh, NC · On-site
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 ...
Revlon is seeking a Director, Quality Control to lead Quality Control laboratory operations at the ... Oversee analytical method qualification, validation, verification, transfer, and lifecycle ...
Revlon is seeking a Director, Quality Control to lead Quality Control laboratory operations at the ... Oversee analytical method qualification, validation, verification, transfer, and lifecycle ...
The Senior Analyst 1, QC Chemistry, adheres to GMP-compliant laboratory operations in accordance with regulatory guidelines. This role generates analytical results and identifies laboratory ...
The Senior Analyst 1, QC Chemistry, adheres to GMP-compliant laboratory operations in accordance with regulatory guidelines. This role generates analytical results and identifies laboratory ...
The Senior Analyst 1, QC Chemistry works with limited direction to execute QC Analytical Chemistry methods used in biological product manufacturing, including chromatography, spectroscopy ...
The Senior Analyst 1, QC Chemistry works with limited direction to execute QC Analytical Chemistry methods used in biological product manufacturing, including chromatography, spectroscopy ...
Quality Control Engineer
Clayton, NC · On-site
QUALITY CONTROL ENGINEER Overview Maintains and adheres to the project-specific Quality Assurance ... Analyze and report the results. * Expand the development of the Plan as the project progresses as ...
Quality Control Engineer
Clayton, NC · On-site
QUALITY CONTROL ENGINEER Overview Maintains and adheres to the project-specific Quality Assurance ... Analyze and report the results. * Expand the development of the Plan as the project progresses as ...
QUALITY CONTROL ENGINEER Overview Maintains and adheres to the project-specific Quality Assurance ... Analyze and report the results. * Expand the development of the Plan as the project progresses as ...
QUALITY CONTROL ENGINEER Overview Maintains and adheres to the project-specific Quality Assurance ... Analyze and report the results. * Expand the development of the Plan as the project progresses as ...
The Senior Analyst 1, QC Chemistry, adheres to GMP-compliant laboratory operations in accordance with regulatory guidelines. This role generates analytical results and identifies laboratory ...
The Senior Analyst 1, QC Chemistry, adheres to GMP-compliant laboratory operations in accordance with regulatory guidelines. This role generates analytical results and identifies laboratory ...
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 ...
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 ...
Quality Control Engineer
Raleigh, NC · On-site
QUALITY CONTROL ENGINEER Overview Maintains and adheres to the project-specific Quality Assurance ... Analyze and report the results. * Expand the development of the Plan as the project progresses as ...
Quality Control Engineer
Raleigh, NC · On-site
QUALITY CONTROL ENGINEER Overview Maintains and adheres to the project-specific Quality Assurance ... Analyze and report the results. * Expand the development of the Plan as the project progresses as ...
Quality Control Engineer
Morrisville, NC · On-site
QUALITY CONTROL ENGINEER Overview Maintains and adheres to the project-specific Quality Assurance ... Analyze and report the results.Expand the development of the Plan as the project progresses as ...
Quick apply
Quality Control Engineer
Morrisville, NC · On-site
QUALITY CONTROL ENGINEER Overview Maintains and adheres to the project-specific Quality Assurance ... Analyze and report the results.Expand the development of the Plan as the project progresses as ...
Director, Quality Control
Oxford, NC · On-site
Revlon is seeking a Director, Quality Control to lead Quality Control laboratory operations at the ... Oversee analytical method qualification, validation, verification, transfer, and lifecycle ...
Director, Quality Control
Oxford, NC · On-site
Revlon is seeking a Director, Quality Control to lead Quality Control laboratory operations at the ... Oversee analytical method qualification, validation, verification, transfer, and lifecycle ...
Quality Control Analyst Per Diem information
See Raleigh, NC salary details
$16.36 - $18.50
3% of jobs
$18.50 - $20.65
10% of jobs
$22.41 is the 25th percentile. Wages below this are outliers.
$20.65 - $22.79
15% of jobs
$22.79 - $24.94
20% of jobs
The median wage is $25.23 / hr.
$24.94 - $27.09
16% of jobs
$27.09 - $29.23
11% of jobs
$29.35 is the 75th percentile. Wages above this are outliers.
$29.23 - $31.38
10% of jobs
$31.38 - $33.52
5% of jobs
$33.52 - $35.67
3% of jobs
$35.67 - $37.81
4% of jobs
$37.81 - $39.96
3% of jobs
$16
$27
$39
How much do quality control analyst per diem jobs pay per hour?
What is a quality control analyst per diem?
What does a quality control analyst per diem do?
What skills and qualifications are needed to thrive as a quality control analyst per diem?
What is the difference between Quality Control Analyst Per Diem vs Quality Control Analyst?
| Aspect | Quality Control Analyst Per Diem | Quality Control Analyst |
|---|---|---|
| Work Schedule | Temporary, on-call, or daily assignments | Full-time, permanent position |
| Certifications | Typically requires industry certifications (e.g., GMP, GLP) | Same certifications as Per Diem role |
| Work Environment | Laboratory or manufacturing settings, often in multiple locations | Consistent workplace, often in a single facility |
| Employment Type | Per diem, often with flexible hours | Full-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:

Fujifilm rating
8.4
Based on 68 frontline employees who took The Breakroom Quiz
50th of 540 rated manufacturers
Job description
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 OverviewFUJIFILM 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 DescriptionWhat 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 InformationFujifilm 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 InformationIf 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: OTHERAbout 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