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Day Shift Mqsa Inspector Jobs in Raleigh, NC (NOW HIRING)

Shift: 1st Shift, Day Shift (8:00 AM - 5:00 PM) Pay: $17/hour - Weekly Pay Location: Morrisville ... You will work hands-on with small precision parts, using benchtop equipment and inspection tools to ...

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Picker Packer

Cary, NC · On-site

$15 - $16/hr

Day Shift: 7:00 AM - 7:00 PM | $15.00/hr. * Night Shift: 7:00 PM - 7:00 AM | $16.00/hr. Job Summary ... Inspect products for defects and ensure quality standards are met * Operate basic warehouse ...

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The Subway Shift Lead oversees day-to-day shift operations to ensure exceptional customer service ... Inspect equipment and storage areas during shifts to ensure cleanliness, organization, and proper ...

The Subway Shift Lead oversees day-to-day shift operations to ensure exceptional customer service ... Inspect equipment and storage areas during shifts to ensure cleanliness, organization, and proper ...

OVERWRAP or SLITTER ALL LOCATIONS

Morrisville, NC

$18 - $23/hr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Inspect, pack, and label products according to job specifications. * Feed products into shrink-wrap ... Day Shift: 7:00 AM - 7:00 PM * Night Shift: 7:00 PM - 7:00 AM WALK-INS WELCOME! Monday-Friday | 9 ...

HVAC Installation Tech

Raleigh, NC · On-site

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Multiple Day / Shift options to discuss / choose from Full-time, year-round work Join ARS, the ... Working knowledge of local inspection codes * EPA certification (or willingness to obtain)

Showing results 21-40

Day Shift Mqsa Inspector information

See Raleigh, NC salary details

$23.8K

$53.4K

$96.2K

How much do day shift mqsa inspector jobs pay per year?

As of Aug 15, 2026, the average yearly pay for day shift mqsa inspector in Raleigh, NC is $53,405.00, according to ZipRecruiter salary data. Most workers in this role earn between $37,400.00 and $61,700.00 per year, depending on experience, location, and employer.

What is the difference between Day Shift Mqsa Inspector vs Day Shift Quality Control Inspector?

AspectDay Shift Mqsa InspectorDay Shift Quality Control Inspector
CertificationsMQSA certification, quality assurance trainingQuality control certifications, industry-specific training
Work EnvironmentMedical imaging facilities, diagnostic labsManufacturing plants, production lines
Employer & IndustryHealthcare, medical imagingManufacturing, industrial sectors

The Day Shift Mqsa Inspector primarily works in healthcare settings ensuring compliance with medical imaging standards, while the Day Shift Quality Control Inspector focuses on product quality in manufacturing. Both roles require quality assurance certifications and involve inspection tasks, but they serve different industries and environments.

What are popular job titles related to Day Shift Mqsa Inspector jobs in Raleigh, NC?

For Day Shift Mqsa Inspector jobs in Raleigh, NC, the most frequently searched job titles are:

Infographic showing various Day Shift Mqsa Inspector job openings in Raleigh, NC as of August 2026, with employment types broken down into 1% As Needed, 68% Full Time, 26% Part Time, and 5% Contract. Highlights an 96% Physical, 1% Hybrid, and 3% Remote job distribution, with an average salary of $53,405 per year, or $25.7 per hour.

Manufacturing Associate 4 (Downstream) - Day Shift (2-2-3)

Fujifilm

Holly Springs, NC • On-site

Other

Re-posted 20 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
Help us deliver reliable, compliant biomanufacturing. We are hiring a Manufacturing Associate 4 to lead and execute manufacturing processing activities in a cGMP environment. In this senior role, you will support both project-phase readiness (procedures, process transfer, testing/commissioning) and steady-state operations in a 24/7 facility-helping ensure safe, consistent, and efficient production of drug substance. You will also assist with daily scheduling and materials oversight for the manufacturing team.
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
  • Contribute to operational readiness for bulk drug substance manufacturing during the project phase.
  • Support procedure review/creation and development or transfer of manufacturing business processes.
  • Provide testing and commissioning support for equipment/systems; travel up to 0-25% (domestic or international) may be required during the project phase.
  • Lead, execute, and document manufacturing processing steps and support activities; perform process monitoring and control per cGMP standards.
  • Perform in-process testing (e.g., pH, conductivity, visual inspection).
  • Execute validation protocols according to cGMP Standard Operating Procedures (SOPs).
  • Maintain required training and qualifications for all assigned activities.
  • Assist and/or lead cycle counts and manage materials for the assigned manufacturing area.
  • Support and/or assist senior-level associates or the supervisor with scheduling daily activities on the manufacturing floor, as needed.
  • Work assigned shifts in a 24/7 operation, including weekends and potential nights.
  • Perform other duties as assigned.

Minimum Qualifications
  • High School Diploma or GED and 6+ years of experience in life sciences manufacturing; or
  • Associate degree and 4+ years of experience in life sciences manufacturing; or
  • BA/BS and 2+ years of experience in life sciences manufacturing; or
  • Equivalent military training/experience.
  • Advanced understanding of manufacturing run cadence and order of shift activities.
  • Knowledge of cGMPs, safety, and operational procedures; strong troubleshooting ability.
  • Demonstrated expertise with operation of specific production equipment.
  • Ability to follow technical instructions, execute operations, and document accurately.
  • Strong verbal and written communication; effective team collaboration skills.
  • Strong time management; ability to adapt in a fast-paced, changing environment.
  • Willingness to work shifts (including weekends/nights) and travel up to 0-25% as needed.

Preferred Qualifications
  • BioWorks or BTEC Capstone cGMP coursework.

Physical Requirements
The physical demands described here are representative of those that may be required to successfully perform essential job functions in a manufacturing environment. Reasonable accommodations may be made to enable individuals with disabilities to perform essential functions. Requirements may include:
  • Standing and/or sitting for prolonged periods.
  • Performing repetitive motions involving wrists, hands, and fingers.
  • Working in proximity to production equipment and utilities.
  • Lifting or moving materials as required by task-specific SOPs and safety guidelines.

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

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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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