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Day Shift Upstream Manufacturing Associate Jobs in Raleigh, NC

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Day Shift Upstream Manufacturing Associate information

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How much do day shift upstream manufacturing associate jobs pay per hour?

As of Aug 8, 2026, the average hourly pay for day shift upstream manufacturing associate in Raleigh, NC is $20.26, according to ZipRecruiter salary data. Most workers in this role earn between $15.87 and $22.64 per hour, depending on experience, location, and employer.

What is a day shift upstream manufacturing associate?

A Day Shift Upstream Manufacturing Associate is responsible for preparing and operating equipment to support the initial stages of biopharmaceutical production, typically involving cell culture, fermentation, and media preparation. Working during the day shift, they monitor processes, maintain sterile environments, and ensure production runs smoothly and efficiently. Their work is crucial in ensuring quality and consistency in the early phases of manufacturing biological products such as vaccines or therapeutic proteins.

What is the difference between Day Shift Upstream Manufacturing Associate vs Night Shift Upstream Manufacturing Associate?

AspectDay Shift Upstream Manufacturing AssociateNight Shift Upstream Manufacturing Associate
Work HoursTypically 8 AM - 4 PMTypically 8 PM - 4 AM
Work EnvironmentManufacturing floor during daytime operationsManufacturing floor during nighttime operations
Required SkillsSimilar technical skills, safety protocols, and certificationsSame technical skills, safety protocols, and certifications
Employer UsageCommonly used in biopharma and biotech manufacturingSame industry usage, different shift timing

The main difference between a Day Shift Upstream Manufacturing Associate and a Night Shift Upstream Manufacturing Associate lies in their working hours. Both roles require similar skills, certifications, and work environments, but they operate during different shifts. Employers in biopharma and biotech industries often employ both to ensure continuous production, with shift timing being the primary distinction.

What are the typical collaboration points between a day shift upstream manufacturing associate and other teams in a biomanufacturing facility?

Day Shift Upstream Manufacturing Associates frequently collaborate with downstream processing teams, quality control, and process engineering staff. Daily responsibilities often involve communicating batch progress, troubleshooting issues, and ensuring compliance with safety and GMP standards. Clear documentation and timely reporting to supervisors and quality teams are crucial for maintaining production flow. This cross-functional teamwork ensures efficient handoffs and rapid response to any process deviations, making collaboration a key part of the role.

What are the key skills and qualifications needed to thrive as a day shift upstream manufacturing associate?

To excel as a Day Shift Upstream Manufacturing Associate, you typically need a background in biotechnology or life sciences, experience with aseptic techniques, and an understanding of Good Manufacturing Practices (GMP). Familiarity with bioreactors, cell culture systems, and process control software is commonly required, along with relevant safety or GMP certifications. Attention to detail, teamwork, and strong problem-solving abilities are valuable soft skills in this role. These competencies ensure the efficient and compliant production of high-quality biopharmaceuticals in a regulated manufacturing environment.
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What cities near Raleigh, NC are hiring for Day Shift Upstream Manufacturing Associate jobs? Cities near Raleigh, NC with the most Day Shift Upstream Manufacturing Associate job openings:
Infographic showing various Day Shift Upstream Manufacturing Associate job openings in Raleigh, NC as of June 2026, with employment types broken down into 1% Locum Tenens, 49% Full Time, 48% Part Time, 1% Temporary, and 1% Contract. Highlights an 96% Physical, 1% Hybrid, and 3% Remote job distribution, with an average salary of $42,131 per year, or $20.3 per hour.

Manufacturing Associate 3 (Upstream)- Night Shift (2-2-3)

Fujifilm

Holly Springs, NC • On-site

Other

Re-posted 7 days ago


Fujifilm rating

8.4

Company rating: 8.4 out of 10

Based on 67 frontline employees who took The Breakroom Quiz

50th of 537 rated manufacturers


Job description

Help us deliver reliable, compliant biomanufacturing. We are hiring a Manufacturing Associate 3 to lead and execute manufacturing processing activities in a cGMP environment. You will support 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. This role requires flexibility with working hours and shift rotations.


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


What You’ll Do

  • Contribute to project-phase operational readiness for bulk drug substance manufacturing.
  • 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/or 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 manufacturing activities.
  • Assist and/or lead cycle counts and manage materials for the assigned manufacturing functional area.
  • 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 4+ years of related manufacturing experience; or
  • Associate’s degree and 2+ years of related experience in a cGMP manufacturing environment; or
  • BA/BS, preferably in Life Sciences or Engineering; or
  • Equivalent military training/experience.
  • Qualified experience on a unit operation (e.g., DPFG Filler or Cell Culture—Seed Train).
  • Knowledge of production equipment operation within assigned unit operations.
  • Basic understanding of manufacturing run cadence and order of shift activities.
  • Knowledge of cGMPs, safety, and operational procedures.
  • Ability to assist in troubleshooting; strong verbal and written communication skills.

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


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.


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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