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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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$11

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$32

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

As of Jul 16, 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, and why are they important?

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.
What are popular job titles related to Day Shift Upstream Manufacturing Associate jobs in Raleigh, NC? For Day Shift Upstream Manufacturing Associate jobs in Raleigh, NC, the most frequently searched job titles are:
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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:
Day Shift Upstream Manufacturing Associate jobs near you
Manufacturing Associate, Bulk Drug Substance - Holly Springs, NC

Manufacturing Associate, Bulk Drug Substance - Holly Springs, NC

Veteran Jobs - 2023 Mar 01 - Veterans Resources

Holly Springs, NC

Other

Posted 14 days ago

Job description

 
ATTENTION MILITARY AFFILIATED JOB SEEKERS - Our organization works with partner companies to source qualified talent for their open roles. The following position is available to Veterans, Transitioning Military, National Guard and Reserve Members, Military Spouses, Wounded Warriors, and their Caregivers. If you have the required skill set, education requirements, and experience, please click the submit button and follow the next steps. Unless specifically stated otherwise, this role is On-Site at the location detailed in the job post.
Manufacturing Associate, Bulk Drug Substance Upstream - Days 
Live 
What you will do 
Let's do this! Let's change the world! In this dynamic role, you will be an Associate in the manufacturing organization at Amgen North Carolina (ANC). The schedule is a rotating 2-2-3,  5:45AM-6:15PM (12-hour shift).  Associates will be completing operations on the floor in our upstream area and are responsible for the manufacturing of cGMP (Current Good Manufacturing Practices) drug substance. 
With general direction, the Associate will support all floor operations in accordance with cGMP practices. 
Responsibilities will include... 
Compliance: 
Completes work in accordance with established cGMP procedures and policies (Standard Operating Procedures SOPs, Manufacturing Procedures MPs, Job Hazard Analysis JHAs, Code of Federal Regulations CFR) with strict adherence to safety and compliance 
Assure proper gowning and aseptic techniques are always followed 
Process/Equipment/Facilities: 
Perform hands-on operations including set-up, cleaning, sanitization, monitoring of equipment and assigned area 
Run and monitor critical process tasks per assigned procedures 
Perform in-process sampling, operate analytical equipment, and complete process documentation (Electronic Batch Records EBRs) 
Identify and escalate issues and concerns regarding daily routine functions related to process and tasks; may engage with team on potential solutions 
Perform documentation for assigned functions (i.e., equipment logs, EBRs) 
Collaborate as part of a cross-functional team (i.e., QA/QC, F&E (Facilities & Engineering), PPIC, Mfg., PD (Process Development), Regulatory, etc.) in completing production activities 
Maintain an organized, clean, and workable space
 

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