Top 6375 Manufacturing support associate 1, documentation Jobs in Raleigh, Nc

Manufacturing Support Associate 1, Documentation
Fujifilm —Holly Springs, NC
- Call employer
- Military
- Bachelor of Science
- No experience needed
Office Assistant
Wake County Government —Wake County, NC
- $25.34 - $30.10 an hour
- Weekends as needed
- HIPAA
- Administrative experience
- High school diploma or GED
10d
Associate Manufacturing - Bulk Drug Substance - Services - Day Shift
Amgen —Holly Springs, NC
- $70,985.20 - $96,038.80 a year
- Overtime
- High school diploma or GED
- In-person
- Associate's degree
- Disability insurance
- Health insurance
CRA 2/Senior CRA 1
IQVIA —Durham, NC
- $90,200 - $175,100 a year
- Full-time
- Bachelor's degree
- Experience equivalent to degree accepted
- 1 year
Associate Manufacturing - Bulk Drug Substance Downstream - Days
Amgen —Holly Springs, NC
- $70,985.20 - $96,038.80 a year
- 12 hour shift
- High school diploma or GED
- In-person
- Associate's degree
- Disability insurance
- Health insurance
Learning & OD Coordinator
Lenovo —Morrisville, NC
- Full-time
- Hybrid work
- Mid-level
- Office
- Psychology
Leave of Absence Specialist
UNC Health —Morrisville, NC
- $23.24 - $33.41 an hour
- Full-time
- Hybrid work
- No experience needed
- Mid-level
- High school diploma or GED
- Parental leave
Associate Manufacturing - (Bulk Drug Substance - Services) - Night Shift
Amgen —Holly Springs, NC
- $70,985.20 - $96,038.80 a year
- 12 hour shift
- High school diploma or GED
- In-person
- Associate's degree
- Disability insurance
- Health insurance
Manufacturing Associate II
Sumitomo Pharma America, Inc. —Morrisville, NC
- $61,500 - $76,900 a year
- Weekends as needed
- Pass drug screening
- Mid-level
- High school diploma or GED
- Paid holidays
- Health insurance
3d
Processing Assistant III - Mailroom Processor
Johnston County, NC —Johnston County, NC
- $38,195.11 - $64,931.66 a year
- Urgently hiring
- Background check
- Pass drug screening
- Office
- Paid holidays
- Health insurance
2d
Manufacturing Associate, Bulk Drug Substance Upstream - Days
Amgen —Holly Springs, NC
- $70,985.20 - $96,038.80 a year
- 12 hour shift
- High school diploma or GED
- In-person
- Associate's degree
- Disability insurance
- Health insurance
Order Management Specialist (Customer Support)
Infosoft-inc —Raleigh-Durham, NC
- $26 - $29 an hour
- Contract
- Microsoft Excel
- Microsoft Outlook
- Research
Quick Apply
Document Control Specialist
Resource Label Group —Garner, NC
- Mid-level
- High school diploma or GED
- Ability to lift 50 pounds
- Paid holidays
- Disability insurance
Quick Apply
QA/QC COORDINATOR
Centian —Raleigh, NC
- $60,000 a year
- Full-time
- Microsoft Excel
- Microsoft Outlook
- Entry level
- Paid holidays
- Health insurance
PLS Entry-Level Lab Tech 1
Pace Analytical Services —Morrisville, NC
- $22 - $25 an hour
- Full-time
- English
- Databases
- Experience equivalent to degree accepted
- Wellness program
- Health savings account
Patient Access Specialist
McKesson —Cary, NC
- $15.93 - $26.55 an hour
- Hybrid work
- Computer literacy
- HIPAA
- Office
- Prescription drug insurance
8d
Regulatory Documentation Specialist I
Grifols —Clayton, NC
- Full-time
- Microsoft Excel
- Writing skills
- Office
6d
Senior Process Operator
GlaxoSmithKline —Zebulon, NC
- Overtime
- Computer literacy
- Mid-level
- Microsoft Office
- On-the-job training
Compliance Analyst I - Third Party Risk Management
UNC Health —Morrisville, NC
- $31.04 - $44.62 an hour
- Full-time
- Hybrid work
- Nursing
- Mentoring
- Business Administration
API Manufacturing Associate I
Novo Nordisk —Clayton, NC
- Military
- Computer literacy
- High school diploma or GED
- Paid holidays
- Disability insurance
2d

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Manufacturing Support Associate 1, Documentation

Fujifilm -
Holly Springs, NC

Apply Now

Job Details

Qualifications

Quality control corrective actions
Quality records maintenance
Technical documentation
Military
Bachelor of Science
Preventive action implementation
Word embeddings
Technical writing experience within manufacturing
Production deviation management
Quality control preventive actions
Corrective and preventive actions (CAPA)
No experience needed
GMP
Mid-level
Factory operations documentation
High school diploma or GED
Change management
Manufacturing facility experience
Maintenance records management
Pharmaceutical company experience
Technology transfer (scale-up process)
Maintenance schedule development
Compliance documentation
Continuous quality improvement (CQI)
Operational excellence initiatives
Technical troubleshooting support
Productivity software
Commissioning phase involvement
Cross-functional collaboration
Associate's degree

Full Job Description

Position Overview:

Help power a world‑class, 24/7 manufacturing operation by ensuring production runs safely, compliantly, and on schedule. As a Manufacturing Support Associate I with a documentation focus, you’ll be at the heart of operational readiness, record accuracy, and continuous improvement—enabling teams to deliver life‑changing products with confidence.

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

During the project phase:

Lead operational readiness initiatives that prepare teams, processes, and systems for start‑up.
Lead site commissioning and qualification efforts to ensure facilities and equipment are ready for compliant use.

In operations:

Support and participate in troubleshooting within assigned process areas to quickly resolve issues and minimize downtime.
Perform documentation updates to maintain accurate, compliant records and enable reliable production.
Create non‑batch activities and develop associated documentation for technology transfer, changeover, preventive maintenance plans (PMs), and column packing.
Support change management records, investigations, corrective and preventive actions (CAPAs), and continuous improvement (CI) activities that strengthen manufacturing performance.
Support inspections and audits by providing requested manufacturing documents and data.
Perform other duties as assigned to meet production and quality goals.

Minimum qualifications

High School Diploma or GED and 4 years of related experience; or
Associate degree in life sciences and 2 years of direct experience; or
Bachelor’s degree (BA/BS) in life sciences with no experience; or
Equivalent military training/experience

Skills and abilities:

Strong verbal and written communication skills
Expertise in Microsoft Office, especially Word
Strong time management; ability to meet deadlines
Ability to adapt in a fast‑paced environment and pivot as priorities change
Critical thinking and superior problem‑solving skills
Team‑based mindset; ability to build relationships and work effectively in a global team environment
Ability to update and create documents on schedule with high attention to detail

Preferred qualifications

Previous current Good Manufacturing Practice (cGMP) manufacturing operations experience
Understanding of change management, investigations, corrective and preventive actions (CAPAs), and continuous improvement (CI)
BioWorks or BTEC Capstone cGMP coursework
Pharmaceutical manufacturing experience

Why this role matters

Make a direct impact on reliable, compliant manufacturing outcomes
Grow expertise across documentation, troubleshooting, and operational excellence
Collaborate with cross‑functional teams in a dynamic, mission‑driven, 24/7 environment

Ready to build your manufacturing career on a strong documentation foundation? Apply today.

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.

#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 ([email protected]).

Apply Now

Refine Your Search

manufacturing support associate 1, documentation jobs in raleigh, nc

Manufacturing Support Associate 1, Documentation

Office Assistant

Associate Manufacturing - Bulk Drug Substance - Services - Day Shift

CRA 2/Senior CRA 1

Associate Manufacturing - Bulk Drug Substance Downstream - Days

Learning & OD Coordinator

Leave of Absence Specialist

Associate Manufacturing - (Bulk Drug Substance - Services) - Night Shift

Manufacturing Associate II

Processing Assistant III - Mailroom Processor

Manufacturing Associate, Bulk Drug Substance Upstream - Days

Order Management Specialist (Customer Support)

Document Control Specialist

QA/QC COORDINATOR

PLS Entry-Level Lab Tech 1

Patient Access Specialist

Regulatory Documentation Specialist I

Senior Process Operator

Compliance Analyst I - Third Party Risk Management

API Manufacturing Associate I

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