From our Bioprocess Innovation Center to our cGMP-compliant manufacturing site, we thrive on ... Associate's degree with 7 years of applicable industry experience OR * Bachelor's degree with 5 ...
From our Bioprocess Innovation Center to our cGMP-compliant manufacturing site, we thrive on ... Associate's degree with 7 years of applicable industry experience OR * Bachelor's degree with 5 ...
From our Bioprocess Innovation Center to our cGMP-compliant manufacturing site, we thrive on ... Associates Degree with 5+ years related experienceBachelor's degree in related field with 2+ years ...
From our Bioprocess Innovation Center to our cGMP-compliant manufacturing site, we thrive on ... Associates Degree with 5+ years related experienceBachelor's degree in related field with 2+ years ...
From our Bioprocess Innovation Center to our cGMP-compliant manufacturing site, we thrive on ... Associates Degree with 5+ years related experience * Bachelor's degree in related field with 2+ ...
From our Bioprocess Innovation Center to our cGMP-compliant manufacturing site, we thrive on ... Associates Degree with 5+ years related experience * Bachelor's degree in related field with 2+ ...
Bioprocess Associate information
See Raleigh, NC salary details
$14.17 - $16.03
9% of jobs
$16.03 - $17.89
0% of jobs
$17.89 - $19.75
0% of jobs
$19.75 - $21.61
0% of jobs
$21.61 - $23.47
0% of jobs
$23.47 - $25.33
7% of jobs
$26.81 is the 25th percentile. Wages below this are outliers.
$25.33 - $27.19
10% of jobs
$27.19 - $29.04
18% of jobs
The median wage is $29.40 / hr.
$29.04 - $30.90
27% of jobs
$31.13 is the 75th percentile. Wages above this are outliers.
$30.90 - $32.76
25% of jobs
$32.76 - $34.62
3% of jobs
$14
$28
$34
How much do bioprocess associate jobs pay per hour?
What is a bioprocess associate?
A Bioprocess Associate is responsible for supporting the manufacturing of biopharmaceutical products by operating and monitoring bioprocessing equipment, following standard operating procedures, and ensuring compliance with Good Manufacturing Practices (GMP). They assist in cell culture, fermentation, purification, and other production processes. This role requires strong attention to detail, problem-solving skills, and the ability to work in a regulated laboratory or production environment.
What does a bioprocess associate do?
A typical day for a Bioprocess Associate involves preparing and operating bioprocessing equipment, monitoring production batches, and performing quality control checks to ensure processes remain compliant with regulatory standards. You’ll work closely with scientists, engineers, and quality assurance teams to troubleshoot any process deviations and uphold safety protocols in a cleanroom or laboratory setting. The role often includes detailed record-keeping and reporting, which are essential for maintaining traceability and supporting process improvements. Collaboration and adaptability are important, as daily priorities can shift based on production needs or urgent issues.
What skills and qualifications are needed to be a bioprocess associate?
To thrive as a Bioprocess Associate, you need foundational knowledge in biology, chemistry, or a related field, attention to detail, and experience with standard operating procedures (SOPs). Familiarity with bioreactors, filtration systems, aseptic techniques, and commonly used software like LIMS is often required; certifications such as GMP (Good Manufacturing Practice) training can be advantageous. Strong teamwork, communication, and problem-solving skills help you excel in dynamic, collaborative environments. These skills and qualifications are critical to maintaining product quality, ensuring regulatory compliance, and supporting efficient bioprocessing operations.
What are popular job titles related to Bioprocess Associate jobs in Raleigh, NC?
For Bioprocess Associate jobs in Raleigh, NC, the most frequently searched job titles are:
What job categories do people searching Bioprocess Associate jobs in Raleigh, NC look for?
The top searched job categories for Bioprocess Associate jobs in Raleigh, NC are:
What cities near Raleigh, NC are hiring for Bioprocess Associate jobs?
Cities near Raleigh, NC with the most Bioprocess Associate job openings:

Investigator 2, Manufacturing
Research Triangle Park, NC • On-site
Full-time
Medical, Dental, Vision, Life, Retirement, PTO
Re-posted 3 days ago
Fujifilm rating
8.6
Based on 71 frontline employees who took The Breakroom Quiz
Job description
Investigator 2, Manufacturing is responsible to perform investigation for Cell Culture, Fermentation and Downstream programs to identify impact for events/minor/major and close PRs within the required standard work timeframe. This role contributes to the creation of effective correctiveand preventative actions (CAPA's) while ensuring timely closure of assigned investigations.
Company OverviewAt FUJIFILM Biotechnologies, we're leading the charge in advancing tomorrow's medicines. If you want to be a part of life-impacting projects alongside today's most innovative biopharmaceutical companies, FUJIFILM Biotechnologies could be the right place for you.
From our Bioprocess Innovation Center to our cGMP-compliant manufacturing site, we thrive on collaboration, creativity, and purpose. Whether your expertise lies in research, manufacturing, or production, you'll find a home here where your efforts directly improve patients' lives. Together, let's shape the future of healthcare.
Situated at the cross-section of Morrisville and Research Triangle Park (RTP), North Carolina, our site is at the heart of a booming biotech hub surrounded by top universities, vibrant communities, and various outdoor opportunities.
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 DescriptionMajor Accountabilities:
- Able to work on event, minor and major investigations with applying site and global compliance SOP's.
- Identify and address corrective and preventative actions (CAPAs) based on root cause analysis and ensure they are implemented and effective.
- Organize, participate in and/or lead cross-functional investigational teams including internal and external (client) members.
- Track and analyze performance metrics to identify trends and develop continuous improvement projects.
- Participate in Problem Analysis (PA) sessions.
- Support document revisions, review/ approval of investigation records and participate in quality improvement initiatives.
- Prepare storyboards for significant deviations and ability to present to regulatory agencies.
- Participate and/or lead difficult discussions to internal team, clients and regulatory agencies.
- Attend and participate in meetings, including tier meeting, internal and external client calls, team huddles, business review meetings, and others as needed.
- Supports junior investigators regarding investigative techniques and best practices.
- Demonstrated knowledge of cGDPs and cGMPs and the requirements to operate in a clinical and commercial manufacturing environment.
- Ability to independently prioritize work based on program needs and deviation timelines.
Minimum Requirements:
- High School Diploma or Equivalent with 9 years of applicable industryexperience OR
- Associate's degree with 7 years of applicable industry experience OR
- Bachelor's degree with 5 years of applicable industry experience OR
- Master's degree 3 years of applicable industry experience
- Understanding of cGDPs and cGMPs and the requirements to operate in a clinical and commercial manufacturing environment.
Preferred Qualifications:
- Understanding of operational excellence and the ability to apply root cause analysis, problem solving and continuous improvement methodology.
- Strong knowledge of Excel, Word, and PowerPoint
- Root Cause Analysis (RCA) training
Knowledge, Skills, or Abilities:
- Knowledge of change management, investigations, CAPAs, and continuous improvement.
- Strong technical writing and facilitation skills.
- Ability to effectively lead cross-functional teams during analysis and CAPA discussions.
- Ability to identify appropriate casual analysis tool for assigned investigations.
- Team based attitude and ability to work in a global team environment and build relationships.
- Ability to effectively present information and findings to others.
- Effective communication, both written and oral.
- Knowledge of performance improvement with a basis in Human and Organizational Performance principles.
- Ability to analyze and extrapolate data, and synthesize and determine recommendations, including the analysis of complex problems.
- Ability to interpret and document technical information and records from multiple subject matter experts (SMEs) into a coherent, clear, and concise narrative to support the investigation process.
Physical Requirements:
- Ability to stand for prolonged periods of time (120 minutes)
- Ability to conduct activities using reptitive motions that include wrists, hands, and/or fingers.
- Ability to conduct work that includes moving objects up to 10 lbs.
Benefits
Our programs are designed to focus on maintaining and enhancing all pillars of health with a robust benefits package including medical, dental, vision and prescription drug coverage with the option of a Health Savings Account with company contributions. In addition, we offer an industry leading 401(k) savings plan, insurance coverage, employee assistance programs and various wellness incentives. We support life-work balance with paid vacation time, sick time, and company holidays. Explore a supportive environment that enriches both your personal and professional growth!
*#LI-onsite
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 (HR_FDBU@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