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Bio Manufacturing Jobs in Raleigh, NC (NOW HIRING)

Sennos

Accounting Manager

Durham, NC · On-site

About Sennos Sennos is rapidly emerging as the global leader in AI-driven sensing, analytics, and control for the Fluid, Fermentation, and Bio-manufacturing industries. With a revolutionary ...

Sennos

Data Engineer

Durham, NC · On-site

$110K - $132K/yr

About Sennos Sennos is rapidly emerging as the global leader in AI-driven sensing, analytics, and control for the Fluid, Fermentation, and Bio-manufacturing industries. With a revolutionary ...

Zifo

Lab Computing Analyst

Raleigh, NC · On-site

Bachelor's/Master's degree or equivalent in Pharmaceutical, Bio-technology, Bio-medical, Chemical ... Zifo is a global R&D solutions provider focused on the industries of Pharma, Biotech, Manufacturing ...

Zifo

Lab Computing Analyst

Raleigh, NC · On-site

Bachelor's/Master's degree or equivalent in Pharmaceutical, Bio-technology, Bio-medical, Chemical ... Zifo is a global R&D solutions provider focused on the industries of Pharma, Biotech, Manufacturing ...

Zifo

Lab Computing Analyst

Raleigh, NC

Bachelor's/Master's degree or equivalent in Pharmaceutical, Bio-technology, Bio-medical, Chemical ... Zifo is a global R&D solutions provider focused on the industries of Pharma, Biotech, Manufacturing ...

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Showing results 1-20

All JobsBio Manufacturing JobsBio Manufacturing Jobs in Raleigh, NC

Bio Manufacturing information

See Raleigh, NC salary details

$34.5K

$77.6K

$109.4K

How much do bio manufacturing jobs pay per year?

As of Jun 13, 2026, the average yearly pay for bio manufacturing in Raleigh, NC is $77,616.00, according to ZipRecruiter salary data. Most workers in this role earn between $69,000.00 and $86,500.00 per year, depending on experience, location, and employer.

What is the job of a biotechnician?

A biotechnician assists in laboratory and manufacturing processes related to biotechnology, including preparing samples, operating equipment, and maintaining lab records. They often work under supervision in cleanroom environments and may need certifications in laboratory techniques or safety protocols.

What are the key skills and qualifications needed to thrive in Bio Manufacturing, and why are they important?

To thrive in Bio Manufacturing, you need a solid background in biology, chemistry, or engineering, often supported by a relevant degree or certification. Familiarity with Good Manufacturing Practices (GMP), bioprocessing equipment, and quality control systems is typically required. Attention to detail, problem-solving abilities, and strong teamwork skills help individuals excel in this environment. These competencies are crucial for ensuring product quality, regulatory compliance, and efficient production in the biotechnology industry.

What are some common challenges faced by professionals working in bio manufacturing, and how can they be addressed?

Professionals in bio manufacturing often encounter challenges such as maintaining strict quality control standards, adapting to rapidly evolving technologies, and ensuring compliance with regulatory requirements. Addressing these challenges involves continuous training, staying updated on industry best practices, and fostering strong communication within cross-functional teams. Many companies also encourage ongoing professional development and provide resources to help employees stay current with regulations and technological advancements.

What jobs pay 10,000 a month without a degree?

In bio manufacturing, high-paying roles such as senior process technicians or manufacturing managers can reach or exceed $10,000 per month with extensive experience and specialized skills. These positions often require technical knowledge, certifications, and hands-on expertise but may not always require a formal degree. Advancement depends on industry experience, technical proficiency, and leadership abilities.

What is bio manufacturing?

Bio manufacturing involves producing biological products such as pharmaceuticals, vaccines, and biochemicals using living organisms, cells, or enzymes. It requires knowledge of cell culture, bioprocessing techniques, and often involves working in controlled environments like cleanrooms. Bio manufacturing roles may also require familiarity with GMP standards and specialized equipment.

What is the difference between Bio Manufacturing vs Bioprocess Technician?

AspectBio ManufacturingBioprocess Technician
CredentialsTypically requires a Bachelor's degree in Biotechnology, Biology, or related fieldOften requires a diploma or associate degree in Biotechnology or related field
Work EnvironmentManufacturing facilities, laboratories, cleanroomsProduction floors, laboratories, cleanrooms
Industry UsageUsed broadly across biotech, pharmaceutical, and biopharmaceutical companiesPrimarily in biotech and pharmaceutical manufacturing
Job FocusOversees entire manufacturing processes, quality control, and compliancePerforms specific tasks in bioprocessing, equipment operation, and sample testing

Bio Manufacturing involves overseeing the entire production process in biotech and pharmaceutical industries, often requiring higher-level degrees and responsibilities. Bioprocess Technicians focus on executing specific bioprocessing tasks, typically with technical diplomas. Both roles work in similar environments but differ in scope and qualifications.

Is biotech a high paying job?

Bio manufacturing jobs in the biotech industry tend to offer competitive salaries, especially for roles requiring specialized skills such as quality control, process engineering, or laboratory work. Salaries can vary based on experience, education, location, and certifications, with many positions offering above-average pay compared to other manufacturing roles.
What are popular job titles related to Bio Manufacturing jobs in Raleigh, NC? For Bio Manufacturing jobs in Raleigh, NC, the most frequently searched job titles are:
What job categories do people searching Bio Manufacturing jobs in Raleigh, NC look for? The top searched job categories for Bio Manufacturing jobs in Raleigh, NC are:
What cities near Raleigh, NC are hiring for Bio Manufacturing jobs? Cities near Raleigh, NC with the most Bio Manufacturing job openings:
Bio Manufacturing jobs near you
Infographic showing various Bio Manufacturing job openings in Raleigh, NC as of June 2026, with employment types broken down into 3% As Needed, 82% Full Time, 12% Part Time, and 3% Contract. Highlights an 97% Physical, 1% Hybrid, and 2% Remote job distribution, with an average salary of $77,616 per year, or $37.3 per hour.

Manufacturing Associate I

Kincell Bio, LLC

Durham, NC • On-site

Full-time

Posted 2 days ago

Job description

Kincell Bio engineers cells into therapies. With manufacturing facilities located in Research Triangle Park, NC and Gainesville, FL, Kincell Bio is a contract development and manufacturing organization (CDMO) with the mission to streamline CMC development, apply expertise in analytical and process development and GMP manufacturing, testing and release from early clinical to pivotal studies and product launch. Kincell Bio is focused on supporting innovative companies developing immune cell therapies, including autologous and allogeneic CAR-T, TCR, TILs, Tregs and CAR-NK technologies. We offer challenging career opportunities, competitive benefits, and an environment that recognizes and rewards performance.
For more information, please visit our website at www.kincellbio.com.
Kincell is seeking a highly motivated Associate I, who will be a key contributor to a dynamic and collaborative Manufacturing team.
As a Manufacturing Associate, you will be operating automatic and manual cell and gene therapy equipment with a variety of complexities in CAR-T, CAR-M, or CAR-NK processes in accordance with standard operating procedures and policies. You will perform quality control analyses as required to complete in-process batches and identify variations. You will be trained in handling hazardous materials and emergency procedures since you will be handling leukapheresis cellular materials.
As part of manufacturing operations, you will be a team member who is relied on to have a good understanding of procedures, techniques, tools, materials, and equipment. Your work and decision-making will be team-based and will focus on the prioritization of workflows centered on the process and available resources. You will follow standard operating procedures to complete tasks which may vary in scope, complexity, and timing. You will contribute to the team's success by sharing knowledge.
Patients need colleagues like you who take pride in their work and look for successful outcomes. You will help ensure patients have the therapies they need when they need them. You will be operating cell and gene therapy process equipment of varying complexity with different processes in accordance with standard operating procedures.
Essential Duties and Responsibilities
Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions of this position.This list contains the major duties and requirements of the job and is not all-inclusive. Incumbent(s) may be expected to perform role-related duties other than those contained in this document.
  • Execute GMP manufacturing operations under approved SOPs and Master Batch Records (MBRs) with strict adherence to GDP and Right-the-First-Time principles.
  • Perform hands-on manufacturing tasks including material preparation, aseptic manipulations, basic cell culture activities, formulation support, and final drug product fill support under supervision.
  • Operate and support manufacturing equipment relevant to cell and gene therapy processing following approved procedures and training qualification.
  • Demonstrate and maintain aseptic technique qualification and comply with gowning, cleanroom behavior, and contamination control expectations.
  • Accurately document all manufacturing activities in batch records, logbooks, and electronic quality systems (e.g., training records, controlled documents, deviation support tools).
  • Perform routine cleaning and sanitization of manufacturing equipment, rooms, and classified areas per approved procedures.
  • Support material handling activities, including material receipt, verification, staging, and controlled introduction into classified manufacturing spaces.
  • Perform basic calculations (volumes, concentrations, dilutions, unit conversions) using approved tools and spreadsheets.
  • Work within established Quality Management Systems (QMS) (e.g., Veeva or equivalent) to complete training, access controlled documents, and support quality records.
  • Demonstrate proficiency in Good Documentation Practices (GDP) across both paper-based and electronic systems.
  • Utilize Microsoft Office applications (Excel, Word, PowerPoint) for documentation, data entry, basic data review, training materials, and operational support tasks.
  • Support Quality and Safety investigations by providing accurate, timely input within approved quality systems.
  • Identify and escalate documentation errors, system discrepancies, or workflow issues impacting compliance or execution.
  • Develop a working knowledge of GxP principles (GMP, GDP, GLP as applicable) and apply them consistently during manufacturing execution.
  • Recognize and promptly escalate out-of-specification conditions, deviations, or atypical events related to equipment, materials, processes, or documentation.
  • Maintain compliance with all required training, qualifications, and electronic learning assignments within the QMS.
  • Maintain personal accountability for PPE use, safety practices, and cleanroom discipline.
  • Collaborate with peers, Manufacturing Leads, and cross-functional partners (QA, MSAT, Engineering) during manufacturing execution, documentation readiness, and issue resolution.
  • Contribute to continuous improvement by identifying process inefficiencies, documentation gaps, or system usability issues and escalating through appropriate channels.
  • Support the development and revision of SOPs, MBRs, and Work Instructions as a technical contributor.
  • Share knowledge and best practices to support team consistency and operational excellence

Qualifications
The requirements listed below are representative of the knowledge, skill, and/or ability required to perform this job successfully.
Required:
  • Education and Experience (one of the following):
    • Bachelor's Degree (BS) in Life Sciences, Engineering, or related field with 0-1+ years of relevant experience in GMP manufacturing, laboratory, or regulated environments.
    • Associate's Degree (AS) in Life Sciences, Engineering, or related technical discipline with a minimum of 1+ year of relevant experience in GMP manufacturing or regulated environments.
    • High School Diploma (or equivalent) with a minimum of 3+ years of relevant experience in GMP manufacturing, regulated laboratory operations, or comparable technical environments.
  • Proficiency with Microsoft Excel, Word, and PowerPoint for routine documentation, data entry, and operational support.
  • Ability to navigate and work within electronic Quality Systems (e.g., Veeva, LMS, document management platforms).
  • Strong attention to detail with the ability to identify documentation, process, or compliance risks.
  • Ability to work independently in a fast-paced, highly regulated environment.
  • Effective verbal and written communication skills.
  • Ability to adapt to changing priorities and manufacturing schedules.
  • Ability to meet physical requirements of the role (lifting media containers, extended standing/sitting).
  • Successful completion of visual acuity requirements as applicable.

Preferred:
  • Prior experience in cell or gene therapy manufacturing, aseptic processing, or cell culture operations.
  • Experience working in cGMP cleanroom environments (ISO 5-8).
  • Familiarity with Veeva Vault or similar enterprise Quality Systems.
  • Exposure to electronic batch records, controlled documentation systems, or deviation support workflows.

Travel Requirements
  • None

Location
  • This position is 100% on-site in Durham, North Carolina. This position requires some non-standard working hours, including early morning or late evening.

#LI-Onsite
Kincell Bio provides equal employment opportunities (EEO) to all employees and applicants for employment without regard to race, color, religion, gender, sexual orientation, gender identity or expression, national origin, age, disability, genetic information, marital status, amnesty, or status as a covered veteran in accordance with applicable, federal, state, and local laws. Kincell Bio complies with applicable state and local laws governing non-discrimination in employment in every location in which the company has facilities. This policy applies to all terms and conditions of employment, including, but not limited to, hiring, placement, promotion, termination, layoff, recall, transfer, leaves of absence, compensation, and training.
NOTE TO EMPLOYMENT AGENCIES: Kincell Bio values our relationships with our Recruitment Partners. We will only accept resumes from those partners who have been contracted by a member of our Human Resources team to collaborate with us. We are not responsible for any fees related to resumes that are unsolicited or are received without contract.

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