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Biopharmaceutical Technology Jobs in Raleigh, NC

KBI Biopharma, Inc.

CSV Specialist II

Durham, NC · On-site

Bachelor's degree in Engineering, Information Technology, or a related discipline. * 3-5 years of ... KBI Biopharma, Inc. is an EEO/AA employer and actively seeks to diversify its work force. Therefore ...

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Biopharmaceutical Technology information

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$12

$26

$48

How much do biopharmaceutical technology jobs pay per hour?

As of Aug 18, 2026, the average hourly pay for biopharmaceutical technology in Raleigh, NC is $26.61, according to ZipRecruiter salary data. Most workers in this role earn between $19.38 and $30.38 per hour, depending on experience, location, and employer.

What is biopharmaceutical technology?

Biopharmaceutical technology refers to the use of biological methods and living organisms, such as cells or bacteria, to develop and manufacture pharmaceutical products like vaccines, antibodies, and therapeutic proteins. This field combines principles from biology, chemistry, and engineering to design processes for producing medicines that are often more targeted and effective than traditional drugs. Professionals in biopharmaceutical technology may work in research, development, or production, contributing to innovations that improve healthcare outcomes. Advancements in this area have led to treatments for diseases like cancer, autoimmune disorders, and rare genetic conditions.

What are the key skills and qualifications needed to thrive in biopharmaceutical technology?

To thrive in Biopharmaceutical Technology, you need a solid background in biology, chemistry, and biotechnology, typically supported by a relevant degree and laboratory experience. Familiarity with bioprocessing equipment, Good Manufacturing Practice (GMP) standards, and regulatory compliance certifications such as those from the FDA or EMA are commonly required. Strong analytical thinking, attention to detail, and effective teamwork are crucial soft skills in this field. These competencies ensure the safe, efficient, and compliant development of biopharmaceutical products that meet industry standards.

What are some typical challenges faced in a biopharmaceutical technology role, and how are they addressed within a team environment?

Professionals in Biopharmaceutical Technology often encounter challenges such as maintaining strict regulatory compliance, troubleshooting complex manufacturing processes, and ensuring product consistency at scale. These challenges are typically addressed through close collaboration among cross-functional teams, including quality assurance, regulatory affairs, and process engineering. Regular team meetings, thorough documentation, and continuous training help ensure that everyone is aligned on protocols and problem-solving strategies. Open communication and a strong culture of knowledge-sharing are key to overcoming technical hurdles and meeting project deadlines.

What is the difference between Biopharmaceutical Technology vs Bioprocessing Technician?

AspectBiopharmaceutical TechnologyBioprocessing Technician
Required CredentialsBachelor's degree in biotech, biology, or related fieldAssociate's or bachelor's degree in biotech or related field
Work EnvironmentLaboratories, research facilities, production plantsManufacturing floors, labs, production environments
Industry UsageResearch, development, quality control in biotech firmsProduction, process operation, equipment maintenance

Biopharmaceutical Technology focuses on research, development, and quality control in biotech labs, requiring advanced degrees. In contrast, Bioprocessing Technicians primarily operate and maintain manufacturing equipment in production settings. Both roles are essential in the biotech industry but differ in responsibilities, credentials, and work environments.

What are the career opportunities in biopharmaceutical technology?

Biopharmaceutical technology offers career opportunities such as bioprocess engineer, quality control analyst, research scientist, manufacturing technician, and regulatory affairs specialist. These roles involve working with bioprocessing equipment, adhering to Good Manufacturing Practices (GMP), and often require knowledge of cell culture, bioreactors, and laboratory techniques.

What does a biopharmaceutical technician do?

A biopharmaceutical technician performs tasks related to the development, manufacturing, and quality control of biopharmaceutical products. They operate laboratory equipment, prepare samples, follow strict safety and regulatory protocols, and document procedures to ensure product consistency and compliance.

What jobs can you get with a biopharmaceutical technology degree?

A biopharmaceutical technology degree can lead to roles such as bioprocess technician, quality control analyst, manufacturing associate, or research scientist in pharmaceutical or biotech companies. These positions often require knowledge of laboratory techniques, Good Manufacturing Practices (GMP), and familiarity with bioprocessing equipment and regulations.

What are popular job titles related to Biopharmaceutical Technology jobs in Raleigh, NC?

For Biopharmaceutical Technology jobs in Raleigh, NC, the most frequently searched job titles are:

What job categories do people searching Biopharmaceutical Technology jobs in Raleigh, NC look for?

The top searched job categories for Biopharmaceutical Technology jobs in Raleigh, NC are:

What cities near Raleigh, NC are hiring for Biopharmaceutical Technology jobs?

Cities near Raleigh, NC with the most Biopharmaceutical Technology job openings:

Biopharmaceutical Technology jobs near you
Infographic showing various Biopharmaceutical Technology job openings in Raleigh, NC as of August 2026, with employment types broken down into 1% As Needed, 78% Full Time, 17% Part Time, and 4% Contract. Highlights an 86% Physical, 3% Hybrid, and 11% Remote job distribution, with an average salary of $55,348 per year, or $26.6 per hour.

Process Engineer II

Asklepios BioPharmaceutical, Inc.

Durham, NC • On-site

Full-time

Posted 14 days ago

Job description

AskBio Inc., a wholly owned and independently operated subsidiary of Bayer AG, is a fully integrated gene therapy company dedicated to developing life-saving medicines and changing lives. The company maintains a portfolio of clinical programs across a range of neuromuscular, central nervous system, cardiovascular, and metabolic disease indications with a clinical-stage pipeline that includes investigational therapeutics for congestive heart failure, limb-girdle muscular dystrophy, multiple system atrophy, Parkinson's disease, and Pompe disease. AskBio's gene therapy platform includes Pro10™, an industry-leading proprietary cell line manufacturing process, and an extensive array of capsids and promoters. With global headquarters in Research Triangle Park, North Carolina, and European headquarters in Edinburgh, Scotland, the company has generated hundreds of proprietary capsids and promoters, several of which have entered pre-clinical and clinical testing.
Our vision: Pioneering science to create transformative molecular medicines.
Our mission: Lead innovative science and drive clinical outcomes to transform people's lives.
Our principles:
  • Advance innovative science by pushing boundaries.
  • Bring transformative therapeutics to patients in need.
  • Provide an environment for employees to reach their fullest potential.

Our values:
  • Be a Pioneer. We are not afraid of the impossible and to innovate to make gene therapies accessible to those in need.
  • Cultivate Collaboration. Strive to be the best teammate, actively listen, openly communicate, and embrace diverse points of view.
  • Embrace Responsibility. We are humbled by the enormity of our mission. We hold a relentless commitment to advance science and clinical outcomes for our patients, families, and caregivers.
  • Raise the Bar. Continuously drive improvements and efficiencies. Seek and provide constructive feedback. Have a bias for learning and action.
  • Act with Uncompromising Integrity. Be honest, transparent, and committed to doing what's right in every situation. Make clear commitments and follow through.

Position Summary
AskBio is seeking a Process Engineer II to join our MSAT Process Engineering team and support current and future commercialization efforts. This position supports scale-up, technology transfer of AskBio's portfolio of gene therapy products into cGMP manufacturing for clinical production, process validation and commercial launch. The incumbent will onboard clinical programs into the MSAT laboratory, perform scale-up runs, and transfer programs to AskBio's contract manufacturing facility. Additionally, this position will be responsible for performing Phase III clinical enabling activities including scale-down model development and qualification, process characterization, and process control strategy definition to enable process performance qualification (PPQ) readiness for both drug substance and drug product manufacturing campaigns. This position is highly collaborative and will require internal and external team interactions to ensure successful process scale-up, technology transfers, and cGMP manufacturing operations to ensure continuity of supply while adhering to global regulations and standards.
This role is based on-site at our RTP (Research Triangle Park) Headquarters in NC and reports to an Associate Director, MSAT.
Job Responsibilities
  • Collaborate with cross-functional teams to transfer small-scale gene therapy processes from Process Development into the MSAT laboratory and subsequently perform scale-up and transfer to the cGMP manufacturing scale
  • Perform process characterization experiments to generate robustness data and define the process control strategy for PPQ manufacturing campaigns. Contribute to process characterization experimental design and data analysis
  • Develop and qualify small-scale models that are predictive of the cGMP manufacturing scale
  • Author technical protocols and reports to support experimental work and maintain clear, organized electronic laboratory notebooks
  • Provide effective communication of experimental results in technical presentations with internal stakeholders
  • Support investigations by contributing technical expertise to root-cause analyses and using a data-driven approaches for driving issue resolution
  • Ensure the laboratory is clean, organized and maintained in an efficient working order, includes scheduling routine preventative maintenance/calibration of instruments/equipment, securing supplies and materials for experiments, and proper scheduling of laboratory work

Minimum Requirements
  • Bachelor's Degree in a scientific discipline with 2+ years of Biopharmaceutical Experience; OR Master's Degree in a scientific discipline; OR High School Diploma with 6+ years of biopharmaceutical Experience
  • Hands-on upstream or downstream biomanufacturing laboratory experience
  • Excellent written and verbal communication skills, with experience interacting with a range of internal stakeholder groups
  • Proficiency in using Microsoft Office Suite (Word, Excel, PowerPoint)
  • Highly motivated, organized, and disciplined, with a strong desire to contribute as part of a best-in-class, collaborative tech transfer team
  • Adaptable and eager to learn, thriving in a fast-paced, highly interactive environment
  • Genuinely interested in building proficiency in upstream and downstream biomanufacturing operations, including process scale-up, technology transfer, process characterization, and process control strategy development
  • Continuous improvement-oriented, seeking opportunities to optimize process operations and performance through proactive problem solving
  • Open to domestic and international travel up to approximately 10%, as needed

Preferred Education, Experience and Skills
  • Prior downstream experience
  • Experience with viral vectors
  • Experience supporting cGMP manufacturing operations
  • Knowledge of the Design of Experiment (DOE) methodology with an ability to design, execute, and analyze experiments with oversight. JMP Statistical Software proficiency is highly preferred

AskBio Inc. (AskBio) is an Equal Opportunity Employer and does not discriminate against any employee or applicant for employment because of race, color, religion, gender, sexual orientation, gender identity, national origin, age, disability, veteran status or any other protected status prohibited under Federal, State or local laws. All employment decisions are based on valid job-related requirements. If you are a qualified individual with a disability or a disabled veteran and are unable or limited in your ability to use or access our website, you may request a reasonable accommodation to express interest in a specific opening by calling us at (919) 561-6210 or sending us an email at careers@askbio.com.
Agencies: Please do not contact any employee at AskBio about this requisition. Any resume submitted by a recruitment agency to any employee at AskBio, through any medium, will be deemed the sole property of AskBio unless the agency was engaged by AskBio Talent Acquisition team to recruit for that position. All agencies must have a prior executed service agreement with AskBio prior to any search engagement. If a candidate who was submitted outside of the AskBio agency process is hired by AskBio, no fee or payment of any kind will be paid to the agency.

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