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Biotech Process Development Jobs in Raleigh, NC (NOW HIRING)

Our technical expertise is paired with an exceptional team of business development, human resources ... biotech processing, and cGMP-regulated clean utilities. This role bridges process engineering ...

Our technical expertise is paired with an exceptional team of business development, human resources ... biotech processing, and cGMP-regulated clean utilities. This role bridges process engineering ...

... biotechnology? At Aldevron, one of Danaher's 15+ operating companies, our work saves lives-and we ... At Aldevron, we deliver world-class CDMO services that accelerate the development of groundbreaking ...

... biotechnology? At Aldevron, one of Danaher's 15+ operating companies, our work saves lives-and we ... At Aldevron, we deliver world-class CDMO services that accelerate the development of groundbreaking ...

Our technical expertise is paired with an exceptional team of business development, human resources ... biotech processing, and cGMP-regulated clean utilities. This role bridges process engineering ...

... biotechnology manufacturing processes. Working alongside experienced engineers and subject matter experts, you will contribute to projects from concept development through detailed design and ...

Job Overview We are seeking a Site Contract Specialist to support the development and execution of ... Strong understanding of clinical research processes and regulatory requirements. * Proficiency in ...

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Biotech Process Development information

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$18

$32

$48

How much do biotech process development jobs pay per hour?

As of Sep 14, 2026, the average hourly pay for biotech process development in Raleigh, NC is $32.74, according to ZipRecruiter salary data. Most workers in this role earn between $26.88 and $40.19 per hour, depending on experience, location, and employer.

What is biotech process development?

Biotech process development refers to the design, optimization, and scale-up of manufacturing processes used to produce biological products, such as pharmaceuticals, enzymes, or vaccines. Professionals in this field work to turn laboratory procedures into efficient, large-scale industrial processes that meet regulatory and quality standards. This often involves selecting suitable equipment, optimizing conditions, ensuring reproducibility, and troubleshooting production issues. The ultimate goal is to produce high-quality products safely, consistently, and cost-effectively.

What are the key skills and qualifications needed to thrive in biotech process development, and why are they important?

To excel in Biotech Process Development, you need a strong background in bioprocess engineering, molecular biology, and chemistry, typically supported by a degree in biotechnology or related fields. Familiarity with tools such as bioreactors, chromatography systems, and data analysis software, along with certifications in Good Manufacturing Practice (GMP), is highly valuable. Strong problem-solving skills, attention to detail, and effective teamwork distinguish top performers in this role. These competencies are crucial for optimizing processes, ensuring product quality, and driving innovation in the biotech industry.

What are some common challenges faced by professionals in biotech process development, and how are they typically addressed?

Professionals in Biotech Process Development often encounter challenges related to scaling up processes from the laboratory to commercial production, ensuring product consistency, and meeting strict regulatory standards. Addressing these challenges typically involves close collaboration with cross-functional teams such as quality assurance, regulatory affairs, and manufacturing. Continuous process optimization, thorough documentation, and robust validation protocols are essential strategies to overcome these hurdles and ensure successful product development and commercialization.

What is the difference between Biotech Process Development vs Biotech Manufacturing Associate?

AspectBiotech Process DevelopmentBiotech Manufacturing Associate
Primary FocusDesigning, optimizing, and scaling up bioprocesses for product developmentExecuting manufacturing processes to produce biopharmaceuticals at scale
Work EnvironmentLaboratories and pilot plant facilitiesProduction floors and manufacturing plants
Required SkillsProcess design, lab techniques, troubleshootingEquipment operation, quality control, adherence to SOPs
Typical CredentialsBSc/MSc in Biotechnology, Chemical Engineering, or related fieldsBSc in Biotechnology, Biology, or related fields

While both roles are essential in biotech, Biotech Process Development focuses on creating and optimizing processes during product development, whereas Biotech Manufacturing Associates handle the day-to-day production to ensure consistent product quality at scale.

What are popular job titles related to Biotech Process Development jobs in Raleigh, NC?

For Biotech Process Development jobs in Raleigh, NC, the most frequently searched job titles are:

What job categories do people searching Biotech Process Development jobs in Raleigh, NC look for?

The top searched job categories for Biotech Process Development jobs in Raleigh, NC are:

Infographic showing various Biotech Process Development job openings in Raleigh, NC as of August 2026, with employment types broken down into 1% As Needed, 80% Full Time, 14% Part Time, and 5% Contract. Highlights an 92% Physical, 2% Hybrid, and 6% Remote job distribution, with an average salary of $68,104 per year, or $32.7 per hour.

Process Piping Designer

Raleigh, NC • On-site

Salas O'Brien, Inc.
Specialized Design Services • 201 - 500 employees

Other

Medical, Dental, Vision, Retirement, PTO

Posted 13 days ago


Salas O'Brien rating

8.2

Company rating: 8.2 out of 10

Based on 13 frontline employees who took The Breakroom Quiz


Job description

At Salas O’Brien we tell our clients that we’re engineered for impact. This passion for making a difference applies just as much to our team as it does to our projects. That’s why we are committed to living our values every day: inspiring, achieving, and connecting as shared owners of our success with a focus on a sustainable future.

Building for the long-term means that all our team members can expect to work on amazing projects with a people-first approach to problem solving. It also means that each member of our team has truly limitless potential to build a unique, meaningful, and high-impact career—and they’ll receive great total rewards along the way.

About Us:

Founded in 1975, Salas O’Brien is an employee-owned engineering and professional services firm focused on achieving impact for our clients, our team, and the world. We know that tomorrow’s requirements are today’s opportunities, and we are here to design lasting solutions for pressing challenges.

We work across a variety of industries providing integrated engineering and consulting services. Our specialized experience includes design for data centers, healthcare, science and technology, high-rise buildings, clean energy, education, and other building types as well as structural and building sciences, infrastructure asset management, advanced robotics, and more.

Our technical expertise is paired with an exceptional team of business development, human resources, finance and accounting, information technology, and marketing professionals, all of whom play a key role in bringing our commitments to life every day.

We’re currently accepting applications for Process Piping Designer candidates to be considered for future projects.

Job Summary:

The Process Piping Designer will assist in the creation, management, and coordination of 3D models and drawings for GMP process utility piping systems. The Process Piping Designer is responsible for developing detailed piping designs and layouts that support pharmaceutical manufacturing facilities, including bulk API (Active Pharmaceutical Ingredient) production, biotech processing, and cGMP-regulated clean utilities. This role bridges process engineering requirements with practical, code-compliant piping design, ensuring systems meet sanitary, hygienic, and regulatory standards specific to the pharmaceutical sector.

Responsibilities:

  • Develop 3D piping models and 2D isometric/orthographic drawings using CAD/BIM software (Primarily Revit & AutoCAD Plant 3D).
  • Design process piping systems including WFI (Water for Injection), Purified Water, Clean Steam, CIP/SIP (Clean-in-Place/Sterilize-in-Place), process gases, and chemical transfer lines, applying sanitary piping design principles (slope, drainability, dead-leg minimization) in accordance with ASME BPE (Bioprocessing Equipment) standards.
  • Coordinate with process engineering, instrumentation and controls, mechanical, and other disciplines to resolve interdisciplinary conflicts.
  • Generate and maintain piping and instrumentation diagrams (P&IDs), line lists, piping plans, isometric drawings, and material take-offs (MTOs).
  • Interface with clients and vendors to clarify design requirements and specifications.
  • Draft clear Standard Operating Procedures (SOPs) and drafting manuals to guide junior designers and external contractors.
  • Assist in building, testing, and maintaining 3D piping material specifications and component catalogs within the plant design software.
  • Create, maintain, and update master drawing templates, title blocks, symbology libraries, and layer configurations to ensure consistency across all project deliverables.
  • Provide technical support, onboarding, and mentorship to team members on software configurations, workflow best practices, and standard compliance.

Qualifications and Experience:

  • Education: Associate's degree in Computer-Aided Drafting & Design, Engineering Technology, Drafting, or a related technical field; equivalent combination of technical training and hands‑on piping design experience will also be considered in lieu of a degree. Bachelor's degree in Engineering is a plus but not required.
  • Experience:3–7 years of piping design experience, with demonstrated experience in pharmaceutical, biotech, or other high‑purity/sanitary process industries.
  • Technical Skills
  • Proficiency in 3D piping design software (AutoCAD Plant 3D, AVEVA E3D/PDMS, SmartPlant 3D, or similar)
  • Working knowledge of ASME B31.3 (Process Piping) and ASME BPE (Bioprocessing Equipment) standards
  • Experience with modular/skid-based pharmaceutical process equipment
  • Knowledge of isometric review and clash detection workflows in a 3D modeling environment
  • Experience with sanitary fittings, tri‑clamp connections, orbital welding requirements, and hygienic design principles
  • Understanding of clean utility systems (WFI, Purified Water, Clean Steam, Compressed Air/Gases)
  • Strong interdisciplinary coordination and communication skills
  • Ability to read and interpret P&IDs, equipment specifications, and vendor drawings
  • Nice to Have:
  • Autodesk Certified Professional (AutoCAD and/or Revit MEP)
  • Familiarity with ASME BPE standards and training
  • Prior experience mentoring junior designers or standardizing CAD/BIM workflows

Location: This position is an office role based in Raleigh, NC.

Travel: Flexibility and willingness for occasional travel based on project needs.

Actual compensation will be determined based on a number of factors including skills, experience, qualifications, and location. This role is also eligible forperformance-based bonuses, and a comprehensiveU.S. basedbenefits package, including:

  • Medical, dental, and vision insurance
  • 401(k) with company match
  • Paid time off and company holidays
  • Wellness programs and employee assistance resources

For more information, visit our full benefits overviewhere .

Equal Opportunity Employment Statement

Salas O’Brien provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state/provincial, or local laws. Salas O’Brien will accommodate the disability‑related needs of applicants as required by law.

Third-Party Agency Notice
Salas O’Brien does not accept unsolicited resumes from external recruiters or agencies. We only work with approved partners engaged directly by our Talent Acquisition team for specific searches. Unsolicited submissions will not be eligible for placement fees.

Qualifications Education Preferred

Associates or better in Drafting and Design CADD or related field.

Experience Required 3-7 years: 3-7 years:3–7 years of piping design experience, with demonstrated experience in pharmaceutical, biotech, or other high‑purity/sanitary process industries.

Equal Opportunity Employer/Protected Veterans/Individuals with Disabilities
This employer is required to notify all applicants of their rights pursuant to federal employment laws.For further information, please review the Know Your Rights notice from the Department of Labor.

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