Process Engineer II
Durham, NC · On-site
Position Summary AskBio is seeking a Manufacturing Science and Technology (MSAT) Process Engineer ... Additionally, this position will be responsible for performing Phase III clinical enabling ...
Process Engineer II
Durham, NC · On-site
Position Summary AskBio is seeking a Manufacturing Science and Technology (MSAT) Process Engineer ... Additionally, this position will be responsible for performing Phase III clinical enabling ...
Position Summary AskBio is seeking a Manufacturing Science and Technology (MSAT) Process Engineer ... Additionally, this position will be responsible for performing Phase III clinical enabling ...
Position Summary AskBio is seeking a Manufacturing Science and Technology (MSAT) Process Engineer ... Additionally, this position will be responsible for performing Phase III clinical enabling ...
Process Engineer II
Clayton, NC · On-site
In NC, we operate three pharmaceutical manufacturing facilities that are responsible for fulfilling ... Coaching & mentoring peers, Engineering & Process Maintenance Technicians * Support technical ...
Process Engineer II
Clayton, NC · On-site
In NC, we operate three pharmaceutical manufacturing facilities that are responsible for fulfilling ... Coaching & mentoring peers, Engineering & Process Maintenance Technicians * Support technical ...
Electrical Engineer 3 Location: Clayton, NC Duration: 12+ Months Position Contributions to Work ... process including; requirements capture, specifications, FMEA, design, development, testing ...
Electrical Engineer 3 Location: Clayton, NC Duration: 12+ Months Position Contributions to Work ... process including; requirements capture, specifications, FMEA, design, development, testing ...
Process Engineer I - SDF
Durham, NC · On-site
In NC, we operate three pharmaceutical manufacturing facilities that are responsible for fulfilling ... Three (3) years of engineering experience in maintenance, design, process improvement, or Six Sigma ...
Process Engineer I - SDF
Durham, NC · On-site
In NC, we operate three pharmaceutical manufacturing facilities that are responsible for fulfilling ... Three (3) years of engineering experience in maintenance, design, process improvement, or Six Sigma ...
Sterilization Process Engineer
Durham, NC · On-site
... 3 years experience in engineering or manufacturing environments Required Experience/Skills ... process validation * Experience working with data analysis software (JMP, Minitab, etc About us:
Quick apply
Sterilization Process Engineer
Durham, NC · On-site
... 3 years experience in engineering or manufacturing environments Required Experience/Skills ... process validation * Experience working with data analysis software (JMP, Minitab, etc About us:
Process Engineer I - SDF
Durham, NC · On-site
In NC, we operate three pharmaceutical manufacturing facilities that are responsible for fulfilling ... Three (3) years of engineering experience in maintenance, design, process improvement, or Six Sigma ...
Process Engineer I - SDF
Durham, NC · On-site
In NC, we operate three pharmaceutical manufacturing facilities that are responsible for fulfilling ... Three (3) years of engineering experience in maintenance, design, process improvement, or Six Sigma ...
In NC, we operate three pharmaceutical manufacturing facilities that are responsible for fulfilling ... Three (3) years of engineering experience in maintenance, design, process improvement, or Six Sigma ...
In NC, we operate three pharmaceutical manufacturing facilities that are responsible for fulfilling ... Three (3) years of engineering experience in maintenance, design, process improvement, or Six Sigma ...
The Principal Process Engineer supports manufacturing operations and capital projects by applying ... This individual will work at least 3 days in the office. Our values-based culture connects to our ...
The Principal Process Engineer supports manufacturing operations and capital projects by applying ... This individual will work at least 3 days in the office. Our values-based culture connects to our ...
The Principal Process Engineer supports manufacturing operations and capital projects by applying ... This individual will work at least 3 days in the office. Our values-based culture connects to our ...
The Principal Process Engineer supports manufacturing operations and capital projects by applying ... This individual will work at least 3 days in the office. Our values-based culture connects to our ...
Associate Process Engineer - Biopharma (JP13416)
Holly Springs, NC · On-site
$30 - $33/hr
Associate Process Engineer - Biopharma (JP13416) Location: Holly Springs, NC. 27540 Business Unit: Engineering & Automation Employment Type: Contract Duration: 12 months with possible extensions or ...
Associate Process Engineer - Biopharma (JP13416)
Holly Springs, NC · On-site
$30 - $33/hr
Associate Process Engineer - Biopharma (JP13416) Location: Holly Springs, NC. 27540 Business Unit: Engineering & Automation Employment Type: Contract Duration: 12 months with possible extensions or ...
Bachelor's Degree in Engineering (Chemical Preferred) * 3+ Years of Experience in Process Engineering * Experience Working in a Greenfield Environment * Extensive Knowledge of Stainless Steel ...
Quick apply
Bachelor's Degree in Engineering (Chemical Preferred) * 3+ Years of Experience in Process Engineering * Experience Working in a Greenfield Environment * Extensive Knowledge of Stainless Steel ...
In NC, we operate three pharmaceutical manufacturing facilities that are responsible for fulfilling ... Drive process monitoring activities for key process parameters and track initiatives * Ensure ...
In NC, we operate three pharmaceutical manufacturing facilities that are responsible for fulfilling ... Drive process monitoring activities for key process parameters and track initiatives * Ensure ...
In NC, we operate three pharmaceutical manufacturing facilities that are responsible for fulfilling ... Participation in design workshops with engineering suppliers * Input & review of Process Module ...
In NC, we operate three pharmaceutical manufacturing facilities that are responsible for fulfilling ... Participation in design workshops with engineering suppliers * Input & review of Process Module ...
In NC, we operate three pharmaceutical manufacturing facilities that are responsible for fulfilling ... Drive process monitoring activities for key process parameters and track initiatives * Ensure ...
In NC, we operate three pharmaceutical manufacturing facilities that are responsible for fulfilling ... Drive process monitoring activities for key process parameters and track initiatives * Ensure ...
In NC, we operate three pharmaceutical manufacturing facilities that are responsible for fulfilling ... Drive process monitoring activities for key process parameters and track initiatives * Ensure ...
In NC, we operate three pharmaceutical manufacturing facilities that are responsible for fulfilling ... Drive process monitoring activities for key process parameters and track initiatives * Ensure ...
Wastewater Treatment Process Engineer
$80K - $180K/yr
... including three or more years leading process design of wastewater projects with full ... engineers, planners, architects, inspectors, designers, and more. Our clients choose us for our ...
Wastewater Treatment Process Engineer
$80K - $180K/yr
... including three or more years leading process design of wastewater projects with full ... engineers, planners, architects, inspectors, designers, and more. Our clients choose us for our ...
Software Engineer III
$128K - $144K/yr
Software Engineer III * Venture III, 900 Main Campus Drive, Raleigh, NC 27606 (formerly 1801 ... We are committed to providing a fair and accessible hiring process. If you have a disability or ...
Software Engineer III
$128K - $144K/yr
Software Engineer III * Venture III, 900 Main Campus Drive, Raleigh, NC 27606 (formerly 1801 ... We are committed to providing a fair and accessible hiring process. If you have a disability or ...
Software Engineer III
Raleigh, NC · On-site +1
$115K - $131K/yr
Software Engineer III * Venture III, 900 Main Campus Drive, Raleigh, NC 27606 (formerly 1801 ... Implement development processes, coding best practices, and code reviews. Operate in various ...
Software Engineer III
Raleigh, NC · On-site +1
$115K - $131K/yr
Software Engineer III * Venture III, 900 Main Campus Drive, Raleigh, NC 27606 (formerly 1801 ... Implement development processes, coding best practices, and code reviews. Operate in various ...
Software Engineer III
Raleigh, NC · On-site
$128K - $144K/yr
Software Engineer III * Venture III, 900 Main Campus Drive, Raleigh, NC 27606 (formerly 1801 ... We are committed to providing a fair and accessible hiring process. If you have a disability or ...
Software Engineer III
Raleigh, NC · On-site
$128K - $144K/yr
Software Engineer III * Venture III, 900 Main Campus Drive, Raleigh, NC 27606 (formerly 1801 ... We are committed to providing a fair and accessible hiring process. If you have a disability or ...
Process Engineer Three information
See Raleigh, NC salary details
$48.1K - $56.3K
2% of jobs
$56.3K - $64.6K
9% of jobs
$72K is the 25th percentile. Wages below this are outliers.
$64.6K - $72.8K
15% of jobs
$72.8K - $81K
18% of jobs
The median wage is $83.8K / yr.
$81K - $89.2K
17% of jobs
$89.2K - $97.4K
14% of jobs
$97.6K is the 75th percentile. Wages above this are outliers.
$97.4K - $105.6K
11% of jobs
$105.6K - $113.9K
6% of jobs
$113.9K - $122.1K
4% of jobs
$122.1K - $130.3K
3% of jobs
$130.3K - $138.5K
1% of jobs
$48.1K
$89.4K
$138.5K
How much do process engineer three jobs pay per year?
As of Jun 8, 2026, the average yearly pay for process engineer three in Raleigh, NC is $89,449.00, according to ZipRecruiter salary data. Most workers in this role earn between $72,400.00 and $100,100.00 per year, depending on experience, location, and employer.
What is the difference between Process Engineer Three vs Process Engineer Two?
| Aspect | Process Engineer Three | Process Engineer Two |
|---|---|---|
| Required Credentials | Bachelor's degree in Engineering or related field; 3+ years experience | Bachelor's degree; 1-3 years experience |
| Work Environment | Manufacturing plants, chemical facilities, or industrial settings | Similar industrial environments, often with less complex projects |
| Employer & Industry Usage | Commonly used in manufacturing, chemical, and oil & gas industries | Used in similar industries, often as a stepping stone role |
Process Engineer Three typically requires more experience and handles more complex projects than Process Engineer Two. Both roles work in manufacturing or chemical environments, but Process Engineer Three often takes on greater responsibilities and project scope, making it suitable for professionals with more industry experience.
What cities near Raleigh, NC are hiring for Process Engineer Three jobs? Cities near Raleigh, NC with the most Process Engineer Three job openings:
Full-time
Posted 25 days ago
Job description
Opportunity for Secondment to AskBio
We're pleased to share an exciting secondment opportunity at AskBio.
This role is available for a time period to be determined by leadership at both Bayer and AskBio. While most assignments range from one to two years, the exact duration will be based on business needs and mutual agreement.
This secondment offers a unique chance to broaden your experience, expand your knowledge, and contribute meaningfully to AskBio's mission: to advance gene therapy and change the lives of patients around the world.
If you're interested in exploring this opportunity, we encourage you to:
We look forward to seeing how our colleagues continue to grow and make an impact across the Bayer-AskBio partnership.
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:
Our values:
Position Summary
AskBio is seeking a Manufacturing Science and Technology (MSAT) Process Engineer II to join our 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
Minimum Requirements
Preferred Education, Experience and Skills
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 talent@askbio.com.
We're pleased to share an exciting secondment opportunity at AskBio.
This role is available for a time period to be determined by leadership at both Bayer and AskBio. While most assignments range from one to two years, the exact duration will be based on business needs and mutual agreement.
This secondment offers a unique chance to broaden your experience, expand your knowledge, and contribute meaningfully to AskBio's mission: to advance gene therapy and change the lives of patients around the world.
If you're interested in exploring this opportunity, we encourage you to:
- Speak with your direct manager to discuss your interest and alignment with your development goals.
- Apply directly using the link provided in the posting.
We look forward to seeing how our colleagues continue to grow and make an impact across the Bayer-AskBio partnership.
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 Manufacturing Science and Technology (MSAT) Process Engineer II to join our 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 the root-cause analysis and using a data-driven approach 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 and 2 years of Biopharmaceutical Experience OR Master's Degree in a scientific discipline and 0 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 upstream experience
- Some prior 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 talent@askbio.com.