Process Engineer II

askbio; Durham (NC); On-site; USD 90,000 - 120,000; Full time

Job summary

AskBio Inc. is seeking a Process Engineer II to join the MSAT Process Engineering team at the RTP, NC campus.

This role supports scale-up, tech transfer of gene therapy products into cGMP manufacturing, process validation, and PPQ readiness for both drug substance and drug product. The incumbent will onboard clinical programs, perform scale-up runs, and transfer programs to the contract manufacturing facility.

Qualifications

• Bachelor’s Degree in a scientific discipline required; 2+ years biopharmaceutical experience in lab settings.
• Hands-on upstream or downstream biomanufacturing laboratory experience.
• Excellent written and verbal communication skills with diverse stakeholders.
• Proficiency in Microsoft Office Suite (Word, Excel, PowerPoint).
• Highly motivated, organized, and collaborative in a fast-paced tech transfer team.
• Willingness to travel domestically and internationally up to ~10%.

Responsibilities

• Transfer small-scale gene therapy processes from Process Development to MSAT lab.
• Generate robustness data and define the PPQ process control strategy.
• Develop and qualify small-scale models predictive of cGMP scale.
• Prepare technical protocols and reports with organized ELN records.
• Communicate results to internal stakeholders through technical presentations.
• Contribute to root-cause analyses and data-driven issue resolution.

Skills

Biopharmaceutical experience

Communication skills

Microsoft Office

Team collaboration

Problem solving

Willingness to travel

Education

Bachelor’s Degree in a scientific discipline

Master’s Degree in a scientific discipline

High School Diploma with 6+ years biopharmaceutical experience

Tools

JMP Software

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 [phone] or sending us an email at [e-mail].

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.