AskBio
From AskBio's careers page
Status: listed on the employer's own careers page when we last checked (daily). Confirm on their site before applying.
This role is based on-site at our RTP (Research Triangle Park) Headquarters in NC and reports to an Associate Director, MSAT.
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.
Advance innovative science by pushing boundaries.
Bring transformative therapeutics to patients in need.
Provide an environment for employees to reach their fullest potential.
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 Sr. Process Engineer, Manufacturing Science and Technology (MSAT) 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, 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
Design, execute, analyze and interpret process characterization experiments to generate robustness data and define the process control strategy for PPQ manufacturing campaigns.
Develop 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 and external stakeholders
Lead cross-functional 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, securing supplies and materials for experiments, and proper scheduling of laboratory work
Bachelor’s Degree in a scientific discipline with 5+ years of relevant work experience in the biopharmaceutical industry OR Master's Degree in a scientific discipline with 3+ years of relevant work experience in the biopharmaceutical industry
Hands-on upstream and/or downstream biomanufacturing laboratory experience
Excellent written and verbal communication skills, with experience interacting with a range of internal and external 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.
Prior upstream experience
Prior experience supporting cGMP manufacturing operations, process characterization, and/or PPQ activities
Knowledge of the Design of experiment (DOE) methodology with an ability to design, execute, and analyze experiments with minimal oversight. JMP Statistical Software proficiency is highly preferred
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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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