Associate Director, Process Development

AskBio Inc.; United States; On-site; USD 180,000 - 240,000; Full time

Job summary

AskBio Inc. offers a secondment opportunity for an Associate Director, Process Development in the Cell Line & Process Development team at the BioPoint facility in RTP, NC.

The role focuses on SME activities for novel rAAV vector platforms, evaluating new cell lines, and developing end-to-end production and purification processes. The position requires a Master’s degree with at least eight years of relevant experience, strong cross-functional leadership, and expertise in AAV biology and QbD

Qualifications

• Master’s Degree in a scientific or engineering discipline with extensive relevant experience.
• PhD preferred in a related field; strong publication/patent record is a plus.
• Experience leading cross-functional teams of researchers and engineers.

Responsibilities

• Lead a team of Research Associates and Scientists in viral vector process development and tech transfer.
• Oversee end-to-end platform development for novel rAAV producer cell lines; apply DOE/QbD to optimize.
• Coordinate GMP cell bank qualifications and materials for vector production.
• Partner with MSAT on lifecycle management of clinical program manufacturing.
• Develop and maintain internal transfer documents and regulatory submissions.

Skills

DOEs

QbD

AAV biology

Cross-functional leadership

Mammalian cell culture

GMP knowledge

Education

Master’s degree in science/engineering

PhD preferred

Tools

Benchling

QbD Vision

JMP

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.

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

The Associate Director, Process Development is a key position in the Cell Line & Process Development team, liaising between the development arms while serving as a subject matter expert (SME) for novel recombinant adeno-associated virus (rAAV) vector platform development. This position evaluates new cell lines in scale down models, develops end to end processes for production and purification with these novel cell substrates and recommends forward looking GMP activities based on development data. This position is onsite at the BioPoint, RTP, NC facility, reporting to the VP of Cell Line & Process Development.

Job Responsibilities

• Lead a team of Research Associates and Scientists responsible for developing viral vector manufacturing processes, scale-up, and internal technology transfer
• Management of end to end platform development for novel rAAV producer cell lines applying statistical approaches for experimental execution and optimization
• Oversee internal qualifications of GMP cell banks and critical raw materials in vector manufacturing processes
• Partner with MSAT on life cycle management of clinical program manufacturing and optimization
• Lead platform fit and/or development activities for portfolio programs, as needed
• Identify and develop new technologies for increased productivity, recovery, product quality and/or improved cost of goods
• Collaborate cross-functionally with other AskBio teams inside and outside of Technical Operations, including our partner CDMOs
• Develop internal tech transfer documents and author/review CMC regulatory documents
• Review and communicate experimental results both orally and in written reports/presentations to colleagues, senior management and at external partners and conferences
• Identifes CapEx needs, develops corresponding budget and justification
• Assists with the development of and adherence to department budgets
• Identifies and executes against personnel plans, including hiring, training, and development in the pursuit of organizational objectives
• Contributes to intellectual property strategies and manages staff to successful IP support
• Author technical and development documents, including relevant sections in regulatory submissions
• Mentors and develops team members by establishing a collaborative and growth minded culture that encourages personal and professional development
• Present scientific data at internal forums and external conferences

Minimum Requirements

• Master’s Degree in a scientific or engineering discipline with a minimum of eight years of relevant work experience
• Prior experience managing cross-functional teams of Research Associates, Scientists and/or Engineers
• Prior experience with recombinant AAV and/or extensive experience in biologics employing relevant unit operations
• Strong understanding of mammalian cell biology, engineering principles and how to interconnect them
• Self-motivated leader with a track record of novel development of biologics demonstrated through publications, patents, posters and/or presentations
• Functional expertise in design of experiments (DOEs) and Quality by Design (QbD) approaches
• Excellent written and verbal communication skills
• Good working knowledge of Microsoft Office suite (Word, Outlook, Excel) and statistical analysis software

Preferred Education, Experience and Skills

• PhD in a scientific or engineering discipline
• Cell line development for the production of AAV, antibodies or recombinant protein
• Strong working knowledge of Benchling, QbD Vision and/or JMP

Equal Opportunity Employer

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 [e-mail]. This portal is for AskBio affiliated company employees to apply for open roles at AskBio. Please ensure that when applying your manager is aware of your application.