What are the responsibilities and job description for the Planner & Scheduler position at AskBio Inc.?
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
This position is office-based in RTP, NC and will report to Associate Director, Facilities Reliability
Job Responsibilities
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.
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.
- 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.
This position is office-based in RTP, NC and will report to Associate Director, Facilities Reliability
Job Responsibilities
- Develop, update, and maintain detailed maintenance schedules using scheduling software (CMMS, Microsoft Project, etc.)
- Coordinate with maintenance managers, engineers, and stakeholders to gather input and align schedules with project objectives.
- Monitor progress against baseline schedules, identify variances, and recommend corrective actions.
- Prepare and distribute regular schedule reports, dashboards, and forecasts to management and stakeholders.
- Ensure resource availability and allocation across multiple work orders.
- Support risk management by identifying potential delays and proposing mitigation strategies.
- Maintain accurate records of schedule changes, approvals, and updates.
- Collaborate with procurement to align material deliveries with maintenance schedules.
- Bachelor’s degree in Engineering, Construction Management, Business Administration, or related field with 2 years of relevant experience in project planning and scheduling within biotech, manufacturing, or related industries.
- Proficiency with scheduling tools such as CMMS, Microsoft Project, or equivalent systems.
- Strong analytical and problem-solving skills.
- Excellent communication and interpersonal skills to work across cross‑functional teams.
- Knowledge of project management methodologies such as PMI, Agile, or Lean.
- Strong attention to detail, organization, and documentation accuracy.
- Ability to manage multiple projects simultaneously in a fast‑paced environment.
- Proficiency in Microsoft Office Suite (Excel, Word, PowerPoint).
- Ability to work both independently and collaboratively.
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.