Associate Director, Downstream Process Development, GT-PD

Novartis AG

Durham, NC

JOB DETAILS
SALARY
$145,600–$270,400 Per Year
SKILLS
Analytical Development, Budgeting, Channel Strategies, Coaching, Conferences, Cost Effectiveness Analysis, Cross-Functional, Gene Therapy, Information/Data Security (InfoSec), Leadership, Manufacturing, People Management, Problem Solving Skills, Process Analysis, Process Development, Productivity Management, Project/Program Coordination, Project/Program Management, Publications, Risk Analysis, Safety/Work Safety, Strategic Planning, Team Lead/Manager, Technical Analysis, Technical Delivery, Technical Presentation, Technical Support, Writing Skills
LOCATION
Durham, NC
POSTED
30+ days ago

Location: Durham, North Carolina #onsite Novartis will not sponsor visas for this position.Novartis is unable to offer relocation support for this role: please only apply if this location is accessible for you.Role Purpose:The GT PD Downstream people manager role provides oversight in process and platform development, improvement/optimization, characterization, and tech transfer to support gene therapy programs/products under DQP. This role demonstrates strong scientific and people leadership skills with deep understanding of gene therapy process and development. Shape and develop its strategic direction and drive operational excellence in line with TRD vision and strategy. Leads and manages all project/network activities and apply scientific/technical expertise to address complex development issues and actively support TRD strategies and goals by participating in cross-functional teams. Lead scientific programs, co-ordinate interdisciplinary projects and teams. Develop long term strategies on science and technologies.Major accountabilities: Responsible for building, leading, and advocating for the GT Process Development Downstream team as well as fostering growth and providing development opportunities for team members.Technical oversights of GT PD projects.Developing plans and roadmaps for future state of GT Downstream, including improvements to ways of working and product quality.Lead teams and coach technical staff to deliver on objectives in a safe and efficient manner.Interface regularly with cross functional team members and clinical and/or commercial manufacturing units to provide support and input during development of various gene therapy programs.Maintain visibility to both process and analytical development activities and contribute to technical assessments and program decisions.Serve as strategic partner and advisor for cross-functional project teams and committees. Author, review and approve process development and related documents to ensure completeness, accuracy, consistency, and clarity.Delivers high impact, technical findings, and concepts to senior leads within the organization.Provides leadership direction, determining and developing approach to solutions by coordinating multiple resources to solve complex problems.Exhibit an exceptional degree of creativity and resourcefulness.Report and present scientific/technical work at internal/external meetings/conferences and publish in peer reviewed international scientific journals including patentsKey performance indicators: Positive customer/ business partner feedbackContributes to achievement of function objectives and strategy -Accountability for costs, quality, quantity, and timelines for all assigned tasks.Reach budget targets, adhere to agreed efficiency increase and cost effectiveness goals.Adherence to Novartis standards, in particular, quality, ethical, health, safety, and environment (HSE), and information security (ISEC) standards.Measurable contributions to the success, efficiency and productivity of the department and new programs/initiatives started and implemented.Accountability for costs, quality, quantity, and timelines for all assigned tasks.Adherence to Novartis standards, in particular, quality, ethical, health, safety, and environment (HSE), and information security (ISEC) standards.Feedback from other team members/leaders.Refer to annual individual and team objective setting.Outcome of risk analyses, process challenge meetings, audits and inspections.Measurable contributions to increasing efficiency and productivity in the work related to assigned projects.Internal and external publications/presentations invited lectures.The salary for this position is expected to range between $145,600 and $270,400 per year.The final salary offered is determined based on factors like, but not limited to, relevant skills and experience, and upon joining Novartis will be reviewed periodically. Novartis may change the published salary range based on company and market factors.Your compensation will include a performance-based cash incentive and, depending on the level of the role, eligibility to be considered for annual equity awards.US-based eligible employees will receive a comprehensive benefits package that includes health, life anddisability benefits, a 401(k) with company contribution and match, and a variety of other benefits. In addition, employees are eligible for a generous time off package including vacation, personal days, holidays and other leaves.

About the Company

N

Novartis AG

Novartis provides healthcare solutions that improve and extend people’s lives. We use science-based innovation to address some of society’s most challenging healthcare issues. We discover and develop breakthrough treatments and find new ways to deliver them to as many people as possible. Our company is focused on industry-leading divisions with innovation power and global scale: pharmaceuticals, eye care and generic medicines Novartis is headquartered in Basel, Switzerland. Novartis Group companies employ approximately 120,000 associates and its products are available in more than 180 countries around the world.

COMPANY SIZE
10,000 employees or more
INDUSTRY
Biotechnology/Pharmaceuticals
FOUNDED
1996