Principal Technical Lead, External Manufacturing - Drug Substance

About Abb Vie Abb Vie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about Abb Vie, please visit us at  Follow @abbvie on Linked In, Facebook, Instagram, X and You Tube.

This role will provide technical oversight for our external manufacturing partners which encompasses drug substance and intermediate manufacturing. The Technical Lead will serve as the primary technical interface between the company and its contract manufacturing organizations (CMOs/CDMOs), ensuring manufacturing processesremainrobust,reproducible, compliant, and capable of consistently delivering product that meetestablishedquality and supply requirements.

The incumbent will provide end-to-end technical stewardship of externally manufactured processes and work cross functionally with Quality, Regulatory, External Manufacturing, Supply Chain and Procurement.

• Serve as the primary technical representative to external manufacturing partners for assigned products and processes.
• Maintain detailed understanding of manufacturing processes, critical process parameters, critical quality attributes, process controls, equipmentcapabilitiesand process performance.
• Review manufacturing performance andidentifyprocess trends, risks, variability,and opportunities for improvement.
• Provide technical leadership for manufacturing deviations, investigations, root-cause analysis, CAPAs, and process related troubleshooting.
• Asses the technical impact of manufacturing changes, including equipment, raw materials,process parameters, scale, facilities, and manufacturing strategy.
• Lead or support technology transfers, process scale-up,process validation (PPQ),continued process verification (CPV), and introduction of processes to new manufacturing sites.
• Provide technical input to change controls,regulatory submissions, validation strategies, comparability assessments, and product lifecycle management.
• Partner with Quality to ensure external manufacturing operations maintain appropriate technical and GMP standards.
• Work with Supply Chain and External Manufacturing toidentifyand mitigate technical risks that could affect product supply.
• Lead technical governance discussions with CMOs/CDMOsand ensure technical issues are appropriately escalated and resolved.
• Develop andmonitorprocess performance metrics and communicate manufacturing performance, technical risks, and improvement opportunities to internal stakeholders.
• Drive process robustness, manufacturing efficiency,yield improvement, cycle-time reduction, and other continuous improvement initiatives.
• Support regulatory inspections and health-authority inquiries related to externally manufactured drug substances.
• Make significant contributions to projectteamthroughlab based, or other work environments, activities, as needed.

• BS or equivalent education and extensive, typically 14+ years of experience; MS or equivalent education with typically 12+ years of experience;
  PhD with typically 6+ years of experience in area or scientific area of discipline.
• Demonstrated experience with GMP drug-substance manufacturing, process characterization, and validation, deviations/investigations, technology transfer, change control, process monitoring, and CMO/CDMO management is highly preferred.
• Comfortability in making technical decisions and influencing external partners and senior internal stakeholders without direct organizational authority.

• The compensation range described below is the range of possible base pay compensation that the Company believes ingood faith it will pay for this role at the timeof this posting based on the job grade for this position.
  
  Individual compensation paid within this range will depend on many factors including geographic location, andwemayultimatelypaymore or less than the posted range. This range may bemodifiedin thefuture.

• We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick),medical/dental/vision insurance and 401(k) to eligible employees.

• This job is eligible toparticipatein our long-term incentive programs.

Note:

No amount of payis considered to bewages or compensation until such…