Adverum Biotechnologies
Adverum Biotechnologies

Associate Director of External QA (Finished Goods) (Contract)

$100 – $110 per hour

TLDR

Oversee external manufacturing operations to ensure compliance with regulatory standards and quality objectives in a fast-paced clinical-stage gene therapy environment.

What you'll do:
  • Leads and participates in cross-functional production teams, internally and externally. 

  • Engages, drives, influences, and leads product teams, internal functions, and external partners to ensure Adverum Quality, Manufacturing, financial and program requirements and milestones are met. 

  • Drive preparation and successful execution of PPQ and comparability production campaigns. 

  • Ensure all quality requirements are planned, completed, and documented in the Quality system. 

  • Lead critical investigations, develop and oversee implementation of effective CAPA. 

  • Provide strategic support and leadership for corporate initiatives, particularly regarding product supply integrity and global GMP compliance. 

  • Actively partner with cross-functional leadership to address challenges, develop solutions, and execute plans for integration with corporate systems and preparation for commercial stage support. 

  • Represents Quality in both internal and external operational forums. 

  • Leads and participates in Quality function and cross-functional teams, focusing on ensuring success in accomplishing objectives through practice of Adverum values and behaviors. 

  • Leverages Continuous Improvement tools and processes to drive efficiencies in delivery of quality product and execution of the Quality Management System. 

  • Stays abreast of evolving multi-regional regulatory requirements and develops strategies to assess and update internal quality processes accordingly. 

  • Provides support for internal and regulatory audits and inspections. 

  • Develops and implements processes and criteria to assess effectiveness of quality initiatives. 

  • Supports periodic presentation of company quality metrics for management reviews. 

  • Other duties as assigned. 

About you:
  • Bachelor’s degree in biological sciences or related field. 

  • 13+ years of progressive responsibility in the pharmaceutical industry, with demonstrated experience in Manufacturing, Quality Control, and Quality Assurance.  Experience in cold and ultra-cold chain is preferred. 

  • Expert knowledge of multi-regional regulatory requirements covering Quality systems. 

  • Ability to read, analyze, and interpret standards, procedures, or governmental regulations/guidance. 

  • Demonstrated consistent accuracy and thoroughness. Ability to apply feedback to improve performance. Monitors own work to ensure quality. 

  • Strong organizational, management and cross-functional leadership skills.  

  • Track record of effective collaboration, effectiveness in team settings, achievement of goals, and deliverables 

  • Experience applying risk management principles to decision making. 

  • Ability to write quality standards, standard operating procedures, work instructions, reports, etc. 

  • Experience with ICH, US and EU Regulatory Requirements. 

  • Previous experience presenting and responding to regulatory agency audits. 

  • Demonstrated ability to develop, coach, and mentor employees. 

  • Excellent interpersonal, verbal and written communication skills are essential in this collaborative work environment. 

  • Comfortable in a fast-paced small company environment with minimal direction and able to adjust workload based upon changing priorities. 

  • Ability to travel occasionally (US and International). 

  • Demonstrate good judgement and escalate important issues to Sr. management; experience and comfort interacting with staff at all organizational levels required. 

  • Demonstrates initiative; ability to undertake additional responsibilities and respond to situations as they arise. 

  • Ability to make independent sound decisions and independently manage priorities in alignment with department and site/global drivers. 

Adverum Biotechnologies, Inc., wholly owned subsidiary of Eli Lilly and Company, is a clinical-stage gene therapy company targeting unmet medical needs in ophthalmology and rare diseases. Adverum develops gene therapy product candidates designed to provide durable efficacy by inducing sustained expression of a therapeutic protein. Adverum’s core capabilities include clinical development, novel vector discovery and in-house manufacturing expertise, specifically in scalable process development, assay development, and current Good Manufacturing Practices quality control. 

At Adverum, Inclusion and Diversity are at our core. We believe in the power of being your authentic self.  We strive to create the space which allows for everyone in our Adverum Community to not only feel safe but encouraged to speak, learn from each other, grow in their professions and be the very best versions of themselves no matter what their age, ethnic background, gender, origin, religion or sexual orientation 

Adverum Biotechnologies is a clinical-stage company dedicated to pioneering gene therapy for prevalent ocular diseases, aiming to provide functional cures that restore vision and prevent blindness. Utilizing its proprietary intravitreal platform, Adverum is developing innovative, single-administration treatments to replace the need for frequent ocular injections, transforming the standard of care and addressing significant unmet medical needs in eye health.

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