Director, QA Systems (Contract)

Adverum Biotechnologies, Inc.•Redwood City, CA

176d

About The Position

Adverum Biotechnologies, Inc., a wholly owned subsidiary of Eli Lilly and Company, is a clinical-stage company focused on developing gene therapy for prevalent ocular diseases. The Director of QA Systems is responsible for optimizing Quality systems to ensure adherence to late-stage clinical and commercial multi-regional regulatory requirements, as well as corporate quality objectives. The candidate will have demonstrated successful development, implementation, and execution of robust Quality systems and processes covering CMC, Clinical, Regulatory, and IT functions. The individual must provide strategic leadership within internal and external CMC functions, along with cross-functional leadership at Eli Lilly, ensuring a successful integration process. This includes the ability to work independently and also as an effective and engaged cross-functional leader and team member in a fast-paced environment. Strong initiative and independent follow-through are essential for this role. The ability to maintain confidentiality and to operate in the role with the highest of ethical standards and professionalism are required.

Requirements

Bachelor’s degree in biological sciences or related field.
13+ years of progressive responsibility in the pharmaceutical industry, with demonstrated experience in Quality systems.
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.

Responsibilities

Assess and optimize Quality systems and processes for CMC, Clinical, Regulatory, and IT.
Drive complete cross-functional adoption of Quality systems and ensure excellence in execution and performance of the Quality systems through active participation and leadership.
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.