Head Of Quality Jobs

Title: Head of Quality

Location: Cambridge, MA

Reports to: Chief Operating Officer

The Role:

Vedanta Biosciences is looking for an experienced Head of Quality to lead the Quality Assurance (QA), Quality Control (QC), and Clinical Quality Assurance (CQA) functions. The ideal candidate will lead a multi-faceted team of Quality professionals and deliver phase-appropriate GXP Quality guidance for Vedanta's full roster of investigational programs. In particular, the Head of Quality should have experience leading an organization through the maturation of early-phase development into later-phase and commercial programs.

The successful candidate will oversee clinical trial and product compliance globally by managing and improving existing quality systems and ensuring appropriate controls for Vedanta's in-house cGMP manufacturing capabilities. This includes expanding the existing Quality Management System (QMS), development of documents, training of personnel, and quality oversight of Live Biotherapeutic Product (LBP) manufacturing. Vedanta uses third-party vendors for analytics and final fill/finish manufacturing; the Head of Quality will handle QA aspects of these vendors through site audits, establishment of Quality Agreements, major deviation review, and batch disposition/release. Additionally, the Head of Quality will oversee and guide QC personnel responsible for external analytical testing for Drug Substance / Drug Product release, stability, and product characterization. The Head of Quality shall manage PAI and BIMO inspection readiness and QA support of post-approval pharmacovigilance systems. Knowledge of computerized system validation and Annex 11/Part 11 is critical to success in the role.

Here's What You'll Do:

• Drive the use of strategies, technologies, resources, and processes in support of quality initiatives
• Collaborate with executive and functional leaders to ensure understanding and adherence to company and Quality Policies, Guidelines, Programs, and Systems
• Lead the expansion of the QMS, including strategic implementation of electronic systems to support internal CGMP capabilities for our LBPs
• Manage, develop, and build the Quality team and its capabilities
• Establish cooperative relationships with Contract Manufacturing Organizations, parent and affiliate organizations, and internal departments to improve overall quality
• Actively survey and share information on changing regulations and practices that relate to Vedanta's business
• Provide expertise and guidance in interpreting government regulations and guidelines (such as FDA, EMA, and ICH) as they apply to products, procedures, and practices
• Assess and make recommendations to ensure the availability of quality resources to staff the Quality efforts required to ensure both compliance with applicable regulations and support of corporate goals
• Set short-term and long-term goals that are aligned with Vedanta's corporate and quality goals
• Take an active mentorship role in developing the Quality team to best serve the business
• Ensure products, procedures, and practices meet Vedanta's goals, and all quality and regulatory standards
• Report on Key Performance Indicators and make improvements and adjustments as indicated by changes in trends
• Facilitate risk-based decision-making, highlighting best practices and approaches while maintaining a consultative and collaborative approach
• Ensure timelines are met, and costs remain within the established budgets
• Support development and maintenance of operating and capital expense budgets

Requirements:

• Experience in smaller organizations, supporting the development of novel biopharmaceutical technologies and/or products to support creative problem-solving
• A proven track record of leadership, people management, and effective interpersonal and communication skills
• Deep knowledge of cGXP requirements, with an understanding of phase-appropriate clinical and commercial expectations
• Some technical knowledge of biologics manufacturing areas, with aptitude to understand the basic science of Vedanta's production processes
• 10+ years' experience in Quality Management with several years in a biotherapeutics manufacturing setting
• Experience with FDA, QP, and EMA/MHRA inspections and audits
• BS/MS in a relevant scientific discipline (e.g., Microbiology, Biochemistry), 15+ years of relevant professional experience
• Experience directly supporting on-site production, including responsibility for product disposition
• A "can-do" attitude with a focus on team success, both within Quality and with cross-functional business partners.
• Ability to prioritize and manage through complex processes/projects

Why join Vedanta Biosciences:

Vedanta is pioneering the development of a new class of therapies that act by modulating the human microbiome. Modulation of the human microbiota holds enormous promise to treat a broad range of immune and infectious diseases in ways that are completely different to existing drug classes. Breakthrough discoveries of our scientific team in the field of mucosal immunology have led to the first rationally designed drug candidates in the microbiome field. Vedanta was founded by PureTech Health and a team of world-renowned experts in immunology and microbiology.

We invite you to explore our site to learn more about our company and how our discovery platform enables identification of bacterial consortia with drug-like properties and their manufacture to GMP standards.

Our Vision:

We are harnessing the human microbiome to enable a new drug modality based on rationally defined bacterial consortia

Vedanta is committed to equal employment opportunity and non-discrimination for all employees and qualified applicants without regard to a person's race, color, gender, age, religion, national origin, ancestry, disability, veteran status, genetic information, sexual orientation or any characteristic protected under applicable law. Vedanta will make reasonable accommodations for qualified individuals with known disabilities, in accordance with applicable law.

Vedanta Biosciences requires all employees to be fully vaccinated against COVID-19 and newly hired employees must be fully vaccinated prior to their employment start date. Vedanta Biosciences will consider accommodations for individuals who are unable to be vaccinated against COVID-19 due to a qualifying medical condition or disability or a sincerely held religious objection.