Associate Director GMP Quality Operations

About Acadia Pharmaceuticals

Acadia is advancing breakthroughs in neuroscience to elevate life. Since our founding, we have been working at the forefront of healthcare to bring vital solutions to people who need them most. We developed and commercialized the first and only FDA-approved drug to treat hallucinations and delusions associated with Parkinson’s disease psychosis and the first and only approved drug in the United States and Canada for the treatment of Rett syndrome. Our clinical-stage development efforts are focused on Prader-Willi syndrome, Alzheimer’s disease psychosis, and multiple other programs targeting neuro-psychiatric and neuro-rare diseases. For more information, visit us at Acadia.com and follow us on LinkedIn and X.

 

Please note that this position is based in Princeton, NJ. Acadia's hybrid model requires this role to work in our office three days per week on average.

Position Summary

The Associate Director, GMP Quality Operations is responsible for support of the GMP Quality Operations department including oversight of cGMP operations performed at Contract Manufacturing Organizations (CMOs), as well as cGMP operations performed at Acadia, for all products intended for commercial and clinical (where required) use. Primary responsibilities include batch record review and batch disposition, support of Product Complaints, Annual Product Review, Continuous Process Verification (CPV), ensuring conformance to Acadia Standard Operating Procedures (SOPs) and Quality Agreements with CMOs, as well as compliance with FDA and applicable international regulations.  Participate in continuous improvement activities with respect to Acadia GMP training program, change management, deviation investigations, CAPA program, GMP audits, and similar related activities.

Primary Responsibilities

• Manages the batch disposition process for all Acadia drug product and substance production.
• May serve as a key point of contact with CMO partners and ensures integrated, coordinated activities related to cGMP production and continuous improvement.
• Leads or participates in formal risk assessment activities.
• Provides on-site quality support at CMOs as required.
• Participates in the design, implementation and management of the Acadia GMP quality management system, based on FDA and applicable international regulations.
• Ensures compliance of the Acadia GMP quality management system with FDA and applicable international quality management system regulations.
• Participates in GMP supplier audits and Acadia documentation control systems.
• Participates in the review of, and ensures conformance to, Quality Agreements with GMP contract service providers for outsourced operations.
• Provides guidance to SMEs and acts as QA lead on investigations, change management and batch record review, and establishing effective CAPA plans.
• Participates in and/or leads QA in continuous improvement of Acadia quality management systems according to GMP and current industry standards.
• Ensures adequate QA representation on all GMP commercial manufacturing, supply chain, and product development teams.
• Recommends changes to policies and establishes procedures that affect the functional area and may also have company-wide effect.
• Participates in Quality Operations functions, such as:  Material Review Board, quality board, strategic planning efforts, etc., as required by Acadia Management.
• Develops and/or contributes metrics to support product and/or process review efforts as needed.
• Other duties as assigned/required.

Education/Experience/Skills

• Bachelor’s degree in Chemistry/Biology or related life science. Targeting 8 years related and progressively responsible experience within the pharmaceutical or biopharmaceutical industry with a minimum of 4 years in a leadership role. 
• Five years in Quality Assurance strongly preferred.  Professional certifications from American Society for Quality (ASQ), or equivalent, are a strong plus.
• Demonstrated knowledge of Quality Assurance activities and International Conference on Harmonization (ICH) and FDA/EU GMP regulations as they relate to clinical trials, product development, commercial requirements and technology transfer.
• Strong problem-solving skills
• Ability to lead a cross-functional team to develop solutions to a complex problem or advance a continuous improvement or preventive action opportunity
• Experience implementing and managing quality management systems
• Demonstra