AMRI provides global contract research and manufacturing services to the pharmaceutical and biotechnology industries. The Manager, Quality Assurance is an integral part of the AMRI team, contributing to our success by supporting the Quality Assurance, Quality Control, and Analytical Services Divisions of the AMRI-R&D/Clinical processes at the Burlington site.
The candidate will ensure compliant phase-appropriate cGMP operations are continuously maintained across the site leading up to project turnover to commercial production. Responsibilities include supporting a partnership with the Quality unit charged with the review and management of departure investigations (i.e., root cause analysis, product impact assessments, and CAPA), GMP document review, on-floor batch review, batch disposition, and also supporting phase appropriate quality oversight during technology transfer. The incumbent will also play a vital role during regulatory agency inspections and client audits pertaining to R&D/clinical products and processes.
The Manager, Quality Assurance will interact with AMRI customers through routine production activities for the R&D business unit. The position assures that all documentation, procedures, and protocols comply with all phase-appropriate GMP, ICH, FDA, and EU guidelines. In addition, the position provides oversight of document control and implementation and enforcing compliance of all the site’s Standard Operating Procedures and FDA guidelines with a phase-appropriate mindset through training and internal audits. The position ensures that any R&D/clinical product produced by the site meets specifications for the final release of clinical materials. This includes but is not limited to method development for Process Development Projects.
The Manager of QA will work on complex issues where in-depth knowledge is required and will participate in strategic decisions for the site’s R&D/Clinical business unit operations. The Manager of QA will interact frequently with AMRI R&D/clinical customers to ensure that their needs are met guaranteeing the quality of the products and services provided. Join our talented workforce, where a commitment to excellence and a customer-focused attitude is everything. We pursue excellence because our work has the power to improve patient's lives with the pharmaceuticals we develop and manufacture.
• Establish and maintain a risk-based and scientific-based phase appropriate quality system to protect the public health and to meet AMRI’s business needs • Through a quality system approach, ensure all GMP operations are in compliance while maintaining an efficient workflow to facilitate operational excellence • Set up and establish innovative solutions for early phase pre-clinical and clinical programs to enable QbD strategies • Oversee, and be ultimately responsible for, the R&D business unit’s quality assurance program. This includes overseeing and assisting with the Company’s training and auditing programs, as well as the review of SOPs, investigations, specifications, methods, validation/ verification reports, analytical reports, and manufacturing records • Lead or assist to deliver monthly Quality Site Management Review Meetings as necessary • Along with the QA team, be responsible for the release or rejection of GMP materials for the R&D/Clinical business unit • Prepare, review, and approve external and internal reports and other documentation required by regulatory agencies, customers, or to support the quality assurance function in R&D • Identify and lead operational excellence initiatives, both in the department and companywide, which result in the overall improvement in both areas • Collaborate with appropriate cross-functional departments to create and implement global corporate standards • Partner with colleagues in other departments to increase the overall effectiveness of the Quality department and identify process improvements/ efficiencies • Assist in cultivating good customer relations that foster profitable new and repeat business for the site • Facilitate communication with customers and the site Quality department Ensure facility compliance with current good manufacturing practices and applicable regulatory guidelines for the R&D business unit
• Bachelor’s Degree in Life Sciences or related field • 8+ years of experience in the Pharmaceutical industry, with at least 5 of those years being experience in Quality • Experience in clinical quality assurance • Superior influential and negotiation skills • Solid knowledge in FDA and global regulations, especially the cGMP for the 21st-century initiatives • The flexibility to adapt to changing circumstances and manage activities to meet the needs of the business while maintaining a focus on quality • Demonstrated ability to manage across departments to maximize productivity, reduce costs and increase profitability through leadership Preferred • Experience in aseptic fill/ finish and sterility assurance programs • Leadership experiences – integrity, experience with operational excellence focus on strategy All interested applicants must apply online.
AMRI is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, or protected veteran status and will not be discriminated against on the basis of disability.
Employer will assist with relocation costs.
Internal Number: 2000178
AMRI is a global contract research and manufacturing organization that has been working with the pharmaceutical and biotechnology industries to improve patient outcomes and quality of life. With locations in North America, Europe and Asia, we provide a complete suite of capabilities in drug discovery, development and manufacturing. We’ve got it down to an exact science.
Working at AMRI, you are part of something greater. As a global company addressing a range of pharmaceutical needs, our reach is expansive. But more personally, it is about making a real, human difference on an individual level. By doing your best work, by solving the toughest challenges – whether they are in the lab, on the manufacturing line, or in a spreadsheet – your work matters