This role will be responsible for leading the GMP QA strategy for both early and late-stage clinical studies. Provide QA oversight of method development, qualification, tech transfer, and validation for Drug Substance and Drug Product conducted at external labs and vendors. Coordinate Quality Events...
Reporting to the Director, QA Drug Product, the Associate Director, QA Operations is responsible for leading the quality and compliance readiness for a state-of-the-art Drug Product (Fill Finish) cGMP manufacturing facility. The Associate Director will play a crucial role in establishing the operati...
Clinical QA Contractor (Associate Director/Director Level). Clinical QA Contractor (AD/Director level). Director Quality Assurance and will be based in Lexington, MA. ...
This role will be responsible for leading the GMP QA strategy for both early and late-stage clinical studies. Provide QA oversight of method development, qualification, tech transfer, and validation for Drug Substance and Drug Product conducted at external labs and vendors. Coordinate Quality Events...
This role will be responsible for leading the GMP QA strategy for both early and late-stage clinical studies. Provide QA oversight of method development, qualification, tech transfer, and validation for Drug Substance and Drug Product conducted at external labs and vendors. Coordinate Quality Events...
This position will require up to 20% travel, domestic and international and report to the Director, Research & Clinical Development Quality Assurance (R&CD QA). Liaison and coordination of audits, hosting of regular meetings with Procurement leaders at comparable Associate Director/ Director level. ...
Anticipate Quality and regulatory needs and adjust QA input to efficiently and effectively drive / support deliverables. Leverage technical expertise and experiences across QA to resolve critical challenges; ensure effective communication and escalation where needed. ...
The Director will be responsible for the program level QA oversight of clinical studies. This position reports to the Senior Director, Quality Operations within Research & Clinical Development Quality Assurance (R&CD QA). Proactively provides GXP QA support and guidance to the Clinical Trial teams b...
Veeva is looking for a QA Director who has an automation-first mindset to grow and lead our QA team for Digital Trials Platform. You will be leading a team of QA and Automation engineers across US and India and working with Development Managers and Product Managers across multiple teams owning all a...
The Assistant Program Director for ACCS Quality Assurance, in coordination with the Program Directors, must provide clinical team support, assessments, determine treatment planning and continually ensure individual's safety through support and teaching. ...
Responsible for oversight and training of Complaint Analysts I, II and III including assignment of complaint related tasks. Provides investigational direction, investigational plan design, direction on investigation execution and review of results to Analysts I, II and III. ...
Our QA lab has a rich history of establishing various testing methods over the past decades. By integrating the expertise of our longstanding lab practices with the enthusiasm and knowledge of co-op students, we aim to establish a cutting-edge QA environment that sets new industry standards and ensu...
The ideal candidate will have a strong background in aerospace engineering, quality assurance principles, and manufacturing processes. Regularly interface with Program Management, Engineering, Operations, and Customers to ensure understanding, documentation, flow-down, and implementation of CPI Rada...
Reporting to the Corporate VP QA/RA, the Global QA/RA Systems Manager is responsible for providing leadership, planning, project coordination, and management to develop a cost-effective electronic Quality Management Systems (eQMS) and harmonized QA/RA information systems while concurrently facilitat...
Lead test strategy, balancing priorities such as test coverage, test quality, competing demands, and project schedule. Identify systemic problems, inefficiencies, risks, and opportunities for improvement; work with workstream leads and vendor to develop and implement plans to address. Work with work...
RBW is partnering with an innovative Biopharma in their search for a Site Head of Quality. The candidate will report directly to the executive team, and this role will be responsible for oversight of the QMS, as well as CAPAs, document control, product complaints, etc. ...
Are you ready to take on a leadership role and make a significant impact on the Quality Function within Operations? Look no further! We are currently seeking a dynamic and experienced Senior Manager to lead our Quality team. As the Senior Manager of Quality, you will be responsible for the effective...
QA Lead Technical Operations, Projects. Provides Quality Assurance (QA) support to Devens Site and reporting Manger through quality review and. ...
Albion Rye Associates are partnered with one of the fastest growing US Biotech's with a rich Clinical pipeline across various indications to recruit a Director / Snr Director, Clinical Quality Assurance. Director, Clinical Quality Assurance. Leading a small team, you will be part of the Quality Assu...
SGA), is searching for an Senior Manager, Medical Device QA for FULL TIME assignment with one of our premier Pharmaceutical Services clients in Billerica, MA . Responsible for all aspects of QA for Medical Device and combination products manufactured either on site or at third party contract man...
If you're ready to join a dynamic team dedicated to excellence in food quality assurance, apply now to become our newest Food Quality Assurance Manager! Together, we'll continue to raise the bar for quality and safety in the food industry. As the Food Quality Assurance Manager, you will play a pivot...
This leader supports the delivery of high-quality programming by establishing protocols and guidelines; conducting regular program audits and assessments; providing support to program directors to improve program quality; and staying current on best practices and innovations. Massachusetts Office of...
The Manager, Quality Control has responsibility for actively overseeing cGMP quality control activities associated with development and commercialization of the company’s small-molecule assets. This function operates within a virtual (100% outsourced) business model and the incumbent will be r...
Minimum of three years in Human Services in the areas of Quality Management or Residential/Day Program Management. Proficient with Microsoft Office. The Director of QI (DQI) is responsible for ensuring that all. Oversee the HCSIS documentation of the agency by reviewing daily alerts in system and no...