Director, Quality Standards Salary at Azurity Pharmaceuticals Inc BETA

Working with Us Challenging. Meaningful. Life-changing. Those aren't words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You'll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams rich in diversity. Take your career farther than you thought possible. Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives. Read more: careers.bms.com/working-with-us. Position Summary This position will support the external supplier au

About the job Director, Clinical Quality Assurance Job Title: Director, Clinical Quality Assurance Job Location: Cambridge, MA, USA Job Location Type: Remote Job Contract Type: Full-time Job Seniority Level: Director Scholar Rock is a biopharmaceutical company that discovers, develops, and delivers life-changing therapies for people with serious diseases that have high unmet need. As a global leader in the biology of the transforming growth factor beta (TGF?) superfamily of cell proteins and named for the visual resemblance of a scholar rock to protein structures, the clinical-stage company is focused on advancing innovative treatments where protein growth factors are fundamental. Over the past decade, the company has created a pipeline with the potential to advance the standard of care for neuromuscular disease, cardiometabolic disorders, cancer, and other conditions where growth factor-targeted drugs can play a transformational role. Scholar Rock is the only company to show clinical

Job Description The Director of CQA-PV is the supervisor of the Clinical Quality Assurance Department with responsibilities for quality oversight of the Post Marketing Good Pharmacovigilance Practices (GPvP) and Commercial Operations that contribute to the PM PV safety data. The position is responsible for the strategy, planning, conduct and reporting of internal and external safety audits. This position is also responsible for Pharmacovigilance inspection readiness and execution. The position will also support the quality oversight of the Prescription Drug Marketing Act (PDMA) for the company Commercial product Sample Management. The role will also support the Global Head of CQA and the CQA GLP and GCP organization regarding quality oversight of safety data and related inspection readiness and execution. This position reports to the Global Head Executive Director of Clinical Quality Assurance and is a hybrid, onsite role at our Waltham, MA office. Major Responsibilities: Develop risk

IDRX is a clinical-stage biopharmaceutical company dedicated to transforming cancer care with intelligently designed precision therapies. IDRX aims to address the limitations of today's precision cancer medicines with highly potent and selective targeted therapies to stop key tumor escape mechanisms and prolong response to therapy. IDRX's lead program is IDRX-42, designed to inhibit key genetic drivers and drug-resistant mutations of KIT in gastrointestinal stromal tumor (GIST). Founded in 2021, IDRX's leadership team has extensive experience in drug development and collectively has been involved in the discovery, development, and commercialization of more than 10 approved drugs. About the role: The Associate Director/Director, GMP Quality Assurance is responsible for leading the Company's GMP Quality Assurance team, ensuring that the highest standards are met for all clinical and commercial products. Reporting to the Head of Quality, this leader will also be responsible for building t

By clicking the "Apply" button, I understand that my employment application process with Takeda will commence and that the information I provide in my application will be processed in line with Takeda's Privacy Notice and Terms of Use . I further attest that all information I submit in my employment application is true to the best of my knowledge. **Job Description** **Job Title** : Principal Archivist, Research Quality **Location** : Cambridge, MA **About the role:** The Principal Archivist is a member of the Research Quality leadership team and is responsible for the strategy, management, operation, and procedures related to archival of information, documentation, records, and other materials associated with Research activities in Takeda R&D. The responsibilities of this position encompass strategic management, efficient operation, and meticulous procedural oversight of the archival function to ensure compliance to company quality standards and global regulatory requirements. The Pri

The Director of Construction Quality Assurance leads the Citys efforts to ensure that all new buildings and major renovations are built to and perform at the highest level. This new position recognizes the critical importance that new construction t Quality Assurance, Director, Construction, Quality, Assurance, Energy

Job Description Job Description Our Mission iSeatz provides digital commerce and loyalty tech solutions that enable travel and lifestyle bookings to global customers including American Express, Expedia, and IHG Hotels. Our proprietary platform processes over $9B per year in transactions. We have a history of long-term trusted relationships and innovation that drives tangible value to our customers through a customizable, scalable, and secure platform, a global third-party marketplace, and loyalty integration. We aspire to put our customers at the heart of every decision and exceed their expectations with best-in-class solutions and business-value innovations. What you’ll do The Director of Quality Assurance reports to the Chief Technology Officer and requires strong leadership, technical expertise, and the ability to foster a culture of quality within the organization. This role is essential to ensuring the delivery of high-quality technology products that meet or exceed customer expec

Director Quality Assurance (On-site GMP) Location: Watertown, MA On-site Requirement HireMinds is seeking your expertise in Quality as an experienced Associate Director/Director of Quality Assurance to lead quality programs in a dynamic cGMP clinical-stage manufacturing environment. In this role, you'll work with an on-site presence in support of the production of cutting-edge radiopharmaceutical therapies for unmet needs in oncology. You'll work with a tight-knit biotech team with backing from pharmaceutical partners. If this sounds like an exciting opportunity to further your career, apply today or contact the HireMinds Biotech team. You'll Be Responsible For: Operational QA Support: Provide onsite QA oversight for aseptic drug product manufacturing, including drafting and reviewing batch records, releasing raw materials and finished products, and managing deviations, CAPAs, and change controls. Metrology Program Support: Develop and review IQ/OQ/PQ documentation for instruments, equ