Director, Quality Improvement Salary at Bridgewaybhs.Org BETA

Job Description Job Description Director of Quality Assurance $170,000 - $180,000 + Bonus Global Manufacturing and Distribution Company Excellent opportunity to join a well-established and growth oriented privately held Global Manufacturing and Distribution company. Company is seeking an experienced Quality Assurance professional with demonstrated leadership skills and sound technical knowledge. In this role you will be part of the leadership team and drive all the quality and compliance related activities. This role will supervise a team and oversee the development, implementation, and maintenance of the Quality Systems and Procedures. You will also be responsible for fostering strong relationships with customers and addressing any concerns they may have. KEY QUALIFICATIONS: Bachelor's degree in related field / master's degree a plus 10-15 years of progressive experience in Quality Assurance in a Manufacturing environment Proven experience leading, training, and managing a QA team and

At Eisai, satisfying unmet medical needs and increasing the benefits healthcare provides to patients, their families, and caregivers is Eisai's human health care (hhc) mission. We're a growing pharmaceutical company that is breaking through in neurology and oncology, with a strong emphasis on research and development. Our history includes the development of many innovative medicines, notably the discovery of the world's most widely-used treatment for Alzheimer's disease. As we continue to expand, we are seeking highly-motivated individuals who want to work in a fast-paced environment and make a difference. If this is your profile, we want to hear from you. Job Summary The Associate Director, GCP Quality Assurance works within the Global Clinical Quality team to conduct GCP compliance activities at Eisai, at our CROs and Investigator Sites, and leading GCP audits and inspection readiness. This position is responsible for ensuring high quality execution of clinical trials from first in h

Reports to: Director, GMP Quality Assurance Location: Princeton, NJ (hybrid) This role is responsible for providing GMP QA expertise, oversight, and auditing support of contract manufacturing organizations of small molecule, oral dosage formulations. Additionally, this role supports PMV’s GxP procedures program, document control, and training activities, utilizing an electronic document management system. Responsibilities Support GMP QA activities spanning across CMC (Chemistry, Manufacturing & Controls) for drug substance, drug product, and clinical trial material, for all outsourced GMP activities. Ensure all API, drug product and packaged and labelled investigational material meet GMP regulations, as applicable to phase of development, and are released in a timely manner. Collaborate with CMC, Clinical Supplies Management, Regulatory Affairs, and other departments to resolve quality issues and implement process improvements. Review and approve GMP-related documents, including master

Our client is actively looking for a Director of Quality Control. This is an on-site position in Cranbury NJ. You should apply if you have: 15+ years of QC experience in pharma/biopharma environment Experience with sterile products Experience overseeing/building out QC labs Previous Director experience

Director Quality Assurance, G-III Warehouses Profile :The Director Quality Assurance is responsible for quality assurance operations at G-III warehouse and 3PL facilities, sampling incoming product to ensure vendors and manufacturers are following quality standards for shipping, packing, labeling, and production. Based in New Jersey, this role focuses on implementing and maintaining quality assurance processes within warehouse environments, addressing quality issues with overseas Quality Control team, and fostering a proactive culture of accountability and improvement .The Director Quality Assurance, G-III – Warehouses will play a critical role in bridging communication between warehouse operations, overseas Quality Control, production teams and vendors to ensure seamless quality control procedures. This role requires strong knowledge of Apparel product QC or QA and process, strong communication skills, analytics skills, and the ability to influence and build trust across cross functio

Job Description Job Description About Us: Callen-Lorde is the global leader in LGBTQ+ healthcare. Since the days of Stonewall, we have been transforming lives in LGBTQ+ communities through excellent comprehensive care, provided free of judgment and regardless of ability to pay. In addition, we are continuously pioneering research, advocacy and education to drive positive change around the world, because we believe healthcare is a human right. Our Mission: Callen-Lorde Community Health Center provides sensitive, quality health care and related services targeted to New York’s lesbian, gay, bisexual, and transgender communities — in all their diversity — regardless of ability to pay. To further this mission, Callen-Lorde promotes health education and wellness, and advocates for LGBTQ+ health issues. About the Role: As the Director of Quality Improvement, you will play a critical role in ensuring the highest standards of care and operational efficiency at Callen-Lorde. You will lead the de

DIRECTOR. QUALITY IMPROVEMENT Job Details Job Location Callen-Lorde Community Health Center - Manhattan - New York, NY Position Type Full Time Education Level 4 Year Degree Salary Range $120,000.00 - $140,000.00 Salary/year Job Shift Any Job Category Health Care Description About Us: Callen-Lorde is the global leader in LGBTQ+ healthcare. Since the days of Stonewall, we have been transforming lives in LGBTQ+ communities through excellent comprehensive care, provided free of judgment and regardless of ability to pay. In addition, we are continuously pioneering research, advocacy and education to drive positive change around the world, because we believe healthcare is a human right. Our Mission: Callen-Lorde Community Health Center provides sensitive, quality health care and related services targeted to New Yorks lesbian, gay, bisexual, and transgender communities in all their diversity regardless of ability to pay. To further this mission, Callen-Lorde promotes health education and well

Job Summary Director, US HEOR & RWE - Field, will develop on-going professional relationships with healthcare decision makers, HEOR & RWE investigators, and public and private payers and policy makers who have an evidence-based medicine and patient population focus as they relate to Company's products and disease states. The candidate in this position will provide HEOR & RWE presentations, clinical presentations as necessary, conduct collaborative research, and enter into evidence-based medicine discussions with healthcare providers, RWE researchers, managed markets medical and pharmacy directors, quality improvement specialists, integrated delivery networks, and managed care formulary decision makers and consultant pharmacists, state Medicaid and Medicare decision makers, guideline developers and others. Responsibilities Identify and interface with regional and national HEOR & RWE experts and organizations, profile data sources and organizations who conduct real world outcomes researc