Vice President, Quality Assurance Salary at Health Concepts BETA

When you join the growing BILH team, you're not just taking a job, you're making a difference in people's lives. The Director, Revenue Finance and Reimbursement, will be a core member of the Revenue Finance leadership team of Beth Israel Lahey Health (BILH). BILH is a new integrated health system with ~$6 billion in revenues and includes academic medical centers, acute and specialty hospitals, outpatient facilities, physician groups, performance networks, and community partners. As part of the leadership team, the Director will assist the VP and AVP to integrate BILH's six separate revenue valuation and reimbursement units to form a unified, enterprise-level department aligned around shared goals and a commitment to: (1)Deliver high quality net revenue valuation and related finance models based on transparent and efficient methodologies; (2)Produce data and analytics that deliver actionable business insights to BILH hospital, physician, and system leaders; (3)Provide strategic solution

Title: Vice President - MEP Reports To: RVP Department: Engineering Location: Charlestown - Hybrid 3-days in office Position Summary: Are you an experienced and forward-thinking engineer looking for an exciting opportunity to lead and shape MEP projects in one of the most vibrant cities in the U.S.? We are seeking an MEP VP to join our client's team in their Boston, MA Office. As an MEP VP, you will be at the forefront of projects, ensuring their successful execution, maintaining the highest quality standards, and fostering a dynamic work environment. Benefits Varied Projects and Strong Backlog Hybrid remote in-office Schedule Commuter Transit and Parking Benefit Program Competitive Compensation Package Gym Reimbursement Tuition Reimbursement Program Professional Development and Training Professional Certification Incentive Programs Medical Insurance including Prescription Drug Coverage Dental Insurance Life Insurance and Accidental Death and Dismemberment Coverage Supplemental Life In

Seaport Therapeutics is seeking an experienced Associate Director, QA CMC to manage GMP quality assurance activities supporting clinical development programs, ensuring compliance with Good Manufacturing Practice (GMP), regulatory requirements, and company policies. This role is instrumental in supporting clinical trials, advancing the development of innovative products, and maintaining a culture of quality across the organization. This position requires a presence in the Seaport area of Boston, with a strong preference for being onsite 3 - 4 days per week to foster collaboration and effective leadership as the Quality function is established. The role will report to the VP, Head of Quality. Seaport Therapeutics has a proven strategy of advancing clinically validated mechanisms previously held back by limitations that are overcome with its proprietary GlyphTM technology platform. All the therapeutic candidates in its pipeline of first and best-in-class medicines are based on the Glyph p

Why this role is important to us The SOC2 & Risk Program Lead will play an important role in Alpha Data Services, responsible for managing the day-to-day engagement with the external auditor and internal process/control owners to deliver an annual SOC2 report. This role will also support the execution of other risk programs including but not limited to the Risk & Control Self-Assessment (RCSA), Control Assurance, and governance reporting. The SOC2 & Risk Program Lead will work closely with business leaders, ERM, and Compliance. Seeking professionals with 5+ years of experience in operational risk, compliance, audit, or managing risk in a direct business role. What you will be responsible for As a SOC2 & ADS Risk Program Lead you will Support the business and its external auditor in initial planning, walk-throughs and testing of SOC2 controls to ensure an effective and efficient process, problem assessment / resolution as needed, and be accountable for the successful delivery of the ann

Job Description Who we are looking for Global Treasury IT is currently seeking a senior functional expert for the Finastra Summit application who will be responsible for delivering functional changes to support our technology architecture roadmap and new business growth. The successful candidate will be involved in all levels of the software development cycle from requirements definition, design/development, and system test and quality assurance. The candidate needs to have a strong understanding for the Finastra Summit application functionality and what we can leverage or not in order to deliver solutions to the business. The candidate will also have strong business and technology acumen, a keen ability to build partnerships and foster close collaboration, and ability to drive solutions with various IT vendors, market service providers, and internal partners. What you will be responsible for As a Summit Application Functional Analyst you will Implement VOLCKER Regulatory Reporting Eng

Overview: Reporting directly to the Vice President of Claims, the Director will oversee our MA and NH casualty and medical claim operations. The Director will have oversight of four casualty and two medical teams and will ensure that claims are handled in a timely and efficient manner. You will be expected to manage litigation activities, 93A process and stay current with changes in the industry that effect our claims operation. The Casualty Claims Director is a key part of the executive team at Plymouth Rock. In this role, you will brief top executives (CCO and CEO) on emerging claims activity, industry trends and large losses. Your input will directly affect not only day-to-day operations, but also the strategic planning for the claims department and Plymouth Rock Auto operations. Our organizational structure and lack of red tape allows the Director to be highly influential and impactful. You will drive the direction and will be a key contributor to the results of our entire operatio

Overview: Lead the Americas Quality Assurance organization, providing long-term strategic direction with the aim of supporting the Waters business in achieving the highest levels of corporate growth, product quality, business process quality/efficiency, operational excellence and customer satisfaction, while meeting regulatory needs, through ensuring that: The Quality Assurance organization within the Americas is aligned to the Waters business and collaborates effectively to support the achievement of Waters long-term strategy and business goals The Global Quality Assurance Strategy is developed and implemented to support high levels of internal and external customer satisfaction through delivery of quality products and an effective and efficient service to the business A strong, globally-consistent culture of Quality is developed and maintained throughout Americas to support increasing inclusion of all Waters staff in supporting customer satisfaction There is ongoing development, impl

About us: Ascidian is redefining the treatment of disease by rewriting RNA. Ascidian Therapeutics was founded to rewrite RNA by editing and replacing human exons. We were inspired by ocean creatures, called Ascidians, who are primordial ancestors of vertebrates. To grow from larvae to adults, ascidians re-engineer their transcriptome through RNA editing via trans-splicing and alternative splicing. In our Brighton/Boston labs, RNA biology meets today's cutting-edge genomics, computational biology, and deep-sequencing technologies to create a new class of medicines that address the underlying causes of disease. We welcome you to come join our vibrant team and help us lead the way into a new gene therapy era. Who are we looking for? As a key member of the executive team, the Senior Vice President (SVP) of Regulatory Affairs, and Quality will play a pivotal leadership role in leading our regulatory affairs and quality assurance function with distinction, integrity, and strategic foresight.