Quality Head Salary at Ensoma BETA

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

nChroma Bio is a pioneering biotechnology company redefining the future of in vivo targeted genetic medicine to treat a wide array of diseases and bring cures to patients. The company's integrated product engine tackles significant limitations of existing genetic medicine approaches by enabling safe, precise and specific in vivo delivery. nChroma's near clinical-stage development candidate, CRMA-1001, is a liver-targeted therapy in development as a potential functional cure for chronic hepatitis B and hepatitis D that leverages the power of epigenetics, nature's innate mechanism for gene regulation. Guided by a world-class team at the forefront of genetic medicine, founded by renowned pioneers in the field, and supported by top-tier investors, the company is uniquely positioned to deliver groundbreaking therapies with programmable tissue specificity, unlocking highly potent, durable and targeted gene regulation for the liver and beyond. We're building a culture and organization to supp

Company Overview Rhythm is a global, commercial-stage biopharmaceutical company committed to transforming the lives of patients and their families living with rare neuroendocrine diseases. We develop medicines for previously untreatable or undertreated diseases and provide meaningful support for healthcare providers and patients and their families. We recognize the courage it takes for patients and their caregivers to begin their journey of advocacy to find the answers they need. Their courage inspires us to challenge convention, ask bold questions and seek answers for them. Every day, we strive for excellence through our willingness to adapt, learn, and our tenacity to overcome barriers, together. Opportunity Overview The Quality Control Manager is responsible for oversight of testing performed at Rhythm's contract sites to support the manufacturing and testing of Drug Substance and Drug Product. The qualified candidate will review testing conducted at CMO analytical laboratories and

Get AI-powered advice on this job and more exclusive features. Were in a unique point in time where the demand from decarbonization and AI data centers have required the world to scale energy infrastructure at rates never seen before in the history of humanity. Luminous Robotics, Inc. addresses this generational problem through flexible, physical AI robot fleets for construction and operations of solar energy infrastructure. We are a fast moving startup having established ourselves as a leader in solar automation. Within the past 12 months, Luminous has developed three generations to LUMI robots and brought online clean energy for thousands of homes in the U.S. the company is now scaling into large scale commercial fleet deployments. We're looking for an experienced leader to oversee the manufacturing of fleets of LUMI robots globally. What you'll do: Build & Scale Manufacturing Operations Design and implement scalable manufacturing systems to support low-volume prototyping through hig

Location: This role is based in the Lexington, MA area with a hybrid schedule of four days on-site and one day remote. We are looking for an experienced Senior Director of Quality Assurance to join a dynamic team. Reporting directly to the VP and Head of Quality, this role will be instrumental in developing, overseeing, and maintaining compliance standards across key third-party partnerships and within the organization’s internal Quality systems. This position holds primary responsibility for ensuring adherence to GMP protocols supporting product manufacturing and distribution, while also overseeing batch disposition processes for both clinical and commercial products. Key Responsibilities: Oversee the GMP Quality Assurance team to maintain quality and compliance standards. Develop and implement Quality objectives, managing risk and ensuring cross-functional compliance. Ensure quality control for manufacturing and distribution across clinical and commercial products. Manage compliance

Global Head of Quality Assurance, Managing Director Who we are looking for We are seeking a Global Head of Quality Assurance to lead the strategic direction and operational excellence of QA across the State Street Alpha and Charles River Development Platform. This individual will play a pivotal role in ensuring consistent quality standards while optimizing for regional market requirements and regulatory compliance. The ideal candidate combines deep technical expertise in modern QA methodologies with strong leadership skills and an understanding of global financial markets and regulatory landscapes. This is an opportunity to influence the evolution of our platform while fostering innovation and collaboration across global QA teams. This role will report directly to the Chief Technology Officer. What you will be responsible for Strategic Leadership - Architect and implement a comprehensive QA strategy aligned with the organization's global expansion and platform sophistication. - Drive m

Receive and review customer requests for product returns, evaluate eligibility based on company policies, and generate RMA numbers for approved returns Administer and process RMAs from all customers as directed by management. Provide prompt and helpful assistance to customers inquiring about the RMA process, status of returns, and product replacement or refund options. Guide a team of Engineers in failure analysis of customer returns and technical report writing. Interface with external customers and Applications Engineering on customer facing issues. Data mining, data reporting and report publishing specific to RMA performance metrics including PPM and cycle time to closure Work with factory quality and manufacturing teams to drive corrective and preventive action for external product related issues Coordinate objectives with production procedures in cooperation with other managers and department heads to maximize product quality and minimize costs. Bachelors Degree in a technical dis

Description As a Dunkin' franchisee, we are committed to our employees as much as we are committed to our customers. We value hardworking and enthusiastic employees and we make it a priority to ensure their success. The Shift Leader will be responsible for coaching Crew Members throughout their shift to execute operational Brand standards and deliver a great and friendly guest experience. They set goals, provide job assignments, and motivate others, celebrating successes and providing timely feedback. Come work and energize your day. Encounter business professionals and busy travelers heading into Boston, New York, and beyond during their morning commute. Be the reason your services leads to our customers' brighter day. We look forward for you to join our team. Benefits of working for a Dunkin' franchisee: Competitive wages Awesome team-oriented environment Lots of potential for growth within the company for those who work hard Health & Dental Insurance Compensation: Starting at $16.50