Quality Assurance Lead Salary at Avenu BETA

The Organization What's happening at Entrada Therapeutics? Entrada is a clinical-stage biopharmaceutical company aiming to transform the lives of patients by establishing a new class of medicines that engage intracellular targets that have long been considered inaccessible. Our Endosomal Escape Vehicle (EEV™)-therapeutics are designed to enable the efficient intracellular delivery of a wide range of therapeutics into a variety of organs and tissues, resulting in an improved therapeutic index. Through this proprietary, versatile and modular approach, Entrada is advancing a robust development portfolio of RNA-, antibody- and enzyme-based programs for the potential treatment of neuromuscular, ocular, metabolic and immunological diseases, among others. Our lead oligonucleotide programs are in development for the potential treatment of people living with Duchenne who are exon 44, 45, 50 and 51 skipping amenable. Entrada has partnered to develop a clinical-stage program, VX-670, for myotonic

**Why This Role is Important to Us:** Reporting to Sr.Manager of Quality Assurance, IT QA lead is responsible for leading the testing efforts for new software applications, system integrations, and upgrades across the organization's technology platforms. This includes planning, executing, and reporting on all testing activities to ensure high-quality software releases that meet business requirements and compliance standards. This role includes overseeing a team of 5-10 offshore resources **Supervision Exercised:** No, this position does not have direct reports. **What You'll Be Doing:** + Develop comprehensive test plans, test cases, and test scripts based on business requirements, user stories, and technical specifications + Lead and coordinate testing activities, working closely with cross-functional teams including developers, business analysts, and subject matter experts to ensure seamless collaboration and successful outcomesDesign and implement automated testing frameworks and to

Job Overview: - Implement and promote use of consistent, efficient and quality processes to meet timelines and deliverables according to requirements and standard operating procedures, and assume accountability for the deliverables - Ensure compliance of operations with governing regulatory requirements - Create, maintain and assume accountability for a culture of high customer service - Nurture and sustain an environment of continuous learning- Take ownership of assigned aspects of quality reviews on projects - Compile metrics and identify quality trends - Assist in addressing periodic client quality reviews and other ad-hoc client quality findings - Prepare initial drafts of Corrective and preventive actions - Take ownership of assigned CAPAs with respect to ensuring that the actions are closed and produce documentary evidence to that effect in coordination with the project managers - Contribute to process reviews, own certain aspects of the reviews and use the results to help identi

Kayem Foods Job Title: Director, Food Safety, Quality Assurance, Environmental Health & Human Safety Kayem is a family-owned and operated craft meat business that has been making New England’s favorite franks, sausages and prepared meats in Chelsea, MA since 1909. This hands on key leader will provide strategic direction and leadership for Kayem Foods’ Food Safety Quality Systems and Food and human safety programs to promote, ensure and enhance our best-in-class policies, processes, standards, initiatives and compliance. Our Director of FSQA will provide oversight to establish all HACCP, BRC, SSOP’s, scientific testing, pre-requisite programs, formulation, testing and development as related to daily operations and will participate at all levels of R&D to collaborate on product development and process improvement. This role will serve as the subject matter expert around all regulatory requirements and provide guidance to leadership, direct team members and other internal stakeholders. S

Direct Hire Onsite - Chelmsford, MA Base salary around $155-178K w/ a 16% bonus and eligible for long-term incentive plan This will be the highest-level quality person at the site **Need someone who comes from the operations manufacturing side along with medical device experience (electro-mechanical medical devices)** PRINCIPAL RESPONSIBILITIES: Team Leadership Develops and leads the execution of the Quality Assurance (QA) strategic plan, ensuring team goals are clearly defined, aligned with business objectives, and effectively communicated to drive focus, engagement, and accountability. Enhances governance and management practices to support continuous performance improvement and delivery of QA goals. Builds strong cross-functional relationships, acting as a quality advocate and ensuring the Quality agenda is understood, valued, and embedded across the organization. Drives talent development through active coaching, mentoring, and tailored growth opportunities, ensuring a strong pipel

Overview: A leading organization is seeking an experienced Quality Assurance leader to oversee and drive quality strategy across multiple sites in the Americas. This role ensures compliance with regulatory standards (ISO 9001, ISO 13485, 21 CFR 820, etc.), and fosters a strong culture of quality and operational excellence. Key Responsibilities: Lead the Americas Quality Assurance function, aligning quality initiatives with overall business strategy and objectives. Develop and implement a comprehensive Quality Management System (QMS) across multiple sites, ensuring compliance with industry regulations and standards. Collaborate with cross-functional teams and key stakeholders to drive continuous improvement in product quality, operational processes, and customer satisfaction. Oversee multi-site QA teams, ensuring they are well-structured, highly skilled, and aligned with corporate goals. Support business development activities, including due diligence for M&A targets and integration of

The CMC QA Consultant will report to the Senior Director of CMC QA and be responsible for supporting cross functional team (i.e. PD, MSAT, CMC, Manufacturing, Regulatory Affairs etc) to confirm the appropriate quality as well as compliant controls are in place for assigned Gene Therapy programs, and working with colleagues to improve processes utilized to ensure product quality. In this role, in collaboration with key stakeholders in Technical Operations, Regulatory Affairs and extended Quality (ie. QC, Supplier Quality), you will provide Quality oversight and support to ensure clinical through commercial development lifecycle activities for drug substance and drug product meet cGMP regulatory requirements and guidelines at GTMF and/or contract manufacturing organizations (CMO). Duties/Responsibilities: Quality Assurance Lead for the cross-functional CMC Sub-Teams Provide quality oversight of process performance qualifications and associated studies Support review and approval of proce

Summary: The CMC QA Consultant will report to the Senior Director of CMC QA and be responsible for supporting cross functional team (i.e. PD, MSAT, CMC, Manufacturing, Regulatory Affairs etc) to confirm the appropriate quality as well as compliant controls are in place for assigned programs, and working with colleagues to improve processes utilized to ensure product quality. In this role, in collaboration with key stakeholders in Technical Operations, Regulatory Affairs and extended Quality (ie. QC, Supplier Quality), you will provide Quality oversight and support to ensure clinical through commercial development lifecycle activities for drug substance and drug product meet cGMP regulatory requirements and guidelines at GTMF and/or contract manufacturing organizations (CMO). Duties/Responsibilities: Quality Assurance Lead for the cross-functional CMC Sub-Teams Provide quality oversight of process performance qualifications and associated studies Support review and approval of process c