QA Test Lead Salary at Aptus Health Inc BETA

Role Overview: A growing life sciences manufacturer seeks a QMS leader to elevate quality systems and ensure compliance to medical device and life sciences regulations. Exciting growth opportunities in a dynamic environment! Key Responsibilities: Quality Systems Management: Manage training programs to ensure regulatory compliance. Oversee the internal audit program. Supervise supplier qualification processes. Support audits and inspections, including compliance with certifications such as ISO 9001. Administer document control processes, including periodic reviews, metadata management, and quality assessments. Maintain and manage the electronic quality management system. Commissioning, Qualification, and Validation (CQV)/CSV: Review and approve CQV and CSV documentation. Maintain and oversee the validation schedule. Operational Support: Provide on-site quality assurance support. Conduct log reviews, audit trail evaluations, and business continuity testing. Assist with quality events and

Job Title: IT CSV Lead Location: Remote (Cambridge, MA) Duration: 12+ months contract JOB DESCRIPTION: IT CSV Lead JOB DESCRIPTION Our client is a small Therapeutics organization seeking a Computer Systems Validation Lead to support the overall IT Compliance and CSV processes. On a day-to-day basis your key responsibilities will be, and not limited to: · Lead and execute the validation activities for other IT Projects like and not limited to Veeva, SAS, VLMS (Validation Lifecycle Management Software), R Studio · Responsible for tracking monitoring and controlling validation processes to ensure timely delivery to meet prescheduled to releases · Provide technical expertise, interpretation, and direction in regard to computer, validation, federal regulations and other quality requirements · Work with business owners to ensure requirements specifications are defined in a clear testable format · Effectively work with cross functional teams (business owners, technical team, project manager)

SUMMARY: 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 key person will provide strategic direction and leadership for Kayem Foods' Food Safety Quality Systems and Health and human safety programs to promote, maintain and enhance our best-in-class processes, ensuring compliance with all relevant local, state and federal food regulations. This position requires an experienced leader who is a subject matter expert and requires limited direction and will report directly to the Chief Operating Officer. Kayem's Director of Food Safety and Quality assurance will provide direct leadership to all team members related to quality and food safety in all Kayem food processing facilities, have oversight to establish all HACCP, BRC,SSOP's, scientific testing, pre-requisite programs, testing and development as related to daily operations to ensure product safety, quality, and regu

Quality Engineer – Medical Device Manufacturing $110k - $130k US Citizens or Green card Holders Our client is seeking an experienced Quality Engineer to join their team and support Manufacturing Engineering and Production Sustaining efforts within a fast-paced medical device environment. In this collaborative role, you'll work closely with Operations, R&D, and other departments to ensure full compliance with the Quality Management System (QMS). Are you an experienced Quality Engineer who thrives in Operations, particularly in Design Transfer, daily manufacturing challenges, yield improvement, and scale-up projects? We want to hear from you! Key Responsibilities: Oversee quality system implementation within manufacturing processes. Provide Design Assurance Engineering support during Product Development or post-market changes. Collaborate cross-functionally to drive continuous process improvements using Quality Systems. Ensure product specifications are met and documentation is complete.

We use science to save lives, and so can you. We are currently recruiting for an Associate Director of Quality Assurance (QA) Operations to join our Quality organization. Reporting to the Head of Quality (US), this position is responsible for the quality oversight of site operations, including manufacturing, facilities, engineering, warehousing, supply chain, validation, and quality control activities. The role is onsite, based out of our Bedford, MA facility and is a key member of the US Quality Leadership Team that works closely with our UK and France teams to ensure OXB is a global leader in terms of viral vector CDMO capabilities. Your responsibilities in this role would be: Provide strategic quality oversight of GMP manufacturing and testing operations in a dynamic gene therapy manufacturing facility driving product release to support client programs. Provide quality expertise on quality management system elements, including but not limited to deviations/investigations, corrective

Hi Friends NO C2C , 1099 , No Transfer Title: QA/Test Lead Location : Boston MA Full Time •Skill: QA/Test Lead Quality Analyst In JUnits, Database Testing tools. Automation Testing. Good Knowledge on data comparison tools. Python Knowledge required. Capital Markets exposure. Jira. Experience on DevOps tools. Test plan and cases understanding. Manage project tracks for QA. Hands on exp on JUnits. Manage project/data dependencies. Provide innovative and creative solutions to problems. Coordinate with offshore team members and work cohesively with them. Team Management. Experience with Agile development methodology. Good Communication and interpersonal Skills. Shashank Chaubey Technical Recruiter 781-552-4337 Bostan MA shashank.c@syntricatetechnologies.com

COMPANY OVERVIEW AIRNA is a biotechnology company with a mission to transform lives, one RNA edit at a time. AIRNA is pioneering the discovery and development of RNA editing therapeutics to realize the therapeutic potential of base editing for patients with rare and common diseases. RNA editing modality is poised to lead the next generation of RNA therapeutics by bringing the precision of gene editing technology with a potent and safe medicine that can be conveniently re-dosed and manufactured. Our RESTORE+™ platform is based on groundbreaking research by academic co-founders Thorsten Stafforst (University of Tübingen) and Jin Billy Li (Stanford University), who were the first to elucidate a therapeutic approach for precise editing of RNA. AIRNA has received $90 million in Series A financing from world class venture capital firms, including Forbion and Arch Venture Partners, and is headquartered in Cambridge, MA with research operations in Tübingen, Germany. JOB DESCRIPTION The Directo

**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