Quality Assurance and Qc Salary at Protec Instrument BETA

Job Title: Quality Assurance Specialist Job Description Manage QC data of multiple programs through external/third party suppliers (CDMO, CTO, etc.). Review raw data from third-party release and stability testing, perform trending for release and stability using applicable software (JMP, iStability, etc.), and draft and review QC documentation including Stability Protocols and Reports, SOPs, Material specifications, CoA templates, and other quality documents. Collaborate with Analytical Development to support method qualification, fit for use, validation, and method transfer activities. Support the reference standard program and draft and execute quality systems (e.g., OOS/OOT, Deviations, Change Controls, and CAPAs). Additional responsibilities and ad hoc projects as required. Responsibilities + Manage QC data of multiple programs through external/third party suppliers (CDMO, CTO, etc.). + Review raw data from third-party release and stability testing. + Perform trending for release a

**U.S. Citizenship Required** **No Corp to Corp** The Global Lead - Design Quality Assurance Engineer will be a multi-site leader overseeing the engineering support required for all new product development and lifecycle management projects. This position will support a global deployment of design control procedures and ensure that projects are adequately staffed to achieve required milestones. This individual will collaborate and partner with peers and senior leadership in other organizations, including Research & Development, Regulatory, Marketing, Supply Chain, and Manufacturing Operations. This role will also be required to support different aspects of the QMS, including quality systems, post-market surveillance, and supplier quality. RESPONSIBILITIES: Lead Design Assurance teams across multiple sites on product development and sustaining engineering projects of significant magnitude and scope. Provide guidance and training to staff, help identify and achieve career goals, motivate

Our pharmaceutical client here in the Woburn, MA area is growing and looking to hire a Manager/ Sr. Manager, QA to their team! This role will provide strategic direction and oversight for the management and development of the QMS to support their combination product development and commercialization! In addition, this role will contribute to the ongoing review, strategy development, and operational planning to ensure that all Quality Assurance programs. Other responsibilities include but are not limited to: Evolve Quality Systems parameters to meet requirements of various drug and device development stages. Partner with GXP Operations to assist in oversight of contract service providers. Assist Regulatory Affairs in the preparation and review of product development data for regulatory submissions. Implement pre-approval inspection readiness program. Manage individual and group workload to meet Company objectives. Write, Review, Edit and Approve Standard Operating Procedures. Write, Rev

Quality Assurance Manager Location: Woburn, MA Vaxess is a NIH and venture-funded company developing a pipeline of next-generation vaccines and therapeutics on the MIMIX platform. With only five minutes of wear-time on the skin, the self-applied MIMIX patch enables up to two weeks of sustained delivery. The platform combines high temperature stability with simplified application to dramatically alter the way that drugs are delivered. Vaxess is committed to enabling products that are not only more effective, but also more accessible to patients around the world. Responsibilities Provide strategic direction and oversight for the management and development of the Quality Management System to support combination product development and commercialization. Contribute to the ongoing review, strategy development, and operational planning to ensure that all Quality Assurance programs meet applicable regulations and standards. Evolve Quality Systems parameters to meet requirements of various dru

About the job Mailroom Quality Assurance Associate Mailroom Quality Assurance Associate needs 1+ years experience required. Mailroom Quality Assurance Associate requires: 3rd shift •Minimum of a high school diploma (or GED) is required, but advanced degree is desired. •Experience of working with teams in a collaborative environment •Must possess excellent communications skills (i.e., interpersonal, written, verbal and presentation) Mailroom Quality Assurance Associate duties: Maintains Quality Management System (QMS) programs and initiatives. •Provides critical information for audits and reviews/analyzes data and documentation. •Maintains all required documentation to meet the required security compliance standards and to meet audit control standards, Standard Operating Procedures (SOP), Forms, spreadsheets, data analytics. •Performs and documents required monthly user reviews for associates access, both data and physical and additional security requirements to meet control objectives.

Job Description Job Description Overview We are seeking a dedicated and detail-oriented Quality Assurance Specialist to join our team here at ACCC! The ideal candidate will play a crucial role in ensuring that our products meet the highest quality standards and comply with industry regulations. This position requires a strong understanding of quality management systems, FDA regulations, and CGMP practices. The Quality Assurance Specialist will be responsible for conducting inspections, analyzing data, and implementing quality assurance processes to enhance product reliability and safety. The Quality Assurance Specialist is responsible for reviewing positive and negative client feedback, phone monitoring, researching and reporting on client complaints, responding to client reviews, file reviews, and utilizing phone monitoring technology to identify innovative ways to scale call monitoring. This role will also assist in streamlining the client feedback process to reduce manual work requi

Join Our Team at KARL STORZ U.S. – Elevate Quality and Drive Continuous Improvement Are you passionate about quality and regulatory compliance in the medical device industry? Do you thrive in a leadership role, guiding teams to achieve excellence? If so, we want you to join our team as a Quality Assurance Manager at KARL STORZ, a global leader in endoscopy, medical device technology, and healthcare solutions. Why KARL STORZ? Be Part of Innovation: Drive continuous improvement and contribute to products that impact healthcare worldwide. Leadership Impact: Lead and develop a talented team, influencing quality initiatives and shaping the future of medical technology. Career Growth: With our commitment to ongoing learning, you’ll have ample opportunities to advance and expand your skill set in a dynamic environment. What you will be doing: Quality System Oversight: Ensure compliance with FDA, ISO, EN, and MDR standards, leading audits, CAPA processes, and driving quality improvement initia

Description The Airborne Systems Operations, part of the Defense Sector at Leidos, currently has multiple openings for a Quality Assurance (QA) Representative located within multiple locations including: Wright Patterson AFB in Beavercreek, OH, Eglin AFB in Pensacola, FL and Hanscom AFB in Massachusetts. This is an exciting opportunity to use your experience helping the Air Force Research Lab, Air Force Lifecycle Management Center, and other DoD missions. Your role will be to support our diverse portfolio of programs through a combination of software design and development, hardware interfacing and integration, laboratory experimentation, ground and flight testing to deploy cutting edge software and hardware solutions. Primary Responsibilities. Responsible for performing software quality assurance including requirements analysis, clarification and tracking, testing, verification and validation of autonomous core system solutions Identify a set of project-specific characteristics, appli