QA Representative Salary at Ab Sciex Llc BETA

Rentschler Biopharma is a leading global contract development and manufacturing organization (CDMO) for biopharmaceuticals. From our headquarters in Laupheim, Germany, and our site in Milford, MA, USA, we offer end-to-end solutions, including bioprocess development and manufacturing, as well as related consulting activities such as project management and regulatory support. In Stevenage, UK, we have launched Rentschler ATMP Ltd. dedicated to cell and gene therapies. We are a family-owned company with approximately 1.400 employees from 25 nationalities. What unites us at Rentschler Biopharma, is the passion for what we do. We empower our clients to help patients with serious or rare diseases. With our dedication and expertise, we convert medical research into outstanding biopharmaceuticals. Thus, we provide an important contribution to the global availability of essential therapies. Going forward, we are expanding our team to ensure our long-term sustainable growth. Join us and be part

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.

Company: American Surgical Company Job Title: Regulatory Affairs and Quality Assurance Associate Location: Salem, MA Summary: Regulatory Affairs and Quality Assurance Associate is responsible for identifying, evaluating, and ensuring compliance with all applicable laws, regulations, and standards. The Regulatory Affairs and Quality Assurance Associate shall also conduct reviews of all and all future target markets to ensure knowledge and fulfillment of establishment registration, device licensing, surveillance, adverse event and corrective action reporting, translation, product standards, and all other requirements necessary to support import, sales, distribution, and support in all chosen distribution markets. Essential Duties and Responsibilities: Remain aware of new or updated regulations, laws, standards and other official enactments that may apply to the company. Provide detailed analysis, official recommendations, and gap analyses for new or revised standards and regulations. Man

The Quality Assurance Specialist will actively contribute to the implementation and maintenance of the Quality Systems Manual and conduct GMP compliance audits as directed. The QA Specialist will have oversight of and involvement in, GMP compliance for production of Clinical Trial Material (CTM), including work performed by Contract Manufacturing Organizations (CMOs). Provide assistance in the audit and oversight of Contract Research Organizations (CROs) as directed. The incumbent will work closely with the Director, Quality Assurance to ensure company goals and objectives are met and compliance risks are identified and communicated to senior management. This position is located in Cambridge, MA. Key Responsibilities: Conduct and maintain New Employee Quality Orientation and Quality Refresher Training with primary responsibility for the Training System including documentation. Develop and contribute to Policies and SOPs in support of the Quality Systems Manual. Review and approve Polic

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

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

Responsibilities: Provides Quality Assurance (QA) support to Devens Site and reporting Manger through quality review and approval of Investigations and Corrective Actions. Decision making of non-conformance through a deep understanding of Quality Systems Regulatory expectations. Reviews and approves Quality, Quality Control, Validation and Automation related documents Review and approve Standard Operating Procedures (SOPs). Review and approval of Validation related documentation such as risk assessments, protocols and test scripts and summary reports. Review and approval of change proposals as well as associated deliverables, ensuring the change deliverables meet external regulatory and internal WWQC guidelines and requirements. Ability to coach across different departments within the subject matter of Investigations, CAPAs, general risk assessments and Validation. Ability to self-manage and prioritize work across multiple competing deliverables, in a remote working environment. Able t

Description Looking for an opportunity to make an impact? Leidos is dedicated to making the world a safer place. This starts with helping our customers in the Defense Industry achieve their critical missions. Our dedicated Defense Group employees are solving critical challenges across the globe. At Leidos, we deliver innovative solutions through the efforts of our diverse and talented people who are dedicated to our customers’ success. We empower our teams, contribute to our communities, and operate sustainably. Everything we do is built on a commitment to do the right thing for our customers, our people, and our community. Our Mission, Vision, and Values guide the way we do business. Are you ready for your next career challenge? The Airborne Systems Business Area, part of the Defense Sector at Leidos, currently has an opening for a cleared Quality Assurance (QA) Representative to work at Hanscom AFB in Massachusetts. This is an exciting opportunity to use your experience helping the A