1 QA Specialist Salary at Web Industries BETA

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

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

Our client, a leader in the pharmaceutical industry, is seeking a Pharmaceutical QA Specialist to join their team. As a QA Specialist, you will be part of the Quality Assurance department supporting various manufacturing teams. The ideal candidate will have strong communication skills, a proactive mindset, and the ability to work collaboratively, which will align successfully in the organization. Job Title: Pharmaceutical QA Specialist Location: Cambridge, MA Pay Range: $50-55 per hour What's the Job? Execute all activities following quality and regulatory standards and procedures. Provide on-the-floor support to manufacturing activities. Review manufacturing batch records for completeness and compliance with cGMPs. Ownership of the following quality systems: Change Control, CAPAs, Deviations, and Self inspection auditing, QA reporting and approval of GMP documentation. Review and approve Standard Operating Procedures, logbooks and QC data. Assist in the coordination of work for the QA

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.

Quality Assurance (QA) Specialist Job Category: Consulting Time Type: Full time Minimum Clearance Required to Start: Secret Employee Type: Regular Percentage of Travel Required: Up to 10% Type of Travel: Continental US * * * What you'll get to do: Serves as a Quality Assurance (QA) Specialist who will be responsible for activities associated with delivery of customer-defined systems and software projects; basic responsibilities include: Develop, evaluate, and implement quality management processes and standards to ensure compliance with organizational standards and governmental regulatory requirements; work with customer quality management representatives to seamlessly design, integrate, and implement quality assurance practices to support achievement of program and customer goals and objectives. Develop and implement a Quality Control Program. Conduct quality audits and implement preventive/corrective actions. Document validation procedures and technical reports; assist with establish

General Summary *Evening Shift* *Overnight Shift also available* The Sterile Processing Quality Assurance Specialist (QA) is responsible for ensuring the accuracy and proper assembly of instrument trays according to pick sheets. This role includes verifying instrument placement, checking for good working order, and preparing trays for processing. The QA specialist provides immediate feedback and coaching, documents data in provided software, and identifies discrepancies/errors in count sheets. Additionally, the QA specialist may assist in developing, recommending, and implementing educational needs, internal standards, policies, and procedures to improve the quality and effectiveness of patient care and sterile processing. Values Statement The Sterile Processing Quality Assurance Specialist embodies the hospital’s core values in all interactions with patients, families, and colleagues. Duties Notice The following statements describe the essential duties of the person assigned to this j