Quality Assurance Specialist Salary at Gale, A Cengage Co BETA

Type of Requisition: Regular Clearance Level Must Currently Possess: None Clearance Level Must Be Able to Obtain: Secret Suitability: Public Trust/Other Required: None Job Family: SCA Job Qualifications: Skills: Quality Assurance (QA), Quality Control (QC), Training and Development Certifications: NDT VT (Visual) - Ship Type Experience: 3 + years of related experience US Citizenship Required: Yes Job Description: Quality Assurance Representative II Seize your opportunity to make a personal impact as a Quality Assurance Representative II supporting installation and modernization of US Navy, Coast Guard, and Military Sealift Command platforms. GDIT is your place to make meaningful contributions to challenging projects and grow a rewarding career. At GDIT, people are our differentiator. As a Quality Assurance Representative II, you will help ensure today is safe and tomorrow is smarter. Our work depends on Quality Assurance Representative II joining our team to engage with the work force,

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

We are seeking a highly motivated and detail-oriented Quality Assurance Specialist to join our team. The ideal candidate will be responsible for reviewing and assisting with the development of written procedures, directives, and publications directly related to the daily functions of all Contract Field Team (CFT) sites. This role involves working closely with the Director of Quality and Program Managers to ensure the highest quality of workmanship is maintained according to standards set forth in our Quality Management System and Standard Operation Procedures. Key Responsibilities: Documentation and Procedures: Review and assist in developing written procedures, directives, and publications. Ensure compliance with quality standards and procedures. Work daily with the Director of Quality and Program Managers. Audits and Inspections: Assist with required audits, audit reports, memos, inspections, and research on safety and OSHA regulations. Develop required spreadsheets and/or databases

Division Overview: Aurobindo Pharma USA, Inc. is a generic pharmaceutical manufacturer and distributor and is a wholly owned subsidiary of Aurobindo Pharma Limited, a leading generic pharmaceutical company based in India. Headquartered in HITEC City, Hyderabad, India, founded in 1986 and becoming a public company in India in 1992. Aurobindo Pharma USA, Inc. is committed to delivering a broad portfolio of quality, affordable generic pharmaceuticals to pharmacists and patients. Aurobindo Pharma USA, Inc. adds value through superior customer service in the distribution of a broad line of generic pharmaceuticals, leveraging vertical integration and efficient controlled processes. Aurobindo has business operations in more than 125 countries around the world. Aurobindo is a global pharmaceutical company with a broad portfolio of generic drugs that includes more than 180 product families and 450 individual product packages. Aurobindo markets over 80% of the top 100 most prescribed products in

Summary See below for important information regarding this job. Additional vacancies may be filled from this announcement. Responsibilities Independently perform audits/surveillance of contractors processes to ensure customer and contractual requirements are met. Develop and implement a surveillance plan which begins with clear objectives supported by a master schedule that includes identification of contractor and sub-contractor production needs. Incorporate a thorough and detailed QA knowledge in applying various methods and techniques for investigating, analyzing, and ensuring corrective action on complex quality problems. Apply a wide range of methods directly related to the quality control/quality assurance fields such as statistical analysis, control and sampling, and quality data analysis and evaluation to determine contractor compliance. Ensure contractor compliance with all requirements related to the design, manufacturing, repair, overhaul, and modernization of a variety of i

Join Sheffield Pharmaceuticals as a Full-Time Quality Assurance Specialist in New London, CT, and be a key player in our commitment to innovation and excellence. This onsite position offers a dynamic work environment where your problem-solving skills will shine as you contribute to customer-centric projects. With a competitive pay range of $20/hr - $25/hr, this role not only allows you to advance your career but also makes a real impact on product quality and safety. Experience a relaxed yet high-performance culture that values integrity and encourages you to grow. You'll be surrounded by dedicated professionals who share a passion for delivering top-notch pharmaceutical solutions. You will be provided great benefits such as Medical, Dental, Vision, 401(k), Life Insurance, Health Savings Account, and Paid Time Off. Take the opportunity to be part of a team that champions excellence and embodies a flexible work approach while driving industry standards forward. Join us today and shape t

Job Title: QUALITY ASSURANCE SPECIALIST Medical Device manufacturer is seeking a Quality Assurance Specialist to join their growing team! Tasks will include supporting key quality assurance processes throughout the quality team and diverse departments. Ideal candidate will have experience working through SOPs, understand FDA regulations and are strong in quality documentation. Company is seeking individual's with strong time management skills, Hands on abilities and excitement for industry! Qualifications: - 3-5+ year's Experience within Quality Specialist/Quality Assurance Roles - Experience Working in Electro-Mechanical Industry or High Tolerance - Background Managing Complaints - Writing, Creating Complaints, Tracking, etc - Experience Working with CAPA's/NCRs - Skilled in Technical Writing (Creating SOPs) - Documentation Experience Top Skills Desired: Quality assurance and ISO 13485 If Interested in Learning More - Please Apply! Top Skills Details: Quality assurance, medical device

Lutheran Services Florida (LSF) envisions a world where children are safe, families are strong, and communities are vibrant. LSF is looking for a talented Quality Assurance Specialist who wants to make an impact in the lives of others. The schedule hours for this role are Non-Traditional hours! Purpose & Impact: The purpose of the Quality Assurance Specialist is to support the Children’s Board Family Resource Center (CBFRC) program goals by managing service delivery tracking systems, collecting, and analyzing data for Children’s Board of Hillsborough County performance and outcome measures. Assumes primary responsibility for the tracking of client services, volunteer services, Use of Facility partnerships, and vendors and subcontracts. Works collaboratively with all CBFRC staff, partners, vendors, and stakeholders, to identify and complete critical tasks needed to effectively plan for service delivery in the CBFRC. Leads the development and implementation of QA practices and data repor