12 QA-Quality Control jobs

TCI delivers innovative content to more than 50,000 K-12 schools across the nation via our award-winning products. As an established EdTech company, we make a difference in the lives of thousands of teachers and students every day through our History Alive! and Bring Science Alive! programs. Position Summary:  We are seeking a detail-oriented and motivated Quality Assurance Engineer to join our dynamic, small team focused on delivering exceptional educational experiences through a flexible online platform. In this role, you will collaborate with software engineers and cross-functional partners to develop and execute testing plans for our customer-facing web application, ensuring the reliability and functionality of both existing and new features. Your contributions will be pivotal in enhancing our quality assurance processes and identifying performance bottlenecks. The Job: You will be working within a distributed team of software engineers and cross-functional...

Site Name: USA - Pennsylvania - Marietta Posted Date: Sep 20 2024 Are you looking for an opportunity to manage projects, identify areas of improvement, and support safety working practices? If so, this is the job for you. As a Validation Engineer/Senior Validation Engineer, you will be responsible for the creation of Validation Strategy; preparation and execution of Installation Qualifications, Operational Qualifications, Performance Qualifications and Process Validation which are harmonized with this division’s corporate standards. This position will also be required to contribute to the development of Site Validation Master Plans. This position will support all validation activities with focus on the aseptic filling areas with qualification associated with manufacturing equipment, including autoclave, washer, tunnel, Sterilization in Place of filling vessels and cleaning validation. This role will provide YOU the opportunity to lead key activities to progress YOUR...

Site Name: USA - Pennsylvania - Marietta Posted Date: Oct 21 2024 As a QU Program Manager , you will lead the development and management of strategic areas within the Quality Unit at the Marietta Site, including but not limited to Governance, Operational Excellence, Quality Risk Management, Project Oversight, and Continuous Improvement. This role will provide YOU the opportunity to lead key activities to progress YOUR career, these responsibilities include some of the following: Leading and ensuring GPS implementation across the Quality organization. Ensure consistency of practices and tools and perform capability assessments. Maintain overview of all projects within the Quality Unit. Assist QU PMs and individuals with PMO preparation as needed. Mentor others on project planning, including financial and resource allocations, monitoring and tracking project status. Develop and track relevant project KPIs and communicate progress, risk and issue. Risk Management...

Site Name: USA - Pennsylvania - Marietta Posted Date: Oct 31 2024 The Quality Compliance Manager is responsible for compliance oversight of quality systems and quality risks at the Marietta facility to ensure compliance with GSK procedures, policies, and standards and the regulations of all markets for which Marietta manufactures product. The Quality Compliance Manager is responsible for oversight of the inspection readiness status of the site and for the internal audit and external inspection programs. This role will provide YOU the opportunity to lead key activities to progress YOUR career, these responsibilities include some of the following: Regulatory and Corporate Inspections: Act as the site regulatory expert, overseeing site compliance and conformance. Manage site inspections, lead teams to resolve audit issues, handle external partner interactions, negotiate workload conflicts, and coordinate and implement CAPA responses. Assess change controls for regulatory...

Site Name: USA - Pennsylvania - Marietta Posted Date: Oct 24 2024 Are you energized by a highly specialized technical role that leverages the latest in quality analytical technology and method development? If so, this Quality Assurance Manager role could be a great opportunity to explore. As a QA Manager, you will be responsible for b uilding and leading the Quality Assurance team that will ensure the transfer of Drug Product processes and test methods to Marietta meets GSK and GMP guidelines. You will also p rovide direct QA support of initial start-up activities (such as facility design and equipment requirements) and will w rive excellence In Quality Assurance Leadership and Management. This role will provide YOU the opportunity to lead key activities to progress YOUR career, these responsibilities include some of the following... During the project phase, the QA Team Leader will be responsible to help drive the Quality oversight for the direction of all Drug Product...

Site Name: USA - Pennsylvania - Marietta Posted Date: Dec 19 2024 Are you looking for a more technical role, where you can directly develop, validate, optimize, and maintain robust manufacturing processes? If so, this Senior Process and Validation Specialist/Process and Validation Specialist role could be an exciting opportunity to explore. As a Senior Process and Validation Specialist/Process and Validation Specialist, you will focus on supporting process efficiency, consistency, and compliance with regulatory and quality standards which involves new product introduction, technical transfers, validation lifecycle, troubleshooting, continuous improvement initiatives, and cross-functional collaboration to support the production of high-quality, safe and cost effective vaccines in line with Site, GSK, and Regulatory requirements, especially in some of the following areas: vaccine’s raw materials, buffer preparation, single use system, homogenization, complexation, formulation,...

Site Name: USA - Pennsylvania - Marietta Posted Date: Dec 19 2024 Are looking for a process and validation leadership role that allows you to leverage your technical expertise to drive quality assurance and compliance in a highly technical manufacturing environment? If so, this MSAT Team Lead role could be an exciting opportunity to explore. As an MSAT Team Lead, you will be responsible for leading a team of Process and Validation Specialists/SME’s to manage and deliver the product and project portfolio, including new product introduction and complex changes to existing products, processes and equipment technologies, to meet business demands. This role will provide YOU the opportunity to lead key activities to progress YOUR career, these responsibilities include some of the following: Develop, motivate, focus, care and lead a highly competent team of Process and Validation Specialists/SME’s to deliver projects, discharge risks, implement complex changes and to maintain...

Site Name: USA - Pennsylvania - Marietta Posted Date: Dec 9 2024 Are you looking for an opportunity to manage validation projects for computer systems cross functionally? If so, this is the job for you. The Computer Systems Validation (CSV) Engineer in the Automation Team is responsible for ensuring that all computer systems and software applications used in the automation of manufacturing processes are validated in accordance with regulatory requirements and industry standards. This role involves close collaboration with cross-functional teams, including IT, Quality Assurance, and Manufacturing, to implement and maintain validated systems that support the production of high-quality pharmaceutical products. This role will provide YOU the opportunity to lead key activities to progress YOUR career, these responsibilities include some of the following: Develop and maintain validation plans, protocols, and reports for computer systems used in automation. Execute validation...

Site Name: USA - Pennsylvania - King of Prussia, Belgium-Wavre, UK - County Durham - Barnard Castle, UK - Hertfordshire - Ware, USA - Maryland - Rockville, USA - Pennsylvania - Upper Providence Posted Date: Dec 4 2024 Job Description The Reference Material and Reagents Director is accountable for ensuring critical reagents and analytical standards are available for the GSK network. They must be of the required regulatory standards and coordination and supply to GSK sites, CMO and LOC to support end to end supply chain of products to the patient. The role will ensure long term availability and lifecycle management of reference materials for existing and new GSK products. You will ensure outsource partners are maintained, ensuring a priority service to GSK is maintained and that bulk materials are effectively supplied to the outsource partner in a timely manner, along with supporting information to maintain a secure supply of reference materials. Also, ensure GSK customer...

Site Name: USA - Pennsylvania - King of Prussia Posted Date: Dec 2 2024 As the Quality Control Data Reviewer, you will perform a technical review of analytical data for Biochemistry, Microbiology, Raw Materials and Compendial testing to support release, stability and tech transfer testing. This role will provide YOU the opportunity to lead key activities to progress YOUR career, these responsibilities include some of the following: Review and approve laboratory data using the ALCOA principles Ensure release and stability data is performed on schedule to support batch release Train other data reviewers to increase capabilities of the team Assist with sample management upon completion of data approval Support or Lead Level 1 Audits and Deviation Investigations Archive Data per local procedures Participate in regulatory audits as an SME in the data review process Identify and lead continuous improvements around the data flow process Review and/or transcribe stability...

Site Name: USA - Pennsylvania - King of Prussia, UK - County Durham - Barnard Castle, UK - Hertfordshire - Ware, USA - Maryland - Rockville, USA - Pennsylvania - Upper Providence Posted Date: Nov 26 2024 Job Description The Reference Material and Reagents Director is accountable for ensuring critical reagents and analytical standards are available for the GSK network. They must be of the required regulatory standards and coordination and supply to GSK sites, CMO and LOC to support end to end supply chain of products to the patient. The role will ensure long term availability and lifecycle management of reference materials for existing and new GSK products. You will ensure outsource partners are maintained, ensuring a priority service to GSK is maintained and that bulk materials are effectively supplied to the outsource partner in a timely manner, along with supporting information to maintain a secure supply of reference materials. Also, ensure GSK customer changes, risks...

Site Name: USA - Pennsylvania - King of Prussia, UK - County Durham - Barnard Castle, UK - Hertfordshire - Ware, USA - Maryland - Rockville, USA - Pennsylvania - Upper Providence Posted Date: Nov 26 2024 Job Description The Reference Material and Reagents Director is accountable for ensuring critical reagents and analytical standards are available for the GSK network. They must be of the required regulatory standards and coordination and supply to GSK sites, CMO and LOC to support end to end supply chain of products to the patient. The role will ensure long term availability and lifecycle management of reference materials for existing and new GSK products. You will ensure outsource partners are maintained, ensuring a priority service to GSK is maintained and that bulk materials are effectively supplied to the outsource partner in a timely manner, along with supporting information to maintain a secure supply of reference materials. Also, ensure GSK customer changes, risks...