7 contracts manager jobs found

Job Description We're on a journey to advance how health happens with technologies that empower patients, support clinicians, inspire innovation, and save lives. Our mission? To create a human-centric healthcare experience powered by unified global data.It's a big challenge, but big challenges are what we do best. We're already transforming major healthcare organizations - helping them turn data into lifesaving decisions and better patient care.We want people just as dedicated as we are to improving health equity and delivering quality care across the globe. If you're excited about making healthcare more human, you've come to the right place.We're looking for a Manager, Federal Testing & Quality Assurance to help us deliver the best Health Care IT Solutions.The role includes: Contributing to the vision, strategy, planning, evaluation, design, development, and implementation of the comprehensive testing program for the Veterans Affairs project. Support testing...

Lensa is a career site that helps job seekers find great jobs in the US. We are not a staffing firm or agency. Lensa does not hire directly for these jobs, but promotes jobs on LinkedIn on behalf of its direct clients, recruitment ad agencies, and marketing partners. Lensa partners with DirectEmployers to promote this job for Mistras Group. Clicking "Apply Now" or "Read more" on Lensa redirects you to the job board/employer site. Any information collected there is subject to their terms and privacy notice. Description Major Responsibilities/Activities: Assess the implementation of the Quality Program and provide guidance on improvements. Provide the Mistras personnel with guidance in the application and implementation of the Quality Assurance Program. Contribute to the process of writing, revising and implementation of the Mistras Quality Manual, Procedures, Forms, etc. Conduct Principal Level 3 activities, and/or support for specific clients or industry (i.e....

Maryland, US Massachusetts, US New Jersey, US Illinois, US Laboratory Chemist 12749 Full-Time Public Trust No - Teleworking not available for this position $67889.77 - $113149.62 Position Description & Qualifications Position Description & Qualifications Do you love Data? Do you have a keen eye for quality? Serco has an opportunity supporting EPA where you could make an impact every day as an environmental data validation lead / quality assurance lead. This is an exciting opportunity leading an environmental laboratory data validation team. The Data Validation / Quality Assurance Lead will assist with the quality assurance, quality control, and data interpretation and validation in Chicago, IL. Serco supports the Environmental Protection Agency (EPA) where every day is Earth Day. Our skilled scientists collaborate with EPA staff at their state-of-the-art Laboratory Services and Applied Science Division (LSASD) in Chelmsford, MA, Edison, NJ, Ft....

Job Description We are seeking a dedicated Quality Assurance Document Specialist to ensure the integrity and accuracy of our documentation processes. This role involves reviewing batch records, completing records in accordance with standard operating procedures (SOPs), and managing quality documentation. The specialist will also be responsible for communicating findings to leadership. Responsibilities Review batch records regularly and ensure they are completed according to standard operating procedures. Manage and maintain quality documentation. Communicate findings and issues to leadership effectively. Qualifications Background in quality assurance. Proficiency in Microsoft Office applications. Detail-oriented with excellent handwriting skills. Ability to read and write in English. About Actalent Actalent connects passion with purpose. We help visionary companies advance their engineering and science initiatives...

Responsibilities Create and update policies and procedures for quality control. Maintain ISO certification. Develop and update General Manufacturing Policies (GMP). Manage internal and external quality audits. Establish and update testing procedures, policies, and methods. Ensure testing equipment is properly calibrated. Maintain production records and documents. Record and retain material traceability. Update disposition of quarantined materials and determine material release. Handle change request forms and maintenance. Manage customer and internal specifications. Participate in the drawdown process with the Ink Department. Ensure staff completes necessary paperwork and data entry. Oversee and maintain accuracy of all records. Essential Skills Proven experience in quality assurance and quality control. Knowledge of ISO 9001 standards. Familiarity with manufacturing...

Job Title: Quality Assurance SupervisorJob Description The Quality Assurance Supervisor is responsible for overseeing and enhancing quality control policies and procedures. This role ensures the maintenance of ISO certification and the creation and updating of General Manufacturing Policies (GMP). The supervisor will manage all quality audits and establish testing procedures, ensuring equipment is calibrated and production records are maintained. Responsibilities Create and update policies and procedures for quality control. Maintain ISO certification. Develop and update General Manufacturing Policies (GMP). Manage internal and external quality audits. Establish and update testing procedures, policies, and methods. Ensure testing equipment is properly calibrated. Maintain production records and documents. Record and retain material traceability. Update disposition of quarantined materials and determine material release....

Job Title: Quality Assurance Associate Job Description We are seeking a dedicated Quality Assurance Associate to join our team. This role involves overseeing supplier quality management programs, auditing compliance, and developing quality agreements to ensure the highest standards in our manufacturing processes. Responsibilities Establish and maintain a Supplier Quality Management Program for CMOs, CTLs, 3PLs, raw material suppliers, and packaging component suppliers. Develop and maintain critical SOPs for supplier management, including supplier qualification, auditing, issue resolution, and change control. Monitor supplier performance through quality metrics, supplier evaluations, and risk assessments. Develop and maintain a supplier qualification and requalification process to ensure ongoing compliance. Plan, coordinate, and execute supplier audits to assess compliance with cGMP, ICH, and regulatory standards. Collaborate with...