Csa Salary at Weebly Inc BETA

**About the Role** Does the art of the deal drive your day-to-day need to succeed? Do you have a way with words thats matched only by your desire to devour new technology concepts and solutions? Are customer concerns always king in your court? If your answer to all these questions is a resounding YES, Canon Solutions America, a leader in print technology, solutions, and services, wants you to take our call. Were in need of a Senior Account Executive, Workplace Technologies & Services (WTS), who can immediately impact the selling of Canons world-class hardware and software technology-based solutions to a dedicated marketplace while solving key business challenges to promote the Future of Work. Enjoy a competitive benefits package, continuous training and education advantages, and an active account base to advance your career. You can also take advantage of a car allowance and merit-based sales achievement trips to exotic locations. So, if youre a pro at picking up on customer needs, hig

This is an exciting opportunity to lead and manage digital quality and data integrity compliance within a cutting-edge biologics manufacturing facility. You will be responsible for overseeing 2 functional teams for Digital QA and Document Management QA up to 30 team members. This is a once-in-a-lifetime Global Expat leadership opportunity within the World’s Largest biologics CMO expanding to 720 KL total mammalian cell culture manufacturing capacity with commercial monoclonal antibody, mRNA vaccine and ADC manufacturing capabilities. Your roles and responsibility will include: Provide Oversight of the newly established Data Compliance group overseeing data integrity compliance efforts consistent with GMP and site Quality policies. Overseeing the DI framework and constituent policies, procedures, tools, and checklists governing DI and Computerized System Validation (CSV) that effectively establish data risk management stewardship and accountability throughout data and system life cycle

This is an exciting opportunity to lead and manage digital quality and data integrity compliance within a cutting-edge biologics manufacturing facility. You will be responsible for overseeing 2 functional teams for Digital QA and Document Management QA up to 30 team members. This is a once-in-a-lifetime Global Expat leadership opportunity within the World’s Largest biologics CMO expanding to 720 KL total mammalian cell culture manufacturing capacity with commercial monoclonal antibody, mRNA vaccine and ADC manufacturing capabilities. Your roles and responsibility will include: Provide Oversight of the newly established Data Compliance group overseeing data integrity compliance efforts consistent with GMP and site Quality policies. Overseeing the DI framework and constituent policies, procedures, tools, and checklists governing DI and Computerized System Validation (CSV) that effectively establish data risk management stewardship and accountability throughout data and system life cycle

This is an exciting opportunity to lead and manage digital quality and data integrity compliance within a cutting-edge biologics manufacturing facility. You will be responsible for overseeing 2 functional teams for Digital QA and Document Management QA up to 30 team members. This is a once-in-a-lifetime Global Expat leadership opportunity within the World’s Largest biologics CMO expanding to 720 KL total mammalian cell culture manufacturing capacity with commercial monoclonal antibody, mRNA vaccine and ADC manufacturing capabilities. Your roles and responsibility will include: Provide Oversight of the newly established Data Compliance group overseeing data integrity compliance efforts consistent with GMP and site Quality policies. Overseeing the DI framework and constituent policies, procedures, tools, and checklists governing DI and Computerized System Validation (CSV) that effectively establish data risk management stewardship and accountability throughout data and system life cycle

This is an exciting opportunity to lead and manage digital quality and data integrity compliance within a cutting-edge biologics manufacturing facility. You will be responsible for overseeing 2 functional teams for Digital QA and Document Management QA up to 30 team members. This is a once-in-a-lifetime Global Expat leadership opportunity within the World’s Largest biologics CMO expanding to 720 KL total mammalian cell culture manufacturing capacity with commercial monoclonal antibody, mRNA vaccine and ADC manufacturing capabilities. Your roles and responsibility will include: Provide Oversight of the newly established Data Compliance group overseeing data integrity compliance efforts consistent with GMP and site Quality policies. Overseeing the DI framework and constituent policies, procedures, tools, and checklists governing DI and Computerized System Validation (CSV) that effectively establish data risk management stewardship and accountability throughout data and system life cycle

This is an exciting opportunity to lead and manage digital quality and data integrity compliance within a cutting-edge biologics manufacturing facility. You will be responsible for overseeing 2 functional teams for Digital QA and Document Management QA up to 30 team members. This is a once-in-a-lifetime Global Expat leadership opportunity within the World’s Largest biologics CMO expanding to 720 KL total mammalian cell culture manufacturing capacity with commercial monoclonal antibody, mRNA vaccine and ADC manufacturing capabilities. Your roles and responsibility will include: Provide Oversight of the newly established Data Compliance group overseeing data integrity compliance efforts consistent with GMP and site Quality policies. Overseeing the DI framework and constituent policies, procedures, tools, and checklists governing DI and Computerized System Validation (CSV) that effectively establish data risk management stewardship and accountability throughout data and system life cycle

About the job Computer Systems Validation Lead At least 10 years of experience supporting and/or performing all aspects of computer systems validation activities including development of scalable validation strategies, documents, and perform document reviews At least 7 years prior experience in computer systems validation within GMP/GxP regulated environments Proven experience developing full validation documentation and testing protocols within the various SDLC phases that is scalable and maintainable to demonstrate continuous compliance Experience with FDA 21 CFR Part 11 Experience with the validation of Enterprise systems SAP and/or MES system Preferred. Validation of Life sciences systems such as Veeva, Trackwise, Argus, Clnical, Quality systems highly desired. Broad understanding of the test management Tools, including experience and knowledge Microfocus ALM, ValGenesys etc preferred. Knowledge and experience around CSA highly preferred.

Responsibilities: Apply your professional knowledge of 21CFR Part 11 systems validation and regulatory compliance with a range of computerized systems. Perform as a project execution and thought leader to provide regulatory guidance regarding compliance with intended specifications. Engage in value-add relationships to deliver outstanding project outcomes and identifying new more optimal opportunities for processes and procedures. Share best practices, industry knowledge, and personal expertise to educate client in formal and ad hoc settings Requirements. Demonstrated capabilities in creating validation documentation, including GxP Assessments, Validation Plans, Risk Assessments, Requirements/Design/Functional Specifications, IQ/OQ/PQ Protocols, Reports, Traceability Matrix, and Standard Operating Procedures. Requirements: Experience with validating SAP, experience in previous SAP implementations. Demonstrated experience planning and scheduling validation and validation lifecycle. deli