Senior Technical Lead

Maximum Salary (US): 151000Minimum Salary (US): 98000Job SummaryExperience with Manufacturing Applications, especially IT tools like Power Platform or equivalent toolsAbility to manage multiple dispositions for multiple J&J Managers with limited supervision.Ability to manage end-end from Inventory, assessments, remediations to final dispositions; 7-10 years of relevant experience; has experience of leading/advising Junior and Senior resources. Specifically in the Pharmaceutical, biotechnology, or medical device industry.Experience in FDA and/or Global regulated environment with good understanding of GxP standards and Risk based validation; Define and implement Risk based validation activities.Experience in writing and executing documentation for all aspects of the validation deliverables (etc. Requirements, Compliance/validation Plans, test protocols, Test Summary reports and Compliance/Validation Reports, SOPs/WIs). Experience in reviewing system test and user acceptance test scripts, Traceability matrix and Design Specs Experience in QA Methodologies, designing, reviewing and approving Test Plans, systems and UAT test scripts and Test procedures.Strong verbal and written communication skills.Ability to work as a team player, lead a team or accomplish tasks without supervision.Ability to work with remote teams and support several changes/projects simultaneously.Ability to provide Validation guidance, timely reviews, and escalations to TQ managementExperience with validation deliverables review, including testing artifacts (e.g., test scripts).Knowledge of Agile Tools (e.g., Jira, Xray, qTest, Service Now etc.).Ability to build collaborative partnerships, work as a team player, including timely escalations to TQ manager.Ability to work with dispersed/remote teams and support several systems simultaneously. Key ResponsibilitiesExperience with Manufacturing Applications, especially IT tools like Power Platform or equivalent toolsAbility to manage multiple dispositions for multiple J&J Managers with limited supervision.Ability to manage end-end from Inventory, assessments, remediations to final dispositions; 7-10 years of relevant experience; has experience of leading/advising Junior and Senior resources. Specifically in the Pharmaceutical, biotechnology, or medical device industry.Experience in FDA and/or Global regulated environment with good understanding of GxP standards and Risk based validation; Define and implement Risk based validation activities.Experience in writing and executing documentation for all aspects of the validation deliverables (etc. Requirements, Compliance/validation Plans, test protocols, Test Summary reports and Compliance/Validation Reports, SOPs/WIs). Experience in reviewing system test and user acceptance test scripts, Traceability matrix and Design Specs Experience in QA Methodologies, designing, reviewing and approving Test Plans, systems and UAT test scripts and Test procedures.Strong verbal and written communication skills.Ability to work as a team player, lead a team or accomplish tasks without supervision.Ability to work with remote teams and support several changes/projects simultaneously.Ability to provide Validation guidance, timely reviews, and escalations to TQ managementExperience with validation deliverables review, including testing artifacts (e.g., test scripts).Knowledge of Agile Tools (e.g., Jira, Xray, qTest, Service Now etc.).Ability to build collaborative partnerships, work as a team player, including timely escalations to TQ manager.Ability to work with dispersed/remote teams and support several systems simultaneously. Skill RequirementsOther Requirements