Associate Manager managing client relations and technical guidance in Private Equity for SS&C. Overseeing financial documentation and supporting junior staff responsibilities in a dynamic environment.
About the role
- Enterprise Quality R&D CSV Manager ensuring quality standards and regulatory compliance for J&J's IT systems. Leading diverse teams and validating system implementations across healthcare solutions.
Responsibilities
- Ensure that all J&J quality standards and global regulatory requirements are being met
- Ensure that building and execution activities include early involvement of quality in the design and development activities, building quality into the work product, building controls within the application/solution, and use of automation whenever feasible
- Own the quality approach for systems and ensure teams are accountable for delivering on an end-to-end support model for systems in scope
- Provide technical and procedural expertise/guidance to the project teams as well as aligning with both internal and external stakeholders
- Plan, task and resource allocations, executing, coordinating and maintaining the validation activities for GxP systems/applications
- Support internal audits and Health Authority regulatory inspections
- Responsible for the approval of SDLC validation documentation deliverables including the approval to release system implementation and/or changes for production use
- Attend project team meetings and provide EQ compliance guidance and support to project and base business support team members
- Lead globally diverse teams in an inclusive environment
- Provide an environment which encourages the company’s credo and the value of a diverse workforce
- Serve as a trusted partner across the Enterprise Quality organization, requiring strong collaboration skills at the senior leadership level, and includes making recommendations for improvements relevant to senior level stakeholders
Requirements
- 8-10 years of progressive experience in the pharmaceutical/medical device/biotech industry, with direct experience in Computerized System Validation activities
- Experience in running large scale end-to-end Validation programs is required such as LIMS, CAPA, MES, PLM, SAP, LMS, Complaints Handling, and Change Control
- Experience authoring or approving validation protocols, non-conformities, Change Requests, SOPs, Validation Plans and Reports
- Proficiency using the following tools is highly desirable: JIRA, HPALM, Xray, Qtest, Jenkins, Selenium
- Direct experience working in a software development environment using Agile, SAFe, CI/CD
- Direct experience in Artificial Intelligence (AI) and Machine Learning (ML)
- Direct experience in CSV Quality and/or CSV for R&D systems
- Thorough knowledge of cGMP regulations related to CSV, including 21 CFR Part 11, Part 210, Part 211 and Part 820
- Knowledge of SDLC Quality Management process and Computerized System Validation/Computerized System Assurance principles
- Proficiency in the English language, both written and oral, is required
Benefits
- 10% travel both international and domestic may be required
Job title
Job type
Experience level
Salary
Not specified
Degree requirement
Tech skills
Location requirements
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