Bachelor's degree in Engineering, Pharmaceutical Sciences, Chemistry, Biology, or related field.
8-10+ years of experience in pharmaceuticals, biotechnology, or regulated environments.
5+ years of experience in Data Integrity/ALCOA+ principles.
5+ years of experience with Computer System Validation (CSV) principles.
Strong understanding of FDA regulations, ICH guidelines, and EU Annex 11.
Responsibilities
Support the creation, review, and approval of CSV deliverables for in-house solutions.
Communicate effectively with stakeholders regarding CSV requirements and project status.
Create documents adhering to established standards.
Facilitate reviews by Business, IT, and Quality stakeholders.
Adhere to SOPs and industry best practices throughout the validation process.
Demonstrate advanced proficiency in MS Office and Visio.
Utilize electronic document management systems (e.g., Qumas, SharePoint) and service management systems (e.g., ServiceNow).
Benefits
Collaboration with a multi-functional team focusing on critical projects in Cell Therapy.
Opportunity to work with current digital tools and AI as part of the validation process.
Engagement in an aggressive project setting that fosters a strong work ethic.
Exposure to regulatory inspections and audits, enhancing professional experience.
Focus on continuous improvements to quality and compliance, encouraging innovative contributions.
Full Job Description
Job Description:
This role will focus on the Computer System Validation (CSV) activities for enterprise GxP systems, specifically for a critical set of projects in the Cell Therapy functional area.
This role will be supporting validation leads to help ensure the required deliverables and testing are complete according to the Client CSV SOP.
Effective communication is key across a multi-functional team consisting of Business, IT, and Quality personnel.
Experience with current digital validation tools is required, use of AI as an accelerator is a plus.
Overall a solid CSV background and having a strong work ethic in an aggressive project setting will be key to being successful in this role.
Responsibilities:
Support creation, review, and approval of all CSV deliverables for custom in-house solutions.
Maintain close communication with stakeholders and team members to keep apprised of CSV needs, interpretation of requirements, impacts on compliance of an application, project status, and other relevant issues
bility to create documents to an existing document standard
Obtain and respond to review by Business, IT, and Quality stakeholders
Follow SOPs and industry best practices
dvanced knowledge of complete MS Office suite and Visio.
Firm understanding of technology platforms as needed for project.
Experience with electronic document management systems (e.g. Qumas, SharePoint etc.); application development and lifecycle management (e.g. ALM, Jira, etc.); and IT service management systems (e.g. ServiceNow)
Excellent oral and written communication skills in English. Strong expertise and ability to interview and accurately interpret communication requirements of team members.
Familiarity with using AI as an accelerator for creation and review of documents and testing.
Requirements:
Bachelor's degree in Engineering, Pharmaceutical Sciences, Chemistry, Biology, or a related scientific or technical discipline.
8-10+ years of experience in pharmaceutical, biotechnology, or regulated manufacturing environments.
5+ years of experience in Data Integrity/ALCOA+ principles.
5+ years of experience with CSA principles.
5+ years of experience with technical writing.
Working knowledge of GMP, GLP, and GAMP 5 principles.
Strong understanding of FDA regulations, ICH guidelines, and EU Annex 11 (as applicable).
Experience developing, executing, and reviewing:
Validation protocols and reportsRisk assessments (FMEA, impact assessments)SOPs, deviation investigations, and CAPAs.
bility to support regulatory inspections and audits (FDA, EMA, internal, or client audits).
Strong technical writing skills with attention to detail and data integrity.
Proficiency with common pharmaceutical documentation systems and tools (e.g., EDMS, change control systems).
Excellent organizational, communication, and cross functional collaboration skills.
Cross-functional experience in one or more regulated areas (i.e. Research, Analytical/QC, QA, Engineering, Manufacturing, Regulatory, IT etc.) is desired.
bility to provide innovative ideas to improve quality and compliance that create value including seeking new information and external insights.
Excellent interpersonal skills, including written and verbal communication.
Strong sense of ethics, diplomacy and discretion.
Commitment to Quality.
Strong critical thinking to analyze complex situations and discern critical issues.
ble to work effectively with highly-matrixed and multi-cultural workforce and build strong relationships by being transparent, reliable and delivering on commitments.
