CSV Specialist
Manati, us-territories - USA
Job Summary
Responsibilities:
- Perform Computerized System Validation (CSV) activities following site CSV Standard Procedure.
- Develop change control records as required following Electronic Change Control (e-CC) Procedure for the Site.
- Communicate to IT and CSV leaders the tasks progress and roadblocks or any requirements not met by the project.
- Collaborate with other department members to review/update documentation related to the projects assigned.
- Develop the testing protocols in the Application Lifecycle Management (ALM) System and/or any other required documentation procedures (such as DCA System for Document Control and Archiving).
- Coordinate meetings with technical or other multidisciplinary teams to develop and revise required documents
Minimum Requirements/Qualifications
- Bachelors Degree in Engineering or Computer Science combined with three (3) years of CSV and Change Control Management working experience.
- Experience must be within a pharmaceutical environment working in the developing of CSV assessments and testing protocols and developing and managing Change Control Records.
- Read and interpret drawings and design specifications and any other technical document.
- Understand and use computers and software packages.
- Knowledge of cGMPs local/federal regulatory requirements and documentation procedures pertaining to pharmaceutical manufacturing plant.
- Bilingual English/Spanish both written and verbal
- Able to interact effectively with people to establish and maintain excellent working relationship with internal and external customers at all organizational levels and disciplines in such a way to facilitate the work.
- Able to plan and prioritize multiple activities simultaneously.
- Customer service oriented and self-starter.
*Weil Group is proud to be an Equal Employment Opportunity Employer.*
Required Experience:
IC
About Company
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