For systems administration in Pharmaceutical GMP regulated lab areas. Implement, monitor and provide technical support of Hardware, Software and Laboratory applications. Assist in managing the implementation and support of all laboratory systems. Provide ongoing Process Improvement, Risk Assessment and mitigation plans. Create, maintain and enforce Policies, Procedures, Documentation, Validation Plans and Test Scripts in accordance with regulatory standards. Resolve daily hardware and software issues in timely manner.
Generate, revise, review and execute Validation documents (VMP, URS, SRS, RA, TM, Protocols, Reports,SOPs etc). Perform hardware and software upgrades as needed and generate the necessary documents to maintain the System validated status. Integration of third party applications and services into the lab environment with knowledge and understanding