Job Description :
Job Title: System Analyst
Job Location: Summit, NJ, 07901
Contract Duration: 7+ Months.
Supports the administration of computerized laboratory systems at multi-use sites.
Experience in Pharmaceutical GxP regulated and non-regulated lab areas.
Implements, monitors and provides technical support of laboratory systems.
Proven track record of customer service, follow through, identifying issues, exploring resolutions, and implementing solutions that are timely, customer focused and in compliance with GMP and IT standards.
Administration and support of Pharm DEV / QC / MFG / Biologics applications including standalone computerized laboratory systems
Ability to link bench-level lab system usage/operation with a corresponding enterprise lab system (i.e. HPLC ? Empower
Deliver support for GMP systems, installing new releases and patches (hot fixes), and performing upgrades.
Responsible for Pharm Dev / QC / MFG / Biologics application’s system efficiency and technical support.
Perform routine backup operations, ensuring all required data files are successfully backed up to the appropriate media.
Repair and recover from hardware and software failures, coordinate and communicate with related vendor or individuals.
Prepare, review and update software/hardware qualification documents, change control, guidelines and SOPs.
Provides technical support to business groups through the use of troubleshooting procedures and testing.
Administration, support and maintenance of Laboratory computer systems adhering to service levels.
Manage project teams with emphasis on solutions to technical and compliance challenges in all phases of the System Lifecycle.
Oversee the Development/Review/Approval of IT Administrative Procedures.
Ensure resources performing IT activities are knowledgeable of and in tune with latest industry regulations and initiatives.
Provide input and guidance for technical strategy as it relates to all GMP computerized systems and address any compliance gaps.
Ensure all computerized systems remain in compliance post-production
Troubleshooting client instrument workstation and information technology issues
Provides feedback and suggestions to the client for future improvements

Ensure all computerized systems remain in compliance post-production.
Required Competencies-Knowledge, Skills, and Abilities:
Skills & Abilities:
Knowledge of cGMP, GXP, GAMP, SDLC regulations, including 21CFR part 11, and good documentation practices.
Advanced knowledge of pharmaceutical, manufacturing and laboratory systems and equipment that support Biologics and clinical manufacturing.
Ability to develop, delegate and motivate others including direct and indirect reports.
Strong written and verbal communication skills.
Excellent interpersonal skills with experience dealing with a diverse workforce.
Strong multi-tasking ability in conjunction with proven organizational skills. Ability to organize assigned tasks in a high paced environment and concurrently monitors tasks / assignments with others that may impact timely completion. Ability to effectively manage multiple tasks and activities simultaneously.
Highly proficient computer skills in Microsoft Office Suite – Word, Excel, PowerPoint and Outlook with some knowledge in database systems. Innate ability to learn new software, such as corporate intranet and enterprise business.
Ability to create and analyze meaningful metrics.
Professional Knowledge
Problem Solving
Team Player / Building Relationships
Customer Focus
Highly Technical
This position requires a minimum of Bachelors’ in Science in Computer Science, Life Science, or equivalent industry experience, and 5+ years of relevant technical experience including supporting lab systems.
Minimum of 5 years’ experience in FDA-regulated industry.
Minimum of 5 years’ experience managing personnel and/ or projects.
Strong IT background and experience in laboratory and manufacturing operations.
Knowledge of cGMP in the pharmaceutical industry.
Excellent computer skills a must