Job Description :
IKCON TECHNOLOGIES INC delivers exceptional IT services and solutions that provide clients with definite edge over competitors and promoting highest standards of quality. We are currently looking for a [System Administrator / Phoenix Technology Partners] with one of our clients in [Summit], [NJ]. If you are actively looking for opportunities, please send us your updated resume with your contact details.

JOB TITLE System Administrator
CITY Summit
INTERVIEW MODE Telephonic/Skype/In person

Supports the administration of computerized laboratory systems at multiuse 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

Regulatory Responsibilities

Ensure all computerized systems remain in compliance post-production.
Required Competencies? Knowledge, Skills, and Abilities
Knowledge, 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 monitor 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.


Bachelor’s Degree or master’s degree in the field of Computer Science or Information Systems or a related field.