Specific Commissioning and Validation support

Katalyst Healthcares & Life Sciences
Summit, NJ, United States
Full-time

Responsibilities :

Maintains all qualified and validated equipment and systems in compliance with policies, guidelines, and procedures.

Support Lifecycle Document Management System.

Develops protocols, and associated reports while adhering to a change management process.

Supports the execution of equipment qualifications and validation protocols

Supervises vendors for qualification functions.

Develops written procedures for calibration and preventive maintenance of equipment

Supports calibration, equipment qualification and validation activities.

Configures and documents the configuration of computerized systems.

Develops validation / qualification deliverables such as Validation Plans, Requirements Specifications, Traceability Matrices, Summary Reports, Change Controls.

Manages projects of varying scope and complexity.

Supports laboratory and manufacturing equipment implementation projects including scheduling, procurement, site prep, installation, qualification, and turn over to business area.

Independent ownership of all lifecycle deliverables in the Qualification of equipment and full CSV for single and multi-user Computerized Systems.

Supports internal customer groups in the procurement, operation, calibration, and preventive maintenance of equipment to meet business needs in accordance with required schedules or dates.

Completes all calibration, qualification and validation documentation with accuracy, completeness and compliance to Client standards.

Provides excellent customer service and support.

Regularly reviews, prioritizes and promptly responds to customer equipment qualification and support requests.

Provides technical support and guidance on calibration and equipment qualification issues. Interfaces with customers to ensure all expectations are being met.

Maintains a positive relationship with all team members and site customers while promoting a positive team environment.

Minimum 50% onsite required work schedule- Normal Business hours.

Requirements :

Strong critical thinking skills.

Ability to learn and function in a fast-paced environment.

Experience executing qualification documents.

Ability to interact effectively with laboratory, QA, and Facilities groups.

Strong 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.

Strong written and verbal communication skills along solid presentation skills. Proficient at writing well-formulated emails and reports.

Ability to follow oral and written instructions, read and interpret engineering manuals / drawings relevant to the assigned task.

Ability to effectively communicate with employees, contractors and vendors. Experience with technical writing and document development / generation Strong computer skills in Microsoft Office Suite ?

Word, Excel, Visio and Outlook, and the ability to learn new software as required for equipment qualification.

Technical / Professional Knowledge

Problem Solving / Troubleshooting

Action Oriented

Attention to Detail

Multi-tasking

Building Relationships

BS degree in Engineering / Computer Science or equivalent.

Working Conditions.

Environment may include working in office or in a laboratory / manufacturing area.

Ability to work safely in an environment with hazardous, radioactive, and infectious materials and waste.

Ability to work safely when working alone or working with others.

13 days ago
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