Commissioning/Qualification Job at Katalyst Healthcares & Life Sciences, Millburn, NJ

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  • Katalyst Healthcares & Life Sciences
  • Millburn, NJ

Job Description

  • Katalyst Healthcares & Life Sciences is hiring entry level candidates for several positions for contract research in Clinical trials of drugs, biologics and medical devices.
  • We have a few immediate job opportunities available in Drug Safety and Pharmacovigilance and Clinical Research field. We work with University hospitals, pharmaceutical companies and recruiting partners.

Job Description



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.
  • Configures and documents the configuration of computerized systems.
  • Develops validation/qualification deliverables such as Validation Plans, Requirements Specifications, Traceability Matrices, Summary Reports.
  • 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.
  • Provides excellent customer service and support.
  • Regularly reviews, prioritizes and promptly responds to customer equipment qualification and support requests.
  • Maintains a positive relationship with all team members and site customers while promoting a positive team environment.

Requirements:

  • BS degree in Engineering / Computer Science or equivalent with 2 years of experience OR.
  • Associate degree with at least 4 years of relevant experience.
  • 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.
  • CSV experience, Draft Qualification/validation documents such as Val Plan, IQ/OQ/PQs, RTMs, Summary Reports, Deviations, Test Plans, worked with change management, cross functional team experience.

Competencies:

  • Technical / Professional Knowledge.
  • Problem Solving / Troubleshooting.
  • Action Oriented.
  • Attention to Detail.
  • Multi-tasking.
  • Building Relationships.

Additional Information



All your information will be kept confidential according to EEO guidelines.

Job Tags

Contract work, For contractors, Immediate start,

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