QP Technologies
Posted 3y ago

CSV Engineer

QP Technologies
Limerick, Munster, Ireland
HybridFull Time
Responsibilities
  • Prepares validation
  • Manages change controls
  • Analyzes testing results
Requirements
  • Requires a BS/BA in Engineering
  • Chemistry, or Life Sciences with 5+ years in automation and IT validation
  • GMP experience essential
  • Biologics experience desired

Job description

Summary:

This position uses policies and procedures to validate/qualify computer systems, including process automation systems, IS applications/infrastructure, and enterprise systems. Plans, coordinates, and participates in a compliant validation process for quality information technology and automation systems which require formal validation documentation under appropriate regulatory requirements and company manufacturing standards.


#This role is Hybrid and will require you onsite in Limerick


Essential Duties and Responsibilities:

  • Prepares/reviews validation documentation related to projects/change controls.
  • Manages change controls and other compliance-related tasks e.g. non conformances. Participates in the review of current and future CSV procedures and policies
  • Analyzes the results of testing and determine the acceptability of results against predetermined criteria.
  • Investigates and troubleshoot problems that occur and determine solutions or recommendations for changes and/or improvements.
  • Identifies current and anticipated requirements for compliant computerized operations and suggests methods for the identification, implementation, and maintenance of the procedures, actions, and documentation necessary to ensure compliance within the operation.
  • Coordinates with other departments or outside contractors/vendors to complete validation tasks. Participates in regulatory audits and communicates the company’s computer validation policies. Assesses the company’s computer systems and identifies any potential Part 11 or Annex 11 gaps. Manages projects and prepares status reports using Microsoft Project and other communication tools.
  • May supervise, lead, or manage lower-level personnel.


Requirements:

  • Requires BS/BA in Engineering, Chemistry, or Life Sciences with 5+ years of related experience within the fields of Automation and Computer systems and IT Infrastructure Qualification/validation; will substitute relevant experience for education.
  • Experience in a GMP environment is essential.
  • Biologics experience is highly desirable



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About QP Technologies

Microelectronic packaging, assembly, and semiconductor engineering services.

Year founded
1992
Employees
150
Organization type
Private
Latest investment
Private Equity (2015) — led by Delphon
Headquarters
US

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