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Lab IT CSV Engineer 1658

icon building Company : Simotech
icon briefcase Job Type : Full Time

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Job Description - Lab IT CSV Engineer 1658



Why SimoTech



What
is it like to work at SimoTech? With a strong collaborative teamwork
culture based on respect, trust, and excellence, we play a critical
partnering role to our clients’ life -changing supply of products to
patients.
 In return, there is excellent salary, benefits, career
progression, educational support and much more.




Lab IT CSV Engineer 1658


SimoTech has a new opportunity for an engineer
with 3+ years’ experience in Computer Systems Validation and Laboratory IT systems
to join our team. The successful candidate will work as part of our client’s Computerised
Instruments team, supporting a variety of computerised instrument systems
across laboratory and manufacturing operations at their state -of -the -art
pharmaceutical manufacturing facility in Cork. The role has a hybrid working
model.

The ideal candidate will have a minimum of 3 years’
experience in a similar role within a GMP / GxP environment, ensuring
computerised instrument systems meet all data integrity, cyber security,
quality, lifecycle management and regulatory requirements.


Key Responsibilities


  • Manage
    and coordinate the Lab System CSV deliverables for new and existing projects
    from initiation to release, prioritising support activities in line with
    project schedules.

  • Generate
    validation documentation in accordance with site procedures and regulatory
    guidelines, including but not limited to, 21 CFR Part 11, EU GMP Annex 11, and data
    integrity guidelines.

  • Work closely with 3rd parties to install
    computerised instrument solutions, ensuring correct configuration to successfully
    integrate with existing onsite IT services and infrastructure.

  • Initiate and implement Change Control activities in
    accordance with quality standards and practices.

  • Follow
    all relevant EHS procedures and assist in incident investigations as required.

  • Recognise
    the importance of the quality control function in pharmaceutical
    production. 

  • Actively participate and contribute to team
    meetings.



Requirements

Qualifications &
Experience

  • 3+
    years’ experience supporting IT Applications including validating laboratory computerised
    systems, writing validation plans, requirements gathering, design
    documentation, system configuration, system testing and troubleshooting.

  • Experience implementing
    changes for IT applications in a GMP environment.

  • Knowledge of 21 CFR Part 11
    and data integrity guidelines.

  • Experience with MS Office and
    software installation knowledge.

  • Strong interpersonal and
    communication skills are required, with proven ability to communicate and build
    relationships cross -functionally.



Benefits

What SimoTech Can
Offer

  • Role provides a
    high degree of autonomy to allow the successful
    candidate to reach their full
    potential.

  • Develop new
    skills and enhance technical ability by working with
    innovative technologies in a multi - disciplined
    environment.

  • Opportunity to
    work with large corporate clients




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