R- Engineer III, Computer Systems Validation

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profile Job Location:

Greenville, NC - USA

profile Monthly Salary: Not Disclosed
Posted on: 2 days ago
Vacancies: 1 Vacancy

Job Summary

Work Schedule

Standard (Mon-Fri)

Environmental Conditions

Adherence to all Good Manufacturing Practices (GMP) Safety Standards Cleanroom: no hair products jewelry makeup nail polish perfume exposed piercings facial hair etc... allowed Office

Job Description

As part of the Thermo Fisher Scientific team youll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life every single day to enable our customers to make the world healthier cleaner and safer. We provide our global teams with the resources needed to achieve individual career goals while helping to take science a step beyond by developing solutions for some of the worlds toughest challenges.

Description:

Join our validation engineering team as a Validation Engineer III (Computer Systems Validation CSV) where you will ensure product quality and regulatory compliance across pharmaceutical manufacturing operations.

In this role you will lead and execute validation activities with a strong focus on automation systems computerized systems and change management for existing commercial manufacturing lines. You will evaluate system and process changes determine validation impact and drive qualification strategies to ensure compliance with cGMP requirements.

You will collaborate cross-functionally with automation manufacturing and quality teams while serving as a technical resource during regulatory inspections and client audits. This role requires a high level of independence technical expertise and the ability to lead complex validation efforts.

A Day in the Role:

  • Lead validation activities for equipment processes utilities and computer systems with emphasis on CSV

  • Evaluate and support change management for existing manufacturing systems and automation platforms

  • Author review and execute validation documentation including IQ/OQ/PQ protocols and qualification plans

  • Perform and lead risk assessments gap analyses and validation assessments

  • Collaborate with automation engineers on systems such as PLC SCADA DCS DeltaV and Allen-Bradley platforms

  • Independently manage validation projects and coordinate cross-functional teams

  • Provide technical expertise during regulatory inspections and client audits

  • Mentor junior team members and support knowledge sharing across the team

  • Contribute to continuous improvement and operational excellence initiatives

Requirements:

  • Bachelors degree in Engineering Life Sciences Chemistry or related technical field

Equivalency:
Equivalent combinations of education training and relevant experience may be considered in place of a degree

  • Minimum of 4 years of validation experience in pharmaceutical/biotech manufacturing or comparable regulated industry

  • Strong knowledge of cGMP regulations (FDA EMA ISO)

  • Experience with Computer Systems Validation (CSV) CQV or automation validation

  • Experience writing and executing IQ/OQ/PQ validation protocols

  • Experience with automation and control systems (PLC SCADA DCS DeltaV Allen-Bradley)

  • Proven ability to lead validation projects and work cross-functionally

  • Strong technical writing and documentation skills

  • Experience with risk assessment methodologies and statistical analysis

  • Advanced problem-solving and root cause analysis skills

  • Excellent verbal and written communication skills

  • Proficiency with MS Office and validation-related systems

Preferred:

  • Experience supporting or contributing to capital (CapEx) projects

  • Experience with regulatory inspections and client audits

  • Knowledge of lean manufacturing and continuous improvement methodologies

Additional Information:

  • Ability to work in cleanroom environments as required

  • Flexibility to support extended hours or off-shift work during project activities or shutdowns

  • May require up to 25% travel


Required Experience:

IC

Work ScheduleStandard (Mon-Fri)Environmental ConditionsAdherence to all Good Manufacturing Practices (GMP) Safety Standards Cleanroom: no hair products jewelry makeup nail polish perfume exposed piercings facial hair etc... allowed OfficeJob DescriptionAs part of the Thermo Fisher Scientific team yo...
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