Computer Engineer - IT Systems (Pharmaceutical Manufacturing)
PHARMIANA LLC, Fort Worth, TX, United States
Job Description
Job Summary
We are seeking an experienced
Computer Engineer
to support IT systems in a
pharmaceutical manufacturing environment . The role focuses on maintaining reliable, secure, and compliant IT and manufacturing systems that support production, quality, and regulatory requirements.
Responsibilities
Support and maintain IT systems used in pharmaceutical manufacturing and quality operations.
Provide technical support for systems such as
MES, ERP (e.g., SAP), LIMS, and QMS .
Ensure IT systems comply with
GxP, FDA 21 CFR Part 11, and data integrity requirements .
Participate in
computer system validation (CSV)
activities including documentation and testing.
Manage servers, networks, databases, and virtualization environments.
Implement user access controls, backups, cybersecurity, and disaster recovery.
Troubleshoot system issues impacting production or compliance.
Work closely with Manufacturing, Quality, and Engineering teams.
Support audits and inspections as needed.
Required Qualifications
Bachelor’s degree in
Computer Engineering, Computer Science, IT, or related field
5–7 years of IT experience , preferably in pharmaceutical or regulated environments
Experience supporting
validated systems
and regulated applications
Knowledge of
GMP, GxP, and FDA compliance concepts
Strong problem-solving and documentation skills
Pay: $37.07 - $44.64 per hour
Expected hours: 40.0 per week
Work Location: In person
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Job Summary
We are seeking an experienced
Computer Engineer
to support IT systems in a
pharmaceutical manufacturing environment . The role focuses on maintaining reliable, secure, and compliant IT and manufacturing systems that support production, quality, and regulatory requirements.
Responsibilities
Support and maintain IT systems used in pharmaceutical manufacturing and quality operations.
Provide technical support for systems such as
MES, ERP (e.g., SAP), LIMS, and QMS .
Ensure IT systems comply with
GxP, FDA 21 CFR Part 11, and data integrity requirements .
Participate in
computer system validation (CSV)
activities including documentation and testing.
Manage servers, networks, databases, and virtualization environments.
Implement user access controls, backups, cybersecurity, and disaster recovery.
Troubleshoot system issues impacting production or compliance.
Work closely with Manufacturing, Quality, and Engineering teams.
Support audits and inspections as needed.
Required Qualifications
Bachelor’s degree in
Computer Engineering, Computer Science, IT, or related field
5–7 years of IT experience , preferably in pharmaceutical or regulated environments
Experience supporting
validated systems
and regulated applications
Knowledge of
GMP, GxP, and FDA compliance concepts
Strong problem-solving and documentation skills
Pay: $37.07 - $44.64 per hour
Expected hours: 40.0 per week
Work Location: In person
#J-18808-Ljbffr