Computer Engineer - IT Systems (Pharmaceutical Manufacturing)

PHARMIANA LLC; Texas; On-site; USD 51,000 - 61,000; Full time

Job summary

PHARMIANA LLC in Texas seeks 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.

The candidate will manage MES, ERP (SAP), LIMS, and QMS, ensure GxP compliance, participate in CSV activities, and collaborate with Manufacturing, Quality, and Engineering teams.

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.

Responsibilities

• Support and maintain IT systems used in pharmaceutical manufacturing and quality operations.
• Provide technical support for systems such as MES, ERP (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.

Skills

Problem solving

Documentation

Regulatory compliance knowledge

GxP knowledge

Cybersecurity basics

Education

Bachelor’s degree in Computer Engineering, Computer Science, IT, or related field

Tools

MES

ERP (SAP)

LIMS

QMS

Job description

Job Description

Job Description

Job Summary
We are seeking an experiencedComputer Engineerto support IT systems in apharmaceutical 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 asMES, ERP (e.g., SAP), LIMS, and QMS.
Ensure IT systems comply withGxP, FDA 21 CFR Part 11, and data integrity requirements.
Participate incomputer 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 inComputer Engineering, Computer Science, IT, or related field
5–7 years of IT experience, preferably in pharmaceutical or regulated environments
Experience supportingvalidated systemsand regulated applications
Knowledge ofGMP, 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