Associate/ Senior Systems Administrator

BioDuro • Irvine, CA

3d

About The Position

Forma is a next-generation Contract Development and Manufacturing Organization (CDMO) based in Irvine, California. The company was recently formed through the acquisition of the Irvine operations from BioDuro and is operating as a newly established, independent entity. As a result, Forma’s standalone online presence is still being built. We are a lean, entrepreneurial organization of approximately 60 employees focused on drug product development and manufacturing for pharmaceutical and biotechnology clients.

Why Forma? Unlike large, highly layered organizations, Forma operates with a hands-on, execution-driven model. Our teams work closely across functions to solve complex technical and operational challenges, move quickly, and deliver consistently high-quality results. Employees at Forma are expected to take on meaningful responsibility, collaborate directly with colleagues and clients, and contribute to building scalable systems and processes as the company grows. This is an environment well suited to individuals who value autonomy, technical excellence, and the opportunity to help shape a growing organization.

Job Overview/Summary The Associate Systems Administrator provides technical and operational support for IT and laboratory computer systems in a regulated environment. This role assists with day-to-day system administration, user support, documentation, and basic validation activities for laboratory and business systems. The position is designed for professionals looking to develop hands-on experience in IT systems support, GxP compliance, and computer system validation while working under the guidance of senior IT and quality professionals. Based on experience this position is available for a more senior role.

Requirements

• Bachelor’s degree in Information Technology, Computer Science, Engineering, or a scientific discipline (or equivalent experience).
• 0–3 years of experience in IT support, systems administration, or technical support (internships and co-op experience acceptable) for junior level.
• 4-8+ years of experience for mid to senior level.
• Basic understanding of Windows operating systems, user account management, and troubleshooting concepts.
• Strong willingness to learn regulated IT systems and validation practices.
• Good written and verbal communication skills.

Nice To Haves

• Exposure to pharmaceutical, biotech, laboratory, or regulated environments.
• Familiarity with laboratory instruments or scientific software.
• Basic understanding of GxP, data integrity, or 21 CFR Part 11 (training acceptable).
• Experience with ticketing systems, documentation, or SOP-driven environments.

Responsibilities

• Provide first-level support for IT and laboratory computer systems, including user account setup, access management, and basic troubleshooting.
• Assist with desktop, workstation, and laboratory instrument computer support.
• Respond to service requests and incidents in a timely and professional manner.
• Escalate complex technical issues to senior IT staff as appropriate.
• Provide hands-on system administration support for laboratory and enterprise applications, including Empower chromatography data systems, spectroscopy software, TrackWise, Ignition, MasterControl, and NetSuite.
• Support NetSuite configuration and ongoing buildout, including user provisioning, role-based access controls, permission sets, workflows, saved searches, dashboards, and module setup, in collaboration with finance, quality, and operations teams.
• Assist with implementation and optimization of NetSuite modules and integrations as the organization scales.
• Support routine maintenance of laboratory PCs, application servers, and virtual environments, including user access, patching, and basic troubleshooting.
• Help ensure laboratory and ERP systems remain available, secure, compliant where applicable, and properly documented.
• Assist with computer system validation (CSV) activities, including document preparation, execution support, and record maintenance.
• Support IQ/OQ/PQ testing activities under direction of senior validation staff.
• Help maintain validation documentation in accordance with GxP, 21 CFR Part 11, and internal SOPs.
• Participate in SOP reviews and controlled document updates.
• Maintain accurate system documentation, logs, and records.
• Follow established IT, security, and quality procedures.
• Support audits and inspections by providing requested documentation and evidence.
• Participate in training related to IT systems, laboratory applications, and regulatory requirements.
• Develop foundational knowledge of GAMP, CSV, data integrity, and regulated system lifecycles.
• Collaborate with cross-functional teams and learn best practices from senior staff.

Benefits

• We offer full health benefits, paid vacation and sick leave, an aggressive bonus structure, and market-competitive salaries to all our employees.
• In addition, Forma provides employees with a variety of engaging employee and community outreach events.
• We strive to reward and promote employees who exhibit our values of Accountability, Respect, Tenacity, Results and Integrity.

What This Job Offers

• Job Type: Full-time
• Career Level: Entry Level