Avid Bioservices Tech Stack

CDMO for mammalian biologics manufacturing with FDA compliance focus

Pharmaceutical Manufacturing Tustin, California 201–500 employees Founded 2002 Public Company

Avid Bioservices operates a Contract Development and Manufacturing Organization (CDMO) for biologics, running mammalian protein facilities and managing a public equity base. The tech stack is dominated by regulatory and operational infrastructure—Oracle, Dynamics 365, LIMS, DeltaV process control, and Six Sigma methodologies—rather than modern cloud or analytics tooling, reflecting a heavily compliance-driven operation. Manufacturing and engineering roles account for ~75% of active hiring, with a stated pain-point focus on process gaps, operational bottlenecks, and scale-up execution, signaling an organization still optimizing core production workflows rather than exploring new platforms.

Tech Stack 18 technologies

Core StackDynamics 365 Oracle ADP Microsoft Office Excel HPLC SDS-PAGE Word Outlook LIMS DeltaV Acronis Veeam Concur Millipore Microsoft Project LabWare LIMS Six Sigma

What Avid Bioservices Is Building

◆Challenges

Compliance with fda and cgmp regulations
Process and system gaps
Operational bottlenecks
Improving existing processes
Process improvement to increase efficiency
Solving hiring needs
Cost efficiency
Lead time reduction
Supply continuity
Support scale up efforts

▲Active Projects

Process tech transfer
Scale-up assessment
Setup of new manufacturing processes
Stable cell line development strategy
High-throughput screening and automation for clone evaluation
Technology evaluations and continuous improvement initiatives for cell line workflows
Strategic workforce planning
Sop improvement team
Method development projects
Validation projects

Hiring Activity

Decelerating65 roles · 10 in 30d

Department

Manufacturing

Engineering

Research

Ops

Quality

Finance

Logistics

Seniority

Mid

Junior

Senior

Lead

Director

Manager

Notable leadership hires: Strategic Projects Director

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About Avid Bioservices

Avid Bioservices is a CDMO headquartered in Tustin, California, focused on manufacturing biologics including monoclonal antibodies, biosimilars, recombinant proteins, and enzymes for pharmaceutical and biotech clients. The company has produced over 250 commercial batches and supports 5 marketed products across 90+ countries. Operations span from early-stage process development through late-stage manufacturing at commercial scale. Active projects center on stable cell line development, high-throughput screening for clone evaluation, process tech transfer, scale-up assessment, and method validation—all pointing to a service model spanning both development support and dedicated manufacturing capacity.

HeadquartersTustin, California

Company Size201–500 employees

Founded2002

Hiring MarketsUnited States

Frequently Asked Questions

What manufacturing capabilities does Avid Bioservices offer?

Avid operates mammalian protein manufacturing facilities for monoclonal antibodies, biosimilars, recombinant proteins, and enzymes. Services include process development, analytical development, CGMP manufacturing, and stability testing across early-stage through commercial production.

What is Avid Bioservices' quality and compliance track record?

Avid reports a 10+ year flawless quality track record and maintains FDA and CGMP compliance across all manufacturing operations. The company has produced over 250 commercial batches with zero noted regulatory failures.

What software does Avid Bioservices use for manufacturing operations?

Avid's operational stack includes Oracle ERP, Dynamics 365, LabWare LIMS, DeltaV process control, Microsoft Project for planning, and Six Sigma for continuous improvement—infrastructure typical of regulated pharma manufacturing environments.