Eva Geygan

Experienced Associate scientist with 4 years supporting complex, regulated programs through strong vendor coordination, documentation oversight, and cross-functional project execution. Skilled in managing workflows,

tracking operational data, and ensuring compliance in fast-paced, highly regulated environments. Recognized for exceptional organization, attention to detail, and communication skills, with a proven ability to streamline processes,

support audit-ready documentation, and partner effectively with global teams. Ready to leverage GMP operations,

stakeholder management, and process improvement experience to drive operational excellence in clinical programs.

Technical Application Sales, OEM at AUTOMATED ENGINEERING SERVICES, INC. (2026-03 – Present)

• Drove revenue growth by combining deep technical expertise with strategic sales execution.
• Developed and expanded relationships with OEM partners and key accounts.
• Delivered tailored application solutions that best meet clients projects and operations.
• Supported customers through the full sales lifecycle.
• Translated complex technical capabilities into customer value, negotiated commercial agreements, and collaborated cross-functionally to ensure successful product adoption and long-term partnership growth.

Associate Scientist, Process Development at AKRON BIO (2023-07 – 2025-09)

• Established post-capture design and execution of scalable downstream bioprocesses for client's recombinant protein production development, targeting <20 EU/mg while maintaining 70% in overall product yield.
• Coordinated with vendors and procurement to align on specifications, delivery timelines, and compliance requirements.
• Authored batch records, bill of materials (BOM) and standard operating procedures (SOPs) for cGMP operations, facilitated tech transfer processes while ensuring full regulatory compliance across all client downstream projects.
• Managed documentation accuracy across Trackwise, supporting deviation review and controlled workflows.
• Conducted 10+ final fill operations under cGMP and aseptic conditions, and also managed label control and reconciliation processes for experiment batches, ensuring product safety and strict regulatory adherence, maintaining accurate records and documentation.
• Helped with preparation and execution of cGMP such as buffer prep, weigh & dispense of raw materials, label control/reconciliation, equipment operation, and column packing while adhering to strong GDP and GMP compliance.
• Monitored process control parameters, maintaining product purity, safety, and potency.
• Managed the efficient scheduling and preparation of lab resources for 3+ experiments weekly, enabling smooth execution and contributing to meeting project milestones, ensuring adherence to project timelines, and generating weekly reports.
• Spearheaded the design and implementation of a ultrafiltration/diafiltration (UF/DF) process for Akron's endonuclease purification platform, reducing buffer consumption by 30% and processing time by 15%, as determined by lab-scale optimization studies.
• Led Design of Experiments (DoE) studies optimizing protein purification process (MMC), enhancing yield by 35% and reducing contaminants greater than 10-fold, leading to higher quality output.
• Trained new staff in documentation, GMP operations, and process workflows.

Associate II, Process Development at AKRON BIO (2022-11 – 2023-07)

• Coordinated and executed experiments for six plasmid development projects, which led to seamless execution to contribute to a 10% reduction in project turn around time via resource allocation.
• Implemented the automation of chromatography scouting workflows for upcoming projects using Unicorn 7 software, developing software solutions that decreased method development time by 40% and improved throughput for AKTA Avant runs.
• Managed data collection and analysis during tech transfer to three cGMP plasmid productions through support to MSAT, ensuring data accuracy and compliance with regulatory requirements.
• Streamlined protein chromatography polishing by screening alternative running buffer pH and salt concentrations, resulting in a 33% increase in product recovery and 15% increase in purity.

Laboratory Technician, Process Development at AKRON BIO (2021-08 – 2022-12)

• Aided senior scientists in downstream processing by preparing buffers, assisting in downstream experiments and conducting analytical assays, meeting project deadlines and exceeding expectations.
• Managed preventative maintenance on over 10 pieces of lab equipment, ensuring optimal lab functionality and contributing to the on-time delivery of critical product development milestones.
• Enhanced laboratory practices by cross-sectional collaborating within departments to resolve discrepancies in analytical assays, leading to an increase in batch-to-batch consistency.

B.S. in Cell and Molecular Biology – UNIVERSITY OF SOUTH FLORIDA (2019-01 – 2021-12)

Certificate in Biotechnology Specialist – STATE COLLEGE OF FLORIDA (2019-12 – 2020-05)