Eric Irby

Biology graduate with hands-on experience in regulated biotech, GMP manufacturing, laboratory operations, and quality-focused documentation. Previously supported Gardasil production as a Biotech II at Merck & Co. and laboratory workflows at Rockland Immunochemicals. Skilled in SOP adherence, batch records, controlled documentation, data integrity, LIMS-supported workflows, laboratory data management, sample/reagent handling, and cross-functional production support.

Seeking QC, QA, laboratory, biotech manufacturing, clinical data, or data-focused roles.

Business Owner & Freelance Writer at Self-Employed (2020-01 – Present)

• Managed day-to-day business operations, including scheduling, customer service, vendor/platform coordination, issue resolution, and workflow planning.
• Maintained records for payments, expenses, orders/projects, and operational activity with attention to accuracy and confidentiality.
• Created written materials, concepts, scripts, and project documentation while managing deadlines, revisions, and client/stakeholder communication.
• Maintained digital records, spreadsheets, operational data, and project documentation with attention to organization, accuracy, and confidentiality.

Biotech II at Merck & Co. (2018-01 – 2020-12)

• Supported Gardasil manufacturing operations in a GMP-regulated environment with strict adherence to SOPs, safety requirements, and controlled production standards.
• Executed routine production support processes and maintained consistency in a high-stakes vaccine manufacturing setting.
• Contributed to accurate batch records, documentation review, data integrity practices, and compliance-focused workflows.
• Collaborated with cross-functional teams to support production efficiency, quality outcomes, and issue resolution.
• Maintained careful attention to detail, cleanliness, and process discipline in regulated operations.

Associate Scientist at Rockland Immunochemicals (2020-01 – 2020-12)

• Supported laboratory workflows involving antibody and biological materials in a GLP-aligned environment.
• Assisted with sample handling, testing support, experimental workflows, and preparation/organization of buffers, reagents, and solutions.
• Helped identify expired or non-compliant laboratory materials and supported audit readiness through improved material organization.
• Supported data integrity, documentation practices, sample tracking, laboratory data organization, lab readiness, and quality-focused scientific operations.

Bachelor's Degree in Biology – Chestnut Hill College