biotechnology facility design
O’Neal is uniquely qualified to design a technically complex cGMP facility that is efficient and fully integrated. With biotechnology facility design expertise and the ability to mitigate risk through facility programming, layout and technology selection, O’Neal can deliver a range of capabilities to fit your needs and budget.
O’Neal’s bioprocess technology expertise includes fermentation, cell culture, perfusion, buffer & media preparation, downstream purification, CIP, SIP, disposables, clean utilities, biowaste inactivation, and manufacturing support systems. In addition, O’Neal has in-house subject matter experts in biologics formulation and aseptic fill/finish operations. Extensive experience in biotech process design, equipment and facilities is leveraged to provide robust and appropriate design solutions for biopharmaceutical and facilities is leveraged to provide robust and appropriate design solutions for biopharmaceutical manufacturers of parenteral therapeutics, vaccines, monoclonal antibodies, and HCT/Ps, as well as industrial applications such as enzymes, probiotics, biofuel and agricultural products.
O’Neal specializes in the design of bioprocess facilities for pre‐clinical, clinical and GMP biologics manufacturing. This engineering core competency is coupled with a thorough understanding of biopharmaceutical regulatory requirements for current GMP and GTP manufacturing. We provide engineering and design services throughout the entire project life cycle, from conceptual design phase through preliminary and detailed design, construction administration, commissioning & validation.