Engineering Services

Multi-disciplinary engineering is our fundamental strength.

Process Design

Biologics, MCC, Vaccines, Plasma Processing, Gene Therapy
Upstream, downstream, fill-finish processes
Oral solid dose, semi-solids and liquid dose
Cosmetics and Neutraceuticals
Cannabis Oil Extraction, Purification and Processing
Batch, Semi-Continuous, Continuous Processes
Process scale up and Commercial Implementation

Critical Utilities Design

High Purity Water (PW and WFI) and steam systems
Process and lab gasses
CIP and SIP
HVAC

Equipment Engineering

Washer & autoclaves, terminal sterilization
Fill finish, lyophilization, packaging, serialization
Chromatography In-line Buffer Preparation, TFF, UF, Nanofiltration, centrifuges, filter presses, Sterile Filtration
Bioreactors and Single Use Technologies
CO2 extraction, rotary evaporation
Compounding / formulation, buffer prep/hold
Chemical storage & dilution skids
Waste handling, neutralization, and bio-kill systems.
Compounding, Granulation, Compaction, Milling, High Speed Mixers, Fluid Bed Dryers, Tablet Press, Encapsulators, Coating Pans

Check out some of our publications on the engineering services we provide.

Designing Stainless Steel and Disposable Hybrid Systems for the Biopharmaceutical Industry

Disposable bioprocessing technologies have existed since the 1970s, originally focusing on filters and tubing sets [1]. Design options have since evolved into complex flow paths including simulated moving bed (SMB) chromatography flow kits, disposable control valves and pre-packed chromatography columns. Options, applications and creativity are bound only by the designer and their materials of choice.
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For any inquiries of our services or previous work, please contact us.

Fujifilm Diosynth Biotechnologies has utilized MMR Engineering at our two US Manufacturing facilities in North Carolina and Texas due to their expertise in Cytiva’s proprietary Unicorn software and Emerson’s DeltaV platform. MMR Engineering was prompt in delivering their proposal, accepting the awarded project and mobilizing their staff on site. Their personnel worked efficiently and strategically within our Automation, Quality Assurance and Validation Departments to deliver a qualified processing system on time and within budget. Their executed protocols were done right the first time all while meeting our stringent cGMP requirements such as adherence to SOPs and training, obtaining access to numerous qualified, electronic systems and supporting change control. MMR Engineering continues to provide Validation and Automation support to both sites at the present time and in the foreseeable future.

Charles Crosier

Sr. Project Manager/Principal Engineer, Fujifilm Diosynth BIotechnologies

MMR’s team has shown great expertise in Clean Utilities when delivering a Global Engineering Guidance project for AbbVie on high purity water systems. Their persistence to meet timelines and deliver projects within tight schedules is also unique. MMR’s technical aptitude and project delivery was instrumental to the successful delivery of our projects, I would highly recommend MMR for Clean Utilities engineering projects.

Chris Peterson

Senior Process Engineer - Clean Utilities, AbbVie

MMR Consulting has demonstrated a profound technical knowledge in clean utilities and other process support systems / utilities, as well as a very unique project delivery model. Their creativity to figure out the real problem and determine a practical solution within a client’s constraints, as well as deliver a project within tight timelines and variable expectations, coped with their technical knowledge, engineering and commissioning skills makes them an exceptional consulting partner. I am fortunate to have worked with MMR on several projects, and would highly recommend them for either technical staff augmentation, or design and commissioning projects, with a specializing in Clean Utilities and Process.

James Meils

Manager Critical Systems Projects, CSL Behring

MMR was contracted to support two high priority projects within our Toronto manufacturing facility: one focusing on chromatography skid upgrades and another on CIP process improvements.

MMR’s management of the two system upgrades was achieved in 9 months, from inception to completion. Further, the actual execution of engineering and IOQ was done during a shutdown period within 6 weeks. The CIP systems were turned over on time without impacting production.

Patrick Bunker

Deputy Director, Engineering Project Management, Sanofi Pasteur