- Registration is OPEN for the 7th Annual Sequence Charity Golf Tournament
Improving the quality of human life is the heart of everything we do.
Sequence has executed a vision to build a fully functional, mock pharmaceutical manufacturing training facility to educate and prepare our team of consultants in a way the industry hasn’t seen before.
At Sequence we’ve developed a cross-functional approach to preparing our consultants through an immersive multi-week training program that includes hands on exposure to equipment and software in our Sequence Training Facility. The result is a pipeline of engineering resources with exposure to manufacturing equipment, utilities, lab instrumentation, HVAC & facilities, and the associated computerized system interfaces that equates to years of experience in a short window of time.
Understands how to navigate the project lifecycle while adding value from design conception through licensure and beyond
Provides project leadership with the ability to proactively knock down barriers to keep the project moving
Understands regulatory requirements and application of industry guidance for achieving and maintaining compliance
Is cross-functionally trained to support the design and testing of any area within the facility: Manufacturing, Lab, Utilities, and IT/Computerized Systems
Our cross-functional approach to training our engineering consultants provides greater value for our clients and employees. We teach risk mitigation through the understanding of implications and impact to all areas within a facility.
Our revolutionary training facility allows us to provide continuing education for our more experienced team members and accelerated learning for newer team members.
By leveraging our Sequence Training Facility, hands-on learning allows our consultants to work with actual equipment, control systems, and processes, giving them the ability to troubleshoot and adapt solutions in real-time before they get to the client site.
We provide targeted training focused on translating product and process knowledge into quality driven design requirements and efficient risk-based testing strategies.
Sequence consultants are exposed to and trained on multiple platforms to ensure they can adapt to different environments and requirements. This knowledge helps them design effective commissioning protocols and perform comprehensive qualification testing across various setups.
Our accelerated training programs create immersive simulations so our consultants can engage and learn in controlled environments. This boosts their ability to perform under real-world pressure as they learn to apply theory to practice in a condensed period, which is crucial when dealing with project deadlines.
We intentionally incorporate all aspects of plant operations to conceptually train our consultants that includes facilities, utilities, lab, IT, manufacturing process (upstream & downstream), filling, automation, and ancillary equipment with a Pharma 4.0 infrastructure. This approach helps our consultants develop a more holistic, integrated approach to problem-solving and risk mitigation to ensure overall project success more quickly and efficiently.
To accelerate our team’s knowledge, our hands-on training facility is set up to represent a mock pharmaceutical manufacturing facility with five core areas of focus for our training: Facilities, Equipment, Utilities, Lab and Computerized Systems.
Our training program is focused on making sure our employees develop an understanding of how to apply both regulation and guidance to the validation lifecycle, specifically focusing on design, commissioning, and qualification of new facilities.
Our training program is focused on making sure our employees develop an understanding of how to apply both regulation and guidance to the validation lifecycle, specifically focusing on design, commissioning, and qualification of new facilities.
We provide exposure to the latest Industry guidance, so they understand what it takes to create strategies to achieve compliance. This includes ISPE, USP, ICH, FDA and ISA.
The rapid acceleration of knowledge is what sets our team of consultants apart by creating a level of understanding that will ultimately increase speed to market for the life impacting drugs our clients are manufacturing.
Exposure to a wide range of Digital Solutions including BMS, PCS and MES.
Incorporates all elements to conceptually train resources on all aspects of plant operations: facilities, utilities, lab, IT, manufacturing process (upstream & downstream), filling, automation, and ancillary equipment with a Pharma 4.0 infrastructure.
We’re establishing an understanding of the engineering principles driving the functionality of common systems involved in converting raw materials into finished pharmaceutical products that meet established quality standards.
To establish an understanding of the engineering principles driving the functionality of common systems involved in utility generation and distribution and functionality of support equipment used for cleaning, sterilizing and solution preparation.
To establish an understanding of the engineering principles driving the functionality of common analytical instrumentation and associated methods. These principles are applied to evaluate system capability to confirm quality standards including purity, potency, stability and safety.
Analytical Instrument Qualification
To establish an understanding of the engineering principles driving the functionality of common microbial identification and detection instrumentation and associated methods. These principles are applied to evaluate system capability to monitor the presence of microorganisms throughout the drug development and production process.
Microbial identification
Microbial detection
Antimicrobial susceptibility
Exposure to regulatory requirements and industry standards that guide microbial testing and handling, specifically USP chapters.
To gain an understanding of data aggregation and system to system interfacing commonly seen in Pharma 4.0 applications. Networking principles, including on-premise and cloud-based infrastructures, are important in ensuring data integrity requirements are maintained during collection and storage over defined retention periods.
Provide a fully integrated digital infrastructure that facilities a deeper level understanding of a wide variety of digital platforms used to support manufacturing processes.
Understanding how to apply both regulation and guidance to the validation lifecycle, specifically focusing on design, commissioning, and qualification of new facilities.
Understanding warehouse functionality as it relates to storage, organization, distribution of raw materials, finished product and other various supplies for operations.
Other Uses
Personnel and material flow and its impact on environmental conditions for classified areas.
Gowning Ante-Room
Supply/Return Corridor
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No Code App Development for Manufacturing Operations
Tulip creates user-friendly and functional apps that improve the productivity of operations, without writing any code. Users can start from scratch or customize an App Template to fit their needs.
Sequence partners with Tulip for implementation and validation of the Tulip platform as well as creation, configuration and validation of Tulip Applications that are hosted on the platform. Our application builds include Electronic Batch Records, Weigh and Dispense, Digital SOPs for training (with embedded videos) and more.
