Job Description

max bill rate ***
max mark up 1.48


Help us improve access to life-changing therapies that can transform human health
We are Cytiva, a global provider of technologies and services that advance and accelerate the
development and manufacture of therapeutics. Formerly part of Client Healthcare, we have a rich heritage
tracing back hundreds of years, and a fresh beginning since 2020.
Our customers undertake life-saving activities. These range from fundamental biological research to
developing innovative vaccines, biologic drugs, and Client cell and gene therapies. Our job is to supply the
tools and services - the pots, pans, soups and sauces - they need to work better, faster and safer, leading
to better patient outcomes.
We are looking for a Bioprocess Engineer - Process Design to work with our Enterprise Solutions Process
and System Design (P&SD) team. Do you have a passion for Process Engineering? Then we would love
to hear from you.
What you ll do
" Process Designer will support the process design efforts for biopharmaceuticals, lactoferrin and
food products manufacturing, and ensure optimal outcomes to support the customer application
and manufacturing operation, in compliance with applicable regulatory requirements. She/He will
provide the necessary technical input to support/enable the design and development of the
manufacturing suite layouts, process equipment design, process equipment layout, clean utility
" Process Designer will be responsible for process design documentations and operational
estimates such as Basis of Design, Mass/volume Balance, Equipment List, Process Flow
Diagrams (PFDs), Production Schedule, Clean Utilities Estimates, Cost of Goods Analysis,
Process Definition, etc. Support customer meetings by providing process understanding from pilot
scale operation, technology transfer, large scale manufacturing and facility design experience.
" Provide Process Design & Engineering support for the Enterprise Project Team. Work closely with
the Enterprise Solutions Project Manager to support the Enterprise Solutions project specific
design development, documentation and execution in alignment with the project scope and
schedule. Provide design input, support and recommendations as needed with qualification test
review and verification and during field execution, commissioning and qualification testing.
" Assure compliance with the Cytiva Quality Manual, Quality Management System, Quality
Management Policy, Quality Goals, and applicable laws and regulations as they apply to this job
" Work closely with Customer's Subject Matter Experts (SMEs) to ensure continuous exchange of
critical and technical information needed to execute design activities on time. Work closely with
Engineering partner companies during Conceptual, Basic design development, installation,
commissioning and testing phase to ensure suitability, applicability and accuracy of Engineering
partner designs, calculations, drawings; ensure they are in alignment with customer requirements.
" Complete all planned Quality & Compliance training within defined deadlines. Identify and report
any quality or compliance concerns and take immediate corrective action as required.
" Work closely with System Designers for the generation of URSs and GSs, and ensure the transfer
of critical equipment requirement specification, design meets customer and process needs, and
the single-use equipment layout is optimized for the customer facility.
" Approximately 10-30% travel depending on project specifics and geographic location.
Who you are
" BS or MS degree in biochemical / chemical engineering or in a related engineering/life Science
discipline or equivalent experience in Biopharma, Lactoferrin and Food industries.Page 2 / 2
" Minimum of 3 years of relevant bioprocess experience. 1 years of direct experience working in a
pilot plant or GMP manufacturing facility.
" Experience in manufacturing of monoclonal antibodies, viral vectors, pDNA and other biologics.
Working knowledge of pharmaceutical, Lactoperoxidase / lactoferrin separation, and other biotech
processes, equipment hardware, and single use technology. Knowledge of biologics CMC, cGMP
manufacturing requirements.
" Working knowledge of pharmaceutical/biotech processes, equipment hardware, and single use
technology. Knowledge of biologics CMC, cGMP manufacturing requirements.
" Experience in working with cross functional teams. Experience with Visio, MS Project, SuperPro,
and AutoCAD. Technical understanding of automation systems used in the biopharma (Delta V,
PLC, PI, etc.).
" Disposable technology design and application experience. Detail oriented, excellent at critical
analysis and problem solving.
" Comfortable working in global business environment. Structured, Organized, Analytical, Team
oriented. Fluent in English both verbally and in writing.
Who we are
Whatever your role, we bring purpose and challenge into our everyday work. If you are driven to make the
world a better place thanks to science and medicine, you ll feel right at home here. If you re flexible,
curious and relentless, you ll belong. If you are excited about a global culture, this can be the place to
further your career.
Want to know more? Experience life at Cytiva on our Careers website, Instagram channel and LinkedIn
Cytiva is a 3.5 billion USD global life sciences leader with over 7000 associates across 40 countries who
are dedicated to our mission to help us improve access to life-changing therapies that transform human
health. As a trusted partner to customers that range in scale and scope, Cytiva brings efficiencies to
research and manufacturing workflows, ensuring the development, manufacture and delivery of
transformative medicines to patients.
Cytiva is part of the Danaher family of companies, a global science and technology innovator committed
to helping customers solve complex challenges and improving quality of life around the world.

Application Instructions

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