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Danaher Corporation Lead Bioprocess Engineer - Consumables Designer in Marlborough, Massachusetts

Be part of something altogether life-changing!

Working at Cytiva in the Life Sciences industry means being at the forefront of providing new solutions to transform human health. Our incredible customers undertake life-saving activities ranging from fundamental biological research to developing innovative vaccines, new medicines, and cell and gene therapies.

At Cytiva you will be able to continuously improve yourself and us – working on challenges that truly matter with people that care for each other, our customers, and their patients. With associates across 40 countries, Cytiva is a place where every day is a learning opportunity – so you can grow your career and expand your skills in the long term. Your health and wellbeing are important to us and together we will not compromise on safety in the workplace or the environment.

Cytiva is proud to work alongside a community of nine fellow Danaher Life Sciences companies. Together, we’re pioneering the future of science and medicine, developing products that enable researchers in the fight to save lives.

We are looking for a Lead Bioprocess Engineer - Consumables Designer to work with our Enterprise Solutions Process and System Design (P&SD) team. Do you have a passion for Consumables Design? Then we would love to hear from you.

What you’ll do

  • Lead Consumables Designer will be responsible for leading consumables design/discussion for Enterprise Solutions (ES) projects including generation of relevant design documents. Lead Consumables Designer will be responsible for maintaining the Qualification Consumables BOM tool (used for quotation and for ordering consumables for qualification), Support Evaluation and Offerings (E&O) team for pre sales consumables discussion, consumables BOM, and quotation. Support generation of consumables lists for FAT/SAT/IOQ and provide consumables forecast. Work collaboratively across teams (E&O, Consumables Application, TCAT, Automation, Qualification, Product Management, etc.) to ensure consistency of offerings.

  • Collaborate with Process Design Engineers (PDEs) and support the make-a-batch workshop. Work closely with the Consumables Application team and coordinate/support the Batch360 exercise for the ES projects. Facilitate alignment of deliverables between pre sales (proposal and technical book) and post sales activities including process and system design. Work closely with the lead System Designer (LSD) and support ES project Factory Acceptance Test (FAT) execution. Assure alignment between hardware and consumables designs.

  • Work closely with customer and internal Subject Matter Experts (SMEs) to ensure continuous exchange of critical and technical information needed to execute design activities efficiently and effectively. Complete all planned Quality & Compliance training within defined deadlines. Lead continuous improvement activities by driving the implementation of process and product quality improvement initiatives. Able and willing to cross train, diversify and expand capabilities.

  • Assure compliance with the Cytiva Quality Manual, Quality Management System, Quality Management Policy, Quality Goals, and applicable laws and regulations as they apply to the job type/position. Identify and report any quality or compliance concerns and take immediate corrective action as required.

  • Approximately 10-30% travel depending on project specifics and geographic location.

Who you are

  • BS or MS degree in Mechanical / biochemical / chemical engineering or a related engineering/life Science discipline.

  • Minimum of 5 years of relevant bioprocess and single use technology experience. 2 years of direct experience working in a pilot plant or GMP manufacturing facility.

  • Working knowledge of pharmaceutical/biotech processes, and equipment hardware. Knowledge of biologics CMC, cGMP manufacturing requirements.

  • Technical understanding of automation systems used in the biopharma (Delta V, PLC, PI, etc.).

  • Experience in working / leading with cross functional teams. Experience with CAD, Visio, MS Project, SuperPro.

  • 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.

* This is a hybrid role with a 1 -4 days in the office a week*

#LI-GCC

When you join us, you’ll also be joining Danaher’s global organization, where 80,000 people wake up every day determined to help our customers win. As an associate, you’ll try new things, work hard, and advance your skills with guidance from dedicated leaders, all with the support of powerful Danaher Business System (https://www.danaher.com/how-we-work/danaher-business-system) tools and the stability of a tested organization.

Danaher Corporation and all Danaher Companies are committed to equal opportunity regardless of race, color, national origin, religion, sex, age, marital status, disability, veteran status, sexual orientation, gender identity, or other characteristics protected by law. We value diversity and the existence of similarities and differences, both visible and not, found in our workforce, workplace and throughout the markets we serve. Our associates, customers and shareholders contribute unique and different perspectives as a result of these diverse attributes.The EEO posters are available here (https://www.dol.gov/agencies/ofccp/posters) .We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform crucial job functions, and to receive other benefits and privileges of employment. Please contact us at applyassistance@danaher.com to request accommodation. If you’ve ever wondered what’s within you, there’s no better time to find out.

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