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Senior Process Jobs in Colorado (NOW HIRING)

Jobtailor

Senior Process Safety Engineer

Boulder, CO · On-site

$110 - $150/hr

Provide process safety engineering technical expertise and leadership to ensure Corden facilities are operated in a manner that protects the health and safety of employees and the public; protects ...

CoorsTek

Process Engineer Sr.

Golden, CO

$107K - $138K/yr

Job Title Process Engineer Sr. Responsible for comprehensively understanding and optimizing process engineering operations within a ceramic powder manufacturing facility. This role serves as the ...

CoorsTek, Inc.

Process Engineer Sr.

Golden, CO · On-site

$107K - $138K/yr

Job Title Process Engineer Sr. Responsible for comprehensively understanding and optimizing process engineering operations within a ceramic powder manufacturing facility. This role serves as the ...

CoorsTek

Global Process Engineer Sr

Golden, CO

$107K - $138K/yr

Job Title Global Process Engineer Sr As the Global Process Engineer Senior, you will be responsible for leading projects aiming to sustain, optimize and develop manufacturing processes. In this role ...

CoorsTek, Inc.

Global Process Engineer Sr

Golden, CO · On-site

$107K - $138K/yr

Job Title Global Process Engineer Sr As the Global Process Engineer Senior, you will be responsible for leading projects aiming to sustain, optimize and develop manufacturing processes. In this role ...

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Senior Process information

What does a senior process specialist do?

A senior process specialist analyzes, improves, and manages business processes to increase efficiency and effectiveness. They often lead process improvement projects, utilize tools like Six Sigma or Lean, and collaborate with teams to implement best practices and optimize workflows.

What is a senior process expert job description?

A senior process expert is responsible for analyzing, designing, and improving business processes to increase efficiency and effectiveness. They often lead process improvement initiatives, utilize tools like Six Sigma or Lean, and collaborate with cross-functional teams to implement best practices. Strong analytical skills, process modeling knowledge, and experience with process management software are typically required.
What are the most commonly searched types of Process jobs in Colorado? The most popular types of Process jobs in Colorado are:
What cities in Colorado are hiring for Senior Process jobs? Cities in Colorado with the most Senior Process job openings:

Senior Process Engineer, Drug Product Development

Umoja Biopharma

Louisville, CO • On-site

$108K - $140K/yr

Full-time

Medical, Dental, Vision, Retirement, PTO

Re-posted 11 hours ago

Job description

Umoja Biopharma is an industry-leading biotech with locations in Seattle, WA and Louisville, CO, focused on transforming the treatment of cancer with a novel integrated immunotherapy platform. Our vision is to develop off-the-shelf therapies capable of treating any tumor, any time. We are a diverse and growing team working in brand-new facilities in downtown Seattle, Washington and Louisville, Colorado, and we are looking for innovative thinkers who are excited by groundbreaking science and technology, and passionate about squaring up to the challenges inherent to cutting-edge drug development. We are committed to our core values and principles that support our overall mission and strongly invite applications from enthusiastic individuals who share our commitment and help position Umoja to deliver on our goals. We at Umoja believe in the importance of stories; we are looking for great people to join our team to help us create more stories for ourselves, for you, and most importantly for patients and their families.
Umoja Biopharma - Your Body. Your Hope. Your Cure.
POSITION SUMMARY
Umoja is seeking a Senior Process Engineer to join the Drug Product Development group within our Process Sciences team. This role will lead the development, scale-up, and tech transfer of lentiviral vector drug product and drug substance processes from lab to GMP scale (250 mL to 200 L), applying Quality by Design (QbD) principles, and supporting transitions through multiple clinical stages. A successful candidate will have a thorough understanding of fill-finish strategies and experience with internal and external tech transfer activities.
This is a fully onsite role based out of our Louisville, CO location.
CORE ACCOUNTABILITIES
Specific responsibilities include:
  • Serve as technical lead for process development and tech transfer activities for lentiviral vector drug substance and drug product fill processes.
  • Represent Process Sciences on CMC program teams, contributing to the process strategy, risk identification and assessment, and project management for Ph1 and beyond.
  • Operate, troubleshoot, and improve lab and production scale processes, consumables, and equipment for drug substance filtration and drug product fill-finish.
  • Evaluate and implement new equipment and process analytical technology (PAT) solutions.
  • Design and execute experiments to support program teams, process characterization, control strategy, and process performance qualification (PPQ).
  • Analyze, interpret, and effectively present data and findings to diverse audiences, including technical peers, external partners, and strategic audiences. This will include experimental, correlative, as well as, continuous process monitoring/trending data.
  • Implement and improve data workflows using tools like Benchling, JMP, and Ganymede.
  • Collaborate closely with the Process Sciences team (upstream, downstream, and optimization), analytical development, manufacturing, supply chain, non-clinical, clinical, research teams, and contract manufacturers.
  • Author technical documentation including SOPs, process descriptions, batch records, IND sections, development reports, and requirement specifications (MRS/URS).
  • Provide person-in-plant (PIP) support during GMP campaigns, mentor junior staff, and be a qualified trainer for Drug Substance and Drug Product processes.
  • Support new product introduction (NPI) activities.
  • Other duties as assigned.

The successful candidate will have:
  • BS/MS in chemical engineering, biochemistry, virology, or related field with a minimum of 5/3 years of relevant experience respectively.
  • Expertise in TFF, NFF, and process analytical technologies, including hands-on experience with the following systems, Repligen, AMBR Crossflow, and sterile filtration operation. Experience with novel filtration methods is desired.
  • Experience with experimental design, planning, execution, and complex data organization and analysis. Specific experience working with Benchling, JMP, Ganymede, INVERT, Python, Smartsheet, and data historians is a plus.
  • Experience with early and late phase implementation of process improvements.
  • Experience with early-phase clinical development and commercial readiness.
  • Experience with QbD, process risk assessments, and process characterization.
  • Proficiency in tech transfer, GMP operations, process description and batch record authoring, GDP, change control, and ALCOA+ principles.
  • Strong communication, collaboration, and technical writing skills.
  • Ability to balance multiple priorities in a fast-paced, cross-functional, and dynamic environment and perform tasks across a variety of programs.

Preferred Qualifications:
  • Working knowledge of lentiviral vector processes, from upstream cell culture through drug substance and drug product storage and filling processes (e.g. Bioreactors, Repligen TFF systems, Pendotech NFF systems, membrane and monolith chromatography) is strongly preferred.
  • Working knowledge of lentiviral vector analytical methods (e.g., flow cytometry, PCR, ELISA, HPLC).
  • Experience managing fill-finish CDMOs.
  • Experience with fill-finish capital projects.
  • Experience identifying and implementing creative and novel strategies to viral vector purification processes.
  • Experience with Aseptic Process Simulations and Hazard Identification Tools risk tools.
  • Familiarity with designing closed-process purifications.

Physical Requirements:
  • Ability to work onsite 5 days/week at our Louisville, CO location.
  • 100% compliance with personal protective equipment (PPE) requirements in laboratory environments for wet lab work, including gloves, protective clothing, and eye safety glasses.
  • Perform physical tasks required for the role, including standing, walking, bending, kneeling, sitting, working your hands in a biosafety cabinet, and occasionally moving materials up to 50 pounds.
  • Ability to work weekends, evenings, and holidays as needed.
  • Ability to travel on occasion.

Salary Range: $108,400 - $133,900
Benefits Offerings
Umoja Biopharma offers its employees competitive Medical, Dental, and Vision plans. Additionally, we offer Umojians access to a 401k plan through Fidelity, with a 100% match up to their first 4% deferral. Umoja also provides a generous Paid Time Off policy, employee commuter benefits, and cell phone stipend. For a full breakdown of our benefits offerings, please see the Benefits section of our website.

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