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Contract Smartsheet Developer Jobs in Colorado (NOW HIRING)

DPR Construction

Scheduler - Traveler

Denver, CO · On-site

Develop contract (baseline) schedule and maintain contract schedule updates with project teams ... Experience with Smartsheet is a plus. Qualifications We are looking for a flexible, detail-oriented ...

Vero Networks

Director of Network Implementation

Denver, CO · On-site +1

$135K - $155K/yr

Identification, bid management & contract negotiation with environmental, OSP engineering, and OSP ... Strong background in Google Suite (Sheets, etc.), Google Maps, Google Earth, Smartsheet PREFERRED ...

EchoStar

Finance Manager

Englewood, CO

$83K - $125K/yr

Our business reach spans satellite television service, live-streaming and on-demand programming ... and Smartsheet tools * Contract & Vendor Management: Partner with Supply Chain and Legal to ...

Araco Group LLC

Be Seen First

Pre-Construction Coordinator

Colorado Springs, CO · On-site

$24 - $29/hr

Software Knowledge: Foundation, Smartsheet, ProEst, Trimble Business Center & Blue Beam ... contract price runs using estimating software, spreadsheet software, hand calculations, etc.

New

Araco Group LLC

Be Seen First

Pre-Construction Coordinator

Colorado Springs, CO · On-site

$24 - $29/hr

Software Knowledge: Foundation, Smartsheet, ProEst, Trimble Business Center & Blue Beam ... contract price runs using estimating software, spreadsheet software, hand calculations, etc.

New

Araco Group LLC

Be Seen First

Pre-Construction Coordinator

Colorado Springs, CO · On-site

$24 - $29/hr

Software Knowledge: Foundation, Smartsheet, ProEst, Trimble Business Center & Blue Beam ... contract price runs using estimating software, spreadsheet software, hand calculations, etc.

New

Onterris

Workday Analyst - Financials & Projects

Denver, CO · On-site +1

$85K - $100K/yr

Our scientists, engineers, field teams,consultantsand professionals collaborate across disciplines ... Support the maintenance of WorkdayPSA (Projects Billing, Project Budgets, Contracts, Invoicing ...

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All JobsContract Smartsheet Developer JobsContract Smartsheet Developer Jobs in Colorado

Contract Smartsheet Developer information

What are the key skills and qualifications needed to thrive as a Contract Smartsheet Developer?

To thrive as a Contract Smartsheet Developer, you need expertise in Smartsheet platform features, workflow automation, and data integration, typically backed by experience in business process optimization or a related field. Familiarity with Smartsheet Control Center, DataMesh, and APIs, and certifications like Smartsheet Product Certification are highly valuable. Strong problem-solving, communication, and client management skills set top developers apart in this role. These skills ensure that you can deliver efficient, scalable solutions tailored to client needs while maintaining clear collaboration and project success.

What is a Contract Smartsheet Developer?

A Contract Smartsheet Developer is a professional hired on a contractual basis to design, develop, and optimize solutions using Smartsheet, a popular collaborative work management platform. Their responsibilities typically include creating custom workflows, automating processes, and integrating Smartsheet with other systems to meet a company’s unique business needs. They often work remotely or as consultants and may collaborate with project managers, IT teams, or business analysts. Contract Smartsheet Developers must have strong technical skills and a good understanding of project management principles.

What are the typical challenges a Contract Smartsheet Developer might face when working with diverse client projects?

As a Contract Smartsheet Developer, you may encounter projects with varying requirements, levels of Smartsheet adoption, and client familiarity. A common challenge is quickly understanding unique business processes and translating them into efficient Smartsheet solutions under tight deadlines. Additionally, you might need to integrate Smartsheet with other tools or systems, which requires both technical adaptability and clear communication with client stakeholders. Effective time management and the ability to educate clients on best practices are also key to overcoming these challenges and delivering successful outcomes.
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Contract Smartsheet Developer jobs near you

Senior Process Engineer, Drug Product Development

Umoja Biopharma

Louisville, CO • On-site

$108K - $140K/yr

Full-time

Medical, Dental, Vision, Retirement, PTO

Re-posted 29 days 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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