Looking for an Elite3E support analyst. 

looking for a business analytics 

JCW is working with a fast-growing fintech bank in Salt Lake City to find a Director of Model Validation to lead their independent model risk function. This is a senior role at the heart of a business that is scaling rapidly where rigorous model oversight is not a back-office function, but a genuine driver of how the bank grows responsibly.

If you have deep credit model experience, a track record of building or leading validation teams, and the credibility to engage senior stakeholders across risk, finance, and technology — this is worth a close look.

What the Role Involves

• Leading the independent validation of credit risk models — including PD, LGD, EAD, and CECL/IFRS 9 — across retail and commercial portfolios.
• Building and managing a high-performing model validation team, setting standards, processes, and governance frameworks as the bank scales.
• Overseeing the model inventory and ensuring all models in scope are validated, documented, and reviewed in line with SR 11-7 and internal policy.
• Engaging senior stakeholders across risk, finance, and the business to communicate findings, limitations, and recommendations clearly and with conviction.
• Partnering with model development teams to shape model design from the outset, promoting sound practice without slowing delivery.
• Supporting regulatory engagement — including examiner interactions — and contributing to the bank’s model risk appetite and governance committee work.
• Identifying gaps in the validation programme and taking ownership of continuous improvement across tools, methodology, and team capability.

Qualifications

• Significant experience in model validation, model risk management, or quantitative credit risk Ideally within a bank or regulated financial institution.
• Deep technical knowledge of credit risk models, including scorecard, PD/LGD/EAD, stress testing, and loss forecasting frameworks.
• Strong understanding of SR 11-7 and OCC guidance on model risk management, and how to apply it practically in a growing institution.
• Experience leading or managing a team of quantitative analysts or validators, with the ability to attract, develop, and retain strong talent.
• Comfort working across Python, R, SAS, or equivalent tools to review and challenge modelling work directly.
• Strong communication skills — able to translate technical findings into clear conclusions for risk committees, senior management, and regulators.
• Comfortable operating in a fast-moving environment where the function is still being built, and where initiative and ownership are genuinely valued.

JCW Group is committed to equal opportunity recruitment. We ensure that no applicant receives less favourable treatment on the grounds of gender, age, disability, religion, belief, sexual orientation, marital status, race, or any other protected characteristic.

I’m working with a pharmaceutical manufacturer in the Greater Denver area on a QA Supervisor opening.

Seeking candidates with:
• 6+ years of pharmaceutical or medical device QA experience
• Experience with deviations, investigations, and GMP compliance
• eQMS/document management system experience
• Strong technical writing skills
• Previous leadership experience

This role will lead a small QA team and partner closely with Manufacturing to support quality operations across multiple facilities.

Process Development / Validation Engineer Medical Device CDMO | Contract (6-9 Months)

About the Role

A leading medical device CDMO has an immediate opening for a contract Process Development / Validation Engineer to support an active catheter production line program. This engagement is driven by a high volume of validation work on a compressed timeline – OQs, PQs, and test method validations – and the team needs someone who can step in and take ownership of a process from day one.

Duration is 6-9 months

Responsibilities

• Write and execute OQ and PQ protocols for a catheter production line in partnership with internal engineering staff
• Execute test method validations including gauge R&R and attribute testing
• Perform statistical analysis and data analysis on validation outputs
• Author clear, complete validation reports
• Serve as the point of contact for the customer on the processes you own
• Interface with production operators throughout execution

Qualifications

Required

• 7+ years of experience in process development, validation, or a related engineering function within a regulated medical device environment
• Hands-on experience writing and executing IQ/OQ/PQ protocols and test method validations
• Proficiency in statistical analysis methods applicable to validation (gauge R&R, attribute testing, etc.)
• Strong written and verbal communication skills – this role interfaces directly with the customer
• Self-directed work style; able to identify what needs to be done and drive it to completion without daily direction
• Must be authorized to work in the U.S. without sponsorship

Preferred

• Catheter or flexible device manufacturing experience is a significant plus
• Familiarity with measurement systems analysis

Work Authorization

Candidates must be eligible to work in the U.S. without employer sponsorship now or in the future.

Engagement Details

• Type: Contract
• Duration: 6-9 months
• Location: On-site
• Start: Immediate

A commercial pharmaceutical manufacturer is seeking a Manufacturing Engineer to join its Northern Colorado site. In this role, you will serve as a key technical resource, supporting aseptic manufacturing operations while driving process improvements and enhancing operational efficiency.

Key Requirements:

• Engineering or scientific degree
• 3+ years of manufacturing experience within biotechnology, medical device, or pharmaceutical environments
• 1+ year of aseptic and sterile manufacturing experience
• 3rd shift is required

If you are interested in learning more, please send your resume and contact details to [email protected]

A commercial pharmaceutical manufacturer is seeking a Manufacturing Engineer to join its Northern Colorado site. In this role, you will serve as a key technical resource, supporting aseptic manufacturing operations while driving process improvements and enhancing operational efficiency.

Key Requirements:

• Engineering or scientific degree
• 3+ years of manufacturing experience within biotechnology, medical device, or pharmaceutical environments
• 1+ year of aseptic and sterile manufacturing experience
• 3rd shift is required

If you are interested in learning more, please send your resume and contact details to [email protected]

Looking for an SVP of ABS to lead credit analysis and structuring of commercial and esoteric ABS transactions.

A growing, regulated manufacturer is hiring a Production Maintenance Supervisor to lead maintenance operations supporting production, packaging, and aseptic processes.

Key Responsibilities:

• Lead and develop maintenance technicians
• Oversee preventative maintenance & equipment uptime
• Manage work orders, scheduling, and spare parts
• Support audits, investigations, and GMP compliance
• Drive continuous improvement across operations

Requirements:

• 5+ years in maintenance within a regulated environment (pharma/med device/etc.)
• Experience supporting aseptic / sterile manufacturing environments
• Prior leadership experience
• Strong GMP knowledge
• Experience with PM/work order systems
• Solid troubleshooting background