We are seeking a QC Supervisor to lead a team of analysts supporting pharmaceutical product testing and release in a GMP laboratory.

This role requires a strong analytical chemistry background, particularly with HPLC and GC, and the ability to support analysts with technical troubleshooting and day-to-day lab priorities.’

This is a on-site position(first-shift) in the greater Denver CO area. Relocation assistance is available.

Key Requirements

• Bachelor’s degree in Chemistry or related science
• Strong hands-on HPLC and GC experience (essential)
• Experience in a pharmaceutical GMP QC laboratory
• Ability to troubleshoot chromatography and support analysts technically
• Knowledge of USP / compendial testing (especially raw materials) is highly desirable
• Previous supervisory experience OR senior chemist ready to step into leadership

We are seeking a QC Supervisor to lead a team of analysts supporting pharmaceutical product testing and release in a GMP laboratory.

This role requires a strong analytical chemistry background, particularly with HPLC and GC, and the ability to support analysts with technical troubleshooting and day-to-day lab priorities.’

This is a on-site position(first-shift) in the greater Denver CO area. Relocation assistance is available.

Key Requirements

• Bachelor’s degree in Chemistry or related science
• Strong hands-on HPLC and GC experience (essential)
• Experience in a pharmaceutical GMP QC laboratory
• Ability to troubleshoot chromatography and support analysts technically
• Knowledge of USP / compendial testing (especially raw materials) is highly desirable
• Previous supervisory experience OR senior chemist ready to step into leadership

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QA Specialist — Deviation Writing and CAPA | Remote | Contract

A well-known biopharmaceutical company is managing a backlog of open deviations that needs to be addressed. This is a fully remote, short-term contract engagement — approximately 4 to 6 months — supporting a small unit of investigators working in parallel to write, analyze, and close a defined body of quality events. The site operates bioreactors, chromatography, tangential flow filtration, aseptic fill lines, and secondary packaging, and has ISO classified and grade-controlled rooms.

Responsibilities:

• Lead end-to-end deviation investigations including initial data review, gap identification, root cause analysis using structured methodologies such as 5 Why, fishbone, and 6M, and final closure in Veeva EQMS
• Review investigation packages to determine whether sufficient supporting data exists to justify conclusions — candidates must be able to recognize when an investigation is incomplete before writing to it
• Work collaboratively within a small remote unit where responsibilities may shift between initiating investigations, writing, and closing depending on workload and stage of each event

Qualifications:

• 4 to 7 years of GMP quality assurance experience — biopharma manufacturing background strongly preferred
• Hands-on experience writing and closing deviations and CAPAs in a regulated commercial manufacturing environment; sterile injectable or aseptic processing exposure is a plus
• Proficiency or familiarity with Veeva EQMS and demonstrated ability to work independently with minimal ramp-up time

Remote. Must be available to start quickly. One-and-done panel interview, 45 minutes. Target pay rate $40 – $45/hr W2.

A boutique asset management firm is seeking an entry level financial analyst to help support the production and maintenance of cash flow models

Senior Electrical Engineer – Transmission Line

JCW Group is partnering with a leading energy company to hire a Senior Electrical Engineer – Transmission Line. Lead high-voltage transmission line projects, oversee engineering deliverables, and ensure safe, cost-effective execution.

What You’ll Do

• Lead design and delivery of 69kV+ transmission lines and EHV projects
• Prepare drawings, bills of material, and specifications
• Apply NESC, ASCE, ACI, IEEE, and industry codes
• Mentor junior engineers and support client projects

What We’re Looking For

• B.S. in Electrical, Civil, or Structural Engineering; PE preferred
• 5–8+ years’ experience in utility transmission line design
• Expertise in PLS-CADD, PLS-POLE, MFAD, RISA-3D, and high-voltage systems
• Strong knowledge of industry standards and structural analysis codes

Apply here or contact [email protected] to learn more.

JCW is currently partnering on behalf of a growing regional bank that’s looking to hire an Audit Advisor for their Treasury, Liquidity and Finance Audit team. Acting as a manager for audit engagements, this role will be focused on the firm’s developing treasury function, which includes resolution planning, liquidity management, capital asset liability management and stress testing.

Responsibilities:

• Plan and execute risk-based audits focused on ALM, capital planning (including CCAR), liquidity risk, and resolution planning
• Lead a team of auditors as an auditor in charge
• Evaluate internal controls, risk management practices, and compliance for Treasury and enterprise risk
• Provide robust and independent challenge to the first and second lines of defense

Requirements:

• Bachelor’s Degreer required
• Demonstrable subject matter expertise in one or more of the following areas: Asset and Liability Management (ALM), Capital Planning, Stress Testing (CCAR/DFAST), Enterprise-wide Stress testing, and FDIC Resolution Planning (including RRP, IDI Plan, or 165(d) requirements).
• Experience working in a bank larger than $100b AUM
• Internal Audit experience ideal

Location: Onsite
Employment Type: Full-Time, Permanent

Overview

We are seeking a Process Development Engineer to support early-stage product development and drive the transition of new medical device designs into validated, manufacturing-ready processes. This role works closely with R&D, Manufacturing, and Quality to establish scalable, high-yield production processes.

Key Responsibilities

• Partner with R&D to translate design requirements into repeatable manufacturing processes

• Develop and mature processes from early development through pilot line and manufacturing transfer

• Design and specify production equipment, tooling, and fixtures

• Lead process characterization and yield improvement efforts

• Develop PFMEAs, process control strategies, and validation protocols

• Execute process validation activities (IQ/OQ/PQ)

• Train operators and support pilot line operations

• Own processes through stabilization and formal handoff to Manufacturing

Required Qualifications

• Bachelor’s degree in Engineering (Mechanical, Biomedical, Manufacturing, or related)

• 5+ years of Process Development experience in medical devices

• Demonstrated experience bringing products from R&D into commercial manufacturing

• Strong understanding of design controls and validation requirements

• Hands-on experience with process characterization and optimization

Preferred Qualifications

• Catheter manufacturing experience

• Electromechanical process exposure

• Experience in small-to-mid-sized OEMs or CMOs

Our client is major regional bank who are scaling aggressively within C&I and seeking seasoned C&I lenders.