I am currently engaged on an Exclusive search for my key client; they are a Tier 1 bank seeking a Counterparty Market Risk VP. This is part of the teams organic and strategic growth. This is an exciting opportunity to be part of one of the largest banks in the USA with clear career progression.
Title: Counterparty Market Risk VP Overview: Organic growth within 2LOD has created a key role within an large existing team. This role will allow direct day to day access to collaborate with Regional and Global Heads of business. Clear and outlined career growth and true autonomy.
Key skills: – Counterparty market risk – Counterparty credit risk – SME knowledge of counterparty portfolio stress testing – Specialization in product areas such as FX options, Equities, Credit Derivatives multiple product knowledge is advantageous – Market Risk Stress testing – Counterparty Risk Portfolio
Work Authority: Green Card or US Citizen preferred Salary: $220,000 – $250,000 bonus: Varies dependant on expeirence Start Date: ASAP, however willing to wait for bonus season Location: Jersey City or NYC WFH: Hybrid, x3 days office based
For further information please contact me: [email protected]
I am currently recruiting X2 Hedge Fund Risk Credit Officers – Director. My client is a leading global bank and actively looking to grow their division due to continued strategic and organic growth across the division. This is an extremely exciting opportunity within a solid and well-established team.
Top skills
Right to work: Ideally US citizen – Green card holders Salary: $200,000 – $250,000 + Bonus Location: NYC Work schedule: Hybrid – x3 days office based For further information contact – [email protected]
Job Description Seeking an experienced Design Assurance Engineer to support product development and ensure compliance with medical device regulations. This role leads design verification/validation, risk management, and design control activities while driving continuous improvement in quality practices.
Responsibilities
Lead design assurance activities, including verification, validation, and risk management.
Prepare and maintain design control documentation (DHF, DMR, technical files).
Develop and execute test protocols/reports aligned with regulatory standards.
Analyze data and support regulatory submissions.
Oversee design reviews and provide team feedback.
Monitor regulatory updates and industry best practices.
Qualifications
Bachelor’s in Engineering (Master’s preferred).
5+ years of design assurance experience in medical devices.
Strong knowledge of FDA, ISO, and IEC standards.
Skilled in risk management, design controls, and statistical analysis tools.
Excellent communication, problem-solving, and teamwork skills.
Position Summary The Equipment & Facilities Engineer is responsible for overseeing the maintenance, calibration, and operational readiness of equipment, utilities, and facilities supporting cGMP manufacturing and laboratory environments. This role ensures the efficient, reliable, and compliant operation of site infrastructure. The ideal candidate will bring strong engineering expertise, hands-on technical problem-solving skills, and the ability to collaborate cross-functionally in a regulated environment.
Key Responsibilities
Facility & Equipment Maintenance & Operations
Quality & Regulatory Compliance
Project Management
Energy & Resource Management
Cross-Functional Collaboration
Documentation & Reporting
Additional Requirements
Location: On-site Duration: 6-month contract to hire Pay: $25–32/hr (flexible for strong candidates)
We are seeking a hands-on Manufacturing Operator to support a growing medical device operation. This role will primarily focus on manual laser welding, with cross-training across additional assembly and finishing processes. The ideal candidate enjoys working in a small, collaborative environment and brings a flexible, problem-solving mindset.
Key Responsibilities:
Perform manual laser welding on medical device components
Assemble delivery systems through multiple build stages
Execute reflow and final assembly processes (bonding, fastening, finishing)
Work across different processes based on daily production needs
Collaborate with Operations, Quality, and R&D teams
Required Qualifications:
Hands-on experience with manual (non-automated) laser welding
Manufacturing or assembly experience in a regulated environment
Strong attention to detail and communication skills
Comfortable working in a small, flexible team setting
Preferred:
R&D or development manufacturing experience
Catheter or micro-assembly experience
Vision systems experience (Keyence, MicroVu, or similar – can be trained)
Schedule:
On-site, 5 days/week
Flexible hours (typical shift ~6:00am–3:30pm)
This is a great opportunity to join a growing team with potential for long-term growth as operations scale.
Contract | Hybrid | Maple Grove, MN
Life Sciences · Quality & Engineering
We’re seeking a driven Supplier Engineer to lead critical remediation activities for contract-manufactured finished medical devices. This is a high-impact, cross-functional role where you’ll own supplier process validation reviews, collaborate with internal engineering and quality teams, and work directly with 10–20 contract manufacturers to close compliance gaps. If you’re hands-on, solutions-oriented, and not afraid to pick up the phone — we want to hear from you.
Important: W2 engagement only — Corp-to-Corp (C2C) arrangements will not be accepted. Candidates requiring visa sponsorship now or in the future will not be considered.
n/a
Location: Onsite Employment Type: Full-Time
We are seeking a Principal R&D Engineer to lead catheter-based medical device development from concept through commercialization. This is a senior technical leadership role responsible for end-to-end product ownership, driving design strategy, leading cross-functional teams, and ensuring successful design transfer into manufacturing. The ideal candidate brings deep catheter expertise, strong design control rigor, and the ability to independently drive complex programs with minimal oversight.
Lead product development activities from concept through commercialization in compliance with Quality System and design control requirements
Serve as technical lead and primary contributor for cross-functional development teams
Translate user, patient, and clinical needs into verified and validated device designs through robust requirements, specifications, and test methods
Drive conceptualization, design, development, and refinement of catheter devices and product line extensions
Own verification and validation activities through regulatory clearance and design transfer
Lead and facilitate design reviews; ensure timely completion of all design control deliverables
Design, assemble, and evaluate prototype devices to assess feasibility and performance
Develop robust test methods, fixtures, and protocols to evaluate materials, components, and designs
Collaborate closely with Process Development, Manufacturing, Quality, Regulatory, and suppliers to ensure scalable, manufacturable designs
Manage multiple projects simultaneously while maintaining schedules and acting as a primary technical point of contact for leadership
Identify technical risks early and implement effective mitigation strategies
Interface professionally with physicians and external partners while maintaining confidentiality and IP vigilance
Contribute to product portfolio strategy, continuous improvement initiatives, and departmental process enhancements
Mentor engineers and, where applicable, manage direct reports
Bachelor’s degree in Engineering or related technical field (advanced degree preferred)
7+ years of medical device R&D experience, including significant catheter development experience
Proven ownership of full product development lifecycles from concept through design verification and commercialization
Deep understanding of design controls, quality systems, and medical device regulatory requirements
Strong analytical and problem-solving skills with the ability to work independently
Excellent written and verbal communication skills
Proficiency with CAD tools (SolidWorks preferred) and standard engineering software
Familiarity with statistical techniques and engineering study documentation
Hands-on experience with common lab equipment (e.g., calipers, micrometers, tensile testers, pressure testers, vision systems)
Advanced knowledge of catheter materials and manufacturing processes (e.g., extrusion, injection molding, machining, tooling, adhesive and thermal bonding)
Demonstrated expertise in generating new catheter designs, materials, processes, test methods, and metrology
Experience supporting regulatory submissions and design transfer to manufacturing
Background in small-to-mid-sized OEMs or CMOs with broad technical exposure
Demonstrated ability to lead and mentor technical personnel
This role offers the opportunity to own high-impact catheter development programs, influence technical and product strategy, and play a key role in bringing innovative medical devices to market. You’ll work in a collaborative environment that values hands-on technical leadership, disciplined execution, and design
JCW is working with a prestigious single family office on a Tax Senior opening. In this role, you will work closely with the tax team and have exposure to the entire business. The team is looking for someone sharp and driven that fits into their collaborative team culture.
Responsibilities for this role include:
Requirements for this role include:
Amanda Esraeilian recruits for Tax professionals across NYC and would be happy to provide further details about this or other positions. You can reach her at 347-293-1534 or at [email protected]
