A global leader in animal health with a multi-million-dollar global footprint is seeking a Senior Quality Associate – Sterility Assurance to coach QA manufacturing operations on the floor. The person will oversee and contribute to Sterility Assurance/Contamination Control Strategy deliverables.

Responsibilities

•  You will serve as the primary technical expert in contamination control, aseptic processing, and sterilization.
•  Coach and oversee the validation and qualification of facilities, processes, equipment, and systems related to sterility assurance, including aseptic processing, media fills, and sterilization cycles.
• Identify and troubleshoot issues related to sterility assurance.
• Responsible for operational excellence/continuous improvement of the site.

Qualifications & Requirements 

• 3+ years of experience in sterile processing, and contamination control.
• 5+ years of QA experience in GMP environment
• Experience coaching on floor as related to QA for manufacturing operations
• Hands on environmental monitoring, medial fills and aseptic training/gowning experience.

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

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

Company Overview

A globally recognised reinsurance business, headquartered in the US, is looking to strengthen its International Reserving function with the addition of a Senior Actuarial Analyst. The organisation operates across multiple European hubs, with reserving teams embedded in key locations.

Key Responsibilities

• Take ownership of reserving analyses across a global facultative portfolio, assessing reserve adequacy and performance
• Support quarterly reserving processes, including monitoring results and investigating key movements
• Contribute to year-end reserving reviews and more detailed portfolio analyses
• Partner with underwriting, claims, pricing, and finance teams to gain a deeper understanding of business performance
• Provide input and peer review within the wider international reserving team
• Play a role in refining reserving methodologies and enhancing existing tools

Key Requirements

• Nearly or newly qualified actuary (or equivalent)
• Around 3 – 5 years of experience in general insurance actuarial roles, ideally with a focus on reserving
• Exposure to reinsurance or a consulting environment would be beneficial
• Strong analytical mindset with the ability to interpret and communicate complex data
• Comfortable working across teams and engaging with stakeholders in different regions
• Self-starter who is confident taking ownership within a lean team structure

Technical Skills:

• Advanced Excel skills are essential
• Experience with tools such as VBA, SQL, or Python is advantageous
• Familiarity with reserving software (e.g. ResQ) would be beneficial

Please note: this role does not offer visa sponsorship.

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.

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Principal Electrical Engineer – Medical Devices | Northwest Minneapolis Metro

We are seeking a Principal Electrical Engineer to play a critical role in the design, development, and testing of electrical and electronic systems for medical devices. This individual will work collaboratively within a multidisciplinary engineering team and engage directly with clients to ensure product excellence and compliance with regulatory standards.

Duties and Responsibilities:

• Lead and manage the design and implementation of complex electronic systems
• Oversee and mentor junior engineers and technical staff
• Collaborate with cross-functional teams to define product requirements and specifications
• Conduct analysis of electrical systems, creating schematics and detailed technical documentation
• Implement testing protocols to verify adherence to performance and functional criteria
• Resolve technical challenges and perform root cause analysis on issues that arise
• Act as the primary technical interface with clients, maintaining strong communication to deliver project updates and address concerns
• Maintain knowledge of industry trends, emerging technologies, and regulatory requirements to drive innovation
• Contribute to design reviews and project planning discussions

Requirements:

• Bachelor’s Degree in Electrical Engineering or a related field; Master’s Degree or higher preferred
• Minimum of 8 years of relevant experience in electrical engineering with a focus on medical devices
• Proficient in electronic hardware design with a strong understanding of both analog and digital circuitry
• Experience with testing equipment and debugging tools
• Familiarity with embedded firmware development, preferably using C and C++
• Strong analytical and problem-solving skills
• Excellent communication and interpersonal abilities
• Demonstrated leadership skills with the ability to mentor junior team members
• Strong organizational skills with the ability to manage multiple projects and priorities effectively
• Knowledge of design software such as Altium is a plus

Instrumentation and Controls Engineer

JCW Group have partnered with a leading organization in the water utilities sector seeking an Instrumentation and Controls Engineer to support the design, maintenance, and optimization of control systems, instrumentation, and data communications for water and wastewater facilities.

Key Responsibilities:

• Support operations teams by keeping process control systems running reliably and efficiently.
• Carry out routine and corrective maintenance on PLCs, HMIs, instrumentation, and associated equipment.
• Assist with SCADA system configuration, upgrades, and integration of new devices.
• Contribute to the design, installation, and commissioning of process control projects.

Qualifications:

• Associate’s degree in Engineering, Industrial Automation, Information Technology, or equivalent hands-on experience.
• Proficiency in PLC programming (Allen-Bradley) and HMI configuration (Wonderware).
• 2-4 years of experience in process control systems, industrial networking, or electrical engineering.
• Familiarity with data communication networks such as Ethernet/IP or radio telemetry is a plus.
• Valid driver’s license with a clean driving record.

For more information, apply here or contact [email protected]

A rapidly expanding life sciences manufacturer is seeking an Engineering Director to lead process engineering operations at a key production site. This is an opportunity to step into a highly visible leadership role with strong long-term growth potential and direct influence on site performance and strategic direction.

The successful candidate will lead a team of 15 engineers supporting equipment and process operations across commissioning, validation, qualification, and continuous optimization initiatives.

Relocation assistance is available for the right candidate.

Key Requirements:

• Bachelor’s degree in Chemical Engineering required
• 10+ years of engineering experience within regulated manufacturing environments
• Prior experience in biologics, biopharmaceutical, or broader life sciences manufacturing
• Proven people leadership experience with a track record of building and developing high-performing engineering teams

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

Sr. Systems Engineer | Medical Device | Electro-Mechanical Systems

About the Role

Are you a systems engineering professional who thrives at the intersection of complex electro-mechanical design and cutting-edge medical device development? This is your opportunity to take ownership of technically challenging projects, serve as a key client-facing engineer, and help bring life-changing medical devices to market.

Location: Northwest Minneapolis Metro
Schedule: Full-time, 5 days onsite

What You’ll Do

• Lead the development of electro-mechanical systems and system architecture, backed by thorough documentation aligned with quality system procedures.
• Own the technical project scope across multiple concurrent programs, serving as the primary point of contact for customers.
• Drive requirement development – both internal and customer-facing – and ensure full traceability through verification and validation.
• Contribute to risk management planning, risk analyses, and Hazard Analysis documentation.
• Coordinate system-level analyses including modeling, algorithm development, simulations, and architecture design.
• Facilitate cross-functional technical discussions and design reviews throughout the product realization process.
• Play an active role in identifying technology reuse opportunities and protecting intellectual property.
• Help shape the team – identify training needs, assess technical talent, and contribute to building a high-performing systems engineering function.

What You’ll Bring

• Bachelor’s degree in Engineering or Computer Science; Master’s degree a plus.
• 5+ years of systems engineering experience, ideally in medical devices.
• Working knowledge of IEC 60601, ISO 13485, ISO/EN 14971, and IEC 62304.
• Familiarity with FDA 510(k), PMA, and De Novo submission processes.
• Experience with Class II and/or Class III medical device development.
• Proficiency with Matlab, Simulink, or similar modeling tools is a bonus.
• Experience with requirements management tools is a plus.

Work Authorization

Candidates must be authorized to work in the United States without sponsorship, now or in the future. This position does not offer visa sponsorship.

Why This Role

This isn’t a siloed engineering position – you’ll be a technical leader, a cross-functional collaborator, and a direct contributor to products that matter. If you’re ready to step into a high-impact role where your expertise shapes both the product and the team around you, we want to hear from you.