Simulacra

Design and draft mechanical central plant boilers and chilled water systems, specify and locate equipment, and assess existing building systems for future designs. | Bachelor's degree in Mechanical Engineering, 5-10+ years of mechanical design experience, P.E. license preferred, strong AutoCAD and MEP knowledge, and ability to lead projects. | Join a rapidly growing engineering company who is looking for a high-performing MEP (Mechanical, Electrical, and Plumbing) Engineer. Overview The ideal candidate will create, draft, and design mechanical central plant boilers and chilled water systems taking into account the customer’s energy plan and usage profiles. This individual will specify, size, schedule, and locate equipment on plans, schedules, elevations, and detail using AutoCAD. Additionally, they will examine existing building systems and recommend alternatives for future designs. This is a remote position with site visits requiring about 15% travel. Responsibilities P.E. (Professional Engineer) license preferred. Applicants must have a minimum of 5-10 years of experience as a Mechanical Design Engineer. It is expected that the assignments will involve, but not be limited to, the following areas of engineering work: • Design of conditioned air, hot water/steam, gas, and plumbing to residential, commercial, and industrial facilities from field survey to construction support. • Knowledge of monitoring and control parameters for the aforementioned systems. • Site Utilities and Central Plant Design. • Knowledge of Building, Energy Conservation, and Plumbing Codes • Familiarity with project delivery methods, and QA/QC procedures • Assess the feasibility of product design. • Review maintenance and operation of existing equipment. Qualifications • Bachelor's degree in Mechanical Engineering or related field • 5-10+ years of industry experience • Strong knowledge of mechanical parts and computer-aided design • Ability to lead projects independently • Great written and verbal communication skills Skills • Mechanical Engineering • Computer-Aided Design (AutoCAD) • Mechanical, Electrical, & Plumbing (MEP) • Design • Engineering • Central Plant Design • Specifications • Capital Plans • Feasibility Studies • Assessments Compensation & Benefits • Competitive base salary according to experience • Collaborative team culture • Benefits package By applying, you give your consent to be submitted to our client for this opportunity. Only qualified candidates will be contacted.

Manage QMS documentation and compliance, support audits and CAPA activities, and handle customer service operations including order processing and customer inquiries. | Bachelor's degree in a technical/scientific field, proficiency in Microsoft Office and Visio, experience with QMS and CRM, understanding of medical device compliance, and customer service or sales experience. | Company Join a high-growth company in the Medical Device industry. They are seeking a high-performing Document Control Specialist to join their dynamic team. Position Overview The Document Control Specialist is a dual-role where you’ll make a direct impact on both product quality and customer experience. You’ll help shape and grow their Quality Management System (QMS), ensuring they meet the highest industry standards, and even take the lead during unannounced audits—keeping their reputation for excellence intact. You’ll work hands-on with SOPs, CAPAs, customer feedback, and supplier files, gaining valuable exposure to regulatory processes. In your capacity as a Customer Service Representative, you’ll be at the heart of operations—partnering with leadership to issue quotes, fulfill domestic and international orders, coordinate with the warehouse, and deliver outstanding service to customers worldwide. This is a unique opportunity to build skills across quality, compliance, and operations in a fast-moving, mission-driven medical device company. Position Details • Status: Full-Time • Hybrid: Onsite 1-2 Days Per Week • Location: Chicago, IL Quality Responsibilities • Support the upkeep and improvement of the Quality Management System (QMS) to ensure all processes, documentation, and records meet current regulatory and industry standards. • Manage controlled documents, supplier evaluations, and training records, ensuring they are accurate, current, and in compliance with company procedures and global regulatory requirements. • Assist with audits, CAPA activities, and product complaint investigations, as well as regulatory compliance for new product development from planning through launch. • Coordinate internal audits and step in to host external audits when leadership is unavailable. Customer Service Responsibilities • Act as a first point of contact for customers, handling inquiries, orders, returns, and account updates in a professional and timely manner. • Prepare quotes, process domestic and international orders, and work with warehouse and leadership teams to ensure accurate, on-time delivery. • Manage order and inventory data in company systems, including e-commerce and accounting platforms, while supporting international shipping documentation. • Assist leadership with high-priority operational tasks, including urgent customer needs and potential product recall coordination. Qualifications • Bachelor's Degree in a technical or scientific discipline • Proficiency in Microsoft Office and Visio • Experience with QMS (Quality Management System), CRM (Customer Relationship Management), and regulatory documentation • Understanding of standards and compliance requirements for medical devices • Sales and/or customer service experience • Interpersonal and communication skills • Strategic mindset with attention to detail Compensation & Benefits • Base Salary according to experience • Benefits Package • Retirement plan If you're an experienced Quality Associate or Document Control Specialist, we invite you to apply and be part of shaping the future of the Medical Device industry. By applying, you give your consent to be submitted to our client for this opportunity. Only qualified candidates will be contacted.