Key Responsibilities. Refine and Optimize Composite Manufacturing Procedures. Utilize Data Analysis and Statistical Techniques. Conduct Experiments and Evaluations. Identify and Address Manufacturing Challenges. Contribute to New Product Development. Manage Multiple Improvement Projects Simultaneously. Stay Updated on Advanced Composite Processing Methods.
Company Overview. ACE Partners is a leader in sustainable building solutions, focusing on innovative composite materials that prioritize energy efficiency and performance in the commercial construction sector. The organization has positioned itself as a frontrunner in the industry by emphasizing continuous improvement and providing a vibrant environment for engineering professionals eager to drive change
Qualifications. Bachelor's Degree in Mechanical Engineering or Industrial Engineering. 4-8 Years of Experience in Process Improvement or Manufacturing Engineering. Proficiency in Manufacturing Software Applications and Analytical Tools. Strong Foundation in Lean and Six Sigma Methodologies. Exceptional Problem-Solving Skills and Detail-Oriented Mindset. Excellent Communication Abilities. Benefits. Competitive Salary with Opportunities for Advance...
Position Overview. The. Manufacturing Process Improvement Engineer. will play a vital role in enhancing manufacturing processes, ensuring optimal production efficiency, and implementing innovative solutions. The ideal candidate will be a proactive problem solver with expertise in composite manufacturing and experience in using data analytics to foster improvements. This position requires collaboration with various teams, including engineering, op...
Controls Engineer - Vineland, NJ - 6 month rolling contract. W2 or 1099 only. Job Description. A leader in pharmaceutical glass manufacturing is seeking a Controls Engineer to join their team in Vineland, NJ. You will be responsible for programming and troubleshooting controllers on the factory floor and diagnosing equipment issues. Key Responsibilities. Maintain, troubleshoot, and program control systems (PLCs, HMIs, etc.). Support new equipment...
Job Title. Process Engineer / Mechanical Engineer – Sterile Filtration SME. Location. Philadelphia, PA (On-Site). Duration. 6 Months rolling for up to 2 Years. About the Role. We are seeking a highly skilled Subject Matter Expert (SME) with deep expertise in Filter Validation, Extractables & Leachables studies, and Sterile Filtration. Key Responsibilities. Lead and support filter validation efforts for sterile filtration processes. Conduct Extrac...
Regulatory Affairs Specialist – Medical Device Industry - $80k - $85k. Remote - Pocopson, PA. US Citizen or Green card holders only. No C2C. A leading medical device technology company is seeking a. Regulatory Affairs Specialist. to join their team. You will specialize in the design and manufacturing of cutting-edge spinal implants and surgical instrumentation. Their commitment to innovation, quality, and excellence has made them a trusted name i...
Regulatory Affairs Specialist – Medical Device Industry - $80k - $85k. Remote - Pocopson, PA. US Citizen or Green card holders only. No C2C. A leading medical device technology company is seeking a. Regulatory Affairs Specialist. to join their team. You will specialize in the design and manufacturing of cutting-edge spinal implants and surgical instrumentation. Their commitment to innovation, quality, and excellence has made them a trusted name i...
Regulatory Affairs Specialist – Medical Devices - $80k - $100k. US Citizens or Green card holders only. No C2C. An innovative medical device company is looking for a. Regulatory Affairs (RA) Specialist. to join their team. This role focuses on developing regulatory strategies, preparing U.S. and international submissions, and ensuring compliance for life-saving cardiac and vascular products. Key Responsibilities. Define and execute regulatory str...
A leading medical device company specializing in surgical and patient positioning solutions is seeking a. Senior Regulatory Affairs Specialist. to support global regulatory strategies and submissions. This role is critical in ensuring compliance with FDA and international regulatory requirements for a range of medical devices, including sterile, wireless, and cybersecurity-related products. Key Responsibilities. Prepare, compile, and submit regul...
Job Requirements. We are seeking a highly experienced Senior Manufacturing Engineer to develop and implement innovative manufacturing processes for single-use medical devices. This role requires strong leadership and organizational skills, as well as excellent communication and problem-solving abilities. Responsibilities. Develop and refine manufacturing processes to enhance efficiency, quality, and cost-effectiveness. Lead process verification a...
About the Role. We are looking for a seasoned Senior Manufacturing Engineer to lead the development and implementation of advanced manufacturing processes for single-use medical devices. This role requires strong organizational and leadership skills, as well as excellent communication and adaptability in dynamic environments. Key Responsibilities. Develop and refine manufacturing processes to enhance efficiency, quality, and cost-effectiveness. L...
