Product Manager Jobs in Massachusetts

Job Title: Manufacturing Manager Company: Genzyme Location: Allston, MA Description: Genzyme Corporation, ranked as one of the foremost biotechnology companies in the world, is committed to providing an exceptional environment in which individuals can excel, and achieve their professional and personal goals. Genzymes people and culture have been consistently recognized for excellence. For example, we have been named several times to Fortunes list of the 100 Best Companies to Work For in the United States. We also consistently rank among the top employers for scientists in surveys of Science readers. Genzymes local offices and facilities in Europe and other parts of the world have earned similar distinction as respected employers. By applying for a position with Genzyme, you are taking the first step toward becoming a part of our dynamic and talented team, and sharing in our continued success.. Manufacturing ManagerJob Responsibilities/Department description:Manages a small to medium size group of employees focused on one or more areas in the planning, development, implementation and maintenance of manufacturing process within a Protein Purification Production environment. Defines necessary resources to meet production schedules that may run across multiple shifts. Applies standard costs and use of materials, labor and machines which can affect standard costs. Investigates labor, cost and process variances and deviations. Contributes to annual budget process through creation of financial schedules for their operation. Implements subsequent changes in methodologies.

Job Title: Manufacturing Manager Company: Top Echelon Network Location: Lynn, MA Description: The Manufacturing Manager reports directly to the General Manager/VP for this small divisional plant. Responsible for leadership of the Manufacturing, Shipping/Receiving, and Materials groups. Ensures all groups function and perform as a team. Supports the flawless launch of new products and processes to production. Attains annual objectives of plant metrics and sales. Requirements BS degree in Engineering or Technical Management. A minimum of 5-10 years of progressive manufacturing experience with medical device, pharma, bio-med and/or healthcare products. 5 years in a people management position. Experience in Lean Manufacturing, ERP/MRP systems, and supply chain management. A minimum of 5 years experience hands on injection molding processes. Familiarity with FDA CFR Title 21, FDA CGMP, and ISO standards including ISO-13485. Material engineering experience with scrap rate and inventory matrixes. Employee performance improvement experience with a diverse workforce. Demonstrated oral, written and interpersonal communication skills, including presentation skills. Proficient PC skills including MS Word, Excel, PowerPoint Facilities management experience.Duties Oversees all levels of manufacturing to ensure smooth operation of departments, leading to 100% On-Time Delivery, 100% Customer Lot Acceptance while maintaining an acceptable level of inventory, and other metrics as determined. Ensures that proper support is provided to production on injection molding of silicone materials and processes, assembly and packaging processes; troubleshoots process issues as required. Ensure adequate and comprehensive training and development of all responsible department employees. Develop training programs and procedures to document adequate training in compliance with internal procedures. Responsible for implementing Lean/Kaizen Systems including engagement of employees and driving continuous improvement within the facility including cost cutting where appropriate Interfaces with customers on product delivery issues, and assures past dues, and overtime goals are met or exceeded. Sets targets to improve productivity, reduce scrap and material waste; for effective training of production personnel using standard work Work with Management to assure that effective quality personnel are hired and developed. Improve set-up reductions, maximize equipment utilization and provide measurements on performance monthly. Assists with maintaining and support of the Quality System to ISO 13485:2003 standards. Develop, maintain and improve as necessary the documentation system for all internal processes, inspection criteria, Bill of Materials, Routers, and other documents as required in regard to GMPs. Work with Sales, Quality, and Program Management functions to coordinate launch of new projects.   See all jobs in Lynn MA