Manufacturing, Production, Operations category and Biotechnology & Pharmaceuticals industry jobs in Massachusetts

. Adecco Medical and Science, a division of the world leader in the recruitment of medical and scientific professionals, has an immediate opening for a Manufacturing Technician on a 12+ Month contract opportunity in Medford, MA. The primary role of this position is to execute and properly document, per GMP, the manufacturing processes required to manufacture textile-based medical devices. These pr...
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. The Allston Landing Facility Support Services Department is comprised of Media Prep and Buffer Prep Departments and is an integral part of the Bulk Manufacturing Organization. Support Services' primary responsibility is to produce and deliver large and small-scale media and buffers to support Upstream and Downstream Manufacturing Operations. THIS POSITION WILL REQUIRE ALTERNATING WEEKEND COVERAG...
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Primary Role Reporting to Systems & Programs as a part of Facilities & Engineering (F&E), this position will be a strategically-focused role, partnering with clients on a daily basis across the various groups within F&E in support of all Rare Diseases BU functions. This role will build and embed processes, methodologies and common tools of a continuous improvement culture. The incumbent will look ...
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Primary Role: Serves as Senior Metrology representative at a specific location. Individual schedules calibration events, performs scheduled and unscheduled calibrations, repairs Measurement and Test Equipment. Acts as the metrological technical representative at a specific location. Responsibilities: Schedule and perform calibrations IAW SOP's or manufacturers procedures on Measurement and Test Eq...
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The Manufacturing Associate 2 operates ancillary equipment process equipment downstream activities. Follows and maintains GMPs and standard operating procedures to comply with regulatory requirements. Receives minimal supervision, expected to make adjustments to day to day operations. Provides guidance to lower level operators on technical/GMP procedure. • Operates BSC's, microscopes, incubators, ...
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. Responsible for ensuring that Manufacturing, Utility, and QC equipment is operating in its validated state. Responsible for managing the Validation-Requalification department consisting of supervisors and validation specialists. Responsible for ensuring "right first time" execution of validation protocols and the generation of final reports. Additional Responsibilities include: Management Provid...
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. Position Summary This position will support Upstream and Downstream Purification Operations including Micro Filtration, Chromatography, Buffer Preparation, Ultra-Filtration, and Final Formulation. The Manufacturing Specialist III uses expert knowledge of compliance and cGMP manufacturing processes to manage investigation and improvement initiatives within manufacturing operations. Core Responsib...
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About the company Our client is a global life sciences company that is experiencing steady growth in the MA market. This client is a well known industry leader in their field. Job description The Associate Director of Supply Chain Planning will develop the functional strategy in direct support of the site objectives and manufacturing plan, ensuring strong functional and site alignment. In this rol...
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Production Control Manager (Boston area) Our client is a fast growth global medical device leader. This is a great opportunity if you are seeking to join a highly innovative and financially solid industry leader that promises challenging leadership opportunities! Reporting into the VP of Operations, you will lead all aspects of the order entry, prep-to-ship, shipping and material control work cent...
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Company: Siemens Healthcare Diagnostics Inc. Division: SMSD - Diagnostics Location: MA - Walpole Req ID: 123334 Position Title: Setup Mechanic - 3rd shift (automated packaging/ filling equipment) Experience Level: Mid Level Education Required: High School Diploma Travel Required: No Company Description: Siemens’ Healthcare Sector is one of the world's largest suppliers to the healthcare industry a...
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Position Summary: The Analytical Chemist will have wide-ranging responsibilities as a member of a late-phase clinical and commercial manufacturing process development group. In support of in-house laboratory trials: perform or coordinate method set-up and training on analytical instruments, particularly HPLCs and GCs; train and assist other lab personnel in the preparation of samples and in the us...
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Position Summary: The primary role will be to develop chemical and purification processes for late phase clinical and commercial manufacturing in the Manufacturing Process Development group. The successful candidate will be responsible for laboratory experiments to support the development of robust, well understood chemical and purification processes. This will involve design of synthesis, identif...
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. The Allston Manufacturing organization consists of the following functional groups: Upstream Operations, Downstream Operations, Scheduling, and the Warehouse. The primary responsibility of the Manufacturing organization is the faithful execution of the current set of instructions, ensuring practice matches procedure, to assure high product quality and compliance with current cGMPs and Genzyme Qu...
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. Job Title: Senior Site Controller The New York Ave 45/51 Management team provides strategic vision, leadership and direction to the New York Ave 45/51 site to ensure reliable supply of high quality medicine to patients. They ensure Safety and Quality compliance of operations. The Management team defines the manufacturing strategy for the site by establishing long range plans and business/operati...
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Primary Duties The Associate Director, Global Clinical Supply Chain & Logistics is responsible for providing leadership and direction to facilitate the planning and execution of Clinical Supply Chain activities globally. This position will oversee operations including clinical packaging, labeling, and distribution. The Associate Director is responsible for developing and formalizing robust process...
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Quanterix is an exciting early stage company whose mission is to develop a game-changing platform that combines proprietary single-molecule sensitivity, multiplexing, and full automation. We are seeking an experienced and highly motivated Manufacturing Technician to join our Manufacturing Operations Group. If you have experience with large or small scale reagent manufacturing, this could be a very...
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About the company Our client is a global life sciences manufacturer that is experiencing steady growth in the MA market. This client is a well known industry leader in their field. Job description In this newly opened role as a Sourcing Manager (Chemicals), you will be responsible for establishing a category strategy and managing a portfolio of raw materials as well as contract manufactured finish...
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. POSITION OVERVIEW/KEY RESPONSIBILTIES: The Manufacturing Specialist uses expert knowledge of compliance and cGMP manufacturing processes to manage and own all process related documents, to include investigation and improvement initiatives within downstream operations. In addition, the Specialist is responsible for: Authoring, reviewing, and improving documentation, utilizing Genzyme's Documentat...
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. Downstream Operations is responsible for Cerezyme protein purification operations at Genzyme's Allston Landing, a large-scale therapeutic protein manufacturing facility. Downstream Operations' main function is multi-stage large scale chromatography operations. In support of our main functions, our additional functions include cleaning and sterilization of process equipment, preparation of bulk p...
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. DEPARTMENT DESCRIPTION: The Purification Operations Department performs multi-stage large scale chromatography, tangential flow filtration operations, cleaning and sterilization of process equipment, final formulation operations, and/or preparation of bulk product for shipment as part of a 24/7 large-scale therapeutic protein manufacturing facility. Position Summary The Manufacturing Supervisor ...
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The Director, Viral Manufacturing will lead the planning, execution, troubleshooting and maintenance of process validations, manufacturing activities, data and documentation to support the manufacturing technology team in the cGMP Processing of ACAM2000 and Japanese Encephalitis vaccines. This position will lead and coordinate the required internal process resources for the Canton Manufacturing un...
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Responsible for the production of viral products to meet established requirements in a cGMP manufacturing environment. Assures that operations are conducted in compliance with cGMPs, CBER, WHO, EP and other regulatory bodies. Manages people within a process team to meet the site goals and priorities. Plans and initiates the production schedule, coordinating activities with Manufacturing staff and ...
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Primary Duties: Operational & Strategic: Under the direction of the Clinical Supply Manager, the Senior Clinical Supplies Specialist manages all drug products and devices; packaging, labeling, Shipment and drug return logistical activities by interacting with both internal and external customers and suppliers in order to accomplish project objectives; develops IMP distribution and return drug plan...
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Primary Duties: Production control analysts serve the role as the primary point of contact for manufacturing for all material related needs. They will be responsible for ensuring material is available to manufacturing in support of the production schedule from the warehouse. They will maintain process specs and recipes, release and manage production orders, be responsible for the issuance of mater...
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Primary Duties: The Associate Director of Materials Planning is a member of the Site Leadership Team (SLT) and the Materials Management Leadership Team (MMLT). This person develops the functional strategy in direct support of the site objectives and manufacturing plan, ensuring strong functional and site alignment. This person is a leader in the utilization of the SAP system. Ensures maximum utili...
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