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This client based North of Dayton, OH, has been recognized as a world leader in developing bold products and bringing them to market. Their goal is to produce high-quality products that exceed customers’ expectations. They have a high regard for their employees and have a work culture that excites professionals in all disciplines. The Product Design Engineer will lead the design and development of product specification in 3D, Layout, detail and assembly drawing in compliance with project....


The Manufacturing Engineer (Tooling), requires a person with knowledge of supporting manufacturing processes in a manufacturing plant. This includes supporting production, procuring tools, documenting (drawing) tools, writing work instructions, and quoting new tools/machines. Will maximize efficiency by analyzing layout of equipment, workflow, assembly methods, and work force utilization. Determines parts and tools needed in order to achieve manufacturing goals according to product....


Pharmaceutical company in need of Director or Senior Director to join the Medical Affairs team. The Medical Director will provide support and expertise in the area of psychiatry either Schizo or Addiction as there are two needs In this newly created and high profile role you will serve as the medical affairs strategic lead for our combination oral schizophrenia treatment that is currently in phase 3 clinical development. The Medical Director is expected to establish key medical strategies for....

- Kalamazoo, MI

The Product Manager is responsible for assisting, and managing details as they related to the sales team functions of the food business. Responsibilities: Communicate with VP of Sales, R & D Manager, field sales account managers, customers, and all internal departments.Manage product inventory levels.Make recommendations on present & potential future lines. Assist CEO, & VP of Sales with projects.Establish internal forecast system in effort to maintain inventory levels.Provide....


Sr Principal Engineer - Clean Room Development Industry leading medical devices company seeks a Sr Project Manager to lead global design and construction of medical device clean rooms. This is a sole contributor role. TheSr Principal Engineer/ Project Manager - Clean Room Development will essentially be the company's subject matter expert on clean rooms globally and will be responsible for leading international teams from design through qualification of both new clean rooms as well as....


Our client is a world leader in the manufacturing and distribution of analytical instrumentation used in R&D Laboratories. They have an opening for a Field Service Engineer to be based in the Chicago area or Milwaukee. The Field Service Engineer provides on-site service including preventative maintenance, calibration, installation, and training across all product lines.Responsibilities & QualificationsThis position will be based in or near the Chicago area but will also conduct....


Our client is a world leader in the manufacturing and distribution of analytical instrumentation used in R&D Laboratories. Due to continuing growth they have opening for a Field Service Engineer to be based in the Kansas City, St. Louis or Springfield. This position may also conduct supplemental travel into other territories on a regular basis.Requirements:Duties include the preventative maintenance, troubleshooting, repair, and calibration of instruments in R&D Labs in the assigned....


Here is an excellent opportunity with a new food products plant, a division of a thriving national company, located in Wooster Ohio. Quality Assurance Analyst -- $60-75,000 -- experience required with SQF in food or dairy or beverage or pharma manufacturing -- relocation paid! Requirements for the QA Specialist: - Bachelor degree - 2-5 years of Quality Assurance experience in food related manufacturing. - Proficient with SQF - Must be US Citizen or Green Card. Sponsorship is not available The....


We are looking for an Incoming Associate who will be responsible for inspecting and sampling materials.Responsible for reading and understanding all the accompanied paperwork, which includes but is not limited to: Packing Slips, Bills of Lading, Certificates of Analysis (CoA), Certificate soft Compliance (Coca), Printed Material Proofs, & Material Safety Data Sheets (MSDS). The QCIA will inspect all received materials for identity, quantity, and damage. Processing and bookkeeping of all....


Provide technical expertise to department & senior level analysis to site managers in a wide range of environmental, health & safety disciplines to achieve compliance w/ company EHS standards (national, provincial/statewide & local requirements). EHS Programs Specialist be directly responsible for ongoing support & coordination of multiple key EHS programs the plant level. Programs include, but are not limited to PSM/RMP, VPP, ISO, Radiation Safety, chemical management (TSCA,....


Well-established Medical Device manufacturer has a unique opportunity for a Technical Service Manager for their line of Dialysis equipment. The Technical Service Manager will develop and manage end-to-end service of dialysis equipment in North America. This includes the installation, service and repair, and assisting with in-servicing the Sales and Clinical teams, and with external customers, on the (non-clinical) use of equipment. The Technical Service Manager will be responsible for managing


The Quality Assurance Generalist I (QAG I) reports to the Quality Assurance Supervisor. This position is responsible for the daily Quality Assurance support in the Manufacturing and Packaging process on site. They will be required to review all appropriate documents during the production process. In this role, the QAG I will be readily available to support the production process; therefore, this position requires that the associate stays on the production floor for the majority of the work....


Summary of the Position: The Batch Record Reviewer is responsible for the review and release of batch records, Certificates of Analysis and other pertinent document and relaying this information to the appropriate departments. Roles and Responsibilities:Communicating accurate and up-to-date status reviews to appropriate personnel and updating the Finished Product Release spreadsheet. Additionally on a daily basis, the Batch Record Reviewer will assist in the correction of deficiencies found....

- Lancaster, SC

We are looking for a Quality Control Chemist to work in a cGMP laboratory who will operate laboratory instrumentation, troubleshoot and generate/revise SOPs and test methods.The Quality Control Chemist (QCC) reports to Quality Control (QC) Management.The QCC will stay current on publications released by USP, FDA and other pertinent regulating bodies to ensure the Quality Control Chemistry Laboratory complies in the areas of analytical applications, release specifications, and documentation....


Principal Injection Molding Process EngineerCompany: Our client is a leading manufacturer of injection molded proprietary products located in the Northeast US. This company is a leader in their market, and their products are highly innovative. You will be the resident molding and plastics expert, and will be responsible for specification of materials, ensuring appropriate tooling designs, ensuring proper manufacturing equipment and justifying the purchase and installation of Capital Equipment....


The Senior Manager Clinical Operations is responsible for developing operational strategy for one or more clinical studies, and leading the cross functional Study Management Team to align and deliver on study goals of data quality, timelines, budget and GCP compliance in support of overall program level plans. Responsibilities: The Senior Manager Clinical Operations Lead will independently plan all aspects of the clinical operations for one or more clinical studies and oversee the execution of


Job Category: Research & Development The Senior Clinical Program Leader I3 (Inflammation, Immunology and/or Infectious Disease) is accountable for the operational strategy, planning and execution of the clinical development portfolio up to LIP for the designated Discovery and Translational Area (DTA).You provide the primary interface between the I3 DTA and pRED’s the Clinical Program Execution (CPEX) function in Clinical Operations, oversight for program and study management, line....


We are looking for a Quality Assurance Document Control Associate to provide assistance with maintaining a GMP documentation system. Roles And ResponsibilitiesAssist in implementing information systems for managing document tracking, controlled document distribution (issuance) and records management.Oversee the issuance and maintenance of logbooks.Facilitate the final review of production batch records.Assist in administering the change control system (issuance, tracking, and....

- Charlotte, NC

Perform release and stability testing on raw materials and finished products following Standard Operating Procedures (SOPs), in-house test methods, and/or compendial methods.Train in the operation of the following instrumentation: Laboratory Balances, High Performance Liquid Chromatographs (HPLCs), Gas Chromatographs (GCs), Automated Titrators, and Dissolution and Disintegration Instrumentation. The operation of additional instrumentation and/or the performance of additional test methods may....

- Lancaster, SC

Perform release and stability testing on raw materials and finished products following Standard Operating Procedures (SOPs), in-house test methods, and/or compendial methods.Train in the operation of the following instrumentation: Laboratory Balances, High Performance Liquid Chromatographs (HPLCs), Gas Chromatographs (GCs), Automated Titrators, and Dissolution and Disintegration Instrumentation. The operation of additional instrumentation and/or the performance of additional test methods may....

61-80 of 91 results