Baxter International Jobs in Bethlehem

Currently, there are no Baxter International jobs available in Bethlehem, West Virginia. You may wish to explore jobs in nearby locations on the Baxter International jobs in West Virginia page or view related jobs below.
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Quality Associate III Job description This position is responsible for serving as subject matter expert for assigned Quality Systems processes, including but not limited to change control of product, process, and documents. Take leadership and/or subject matter expert role in normal day-to-day activities, routine and special projects, and continuous improvement efforts supporting assigned Quali...
Sr. IT Manager, Clinical & Medical Affairs Baxter Healthcare Corporation Round Lake, IL Overview • Baxter develops, manufactures and markets products that save and sustain the lives of people with chronic and acute medical conditions. As a global, diversified healthcare company, Baxter applies a unique combination of expertise in medical devices, pharmaceuticals and biotechnology to create pro...
Job Description: This position will consist of managing sterilization process before products are released as well as managing how the production process works. This role would be best fit for an Engineer that possesses sterility assurance/ science experience as well as project management skills. The position may require up to 20% travel, but mainly supports global manufacturing facilities from R...
Baxter’s products save and sustain the lives of people with hemophilia, immune disorders, infectious diseases, kidney disease, trauma, and other chronic and acute medical conditions. As a global, diversified healthcare company, Baxter applies a unique combination of expertise in medical devices, pharmaceuticals and biotechnology to create products that advance patient care worldwide. We ar...
Baxter’s products save and sustain the lives of people with hemophilia, immune disorders, infectious diseases, kidney disease, trauma, and other chronic and acute medical conditions. As a global, diversified healthcare company, Baxter applies a unique combination of expertise in medical devices, pharmaceuticals and biotechnology to create products that advance patient care worldwide. We ar...
Baxter’s products save and sustain the lives of people with hemophilia, immune disorders, infectious diseases, kidney disease, trauma, and other chronic and acute medical conditions. As a global, diversified healthcare company, Baxter applies a unique combination of expertise in medical devices, pharmaceuticals and biotechnology to create products that advance patient care worldwide. We ar...
1) Make decisions regarding feasibility of marketing projects based on sound financial and market analyses. 2) Deliver expected results on complex, multifaceted marketing projects. 3) Lead cross-functional teams to develop strategy and deliverables for specific product areas. 4) Assist in the integration/transfer business development projects into Baxter business. 5) Solicit market research and ap...
BioPharma Solutions facility in Bloomington, IN is one of the largest contract manufacturers of sterile products in North America, with a state of the art 600,000 square-foot facility campus. As a full-service contract manufacturer, our Bloomington facility serves client's needs with clinical development through commercial launch. These include manufacturing, packaging, quality systems, expe...
This laboratory supervisor position will work second shift supervising the Serological tesing and personnel during this shift. Job duties will include but not be limited to: • Provides day-to-day supervision of operations and moderate or high complexity test performance by all testing personnel in their laboratory area • Must be accessible to testing personnel at all times testing is performed t...
Summary: The Director, Operations is responsible for the Hoover, AL facility and all laboratory operation at the facility, in accordance with established Standard Operating Procedures (SOPs), applicable sections of the Code of Federal Regulations (CFRs), with emphasis on Good Manufacturing Practices (GMPs), the Clinical Laboratory Improvement Amendments (CLIA), and applicable Baxter and BioLife p...
Responsible for the strategic planning of the Risk Based Life Cycle Management Process (RBLCM). Leads the development of new ideas, processes and techniques as part of the continuous improvement and evolution of the RBLCM Process. Sets the direction to execute the vision and strategic plans related to RBLCM Process output: data architecture, process control management and risk mitigation plans t...
This section focuses on the main purpose of the job in one to four sentences. Conducts reviews of documentation and reports for conformance to procedures, protocols and regulatory requirements. Essential Duties and Responsibilities: This section contains a list of five to eight primary responsibilities of this role that account for 5% or more of the work. The incumbent will perform other duties ...
The Manufacturing Associate 3 operates process and ancillary equipment, in compliance with cGMP regulations, to support the production of OBI-1, a hemophilia therapeutic drug scheduled for commercial launch in 2014. The final title may differ and will be commiserate with experience and in alignment with our current internal team. Essential Duties and Responsibilities Functions in a leadership r...
Summary: The highly-experienced QC Analyst III conducts a wide range of biological, chemical and physical analyses on pharmaceutical products (biologics and drugs) in accordance with approved and/or compendial test method procedures in support of all stages of the GMP drug manufacturing process from incoming raw materials to finished goods and stability. Essential Duties and Responsibilities: • ...
The Quality Control Analyst II in Microbiology is responsible for microbiological analysis of in-process, release and stability samples to support the manufacturing of biologic drug substances. In addition, the Quality Control Analyst II is responsible for performing environmental monitoring of cleanrooms and water system sampling/testing. Position schedule is Second Shift, Monday-Friday, 2:00 – ...
Summary: The QC Analyst III in the QC Raw Materials group conducts a wide range of biological, chemical and physical analyses on pharmaceutical products (biologics and drugs) in accordance with approved and/or compendial test method procedures (USP, EP, JP) through all stages of the manufacturing process from incoming raw materials to finished goods and stability. Essential Duties and Responsibil...
Summary: The Documentation Specialist is responsible for document issuance, review, and archival in the QA Doc Centers. Responsibilities include batch record issuance, batch record review, document issuance within BPLM, and review of other GMP documentation. The Document Specialist has responsibility for management, organization, and archival of GMP Documentation within the Document Center. He or...
Lead and manage cross functional teams in complex Process Automation engineering assignments, on a project by project basis. Manage successful completion of projects within boundaries of quality, time and budget. Work directly with customers to develop detailed requirements definitions, and execute the project(s) based on these requirements. 1) Independently plan, execute and direct cross f...
The Medical Information Associate II will receive, research, and respond to internal and external medical information inquiries related to the Baxter Renal product portfolio. The Medical Information Associate II will have clinical knowledge of these products and is responsible for all aspects of Medical Information support of these products. 1. Provide high quality, balanced and timely clinical, ...
Summary: As part of the Quality Assurance team, the experienced Quality Associate III serves as a manufacturing process expert with responsibility for identifying and assessing regulatory and quality risks to ensure that all GMP processes are performed according to Baxter’s rigorous quality standards and all relevant regulatory agency rules/guidelines. Position schedule is Monday-Friday, 3:30 pm ...

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