Baxter International Jobs in Ada

Currently, there are no Baxter International jobs available in Ada, Oklahoma. You may wish to explore jobs in nearby locations on the Baxter International jobs in Oklahoma page or view related jobs below.
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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 – ...
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 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...
Develops HR plans and strategies to support the achievement of business objectives and achievement of desired organizational culture. Drives overall implementation of plans and strategies, continually monitors effectiveness Consults with management on a variety of HR and business related issues, both strategically and operationally. Continually assesses the effectiveness of the organization’s b...
The primary responsibility is to proactively manage and ensure clinical development and operations compliance to established procedures, provide expert knowledge on operating processes around clinical operations, and document management for both drug and device studies. The responsibility may include managing several employees globally. This position will support Clinical Project Managers to ensur...
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, ...
1) Coordinate marketing activities for a specific product or product line. 2) Establish project plan budget/resources. 3) Conduct market research and assist in development of short- and long-term plans and marketing strategies. 4) Draft informational and promotional materials for internal and external customers. 5) Prepare and deliver presentations to management, nurse or physicians. 1) Bachelor'...
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 ...
The Senior Manager of Marketing Communications will be responsible for: Strategic Communication Plan Development – Partner with Marketing team to develop communication plans to address focused needs of business. Clearly articulate plan objectives, strategies and tactical approaches. Manage project performance to budget and identify potential issues. Writing & Editing - Assist business partners i...
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...
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...
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...
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...
• The primary focus of the job is to ensure the Medical Products North Cove Equipment and associated systems are in compliance with regulatory quality standards through the life-cycle validation activities • Prefer experience with TQM methods (e.g. "six sigma") • Work with teams to gather requirements, create procedures and develop new solutions or enhance existing quality engineering systems. E...
Summary: Experienced Design Lead responsible for driving cross-functional development of Container Closure System platforms or components. Applies a solid understanding of theories/practices utilized by other disciplines outside the primary area of expertise toward the development of new or enhanced products. Through disciplined application of best practice product development techniques, indepen...
Lead the Human Factors Engineering team, within the Device Engineering organization, which is a strategic function leveraged across multiple franchise product lines and therapies. • Own the compliance and implementation to global usability standards and Human Factors requirements for all products through product lifecycle management (from ideation, development, risk mitigation, sustainability, an...

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