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company:(csl behring)
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Job DescriptionThis position is responsible to lead operational excellence and data analytics initiatives on the Kankakee site, and manage cross functional teams to ensure projects are rolled out and delivered..
Job DescriptionResponsibilities:• Under general supervision, carries out production-related tests and inspections to control quality• Tests or analyzes components, raw materials, and products to monitor quality following established methods• Properly documents..
Job DescriptionThe Sr. Principal Process Engineer is accountable for supporting day-to-day business with process engineering and scientific knowledge and resources; focused on site and/or project execution and support.. S/He works..
Job DescriptionResponsibilities:• Oversees and directs regulatory activities for new and mature products to ensure alignment and compliance with local and regional registration requirements as well as with company policies.• Interface..
Job DescriptionJob Description Summary This position provides immediate support to the Assistant Manager of Quality in monitoring plasma center processes to ensure overall compliance with CSL Operating Procedures, as well..
Job DescriptionPosition Purpose:Provide an overview of the responsibilities of the position by providing a summary of the most important aspects and duties of the position.Responsible for investigating deviations. Responsible for..
Job DescriptionPosition PurposeThe position holder is responsible for both scientific input to clinical development strategies, acting as the primary liaison between the assigned therapeutic area and key stakeholders to ensure..
Job DescriptionLead the team responsible for design and management of US forecasting and performance analysis at CSL Behring that is synergistic with strategic and tactical brand planning. Incumbent will be..
Job DescriptionThis role is responsible for leading investigations to ensure the written investigation report contains the technical merit and completeness according to regulatory expectations. This position will be responsible for..
Job DescriptionThe Quality Assurance Specialist: Will Manage deviations, investigations, CAPAs, product technical complaints and change controls associated with the manufacture of R&D Gene Therapy Investigational Medicinal Product. You will ensure..
Job DescriptionThis role is responsible for owning and executing changes within the Value Streams, from beginning to end, collaborating with a network of Subject Matter Experts, to ensure the cGMP..
Job Descriptionrnrn rnrnThe Global Competitive Intelligence Lead will be responsible for generating, integrating and translating insights and analytics into growth opportunities and tactics that help guide decisions and drive organizational..
Job DescriptionResponsible for owning and executing changes within the Maintenance Value Stream, from beginning to end, collaborating with a network of Subject Matter Experts, to ensure the cGMP documentation exists..
Job Descriptionrnrn rnrnThe Engineer is responsible for improving the reliability of equipment, utilities, critical systems and maintenance processes by applying the principles of Reliability Centered Maintenance. Apply Root Cause Analysis..
Job DescriptionResponsibilities:• Under general supervision, supports Clinical Quality Assurance CQA programs for the assigned therapeutic and compliance area• Completes audits to assess quality of scientific data and ensure compliance with..
Job DescriptionResponsibilities:n• Responsible for developing and implementing Quality Assurance Systems to ensure compliance with company standards and regulatory guidelinesn• Establishes and maintains GMP-related quality systems including standard operating procedures (SOPs)..
Job Descriptionrnrn rnrnThis position is for the Chemistry In-Process laboratory. This group works 24/7. This position is for 3rd shift. (11pm-7:30am). Shift differential is available for 3rd shift.rnrn rnrnResponsibilities:rnrnrntPerforms required..