• Penske Truck Leasing Co., LP (Obetz, OH)
    …but we also make sure you have the time you need to do the job right. Safety and reliability are our top priorities. Yes, we know you are experienced, and we will ... in non-climate-controlled conditions * Basic computer skills * The associate will be required to understand and comply with...all work adhering to DOT, OSHA, and all Penske safety and maintenance policies; including but not limited to… more
    JobGet (05/04/24)
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  • Penske Truck Leasing Co., LP (Columbus, OH)
    …a week based on business needs. Major Responsibilities: * Follow appropriate safety procedures while driving trucks to destination of Penske location or customer ... locations * Check vehicles to ensure that mechanical, safety , and emergency equipment is in good working order,...(to include past employment, education, and criminal history) and drug screening are required. This position is regulated by… more
    JobGet (05/04/24)
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  • Penske Truck Leasing Co., LP (Columbus, OH)
    …foundation in sales and operations. You'll enjoy flexible schedules, excellent benefits, associate incentives and discount programs. You'll be on the fast track to ... (to include past employment, education, and criminal history) and drug screening are required. This position is regulated by...regulated by the Department of Transportation or designated as safety sensitive by the company, and the ability to… more
    JobGet (05/08/24)
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  • Merck & Co. (North Wales, PA)
    …Management Safety Teams.- Lead and provide statistical support for related drug /vaccine projects in Clinical Safety StatisticsInteract with Safety ... analysis methods fundamental to effective pharmaceutical R&D.- The Clinical Safety Statistics (CSS) group within BARDS supports proactive assessment, transparent… more
    HireLifeScience (05/14/24)
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  • Catalent (San Diego, CA)
    Quality Assurance Associate I, ManufacturingCatalent Pharma Solutions in San Diego is currently hiring a Quality Assurance Associate I in our QA Manufacturing ... group. A QA Associate I must be familiar with applicable GMPs. This...pharmaceutical and biotechnology industries. We focus on bringing client drug compounds from discovery to the clinic with services… more
    HireLifeScience (05/13/24)
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  • Penske Truck Leasing Co., LP (Lockbourne, OH)
    …and long-term disability; life and AD&D insurance * Company-provided uniforms and safety footwear * Employee discount benefit program * Driver referral bonus program ... up to $5000 per referral * Safety incentive program * Premier Driver Recognition Program Why...(to include past employment, education, and criminal history) and drug screening required. * This position is regulated by… more
    JobGet (04/29/24)
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  • Merck & Co. (Boston, MA)
    Job DescriptionWe are seeking an experienced and innovative Associate Principal Scientist with a strong background in In Vitro Pharmacology to join the External ... notebook entries.Participate in partner site visits to evaluate processes, capabilities, safety procedures and compliance standards as well as build workflows to… more
    HireLifeScience (05/14/24)
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  • Merck & Co. (Rahway, NJ)
    Job DescriptionThe Associate Principal Programmer leads the statistical programming activities for multiple and/or large/complex late stage drug /vaccine clinical ... the development and execution of statistical analysis and reporting deliverables (eg safety and efficacy analysis datasets, tables, listings, figures), the span of… more
    HireLifeScience (05/09/24)
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  • Catalent (Manassas, VA)
    Associate Director, Regulatory Affairs Position Summary: Catalent is a global, high-growth, public company, and a leading partner for the pharmaceutical industry in ... to a Patient First culture through excellence in quality and compliance, and to the safety of every patient, consumer and Catalent employee. The primary duty of the … more
    HireLifeScience (05/03/24)
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  • Catalent (San Diego, CA)
    Quality Assurance Associate II - Manufacturing Catalent Pharma Solutions in San Diego is currently hiring a Manufacturing Quality Assurance (MQA) Associate II ... regulatory requirements; to advance the development and manufacture of drug candidates. This will include documentation review and approval, dispositioning… more
    HireLifeScience (04/25/24)
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  • Penske Truck Leasing Co., LP (Columbus, OH)
    …and long-term disability; life and AD&D insurance * Company-provided uniforms and safety footwear * Employee discount benefit program * Driver referral bonus program ... up to $5000 per referral * Safety incentive program * Premier Driver Recognition Program Why...(to include past employment, education, and criminal history) and drug screening required * This position is regulated by… more
    JobGet (04/29/24)
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  • Merck & Co. (North Wales, PA)
    …to discover the next medical breakthrough.Position Description: The Associate Principal Scientist Statistical Programming leads the statistical programming ... activities for multiple and/or large/complex late stage drug /vaccine clinical development projects.- Accountability predominantly includes the development and… more
    HireLifeScience (04/25/24)
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  • Aequor (South San Francisco, CA)
    …closely collaborating with scientists across the organization to support the overall safety assessment for our Client therapeutics spanning drug discovery ... position is in the Investigative Toxicology Group within the department of Safety Assessment in Genentech's Research and Early Development organization. The mission… more
    HireLifeScience (04/27/24)
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  • Legend Biotech USA, Inc. (Raritan, NJ)
    …in the treatment of multiple myeloma. Legend Biotech is seeking an Associate Director for Operations Compliance and Investigations Managementas part of the Technical ... Operations team based in Raritan, NJ. Role Overview The Associate Director for Operations Compliance and Investigations Management will provide strategic direction… more
    HireLifeScience (04/19/24)
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  • Catalent (San Diego, CA)
    Job Title: Quality Assurance Associate , Analytical City: San Diego State : CA JOB DESCRIPTION:Review of analytical release and stability data, involving review of ... and external audits.Lead or support client audits along with the Director and Associate Director of Quality AssuranceManage a direct report and train the direct… more
    HireLifeScience (03/22/24)
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  • Daiichi Sankyo, Inc. (Basking Ridge, NJ)
    …opportunity employer including veterans and people with disabilities. Summary The Associate Director, External Data Management, is accountable for the end-to-end ... data in Daiichi Sankyo R&D collaborating with clinical and medical teams, clinical safety and pharmacovigilance, CROs and External Vendors for the data services they… more
    HireLifeScience (04/20/24)
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  • Legend Biotech USA, Inc. (Raritan, NJ)
    …to resolve issues. Perform tasks in a manner consistent with the safety policies, quality systems and cGMP requirements. Require minimal direction to complete ... citizenship status, uniformed service member or veteran status, or any other characteristic protected by law. Legend Biotech maintains a drug -free workplace. more
    HireLifeScience (04/17/24)
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  • Legend Biotech USA, Inc. (Raritan, NJ)
    …in the treatment of multiple myeloma. Legend Biotech is seeking an Operations Associate (2nd Shift) as part of the Technical Operations team based in Raritan, ... a clean and safe work environment. Take necessary action to eliminate safety hazards and communicate to others any observed unsafe behaviors Ensure materials… more
    HireLifeScience (03/15/24)
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  • Lovelace Biomedical Research Institute (Albuquerque, NM)
    …basic research findings to in vivo models. Our well-established pre-clinical investigational drug safety program allows opportunities to extend work into human ... Comprehensive Cancer Center. We are currently seeking Tenure-Eligible Faculty members at the Associate or Professor level to join LBRI and be a part of our… more
    HireLifeScience (02/28/24)
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  • Daiichi Sankyo, Inc. (Basking Ridge, NJ)
    …develop programming submission strategy, perform integrated analysis of efficacy and safety , generate submission data package, create TLFs to support submission QAs, ... and reporting of clinical trials preferred- Knowledge of all phases of drug development, including early and late phase clinical development and submission… more
    HireLifeScience (04/03/24)
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