• Associate Director, MSL Communications-Hematology…

    J&J Family of Companies (Horsham, PA)
    …accuracy of proactive and reactive decks and facilitate their review and approval process . + Stay abreast of innovations and novel formats that are being used ... + Support the development and review of, and approval process for, compliant materials for proactive and reactive usage...or medical writing experience or 6 years of related ( pharmaceutical ) work experience or an advanced degree (MS, PhD,… more
    J&J Family of Companies (01/08/26)
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  • Chemist I - Incoming Quality

    Endo International (Rochester, MI)
    …in- process materials, stability & finished products, and testing to support process validation . May participate in investigations. Learns and stays current ... with regulatory guidances and compendia relevant to laboratories and pharmaceutical manufacturing. **Job Description** Scope of Authority _- span of control_ _(work… more
    Endo International (12/20/25)
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  • Manager, Quality Systems

    Curia (Albuquerque, NM)
    …organization (CDMO) with over 30 years of experience partnering with pharmaceutical and biotech companies to provide life-saving treatments to patients. At ... materials, products, computer systems, quality systems, regulatory submissions, calibration, and validation + Oversee the site's Quality Event and Corrective and… more
    Curia (12/13/25)
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  • Manufacturing Engineering Sr. Intern

    ThermoFisher Scientific (Indianapolis, IN)
    …manufacturing equipment. Quality Assurance: Support quality assurance activities, including process validation , equipment qualification, and root cause analysis. ... contributing to the development and optimization of manufacturing processes for pharmaceutical products. Key Responsibilities: Process Improvement: Assist in the… more
    ThermoFisher Scientific (12/12/25)
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  • Senior Manager, Global Product Quality - Biologics

    Otsuka America Pharmaceutical Inc. (Baton Rouge, LA)
    …support OPDC R&D products; including LIMS data, method development & validation , method transfers and testing (release, stability). + Maintains KPIs/quality metrics ... related Science. + Four years of combined experience in pharmaceutical /medical device industry as a manager in Manufacturing, QA...Thorough understanding of GMP requirements and the Drug Development process . + Knowledge of FDA 21 CFR Parts 210… more
    Otsuka America Pharmaceutical Inc. (12/03/25)
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  • Mechanical / Electrical Engineer

    Unither Pharmaceuticals (Rochester, NY)
    Mechanical / Electrical Engineer Who we are? We are a French pharmaceutical industrial group, recognized for making affordable healthcare products that improve and ... Rochester (NY), specializes in the manufacture of Blow-Fill-Seal, Liquid Stick-Packs, Pharmaceutical bottles, Tablets and Capsules. It has more than 300 employees.… more
    Unither Pharmaceuticals (11/27/25)
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  • Director, Quality Operations

    Curia (Albuquerque, NM)
    …Curia provides global contract research and manufacturing services to the pharmaceutical and biotechnology industries. Join our talented workforce, where a ... the Director also supports other quality functions, including QSYS, QC, and Validation , during external engagements. This role is central to maintaining compliance,… more
    Curia (11/22/25)
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  • Associate Director - Business Solutions - MQ Tech…

    Lilly (Pleasant Prairie, WI)
    …Identify and prioritize innovative technology initiatives that support the pharmaceutical manufacturing site's growth and compliance requirements. + Collaborate with ... globally and locally defined targets. + Maintain robust computer system validation and data integrity capabilities, following globally defined standards, to protect… more
    Lilly (01/16/26)
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  • Microbiology Analyst

    Actalent (Hercules, CA)
    …per client requests. + Develop, modify, verify, and assist with method validation testing. + Participate in method transfer activities and suitability studies under ... first attempt. Essential Skills + Proficiency in aseptic techniques and cleaning/disinfection validation . + Experience with GMP and GLP standards. + A background in… more
    Actalent (01/13/26)
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  • QA Reviewer

    Actalent (Cherry Hill, NJ)
    …documents. These include Standard Operating Procedures (SOPs), Change Controls, Validation protocols, General Test Requirements (GTRs), Engineering Drawings, and ... environment. Responsibilities + Review and approve SOPs, Change Controls, and Validation protocols. + Evaluate and approve General Test Requirements (GTRs). +… more
    Actalent (01/10/26)
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