• Senior Packaging Operations Manager

    Catalent Pharma Solutions (Philadelphia, PA)
    …to maintain robust processes and high functioning teams + Partner with Validation and Engineering to identify, implement and effectively use Packaging Equipment and ... + Three years of Supervisory and/or management experience required + Pharmaceutical Packaging and Manufacturing experience required + Detailed knowledge of the… more
    Catalent Pharma Solutions (09/10/25)
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  • Associate Director, MES and Enterprise IT Systems

    Bristol Myers Squibb (Devens, MA)
    …21 CFR Part 11) and internal standards for system design, validation , and data integrity. + Collaborate cross-functionally with Manufacturing, Quality, Engineering, ... Science, Engineering, Information Systems, or related discipline. + 8+ years' experience in pharmaceutical or biotech manufacturing IT, with at least 3 years in a… more
    Bristol Myers Squibb (09/09/25)
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  • Formulation Technician III

    PCI Pharma Services (Madison, WI)
    …with aseptic and non-aseptic personnel. Works closely with Quality Assurance, MTS, Validation etc. + **_TRAVEL -_** < 10% **Qualifications:** The requirements listed ... work experience in a GMP environment, preferably in fill finish pharmaceutical operations + Demonstrated ability to prioritize multiple projects and activities… more
    PCI Pharma Services (09/09/25)
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  • Construction Quality Manager

    CBRE (Indianapolis, IN)
    …activities. + Familiarity with construction-related codes, standards, regulations, and validation requirements. + Proficiency in Microsoft Office Suite (Word, Excel, ... Experience:** + Construction quality oversight in regulated industries such as pharmaceutical , life sciences, or advanced manufacturing. + Working within or… more
    CBRE (09/09/25)
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  • Inspection Data Quality Analyst - INTL…

    Insight Global (New York, NY)
    Job Description Our pharmaceutical client is seeking a Data Quality Analyst (Inspection Analyst) to support the migration of risk management files from Excel into a ... in Pharma and/or Medical Device industry * Proficiency in Excel and data validation techniques. * Familiarity with risk management tools and methodologies (eg, FMEA,… more
    Insight Global (09/09/25)
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  • mRNA CoE Resource Management Officer - Vaccines

    Sanofi Group (Waltham, MA)
    …BSM for updating the algorithm in RDPM. Oversees continued definition and validation of standard functional-based deliverables, related activities and metrics for NV ... regarding planning & resource management/allocation + Experience in biotech or pharmaceutical R&D, including knowledge of value chain and key contributing functions… more
    Sanofi Group (09/09/25)
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  • Project Engineer - Global Robotics

    Lilly (Indianapolis, IN)
    …Minimum 5 years of relevant manufacturing experience, preferably in discrete pharmaceutical manufacturing: + parenteral filling and/or inspection processes + device ... automated systems + Experience in Project Delivery, Commissioning & Qualification, Validation Activities, and cGMP Regulations + Experience in control system… more
    Lilly (09/09/25)
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  • Scientist IV

    The US Pharmacopeial Convention (USP) (Rockville, MD)
    …skills in developing and implementing appropriate chemometric models, s and validation , interpreting model output. + Data visualization and modeling skills (ex. ... and concurrent management of multiple tasks. + Experience working in the pharmaceutical , chemical and/or biotechnology industry. + Experience working in GLP or… more
    The US Pharmacopeial Convention (USP) (09/09/25)
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  • Sr. Manufacturing Engineer

    Edwards Vacuum, LLC (Buffalo, NY)
    …processes into new plant in Genesee, NY including qualification, installation, and validation of new equipment and associated documentation. + Assist with the ... including power, glass and other coating applications; steel and other metallurgy; pharmaceutical and chemical; and for scientific instruments in a wide range of… more
    Edwards Vacuum, LLC (09/09/25)
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  • Senior Manager, Risk Remediation Process

    Insight Global (Bedford, MA)
    …quality and process reliability, supporting new product development and validation , and assisting with complaint investigations and resolutions of non-conforming ... field. - 10 years of experience within a regulated medical device or pharmaceutical environment. - 5 years of risk management experience in the medical device… more
    Insight Global (09/09/25)
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