• GMP Data Reviewer

    Eurofins (King Of Prussia, PA)
    …Testing. + GMP review of Qualification and Media Release testing. + GMP review of facility cleaning data and in-processing testing, including but not ... stocks in Europe over the past 20 years. + Water Systems + GMP review of microbiological testing of the facility and/or laboratory water purification system… more
    Eurofins (07/12/25)
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  • Director Quality Assurance

    Merck (West Point, PA)
    …consultation services for regulatory reporting (eg, BPDR, DPR) + Author and/or review global standards and procedures related to biologics, vaccines, and finished ... pharmaceutical, vaccine or medical device industry experience; + Expert knowledge of GMP requirements for multiple regulatory agencies + Expert knowledge of large… more
    Merck (07/04/25)
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  • Scientist, Integrated Systems

    West Pharmaceutical Services (Radnor, PA)
    …integrity (CCI) assessments in compliance with Good Manufacturing Practice ( GMP ) regulations. This role involves method execution, documentation, and collaboration ... strong analytical skills, and a thorough hands-on understanding of GMP requirements. **Essential Duties and Responsibilities** + Conduct performance and… more
    West Pharmaceutical Services (05/22/25)
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  • Supervisor Quality Assurance

    Charles River Laboratories (Wayne, PA)
    …pertinent regulatory requirements and to departmental policies, practices and procedures. + Review , revise and approve ( GMP QA) SOPs, protocols/batch records, ... and understanding of regulations and quality principles. + Perform data audits to assess that records are attributable, legible,...suitability of materials and supplies for compliance with specifications ( GMP QA). + Review and approve all… more
    Charles River Laboratories (06/25/25)
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  • Chemist - II (Associate)

    ManpowerGroup (Lansdale, PA)
    …high quality data . + **Experience with HPLC is required.** + ** GMP experience is required.** + Successful performance requires a sound basic knowledge of ... more senior staff member, the incumbent will carry out GMP and non- GMP testing on pharmaceutical drug... electronic notebook in compliance with regulatory requirement for data integrity, author/ review technical document. + May… more
    ManpowerGroup (07/10/25)
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  • Associate Director, Technology Partnership

    Merck (West Point, PA)
    …Skills:** Automated Manufacturing Systems, Business Process Improvements, Capital Projects, Data Collection Methods, Digital Manufacturing, GMP Compliance, ... include the resolution of automation problems, implementation of process control, data collection and analysis, and troubleshooting in compliance with System… more
    Merck (07/12/25)
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  • Manager, SAP Support Services

    Pfizer (Collegeville, PA)
    …markets and applications under his/her responsibility. + Design, develop, test, and deploy data services using SAP data management tool and Syniti ADM toolset. ... audit meetings to ensure all teams involved are following appropriate SOX and GMP audit procedures and policies to maintain good compliance posture. + Provide… more
    Pfizer (07/09/25)
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  • Process Engineer

    Endo International (Horsham, PA)
    …and assist in completing process deviation investigations/unplanned events. Author, review , and approve cGMP documentation - manufacturing process and equipment ... programs. Utilize statistical control software to analyze and trend process and facility data and results. + Support the Horsham site validation program - Author/… more
    Endo International (07/08/25)
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  • Specialist, Operations

    Merck (West Point, PA)
    …to motivate others to do the same **Business Expertise:** + Perform a thorough review of batch records and related GMP documentation, identifying and resolving ... timely manner and implementing corrective actions to improve the batch record execution/ review process + Work with Subject Matter Experts (SME's) to provide/track… more
    Merck (07/12/25)
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  • Analytical Chemist III

    Catalent Pharma Solutions (Malvern, PA)
    …derived in support of CMTI Operations or external sample submissions. Conduct peer data review of raw data /documentation. + Provide technical training ... testing activities with clients as needed. Able to individually evaluate data and communicate information with internal and/or external stakeholders to drive… more
    Catalent Pharma Solutions (06/13/25)
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  • Senior Project Controls Manager

    Turner & Townsend (West Point, PA)
    …**Responsibilities:** + Manage Cost / Change Control, including change order review , negotiation, recommendations, and delay analysis. + Track and review ... Contractor. + Produce monthly reports for management. + Providing review reports. + Produce earned value reports. + ...cost tracking reports. + Reconcile GC actual costs with GMP / Schedule of Values. + Contract Administration (retention, T&Cs,… more
    Turner & Townsend (06/28/25)
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  • Quality Assurance Associate - Batch Release

    Glenmark Pharmaceuticals Inc., USA (Allentown, PA)
    …are not intended to be an exhaustive list of all responsibilities and duties. + Review of Data logger communication (DLC) form along with data logger ... data , Packing slip and other related documents. + Review of Certificate of analysis, Batch records, Certificate of conformance and Investigation reports. +… more
    Glenmark Pharmaceuticals Inc., USA (06/27/25)
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  • Quality Assurance Associate II

    J&J Family of Companies (Spring House, PA)
    …ensure inspection readiness at all times. **Key Responsibilities:** + Provides Quality review and guidance associated with review and approve investigations and ... corrective/preventive actions (CAPA) are implemented in a timely manner. + Review and approve controlled documents including standard operating procedures, work… more
    J&J Family of Companies (07/08/25)
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  • Senior Scientist, Laboratory Automation

    J&J Family of Companies (Malvern, PA)
    …with Method Development, Assay Automation, Integrations, Orchestration, Information Technology, Data Science, and Operations to increase sample testing volume while ... end-users to independently execute automated workflows + Partnering with Information Technology and Data Science teams to automate data flows to ensure data more
    J&J Family of Companies (04/23/25)
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  • Quality Assurance Associate - Inspection

    Glenmark Pharmaceuticals Inc., USA (Allentown, PA)
    …intended to be an exhaustive list of all responsibilities and duties. + Pull out data loggers from the batches, download the data , enter the temperature entries ... in SAP and generate Data logger Communication Form for each batch. + Forward...all DLC Forms to respective manufacturing sites for their review and disposition recommendation. + Upon receipt of the… more
    Glenmark Pharmaceuticals Inc., USA (06/27/25)
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  • Integrated Lab Solutions Technician - Life…

    CBRE (King Of Prussia, PA)
    …Manage and improve the service logging process and asset database. Create, and review supporting documentation like service reports. + Track the performance of the ... systems to keep accurate records of all equipment-related faults. Support data -related initiatives such as contract renewal, asset replacement, etc. + Maintain… more
    CBRE (05/15/25)
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  • QA Technician -Fabrication

    JBS USA (Souderton, PA)
    …TECH I - 1st SHIFT - SOUDERTON, PA + Monitor SOP's, SSOP's and GMP compliance of associates, perform HACCP procedures to comply with federal regulations + Perform ... present records to them at the agency's request + Review records to ensure accuracy and be held accountable...accuracy + Aid QA supervision and management in gathering data and investigating items outside of regular technician responsibilities… more
    JBS USA (06/14/25)
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  • Associate Director, External Manufacturing…

    Merck (West Point, PA)
    …Reliability, and Lifecycle Management). - Lead Periodic Business and Operations Review Meetings (with External Partner). . **Compliance:** Achieve compliance goals ... budgets (Expense, Capital/Prepaid, and Product Cost). Understanding of industry and economic data to make business decisions that drive value for our Company and… more
    Merck (05/19/25)
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  • QA Technician

    Staff Management | SMX (Chalfont, PA)
    …discover issues and to verify the accuracy of information, results, and data + General knowledge of ISO9000, Quality Management Systems, Good Manufacturing Practices ... & vendors to Nexus + Associate training requirements + Shift Conformance + GMP Audits, Internal Audits, GBP Audits, and Perion/Quarterly Metric Reporting + Quality… more
    Staff Management | SMX (05/09/25)
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  • QC Analyst

    Kelly Services (Fort Washington, PA)
    …they conform with specifications and standard operating procedures (SOPs). + Support the review , data generation and/or writing of technical documents such as ... Medical Technology, or related science is preferred. + Minimum 1 year of GMP /GLP quality control lab experience in a pharmaceutical and/or OTC and/or regulated… more
    Kelly Services (06/17/25)
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