Batch Records Jobs in Philadelphia, PA

Manager Pre-Production and Label ControlPosition SummaryCatalent Inc. is a leading global contract development and manufacturing organization (CDMO) whose mission is to develop manufacture and supply products that help people live better and healthier lives. Catalent is dedicated to d More...

Clinical Production SpecialistPosition SummaryCatalent Inc. is a leading global contract development and manufacturing organization (CDMO) whose mission is to develop manufacture and supply products that help people live better and healthier lives. Catalent is dedicated to delivering More...

Clinical Production Specialist Position SummaryCatalent Inc. is a leading global contract development and manufacturing organization (CDMO) whose mission is to develop manufacture and supply products that help people live better and healthier lives. Catalent is dedicated to delivering More...

Data Labeling AnalystThis is a contract position.This is a remote opportunity. About this positionAre you detailoriented and passionate about data quality As a Data Labeling Analyst you will help drive better product decisions by ensuring data labeling accuracy and maintaining hi More...

OverviewThe Manager Quality Assurance (QA) IOVAA QA Ops is responsible for supporting daytoday GMP QA Operations activities that support manufacturing testing and release of iPBMCs in a GMP compliant manner. The individual is collaborative organized innovative flexible with a strong d More...

OverviewIovance Biotherapeutics is seeking a Training Specialist I to join the Operations team at 700 Spring Garden St Philadelphia PA. Colocated at the American Red Cross Penn Jersey Region this Iovance facility produces a critical raw material used in the companys tumor infiltrating More...

OverviewThe Supervisor Quality Control Sample Management will be responsible for sample inventory management as well as internal and external sample distribution including storage and shipping of QC samples under appropriate conditions. This role will be responsible for developing sta More...

Senior Quality Assurance Document ControlPosition SummaryCatalent Inc. is a leading global contract development and manufacturing organization (CDMO) whose mission is to develop manufacture and supply products that help people live better and healthier lives. Catalent is dedicated to More...

OverviewThe Senior Quality Release Specialist will support review of documentation and support releasing of materials and products. Th Sr Quality Release Specialist will also ensure compliance to Iovance procedures by supporting lot closure and deviation reviews.Shift: Wednesday to Sa More...

OverviewIovance Biotherapeutics is an immunooncology company focused on the development and commercialization of novel cancer immunotherapies based on tumor infiltrating lymphocytes (TIL). The Lead Aseptic Manufacturing Technician role is crucial for the autologous cell therapy manufa More...

OverviewThe MSAT Specialist I is a Manufacturing Operations cell therapy subject matter expert. The MSAT Specialist I reports to the Senior Manager MSAT and EM and is responsible for manufacturing data analysis contributing to deviation root cause analysis and owning steps of the manu More...

OverviewThe Supervisor for Aseptic Manufacturing oversees the production process to ensure that all materials are produced safely and follow the companys standards. This position requires timely document review and ensuring all targets are met. In addition the supervisor will be respo More...

OverviewThe MSAT Specialist is a Manufacturing Operations cell therapy subject matter expert. The MSAT Specialist reports to the Senior Manager MSAT and EM and is responsible for manufacturing data analysis contributing to deviation root cause analysis and owning steps of the manufact More...

OverviewThe Senior Quality Assurance Specialist will report to the Manager Quality Assurance. The position will support the quality and regulatory compliance of commercial and clinical products including manufacturing testing and release at contract service providers. Further the posi More...

OverviewThe MSAT Supervisor/Managers role is integral to ensuring effective of manufacturing related investigations according to regulatory guidelines as well as and development of protocols related to process improvement. The MSAT Supervisor/Manager will also lead the development a More...

OverviewThis position reports to the IT Manager Manufacturing Systems. The MES Analyst will serve as a key liaison between the MES IT group and various business functions (Supply Chain Manufacturing Quality MSAT) ensuring business requirements and requests are gathered documented impl More...

OverviewIovance is seeking an MSAT Specialist II who is a Manufacturing Operations cell therapy subject matter expert. The MSAT Specialist II will report to the MSAT Manager and be responsible for manufacturing data analysis contributing to deviation root cause analysis and owning ste More...

OverviewThe Supervisor Aseptic Processing is a part of the Manufacturing team at 700 Spring Garden St Philadelphia PA. Colocated at the American Red Cross Penn Jersey Region this Iovance facility produces a critical raw material used in the companys TIL process. The critical raw mater More...

OverviewThe Quality Assurance Specialist I Raw Material Release will support review of documentation and support releasing of materials and products.Schedule & Hours: Wednesday to Saturday 7am to 6pmEssential Functions and ResponsibilitiesEnsure compliance to cGMPs and facility pr More...

OverviewIovance Biotherapeutics is seeking an Aseptic Processing Technician (contracttohire) to join the team at 700 Spring Garden St Philadelphia PA. Colocated at the American Red Cross Building this Iovance facility produces a critical raw material used in the companys TIL process. More...