- ATS Automation (Warminster, PA)
- …Requisition ID: 13624 Location: Warminster, PA, US, 18974 Date: Dec 14, 2024 Validation & Documentation Specialist ATS Scientific Products is seeking ... a full‐time Validation and Documentation Specialist in Warminster, PA to create and maintain various technical documents (eg, user manuals, equipment… more
- WuXi AppTec (Philadelphia, PA)
- …resource for the development, execution, review, and approval of Computerized Systems Validation , System Life Cycle Documentation ( Validation Plans, Design ... assessments, risk assessments, requirements traceability, URS, FDS, procedural mappings and Validation Project Plans. + Stay current with changes to GXP, including… more
- Insight Global (Philadelphia, PA)
- …Quality Assurance resource. Review and approve system lifecycle documentation , including Requirements Specifications, Configuration Specifications, Risk Assessments, ... Protocols, and Summary Reports. Perform QA review and approval of validation non-conformances. Collaborate with process owners and SMEs to resolve compliance… more
- Sokol Materials & Services (Skillman, NJ)
- CQV Technical Writer / Validation Engineer Apply Now (https://forms.monday.com/forms/3cdf5bfb73703e4a3aa29c55653510f4?r=use1) Job Type Validation Engineer ... at times. About the Role As a Technical Writing Specialist at Sokol GxP Services, you will play a...the creation of technically accurate documents in line with validation programs. - Process-oriented with strong critical thinking and… more
- J&J Family of Companies (Titusville, NJ)
- Johnson & Johnson is currently recruiting for Equipment Lifecycle Management (ELM) Specialist ! This position will be located in Titusville, NJ. At Johnson & Johnson, ... at https://www.jnj.com/. Position Summary: The Equipment Lifecycle Management (ELM) Specialist performs the technical execution of ELM Quality Control activities… more
- University of Pennsylvania (Philadelphia, PA)
- …wellness programs and resources, and much more. Posted Job Title Research Specialist C/D (Center for Cellular Immunotherapy) Job Profile Title Research Specialist ... C Job Description Summary The Human Genome Editing Research Specialist will play a key role in managing the...duties, the individual will contribute to the development and validation of standard operating procedures (SOPs) critical for modifying… more
- Penn Medicine (Philadelphia, PA)
- …at the Hospital of the University of Pennsylvania is seeking a Technical Specialist in Electron Microscopy to join their team:** **Summary:** The incumbent's primary ... functions of the electron microscopy laboratory. Using an ultra-microtome, the specialist will perform gross microscopy, fixation, processing and embedding of… more
- Merck (West Point, PA)
- …process design/definition, engineering studies, process demonstrations, change control and validation . + Prepare documentation to support regulatory submission ... looking to make a difference in vaccine manufacturing? As a Senior Specialist , you'll play a critical role in providing technical guidance, leading projects,… more
- Integra LifeSciences (Princeton, NJ)
- …patient outcomes and set new standards of care. The Sr. Regulatory Affairs Specialist is a seasoned senior professional role responsible for contributing to and ... regulations in the US, EU, Canada and globally. The Sr. Regulatory Affairs Specialist is responsible for providing advanced level regulatory input for regulatory … more
- Kelly Services (Fort Washington, PA)
- **Quality Assurance Specialist ** Kelly(R) Science & Clinical is seeking a **Quality Assurance Specialist ** for our client, a top consumer product company, in ... 12 months **Pay:** $33-35 an hour Depending on experience The QA Specialist is responsible for providing daily Quality Assurance support to the manufacturing… more
- Bank of America (Pennington, NJ)
- Sr Business Control Specialist - Consumer AML Operations Fort Worth, Texas;Pennington, New Jersey; Plano, Texas; Phoenix, Arizona **Job Description:** At Bank of ... as required by the BSA. _Position Summary:_ The Senior Business Control Specialist will provide oversight and support in executing internal control discipline and… more
- University of Pennsylvania (Philadelphia, PA)
- …programs and resources, and much more. Posted Job Title Cell Therapy Specialist (CVPF)(Center for Cellular Immunotherapy) Job Profile Title Cell Therapy ... Specialist Job Description Summary This position carries out day-to-day...Aseptic cell processing following established Standard Operating Procedures. Accurate documentation following Good Documentation Practices. Prepare cell… more
- Highmark Health (Trenton, NJ)
- …and Medicaid Services (CMS) coding guidelines, and Risk Adjustment Data Validation (RADV) Audits. Works closely with physicians, team members, Quality, Compliance, ... projects to comply with all CMS requirements by analyzing physician documentation and interpreting into ICD10 diagnoses and HCC disease categories. Supports… more
- Endo International (Horsham, PA)
- …from the local, contract manufacturing, filling, and packaging facilities. Quality Documentation /Reports Review + Contributes to preparation and/or review of annual ... that require developing options to solve moderate to complex issues. Quality Documentation + Prepares and/or reviews controlled documents (eg SOPs) required for… more
- PCI Pharma Services (Philadelphia, PA)
- …for the Philadelphia facility. This Quality Management System includes Documentation Control, Investigation and CAPA Management, Training, Internal/External Audits, ... Customer Correspondence, Validation . This position reports to the Senior Training Manager,...documents include SOP's, forms, regulatory documents etc. Wherever possible, documentation best practices should be applied consistently across the… more
- Merck (West Point, PA)
- …Projects, Maintenance, Safety, Process Development, Technical Services, Utilities and Qualification/ Validation . This position is a support role for utility systems ... design, and supports commissioning and start-up activities ranging from documentation to equipment inspection. + Optimizes equipment maintenance activities including… more
- Integra LifeSciences (Plainsboro, NJ)
- …status of all documents. + Maintains hard copies of all approved documentation . + Maintains appropriate templates for access. + Tracking, follow-up, and ... including but not limited to, ECRs, DCRs, ECOs, DCOs, and MCOs.deviations, validation records, batch records, and notebooks. + Responsible for processing change… more
- Actalent (Philadelphia, PA)
- …data obtained for compliance to specifications and report abnormalities. + Execute validation protocols, laboratory test plans, and report results to management. + ... Prepare documentation for presentation to Regulatory Agencies. + Apply knowledge of good manufacturing practices and good laboratory practices on a daily basis.… more
- Integra LifeSciences (Plainsboro, NJ)
- …employees at CMC. This role works closely with the Sr. Training Specialist assisting in the development of training materials, coordinating and delivering training ... GDP training. + Supports training management system enhancement activities and validation efforts. + Provides support during regulatory inspections by assisting with… more