Joseph Rapley

Joseph Rapley Email and Phone Number

Manager Technical Operations at Siemens Healthineers @ Siemens Healthineers
Joseph Rapley's Location
Boston, Massachusetts, United States, United States
Joseph Rapley's Contact Details

Joseph Rapley personal email

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About Joseph Rapley

Highly experienced in the processes of manufacturing immunodiagnostic reagents, scientific research and assay development. Please see the experience section for an in-depth breakdown of achievements, knowledge and skill sets

Joseph Rapley's Current Company Details
Siemens Healthineers

Siemens Healthineers

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Manager Technical Operations at Siemens Healthineers
Joseph Rapley Work Experience Details
  • Siemens Healthineers
    Technical Operations Manager
    Siemens Healthineers Apr 2024 - Present
    Forchheim, De
  • Siemens Healthineers
    Senior Biochemist
    Siemens Healthineers Jun 2020 - Apr 2024
    Forchheim, De
    I am currently involved in manufacturing reagent troubleshooting, process development of chromatography scale up procedures to increase throughput by design and process change implementation. Duties also include raw material qualification for use in manufacturing builds as well as authoring and reviewing Temporary Manufacturing Deviations (TMD), Quality Notifications (QN), feasibility/verification/evaluation reports and miscellaneous compliance documentation.I am also training and mentoring new hires as well as junior team members who can work independently as well as assist me with my projects. Previously led the Technical Operations team in the support of our new COVID immunoassays during the pandemic. The project involved supporting Manufacturing, Technology Transfer and Global Assay Development in the co-ordination of reagent builds while new procedures were implemented. Additionally I worked closely with Quality Control for testing and subsequent product release of these brand new assays.
  • Siemens Healthineers
    Biochemist 2
    Siemens Healthineers Feb 2016 - May 2020
    Forchheim, De
    My principal work revolved around troubleshooting, feasibility testing and purification of biological raw materials which are used in our biochemical diagnostic assays. Assay development has also been an integral component of my work to assist in optimizing procedures to ensure top quality materials were provided for our product builds. Assays included, infectious diseases, endogenous proteins as well as small molecules
  • Minerva Biotechnologies
    Senior Scientist
    Minerva Biotechnologies Jun 2014 - Aug 2015
    Waltham, Ma, Us
    Performed research using immunotherapeutic techniques to inhibit cancer cell growth and metastasis by the use of therapeutic antibodies, Chimeric Antigen Receptor T-cell technology (CAR-T) and purification of growth factors.
  • Massachusetts General Hospital
    Assistant In Biochemistry
    Massachusetts General Hospital May 2011 - Jun 2014
    Boston, Ma, Us
    Performed research in the field of molecular signal transduction and cell cycle regulation. Our work focused on mitotic regulation by the NIMA kinases and regulation of the mTOR pathway. We identified that Nek6 regulates the essential mitotic motor protein Eg5 and that this phenomenon is required for cell division. We discovered that the RNA binding protein IMP2 is a substrate for the mTOR kinase and consequently became the first reported evidence of mTOR regulating CAP independent protein translation. IMP2 is implicated in type-two diabetes and highlights a further mechanism by which mTOR may impact human disease. We also analyzed the mechanism which controls substrate binding to mTOR and determined that enhancement of substrate binding does not control mTOR signaling. We also identified that Calmodulin dependant protein kinase II (CAMKII) is capable of phosphorylating CARMA1 and that this procedure is required for T-cell receptor signalling to NFκB.My final project focused on new mechanisms of how amino acids and insulin regulate mTOR signalling and how these phenomena contribute to disease phenotypes. Duties also included supervising and training undergraduate students as well as preparation of scientific manuscripts.
  • Massachusetts General Hospital
    Postdoctoral Fellow
    Massachusetts General Hospital May 2004 - Apr 2011
    Boston, Ma, Us
    See Assistant in Biochemistry for details
  • Harvard Medical School
    Instructor In Medicine
    Harvard Medical School May 2011 - Jun 2014
    Boston, Ma, Us
    Performed research in the field of molecular signal transduction and cell cycle regulation. Our work focused on mitotic regulation by the NIMA kinases and regulation of the mTOR pathway. We identified that Nek6 regulates the essential mitotic motor protein Eg5 and that this phenomenon is required for cell division. We discovered that the RNA binding protein IMP2 is a substrate for the mTOR kinase and consequently became the first reported evidence of mTOR regulating CAP independent protein translation. IMP2 is implicated in type-two diabetes and highlights a further mechanism by which mTOR may impact human disease. We also analyzed the mechanism which controls substrate binding to mTOR and determined that enhancement of substrate binding does not control mTOR signaling. We also identified that Calmodulin dependant protein kinase II (CAMKII) is capable of phosphorylating CARMA1 and that this procedure is required for T-cell receptor signalling to NFκB.My final project focused on new mechanisms of how amino acids and insulin regulate mTOR signalling and how these phenomena contribute to disease phenotypes.Duties also included supervising and training undergraduate students as well as preparation of scientific manuscripts.
  • Harvard Medical School
    Postdoctoral Fellow
    Harvard Medical School May 2004 - Apr 2011
    Boston, Ma, Us
    See Instructor in Medicine for details
  • University Of Leicester
    Ph.D Studentship
    University Of Leicester Oct 2000 - Mar 2004
    Leicester, Gb
    Performed research as a graduate student in the field of cell cycle and centrosome regulation. My work focused on how the NIMA kinase Nek2 controls mitotic progression by regulating a novel centrosomal protein called Nlp. We also demonstrated that Nek2B promotes the formation of zygotic centrosomes in Xenopus egg extracts, these in turn are required for early development and highlights a structural function for Nek2B prior to somatic cell division. Duties also included demonstrating experimental techniques to undergraduate students as well as preparation of scientific manuscripts

Joseph Rapley Skills

Molecular Cloning Cell Protein Purification Western Blotting Protein Expression Transfection Cell Culture Biochemistry Molecular Biology Immunoprecipitation Cell Biology Fplc Immunofluorescence Rnai Dna Extraction Rna Isolation Southern Blot Cdna Library Screening Yeast Two Hybrid Pcr Amplification And Mutagenesis Sds Page Antibody Generation/characterisation Stable Cell Line Generation Enzyme Kinetics Lentivirus Mouse Handling Elisa Genetics Protein Kinases Adenovirus Baculovirus Cart Cell Technology Humanizing Antibodies Scfv And Fab Production/purification

Joseph Rapley Education Details

  • University Of Leicester
    University Of Leicester
    Biochemistry
  • University Of Sussex
    University Of Sussex
    Molecular Genetics In Biotechnology

Frequently Asked Questions about Joseph Rapley

What company does Joseph Rapley work for?

Joseph Rapley works for Siemens Healthineers

What is Joseph Rapley's role at the current company?

Joseph Rapley's current role is Manager Technical Operations at Siemens Healthineers.

What is Joseph Rapley's email address?

Joseph Rapley's email address is jo****@****ens.com

What is Joseph Rapley's direct phone number?

Joseph Rapley's direct phone number is +178148*****

What schools did Joseph Rapley attend?

Joseph Rapley attended University Of Leicester, University Of Sussex.

What are some of Joseph Rapley's interests?

Joseph Rapley has interest in Specifically Cycling And Hiking, Outdoor Pursuits.

What skills is Joseph Rapley known for?

Joseph Rapley has skills like Molecular Cloning, Cell, Protein Purification, Western Blotting, Protein Expression, Transfection, Cell Culture, Biochemistry, Molecular Biology, Immunoprecipitation, Cell Biology, Fplc.

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