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# 8231 English-speaking jobs in Italy

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[### Regulatory Affairs Consultant - CMC vax/bio](/clickout/80b4d1c534935f0c?ql=l&sig=aed6ea163501e9a386bd3902cd06cb332f2951d9&e=ZrRgo2aDy_ZFnfjfxCfm3-8P6i6ccDzCF0x1apxcNu9dfz9Rta5kzMBwoZcrBVVCTTR4Cp0KzR_MDoEXaLSNgpjYGaugtoRvbJwAHYkFjbvb4MNQH1CLE7dCvbovcummHKXL2ZTnFkAA5dGluUQZf2dd9gflbNZKJ-5AqyiPSboSW1VcFnZboM9TVTTD8TuMz0CuBaLr7MB4nvNEfZGA2rtXQr8BPKp_-0n76NJnomy9GXAHR3J6MvolH5OIVEM0PL6pnBlRtTQ_fqvygBhKOUXapZ9biDJlCLIii7gRln6Wi0woqSUCvO_ydFUytEO4vXt8U7J4p01JRDGpDLxscTm4HC919oZ3mcwEcEFIGPJiD2P5hkvbpWwVIt1_MgPWTKUgq6_jGzphqNdRWvdz7-Iea7h5naFztdxEG1piBfD6sGPXlWuTVIfTHvRJwYF-r3H9Y_-gKJmeU4yOPCGnVGcigMsGTr85JbgUg4N6Ja6_RwtukLAbf4R57dcRNaoTn-kvubRLrTTX0pwQ8Njhy1v-uJm92g3woXAtboaWKk7cTXPAqVqWkpIxkGupIZ9eHH2L4MNP7QiwXofTSZFd6KFYmH6WMjYFAJpyMPONqvMEpZwDdA_zRTR48bTbmlQ3yjzaHQMExwk9gn0RBaXT5ILJiScHDIugTCrtQrsFhZ2mYeCVT9xY3XawyNpYhebYFxWLESDXrrJY4i67HT2mfwaYvGElUreUVymxqUK6QoqWNTVCUrPKA3crQYP4RaIssi2y0VE3iPlPH0cxO4WdLrB4gPuXpA6fp8zb_w4GrHZA8o4NLfraWJdcaGVHL7EeZekpoaahqODebcZED04wtN2F-fABdl33SESOMjUl13XZpCTS1UZI9Ql-PQmgfEqJmBp6JEoBAUZhKncvq4Ywg4bTUHwpUBD1gl5Qsa67Qeszx662qxq34pLu4exgefkRYyXccdz1D23wFlVw7B53tobE8kbD69UqvpIZXKJ-B7W1lRPnoydjFVbaI2I4nDWILt58BR0F4xrTW-bSXvB1AcEQouA7O8bkElj1yTslg3e9wKqHHH3zcflmleR-CZluHk_sERpxvWlaIXPJorpMqEzSacZb-Q8I3hQ0W3002QiIo4gKRUs9R4-6DWFAXzzIPCGTHs6LkTr4gvvN82_ZOZ29cZ_9zNt1WupFlGTn3llf7QGG13TbqVXhc90VHrgpygkHqY0dB7wzOHcepI1smrwYxU0t2_fbFGrVBL9f-yfCOWJu6hw72V7P_bpbY6vz19STJvGStA0NiTCbWOKbhEXUPBo4_OsYRqCFZzutLexxXTAad67gjlSk0uo2FEUF3uzBQ9n0THKc_fUAfJDcVTtLdTRRhvepVZgoIz3SnjxdDmndN8saOEtoQRcl27rcCF2OACVcDlQYAON9t7bQyEIbzxg4B7DJdSMhSP6581BriokgzBwGV83ae_HpJenPEHHN2PuOLG098KkW&prev=RQ1C1BBE42909B1C&p=1&pg=317)

* Italy
* PAREXEL
* Bergamo
* October 16
* remote work

Support worldwide post-approval regulatory activities focused on CMC for vaccines or biological products. Develop submission strategies, assess quality changes, and coordinate cross-functional input for regulatory dossiers. Requires Life Sciences education and experience in technical/CMC/quality regulatory affairs.

report problem

[### Regulatory Affairs Consultant - CMC vax/bio](/clickout/d92eabc2fee0f96e?ql=l&sig=a1eb822815d05e904ae99242c3b6e39bf30009c0&e=qib_ErBWm2Xqhf2eczJ0KJaSmYowB5EZZyEaVRvcr4vlOxiiBnt646aV7SFGfnlXoZOUszcCydNxv8pL41vT7qcOA-EE475AP67lyxMedJLvNJHORqMeNZmykdRi--Ig2E1rq3yZXugPW7T0mC1j4InqJHxsfdEA4qeYo_IozSBzn4cQriQ26CIHu3Ew726wTRG_3R3vR2xQMySWzWvHj2Xk25_ceDJ5_TLr8rdvyt1l0Mbg7UbQzK_tpoQbhCJGDQ5o2xkI6-Nu74xMhWZxqFCj6GvOVb29TejVhwSI9abmjPOdIGVfe2JtcmARKsTYNYp7N5vHXwIZJrJ4TbRttLP1XtWOyWZgdRPRNq0fqb-uCwp8AqiGzARWv-0aZGjv4_gMAILHKwH1shDTOc21oBnm0ywVBfHi9s-2uYcGzWAgFJduban7Z5a07rY4vB4TsM850gaZI1SuDDYogrfwlg-dEI1mwy2gbDX4Rc_OzfQCcMN5KtDOvyTg55OUKgPcP8AoJLmKtYq1HcaYN7b6SWUZGqAJwg1fTUxop8P3Msl_slkXcfyAq_9pZTj4y__SXyproWxtiOvCPHLgyxgsl42ywc3die2n3VWREDsZOJlevx0JBKcWHZFGKP1Of4EI5XmvJ74xlPeIzg9nYZHLiDxa8M_6sa5YkqiwRh33a8jbYNt2B0JfGR-hXcX088ApQOD6NjMZT7MJYv_usVW-Q_-D6NPkTdNIbtyEov2ske5AevrrN_VEp9NcGtpo0Jq4YiGFRBj-SZDRvPYdeXI1fSS4zgKQvlcKeS3AlE6NKX5rSmQtLN2Zr-Uf7uHmSTWSdm1taDbztb92jG5jcnBg37afiQxeQlSol9ab6zOEuZfNE5zbKFTaPgUx_6HgzCM1dgOuq8m91WFtVWzE0j6jDgc-scywZNbNccA7vSmJE_8jUGnSemNRLRY5cS3nka4eMx9nTod2bxzHgEFz2CL4tHwSHHr96ADeCqmkEhIrO9P--emQBXHtVjMgILMAjZtpupDVzZL2PBSCCUDKIAV65wE1Sj8vBVR1cFIrKkwSzC7ZLBwgaT5bkGE3JdFNg5nzh-K9zlktjCSORejXvD-2kwXAkpcPGK9G525VVn0n7eJM86fG-N4UY07un1tO8iZLOwkKhllsRH42sUQgysanJowQfVl7p3aOLeuRw-KLvKwq7CBiuW_htmGGAH3bKRHmDmE3IBPp7mkzc8ywDto3eaunyVDhWKXS_wxrm0dOb9XRRemvQBnpcPO1z1ejcfCCS0AfCi0JI3-DQs3_bxJxB4e50TolLm5rpXJ4AlvW9oc-PuWtIxWmfVVb1yURiEjfm4Vi2PLrzAbk9lSZqDjvl1BffnM1i9IfUuC3sYJ7YH-HUkfP8S2m6zMLA3II6uPKgwNxVvdDKMtLj-4WCaakWhBIsWaER_nNZVGy1dtmYqQVw51OZ2tlASSbhmz78FQKQMs5lJkw6gmLnB0&prev=RQ1C1BBE42909B1C&p=2&pg=317)

* Italy
* PAREXEL
* Venice
* October 16
* remote work

Support worldwide post-approval regulatory activities focused on CMC for vaccines or biological products. Develop submission strategies, assess quality changes, and coordinate cross-functional input for regulatory dossiers. Requires Life Sciences education and experience in technical/CMC/quality regulatory affairs.

report problem

[### Regulatory Affairs Consultant - CMC vax/bio](/clickout/c1855b5b0fdf2e47?ql=l&sig=0e201356eedb3eece0f99011f9f25f78aff0eca2&e=Siud4Kyqf7pNFYLyt2qGzSj6Gtg4E5S6bpeP0tWCU7eIrEBHRQDzNIkh8t-mVG7C-r5hNnOk0gPqwnohUZBuzEeVfVb6CjQj_t_URWsYK1gZ9T5lo1FwimVynHvqJQ-NuR9-vcfWjNIRnh2xG3fhaFzgxew_xi5KgfFfo_mhZykF6cJ7NFrXOwxw0HGWm35p30b0tz3LtQeZGTfQo3aEPtn7PpyAVZKm6eXSTNie7PdatqYRQHNSzdHDRotWZqTCVh84oT6ji1tKGyfoeGxOGSq2uvBZqfrTizmKneyQZ1dZlY1MGxyuf2AMWyeCONLgnIQ7ld8yTdjrC2Al0T0GueOl0nvYZuxQW0pqjhdf4QlRDMbccZMwvuR7SsDQXV8k7JAaKTldmaR6FwgyNri7vY49FM6j9o1Oc-bgmytQQgKGlc3GdbIsyFus7MXxGbiHYb7uAiHk6dY1CfIMBc-cLzJ-wTCjj8xrUvR89-58m-c6ohmnMAUBzic1zdF22id7Asm6rPEYdAwvdbI8kq9IjiJWovyvffYfJw4FG3qOJYjZy9luagJwo2ysjbxtN28E_p0UkJAIBaGvk6anQpWRtvjNKVp5hy2B-XWN4ighWnduXTUVptBKEKkXFcMLGa-3vOL9T6MdqLJy2_pk5APoiIuPSyHhA5_GgLttBo_mZxFzIU5a624eNCjmw17XPnLdbQ67GkcHPBX0THTE1vIoYa1WjS5j6izW5GZbulwEqn2aFv4fY5rV-Ps95No333PK8o6A1XBOrZegroiiJUWdsM110vJ1ore_PzKJD55vok5YuTKDj1FlgclACL1JSB2yHRmrnGWCg4fO3PT31oW7XWKx5p6S1sL8Z7f73vmIxPIgmchLkfVUYOlhiEpVGDSr-CSeTgRgbHWsJU9qhi3uVR_3SQ4jwaa7_oHoyVVqYCJykuh0MOAVY6ouK-kr-yzpsjQzQIzqn3ajWnTlq2LXW-jamxvi_7rpDxoj4HvLWRuZGQfGEMezxWa1A6BAy5BuE9kPD3DGolDFqZnYfrothvFM5AY2ojCcrMqi71gF2kaR87bsY4CfwyXNj_w_d8pgoD0ldtpRRjuH0NLMzmze_V6fPub2n21z_LqXBGBL-ix2ZQxPyKmOIzeYRSq_PeGTQNjJWNoZerupSKgX4a_5kEP9eU2DSICFrD3BhUAWnjiQ0f_bKWW9ENa3wAoq5vT-GJnPbMITqCrcNNY4al39Z1AJZv-ZqsL8TZZURSgSddtsuBo6apXSvLQuIabflKn7OsK4MSPzJ56Fi__tTRQYFmMzPzvCG-xsAZR3wVIdsBnLKt1U3qdcG5sTtyD2zxxlCDclRw9YFG0oVTTfwC3MADL3xgkNG4SR2cSf-NhZOi3LAmYKr13zywtTwar_kudd5Pa5nn-pRdG86GjCAA8GNeUNLUE4RqIbMsUhxoqJllrOapHfiE1XP9q72ugTFN-xnmpmyEwiEwV1rQ&prev=RQ1C1BBE42909B1C&p=3&pg=317)

* Italy
* PAREXEL
* Modena
* October 16
* remote work

Support worldwide post-approval regulatory activities focused on CMC for vaccines or biological products. Develop submission strategies, assess quality changes, and coordinate cross-functional input for regulatory dossiers. Requires Life Sciences education and experience in technical/CMC/quality regulatory affairs.

report problem

[### Regulatory Affairs Consultant - CMC vax/bio](/clickout/096673c3fde12f29?ql=l&sig=049a2445853fde68f3936728322fed37cf6b49a5&e=XoI6C6JJAF4wHVI6lK9Xk7fcd5WVfl71PRYxYOWtEPmPFyDal44TcxCDkPmpgdhFAEpYZjzm7fWghKj9HsyOldE67MZR6vqTeAO6zcqUNU74KCRsu12NNUjGkr5znaYFEN0BOOdx-yOGEIQM5KgL2rbYv3Z4xuuOv6pHHmuQ69wTtSImP0Arfj0E1LBIAQ5OKAaCxLQfOa_sxQpLzGnHY4Fg2nhELft5mWwWz6YuwbTdM1WD2094YGJIuLnROQwn3_ZAWsVlHewwbBqNXk-wES563WVQNBx_IIAcr4Aj7AHBf-2iuUsHmUL1hRNcZvBhOOW6r5C61wrLtVk91U_sY0Yu9R12I0A4xqXAxvo8pMPqTdjyn-CduA6aBi47dtcwgCM0WzqX3Mh3ATbIBjXcdyJIgi-NfyrXN0fK7HQSSuAwBcK1cALoRLsg-deWJxUmJKb-lY6kegdcpyctJ3SgC3oUcuNAfLqZNT6NdG7_JB0Fosv3DSHx5kX2CMI2pu0PF-a_ANoqnBxnjf1tutxaeXUEiUz4BDY4konSn29zRW2EGtYBhMs1BuKHsEDhcVAZXsM9pxukSBJEKFd-14Yc4FlVNkTEJGkLijvVFNsvwC2Goy8eOAa8MyFfKIFn_HTQSJdmTiZDZ9jQDtHZe0CqXZduIlOR8fo1KOIILDGBL__jS5CiIh37HQMTLYDRHJGdlT5stt2_frw1_I5TRdGyONnB9fdXK1zS_hAiCWvUvzbjlWNsq4_h7YFitVlkYMuv_eYzKviF7YFeBlpKYxletPSPG2b5sRXLESeTsPWAWQOHr_Ik4dsIhXijSBcWhHtZSWScnxcjOC2xhVnSaPmeRkRxrBFRjszBjtEsr0hsYidO9zOFeGa5G65cM0P_fjAUPbD7Y9nlQduvzXCxEEJlihHHr5HyE8IJ3XHQQViRj4fABFVG7HBqElrDtctxy6sHNuu6d5_d_Bj7GHZX1C1B2O1DQv5LXZAv08HXpEozeZJktZMGkuAFnjLEmgfqODKFxicyEsyyJvjWbtVzIG7j3BYd4k4YT-HgAZceAyAEVdpkMyDx3gVoD02ZydwUHbdSrCFFI0l9_Z08Oer98IGmHXQQFCmiY8Pp2jO0zC1iEIqGy_bKLD40PeY4Y5Vy6I3DFq_j_xaR5ul_11VIPpwEf7_VTly2nA3CAZp9nRNRWutNsj5VnmzT77j7O0gtiJVU8pK5oTZ4V53CkZpaRSGTEBGJ1niHezl54e8ClDhYJSC_mmhI88oXiDyeajv2wssvtFViSer_6-mzYw0qs_ryZpC4iStnOOsILwS7oETcGgGInK0iFTKMscjIZdRw7s28XrktJG_bnYoscr0kpZfhr8MFDrd7ekfTq_DwHVjdxAmZNCA6jg6Tv-7qz40Ug5pqH-lVkUpEPIjLWvERmLNAqxQXEgYUjVBi1jcS_XQCx8nF6UdwxJSVMx4LDLhlrYx1xg_BowM6Jv-essTo&prev=RQ1C1BBE42909B1C&p=4&pg=317)

* Italy
* PAREXEL
* Vicenza
* October 16
* remote work

Support worldwide post-approval regulatory activities focused on CMC for vaccines or biological products. Develop submission strategies, assess quality changes, and coordinate cross-functional input for regulatory dossiers. Requires Life Sciences education and experience in technical/CMC/quality regulatory affairs.

report problem

[### Regulatory Affairs Consultant - CMC vax/bio](/clickout/33b53b454e101f60?ql=l&sig=d8294eb433d0184fb96ebb293bd88a6d7a67b346&e=ADEQ63Ahk416p81eSAux0nDuLOjQXgHR3RQzf0SMGKL9gUYM9yfCCnwhKho6j69wpjFlkcAAS-urVs8AVXzaBRY-n79ndJ2CVKARgsOP6rRguLDpngQD65tZMYiCdNa1KfcXAAHkap5-iIAVfIO891nDieiE3yeunJRD7CCIQjHfCsrVWPR7_2iYLCgxO122ug7J-q_E6KG22Bn2YP2EE4t5w3WxcexSUrvMnF07MPdZrGXioJtxdDKKBietb0TwkBtEsdz0ENl6WR8PAgwbe5fop6IQ-4NtSeYOl7gYf01lw_LfaQqGpnveONuf-u9Vo_sdQjvZPdjjL8yzyMzfzkpzOSsUlqbDPFtdJhTSzIX8XABwguW6cM8lKLa4xHqzhEiUvFu6fGdtdPhg0-C6mlyQefxY5Fohp6-obFBPxFAh2uyfpTdrK5EQl7etQBI9M9T2AN-j-JCzgoccdva20MopNG08m98_-oLoHKGm7za_yq9BIkUNEkPXWHm5zKr9vcrHjTKIHzk3aQOCizaiPtB29VuxBYaCDXAw1bSR2YTzljcYqZcOURc62XPiksh8Ub0bPzZXIb5AmY8OxzFxGnLCpCBYwarMLeqpGVTe74nwozJH6CkUnBR-10AQvcwAap87ehPleXNJQ_ZQu52X6-gbaU8G0kFTQDL-1VFhBdipjUAIFHH88X57Kl98SGfV15F50bRg978rt7nWpN9xtFdU2i404MxWvXjogIRpTKLTaxZc9Ji3pIIXQ_xIoeU_PRs3NQC3yYXxnjrdKQv7-LkyZopSNM9SDFF3kGAw7c570ryKfHVuyNtXl79p9jmmWe-yajtiUXBpeII-cKy3J7vuRXwZfepJWGtSL9mlodD0ElDJHdkn6ciz6UwGWduNp0J3LH6txncRWvbvg9IJIYrFDZ9aF6CUJ6eAYbm1IRqSn3MeexrlhbwlSL7PRW7L8GWSwp51hRrMvSnIJK4ixOTlHjpyZbBcJSsldCHvV9NcpIZSbk9lnCE5EBYQeJPvybGnjquNTbmQZKx9HLRPoj42y4Icv-hNytkxPV_TCIW0yh4rVw0NJIqmU9I-ClU_VgnKnd38MRg4ZJH-iya0IrHkz2Y_VHs2yFcctoK0KY5dZkmCf2pDSWMLjFZ-WFrmOneP0NNvDpr6i2EpK7zsn8uPRE0KX3lkJ1wzxo-Ymkj2V0HkyDLPoIlMYQmtQMQb-hgEYZOxuw4viTTm4H2w04I_Bs5H2faII6yRaL_SAsHmeaJPaqixKCcp5YjQv-a8cbqMS5eZPe_HCHLShtluiiFXkfin8xOVoIoM0jUM_KYUP3m0Cl4xYkr6dds9iE7ACcpQ52CV4lZivJETtAQyitntcWYscksw6eMhO0V4oYGsBtFer8AIkb6Qfcvi6II6Zv3d31vIql4rJVtGC9gdygp-rzPA91kHhNkardZXNJLp68k6E_CO6OYiYx0rmTDP6rfvNHDu-rncWA&prev=RQ1C1BBE42909B1C&p=5&pg=317)

* Italy
* PAREXEL
* Parma
* October 16
* remote work

Support worldwide post-approval regulatory activities focused on CMC for vaccines or biological products. Develop submission strategies, assess quality changes, and coordinate cross-functional input for regulatory dossiers. Requires Life Sciences education and experience in technical/CMC/quality regulatory affairs.

report problem

[### Regulatory Affairs Consultant - CMC vax/bio](/clickout/98ee0767d7dbb547?ql=l&sig=e9055e875bc310183a882f1c2223f57ace715c80&e=HEI8sdDOIY2ovC9o5vktbN1x7I4dNc9f9N66aMv8wxT-YhNSRyUp0wOrLtjljhQ5j5iWeISJPxI_yD6ZpNf7I-ejMp5h124V0JigmSJOvzCcKOquaWEffuT-Y0__Gl-vOhCyOTbv5CMU9Fe2EtT3JAKb0OeRKAKmh70T5yJGlb26akfCQCvLmqU-Z9K7qa7dyTR6XKx0kJPhD-ECrqPldm1STzMUfR0t--So_LeqnJmn-M_wN5prgV_ftBvSoim4d0KMRfvYWegWZjCy1DEUrep6boxMsX-STPVh5PDi89XNn-jEancJ-TW31rOsXhkE5d9HVEKhAUw2T7Z4bNCzoswvaFMot_xCAPrgI9ehBJ0HFAfJwbq_dJl4QgL8J1ffxN8L5Ii7Q-CJPW68c6xJK19v2mVCVMNVM7J9r-wbP2j34S6m1M7CR7dWAXXmgDO_RZke2AgGXrwwxdq9BfsT8MdMLQdLbMqH3TWWb9rrEg_szQAcermawcE1hJup_8lUVQeXCQGnS5BDaGcop3FVM1Qdpla1mIBw40T79HOerNGx2YJBuEPzl1itDBEk82Lsfz1bJyxMG-yzpdt2r5U1HhkZlACFZ7R78RPXJAVglpNqq6IxLsGzN1lPhfEfR_tymStzecUAuh908BSYsueE5K_VP_tYwxlp-O6MnlYEaD3vWPzrg-nkvc0U9lk7tdOh3ih7xfoTCqs5w0fpCHmNIplVNhZcLCuSKKu92Z15zSnIPRB3qXhDUzst4IlEh1JbVUJhAF9QycZpIkgFx8y0r4afLLy3LFklPRK0gQcMVlOnDSbDuOO0YcSJy7OQtV7wU3vObhG83rKlwok2Cm3N0VeY4rBzlrb2Wo6kSZguu1kcrf2mdQgH4z6_sIQ2pkq1IrMTXfe_6RX3PwsS1j6f_T0uVmtkx7A4NYN8WQhmhonjnGuynsbfbykqExmNeDf00rSGZh_7IAqtnGff5IVy7UOI83Hmhi1XDyBkBTWG3MtdDDTEBSyXaj-1vD61tr6m0AoTyRAD128JFa_YqFyjyxSliqhXNu1K_JtO9Rei3FoFo2nrBxStuWbhz6_SGrefudEHB92z3d7h6EW-DzQOq0IVNoj3P7WnC9yYa3wghOBd4IJvfzDu2oqENo_-Q2MA_7IjGr2FHpflp1G_iQGRN6IZ3I0pvxUguoNa4EGoi4B7RQsgUzRC9zNE6RZClMBYLULK7o5mMSvXqeMKeIZFsxyQ_9P_pqEgAdzntKEZdmiAu7M82t8en5gV4yXYa-4fIXXsAcZZ7iVQMfckp-4zu6jyLCz2oAIOkcUUB6OzJJUGTSayZnxLlo5SuOnQGO_2YAArVeQ7RfPJkB7P0cPoy56fWwc9rQm_W8rQjkfxZ77XP5TncPch76NluMOh0vgEdpnpFWByK90VqZ2LpfiAodViKFzuMIwmeKUwKKcjK1DMAae83LeX2eMd0LXKHKhXxHFztSayNDPkGfkt&prev=RQ1C1BBE42909B1C&p=6&pg=317)

* Italy
* PAREXEL
* Treviso
* October 16
* remote work

Support worldwide post-approval regulatory activities focused on CMC for vaccines or biological products. Develop submission strategies, assess quality changes, and coordinate cross-functional input for regulatory dossiers. Requires Life Sciences education and experience in technical/CMC/quality regulatory affairs.

report problem

[### Regulatory Affairs Consultant - CMC vax/bio](/clickout/4f14167a96008b53?ql=l&sig=b52757f4a6c0c0341d2f5f2b84956d80811f2fc4&e=xUIvtQC05uI6_KDobmCi6QK5iofqiDbnIPQLTECZ7HIZTAF8csi3EXu-CEDurTQGVAZiN59xtclhMt5pVKWRI1L1U1lWH2MDaCeoeLYf5ighbqHcp14r9HDVsht5tRJyGIsU2HVseNDAmzGbMUqsxIry3AZ0ekWEVb5B8B1AEp6E2OLvvTeQoMpN86zFvs9_gEeebd4RiJjVr94oUrFmzJyKz2nUggILa-VWhJc6TLiuYHbK_Q2b8valtzWALk8y9cJAf96DLwwrUfvj5S3PN-OyuGdgP27bjxSHxjbeJexytW97AnrdrjfiMtPbVv5di_30XbJkGzsxKUNOXEQuM-z2bLqX6RpmaF0delCZxo-dYbtkU4QkMrSorDeK2aZ62PVVjSMCf-x1-W507E-pq-2nAL1PPzU0mddKQ9AsStDxKnsrUs6_aZ58IiY0nh-HuhOL7T6WDTgHCuut3-CzGo4Al3EDkjs4UOy11ZRgQ8PovA18SDPID0vG5Ni4t76LbcaQeNJcXBpqyRN6SYVGD0RBaT9UHqTVfk1tLzETkfTsMaJXspFNe6YZZyBrZJocr4sJTu4rxLez-beTgsfTnTvVVryKPYUt5azXTKXQNiiX5yn208FUm7RjV4ZNlcejt9T7gcsrgFxUQIRsj0r-KARzln5fiRXT7eU2bOy4i9XZj5ayRocAJRKGJnll_dRqBshs13t8yWygc70tHxxPjdZXehldctpmrhHdIzMxf6VE3nJcgLWoEN2vzD7atacc9IEpxCicOspgLOYgFhz9nl8xyS2-SFy5L1VxLC9jNG7CXi2OXl3Qa3PQZvpRji2mn8WfVQP_GNSEksaoD1Q_Xli4soBLihVnluBqXtATVbPi32LKiDvnK48cKiys97SBlAaLElA46x0dDjct8ZOXxr2WjF-Qv15pzZy2bEfbwKdfnhx_1oBN4X6-E7_pvwV_tzarV7YUJDvzS9jZdKdsbbvZo8LIDBUuZQr-gBOKgwbue1TmbOwJArGqDvPCOwHNClgXHylwnYzB5UL9Zbtfj7Dzr9WH0pjGQJ9lKFD2EpsmJlbgu0nLpkRoPHJ-gdKiYuI9pAcGkrwzOCXW_1BdcgV6QEXsIdFgn2IEvJZ25180SgLFVpuyt3kWJoUI4g9rOcVPCcnyZV1_p6Dd_QE03ybG_bAM1Jwz2ExbsV3di7Ivl-pFcJJHONcs1mHlV4lwDdA1E-rz69gGVKMg0ZCrkgBnePv3ZJp9uZIwXb7slannxP-7wuCFVd1lQ9OJ1Pz9wQTs4n3qLt_qMfF4QWs2qSpwEQQ-RstdtC5NMCBAMXQQ0NuvC9H5c-bJbI-5mWlU75YmNbdl0AdnOXIOI39ERgKKch-nWgFuxjBJXYMpF5vcnU5XfyyPDuvowwkSIZuW49fDuc1aq5KTAuilzBv05ThGjeG0kt_n8ajc6b3j_jOIUV4Z68ag50Bj5BprkX1ZjWZ1SSctMX-mId0dl97kX_Au&prev=RQ1C1BBE42909B1C&p=7&pg=317)

* Italy
* PAREXEL
* Reggio Emilia
* October 16
* remote work

Support worldwide post-approval regulatory activities focused on CMC for vaccines or biological products. Develop submission strategies, assess quality changes, and coordinate cross-functional input for regulatory dossiers. Requires Life Sciences education and experience in technical/CMC/quality regulatory affairs.

report problem

[### Regulatory Affairs Consultant - CMC vax/bio](/clickout/e18d4f5cc7a1d895?ql=l&sig=06e8d52a1d847afd16ef3ce88bb50dfc959cab2f&e=sL6_FDDT2ooolGhWuuVPV23eEdYJ99k2Jzi6TxyDmOs5JwQqTpeIih_BUkDWeKiZ-B3s-bLTi4sAgyViAtdno_RIWf5mHhyEYl9mKQ4mxp_hXqtW6sQRNft881caugWmlcKIA0-qSpclakyTHZK0N5kWTr4UuLzyyqePiiisOpSm9wQGvWjZxACDneu6VZ3jQX5W2hTMzsYGb6_iv6-UU0T-j7o8cXG6kSHFUjBMtcVZ7KSVEfEddmj4t2UuslPAFZ0rw8rZGzcMYQT2nG7FzQnrs3UnLpy3AfomxF9jmeOu1HOO2jMX-PTN96f0d3gg8X7paRiKrgpYNbLiaFlJC2f5f1Zev8G1QM1RyvFxZz8yGfKtDuKqANKd1j6wugMQ24P_nqcqdp3b9cVvfKaLQRVM_qRD2gnMmEYevHs9sozOVtry_rwQAJQHkZk2EpcOsGcfj7YFU_54VW5sg5vckGJz94wDkEVcCka_r_m_gzQSzOqWQTHI2SOAhfW2vUqKhCpGhkQ1-ATAbW1RleqQ5xY-4siwtGRxcvHp324ipR9nACOQX2rb9c_6t5Y6ZA4UfqK6G3_w_jxzqe2o0M_qz0VpTtR4K2NALHxz1d3xP4P5BAIWRqj0xg7PUBbGVbigOLzjTFGmGh_cVZla7WSbzF6cPxht8dhjuV9If5giPzRVwa_9KgVYBoWOQWTPw1LPrYt8Si_w5xuFxyU9W-N6FkY9r_EJ-_O4eSbFGbcCBz2lkBniZIWOvRs5lBrHLXO2YcSCsif_YASO1k1MNgbwsH3OObCBNgx3KzgBZkZsjyfNxQ0svCtlCDuaEhpDvOD48fd2BT0dp7zg-IPq8Khd5qgZCQ_ZbnlqcFgt5ystY65D64HDbul1QJyYMA1arOZclitqbyBJ55HmowyrENzjl2rUXyo1-zJGSkQ931h-gWs3Aw5OOa9Tc-7wplnqrtxxkLtWs-US-w_DOpQrr-sYo_jbbEHIfUWNrIrqkWRwbenWjdqKXkKSkoynIxTrt9qTG-a8WOOTKL5ksZxcyjZIttFHKPPHXNx4GkXq3CRFnqfwGiJnncxvaUt4FADxNrPJgVPjInRwVGNNEqakrKwn44EXhTtD5F13f957DfYVqEtN1Z7pCAQhKswfX8VYFZjSMxgjDBhXC67n-TMCwP3Mv2xNXu4nCGZtVNlht8mIK80hVPw9T-iTrRg_HdZSzm_BPD6dfupcumqL7kvvAWVdRaMMbrDDjF82ZvYdGOpRxvHfaOTmqMTep6Pn7QjDdsj3a-99QWxutqCbugG1PKP5PhtNtOjAh3OY7_i6vHohQl-_Tx4NLbR421S7Up49z5hwSVC0UDdhKS4-Bi43qUJZKHKZG6f60_ToAJJ2bBHjYgZ8qh-GA_TzYNYUkmBt-QxZ3whuOKjV6FPhFNn8h_E8gfJ798rD8-XedY-zWNdpWFSwTxTLKRbLWsoPdXgz6YNkFYRjDYWPqfzE&prev=RQ1C1BBE42909B1C&p=8&pg=317)

* Italy
* PAREXEL
* Bari
* October 16
* remote work

Support worldwide post-approval regulatory activities focused on CMC for vaccines or biological products. Develop submission strategies, assess quality changes, and coordinate cross-functional input for regulatory dossiers. Requires Life Sciences education and experience in technical/CMC/quality regulatory affairs.

report problem

[### Regulatory Affairs Consultant - CMC vax/bio](/clickout/e4e2e1fc5e7f8540?ql=l&sig=26d390d5425bec45d559b889eb312cbd479f134e&e=bd9SW6qxZDD6aQsO6-Z9EV4xq6PY_dnpt0gvobsy5njh327i_R9Q2vNdN_I9eenmUC9IMtQbdCFrtiG0MHvCTgJedctWVtTtHKVIyrO1A-jVRV78F04AiPY2bpsM69i2MLQ2GcQ8wzN7qmbuaVkK6-7lHRjWfbdmfa0haoqAvkMjNwNcqJzIhSbOkuMRnGjzCqQ_WrKD7C8NMDfxTf2BIedmK0arD5NTN6tyBAOTJMd6TO36XiLHYPTMcV8wuy9Y4nWGmiooY6BLMxnHl4XHUXpcXBb_USq_PEutTQWK8hpcUT0Y5_r706BeZKKeBaN9upz-DV9slJdTbKI6cFKpgSi0GIYWoMAWG99xQOMO1ojvPcOqwkKCOQWhsbeLLuluTQ3fYRB1j2NomCdTo6n2JJAmjJlXR3V4YJ1qoug3o_X8shPuG62pxRKOo1XabuUasRYVO_GafYquVDFAyR_MOTXzqPcYTajuJlDBzRlUi7O_cuTeRBHVlEBVlZTQWsCdPx7pMCVqj4OiIkrnxT1GarzoJcjoAswhA_u6NvVtCm3mL4Def1MWQIuaf7bpDvOL40AZungL5yTyLBClQtmKJmcxBm5Qs5OHWTYX-ZP-I-Ynnkgi9ajeVu85gcDCwRk0fLNala601ThSDLPXpWb8KbIr-aQ7GTQjIvC83-aoUOpgus8NNeMnV8hL1_VkoHWAq66QmruVjTY773GLel1Y1CdtGATI0tEMWHOHfQvuHAx8Twri8xuKbJ6_TV-7lxizmI01E2rYMuGM7QyAardX87pRmpSq9I2NC5pQgL43v2u-z5lJmf4Mb_43KusIk8rzaESusFWK6MRe2tRRAiBw8NYZWsMoZEoe_L35SVXmFNJF70FwjUPEAX_5ucpZyN91OJpU4ZPITLCp05BPJZxwJ6iZQRNlWAsRhPDFrkt-ogM5R1oACEgCMUh8cdq1hpJmYM5TdYTlv9n5O1I_XMiBnaN_kw5_A-AN3nHHRgFnDicFR8602XI3BjBdeWaNw3fZ34Eid4HOhJMXM6eIIZvsVTnTwzvNnAUoiTrVlsfEeEDF_a5d_SUo2YYSioj9GmYw5uHUBrEzd-l4sg-lD1Xg34wti--VlepoFviN3Kj-XVVfKITwib62Nl7iUOU1BdESFsRtaIS2FskS1LTt-ThDA1qftBURp1aSB78AnhjAtMvlacXX6CkbnYOQMs5wZNnx3RRQqGcY1Pcu3A7RcSNB8URTQ7hMHrJAhTMGekImvYvt_RSXDPPgmwgYEns-e2Z68oIwy4hJctFYkTGNBL6Np1BuxtRzzGNq9eqXOKH7b72dR8a2DAQ7zxGs1iAbnwVXBgmU99yadTwh1m-UNoT-EJ9m1Xe_sTOtlIqasisaBsfeDVyB28IACR7FAK5lDlkn4jMnz-JlLiBWHPhPg-_z4NmyJLvnRhMYDkWVql9P8brUWh1yguZxvFhKfPE-7g7YVBYFVmVMCkRsSw&prev=RQ1C1BBE42909B1C&p=9&pg=317)

* Italy
* PAREXEL
* Udine
* October 16
* remote work

Support worldwide post-approval regulatory activities focused on CMC for vaccines or biological products. Develop submission strategies, assess quality changes, and coordinate cross-functional input for regulatory dossiers. Requires Life Sciences education and experience in technical/CMC/quality regulatory affairs.

report problem

[### Regulatory Affairs Consultant - CMC vax/bio](/clickout/4664cf8c9c6afaca?ql=l&sig=c07ab43d66aaca0771fd020e0a23ff3d91ce376f&e=dCzOJTyK8RoaTqL2fqAkQZKJCCnaBlVEPNn4qd3egb2XroaIBV1sMLhzFcGi4evIrkQDYbQ1oE_05pfGqrDXzgc0h5jefuw0GLbPze9yl_s6YWjGlCBZh3NSHYO4Ywdre4HGFiQDvx753IUJnvWSZUCnfkcfXdKg7kgvaKPXrRGAi2711qth_TNHJHKfmRuLxLbeLzOUGVzToDF-1jQrld7_ICYWbr5_b_DvPH4gVavkvo4dJ1dG1LSvoYTr2_JywVSemycx-06JSAS_PFBPiqOI5wv-w_BYjgpgMHtJ7JU2KLV9TY5wUcmenDd6d_Nd9j7yJWSYVSVYmUbMEHs50SuIzw61oViF75xHt6TxmJb1-GRamL2XqFUC8N8aXLM29FmYyRiJ9nEQfHY_XXGbweeHq1U5Ao3ZCWSPnjd4L7YNyL4y5Dhq51Lygl1HykLhKz-X4opCUKeDtum5FlC1OP8_QuNktNQ_iRPmzxeziithKvYmW4BCEHW9RoNGBLAwQEqZL6ErEgP94YutYLFEPF2nD3vZ6GDlha69M3i2BPWbPaLUX9QORNrYjFthVZxPn5P_d_AwqMMYvNNtuUFXVXYqR5D3kBAp_1i4A8ddn_DdXf2JK1d37OeUqnEiNaV60P5Hz5wmp7nl9GKPuxTDd3aQPZwlJKXdfP4U8xU0mvQMD4kSAshISETbxQ-sJlzm06MJLCblFaoMnKOPOBwgYhXaHgtNUouBjXz3K2J3V94S-o8buE3C_z0Q83xcBOv0iUq-KD-RsFNXIK9smF3gXm2M8SEdBa0GGRzp5y-2LObkKL__aOIyI69TTZ8D4iRhjwqeb102cXlHPrnl7F1vtNSX1wJ9YPsqCSob9sIO5fg2HkB5pmdcRQ5v_NjsprAik73j2tmMKGjASWclRObXesF5YkIdhoTw9zCLeeaeku-Hj_Mt154jpV1V6psZB1OsnLoQDo9IYYTofp4VxBVO46tKk1T8zStgpJpv4SYI2cAC12GmaBIVrtO4K3Zrxz_1d96zbrNvxVFYy8acGWI4v9WorWFCBMv2mFbw3FeMh2ksDcdS6RgnZJhJsIT7CoAa47Hm-NgB6UjKCb2FQUNK3PGI4g_t4sCm2VM-vh76ztFFk-9a_PWd3-IOoQrGagJg_5vcKgjSknNmOw0B_LiJL76D0oVzVmmZQcivXoQklZNVXxLwwLyl4pZgAOp6vXaBWu86RNu1HOYZPFFs3PDfHhwMhpN8d9YOv8wUoRxNTF11BMC4byeyi-aM1lRXr0t2qOvSYdaSPkAFeqdwdRyf8rSXBLxdvqhE2xSGI6LkY0XrZeWa76staegFVQdBA-BZPcUIxBVrlVE_-2CdPMys5sJ1hSTVmVE8CgK5nNUkQp0feO1UMXy0mGTGYN-GhV9ZeXtSEu9YDafbqNsu2AM5WZbOOArOaaAiRf-LWZgbm87xfPfuKz7cDxeWN-__YptCNZpbTXpi2j1e2A&prev=RQ1C1BBE42909B1C&p=10&pg=317)

* Italy
* PAREXEL
* Monza
* October 16
* remote work

Support worldwide post-approval regulatory activities focused on CMC for vaccines or biological products. Develop submission strategies, assess quality changes, and coordinate cross-functional input for regulatory dossiers. Requires Life Sciences education and experience in technical/CMC/quality regulatory affairs.

report problem

[### Regulatory Affairs Consultant - CMC vax/bio](/clickout/a0cc5b62bfe0a2c9?ql=l&sig=264355f796b11b6881653b3e046aab78ab2bfb76&e=Dcebqr26k0SqsJYrX_i-byDj_doLC629VWcqQo2ZsZTfKQ0YR365hjsNSAgz2stMEx8_IX_BBYEydKNUKMT6ymWteqmfm_D0W6VGgaBr7UdZVtkfxif0MnPNQ9Ot22b8hrN7p2EWhTJ9qj0wayVnHT6wcK26I3OmPpvFMx_-vtmBIJ2dqQpA3PDuvT8gpgywroOV7ZXoAHwQAWErvHrZYMajVIPzOKvlSkV-WO9pMLXRCfNXpSqEhUP1fjb1ak-oOA87WueidWzVrxjgD0xU99dTwlCPHbTNm0rNjfYdi10ROL2fvA-kT3ItXLy_dnPPod10I9LxeAC6NTOMoJvhVpxvQ3enlCzCt_Ue2GGRmOabSeZHyq9G6PKarxLZ2_uE3_idU-Cg6y2ui9JBTrJMNBpLSzCwfeVjz5LjnwiWrtszbE2pD_NFk7vLLUtXQhGKUZQ6oIOuozW6RYwJun00FbGS8Y-wwDvqHc-nzzB1VrdsUIEJtq_Z4M92szBfdAYujSFsPpbuDDLaFQnkZULl5YHq73Yyj3BVwvrMasNqhSbtCYIjylqXqhc0Br6JSx3BYlx1Z1e_Cj66zpU8kyfbcy_dEZEqRV7M5jGuYQ5nCxUqh1fV7I-R5lxrooA_6Xf77lxoOgkvdVmza5iOaSaHrxuI8zJXeSMOxHGpKNs2fdgfPvhH7bbad-Uy7GuqgdhbFTGD10blDWq0qxzIWCzbdh63pgVdToN9hyhGR3OcjFaToyQTL5X8FEoBpgOkE_dXEO6jn75O-zggnfFhKbRednqH4ImYmap5l1qu6fzq0vQcxp3tkJeqmHQnrc4B_nLc2tU9_YJinAS1OalRTFZjtKsLYnpDb61iDS7Ho_EQ1GGfY94eXiAOq5CMzhjp6iD0xtsxu8JaHvERubPKJGoXpj_zZv33nIReVh7e9MCK57gp_szybQRIf86Pf-urgeVvJmjkErDqzDMloIvpIEvqFWz4zmOL5ASTrYzmWJX1r9e91n5mQ-PstOvb9xPNv144O2T995iviP5OkSwXGEvsLE5ttBoVcAw6FPqpQbasYpeGh8-7o-4oT-4yx7w0bKXh_c0b6u_cJ5Tl3xPohIiUj6HB8-dStOlavemRo19ns0ijqB5CfvHMQrB3RdvHDU6OOwk0nIvBXE4K6vBByIW4EYpTjSIh5PDbqmpImgTbFP9EaxTx_slGE0KrQIh5PeqTyjWlVmW2M1Il97uj5SQ5gq-dVsvGINMVJrDv0uFdPr4VuLRhZhONitQVGYWR77GNIC1eVcydTqh4r9HIqzrdX0JRAEJ4QwhDgdEPsE8UbTdcayCP59Q6FUkI7RHtJESmuz_-x3q94tpW0Az7reqFlO0a4ckDGXnFhcBG1PV-YGX0IHIKYch3MC9T7wKfZ1w66n5TVAVRUL0dhGHKhOgS93bAXQ0w8Bol7UYDrKH65ozHGmZtYaJVvyJ5fBA1k-9wCr-sEy6rdBK_YxZB&prev=RQ1C1BBE42909B1C&p=11&pg=317)

* Italy
* PAREXEL
* Bolzano
* October 16
* remote work

Support worldwide post-approval regulatory activities focused on CMC for vaccines or biological products. Develop submission strategies, assess quality changes, and coordinate cross-functional input for regulatory dossiers. Requires Life Sciences education and experience in technical/CMC/quality regulatory affairs.

report problem

[### Regulatory Affairs Consultant - CMC vax/bio](/clickout/158bb6c7afe3da89?ql=l&sig=27874fc2117074921ec598f05b0c28fc0b6ae89d&e=xQIPKF9kyOULF3kWjfh37Ur96tXMM2D42rp1GT_F3myBpE7Dk5BfXL8tJ9N_NhriyLnDfYVxZ1ca5i5oMDWLRYaVSY2lpLkO9cBITOVw4wOFQVB2fxU-PeAYf3jjsJbonwa97IpJg4hSx_NmduWLl7vDQNxiuesGqJsp3GLu3S00hkMxcuoXu0XzVgKuVXRLvpmFPH5_Co9ugANIL3B8PlY_WeuCn_VZopESEBftUtv4qJC7tJ_qUMW_D71mSoXI5fFghkbnLpVWLqlthzSm6VpFliYqGjsxxEMmMjfASBt6IND0re4GAa1_w99dOmGI9TNick2aFxtjGI1QQo3vnEYJSUDt_vA8Edmsj2XAZkrukOHWti9-KRmz7LYA-cn_cO7-dEtoLvNHf6Cqv0B-ewek_5ej_oOoBH4ps5yF1hnGfqkz-c5d3Cbh9iiQ2jUzbMk2XrbC2hgYg_Vnf6Q3RV2Bdyax4g2Ek3a7eIttbBc4i71nCMU1FvWC55ylx91tBeDcO4E1QlFwyjm-zXq7tbyIoihefgQJTe6Il33b1mf_-DSkGbrQYkSX5u8S7zPQ6Zul0MM01SMqyi0FfSBxS6GLvUMKlcgkNtrP5AU05NpLnk6b46FzDJ1mDGNmvqMViqA_6m6qmQlfbm6v2F0ZqupaqFlryRX0vyQgAdpE4erXePvOi47c1NWG9cUrq-oqoz8VGWBK-lDc6ll3WwOXrZcjU-25nFo89tO82ilbNQvYLsvdbM4iZC0kUopfFrLjAJ0XYdV-HYdObIEA4gFk8yvhV-Mv5uO5avLT-3mSWUd8QuFE5o-RwQYQ-BpSL0g_GlwFZKyWJeCXg9ddTpxSTrSYvP_FvvZb9XrrsFFSbAl4z8QC3rSqNELlSgGIWr-s7IYs1ZkKj2-YviwUOsbP894LqkJg1txZMPUNpX-vHl6eT_Lcq6ulm4mhAaOlYjOx5fJEURXPPOZ-XzG49nCC2l-GAqibigJea3-qV3_xqm1oGFSUDHgRUoVq60TzbPZ2gcyfn1wgJ_9sU4uYLmQpT0hfASghCdHpvAHeipV1B8oVIaueagmOsy3aG5174aSvnX0xP03Px3HyRRRZlAELpn-Ko9gJhghe-DIK6YHExzi4ppLI_lTZm9IcY0YgBT1Jj5S2P1IXNPeaDTZoyIOQAAKeFhhamNmHuP5ggx6DHjML9aQhWavn6nUn1OaD3C9CQECfprBipyxqXeQ4SKrn2ecIgUf5UpAZuP9_R_6FPg9GHYRV2mGVW_YV-gUoB_ETGxjvcDr1R4uRWTnxu_tXilU4JFj4mFYeWax51_16IqiJrHQkTpldr-zG0yNl6a3weTKs9fMX3lj9bYbG2KK7mAcSeN9eJG_SDajbQBD3TNcWsVmhk9xeXAa-uighc4zOvpYZOSgVbiNfTA38P25eHh3uHQogEtV8a1i4fFR-EZDGmIq35wS-CS_O9P6JD8okD4nj-6_peZ_oH9jP&prev=RQ1C1BBE42909B1C&p=12&pg=317)

* Italy
* PAREXEL
* Catania
* October 16
* remote work

Support worldwide post-approval regulatory activities focused on CMC for vaccines or biological products. Develop submission strategies, assess quality changes, and coordinate cross-functional input for regulatory dossiers. Requires Life Sciences education and experience in technical/CMC/quality regulatory affairs.

report problem

[### Regulatory Affairs Consultant - CMC vax/bio](/clickout/e48de714af936aba?ql=l&sig=ef105e476e79335854f3d2d3dabf1a8552b60371&e=GHjKDN1IeqfwuR2710SgRlDGd8fq34HpdahaT9V4md1bxaISGiWUDm2eYj6SnpURqE8AoK5S2FEBbSdKKiDzbdiT1onfekYslgWfwM8aZYlbHr5OcGxRYj92YYO3WVNrLwBVUESLdgW0wcihs1hUGrywOLADiEtrT3eBFnQmYrCxLmWhD5sK_nC6whGypd_SrJv1gSs-kpnTK2ev4IRSYC0I3wT72lIy0b5UsJeGh0zIYngQSiUTOl9RnHGFR2k71o4BHgXfic3_VOFqWwh-FUFhyy8mcmidXUUOtqdtSrl17RXmk6V-e_k9hRXytiwYPaDIoTNjEsgfgCT8RZoVdf7j6F2Bb0j0QMRDbmWFZgQCBAkAAs6HUWGhZVcxrcsCj3a4w1fHGlKY5JHvq2MwWmjnh_-W3O3YtG9StrJLWFSTrQUEov4KlVqQsrCDyWOa2fM4iluE8y_XO-UdrYsPvRSjWxOwOTMp4Jsm6DNOrkq39WXN8Y6mXScj73uZ3fXz8HYJKMCms9cXeJoDACSecf6GoICLgZGkO1JH8qjrgKazowmTnKn4rmfu-TPyaUH5__YleHbfFN3bqPgVLjpaANpD5WJ-pWhUpeYJeKq2ASlRs84l_ViufUIs-TZvCatmEknKfCjXHDPBxqg6MbmnBPJzDhWYaRTpKeodxPJRfDOrF12N0euvp_ndXgmqqGDOa2UU48erFLEfJO46gVJWkkJ4zJwahXETwF0CAdUUrU8S3bSqKn8r9MwECez2SkX3833x71pgpktdm_E91xAR6Kt9D5KIA8Gwisr9kCBolvDH43-o542nSmnIg_ZbCLBUn-QFaf753MA9wiSSDYEKM5Y1f6L9LADtAPzF1VYHwA6--gt1Y7K658iPKx_16DdqnX3nZTm8R97q9hzs1rMPE9CvBXVeEqcCPEg18ojO1GYPq-FZdcTvyhqQUU8dj_zKxOarrDvjl0ywOwoWsfhHAlRLFyhfnnbDk_cqIzVhxRsIG6SRpSP1a9kSPlLDH5hb5O1iom58yK_veVt2C4NcuwnRY14m6lBkSJSfKCDCLtVNX5zpkjZ4TezycW7kir_BrufZssC5v34lAPmwRdbKXZG4NjYbXPFlDCcZy0E6p7s6p2g4MqSMfOj42g_OV4DVCusxKTpPjDwMGgTzBKezvwsa5aGHbyZdkQ_vGo50Yh7rANB5k9Wl9bzm-9wO8gBhitJBg-HyilV1hAfOsSNoC39VNdwxEv-Nb_uy1092TtaSRLznLDD-ht_H0n5TD2VZoCY15mXADN8__ZvmcaHWLx6dx4PtzBdmvJXw9KdSsw2svGBxUgkb4Y7KJaUXkBkej_9NUIYxDZg6YsFDFH1Vpz-NdoJ-NjWzCd91CHqtE-VHBZV3ignjsDD68LKEPsbJj9Ls15cXlTzG6utqNW87kZpWaHxRVf3sRXEXQD-0lzSgJJv6Dg3W0Rgmgcmy2dF-bY6_ddmcbZmYtCM&prev=RQ1C1BBE42909B1C&p=13&pg=317)

* Italy
* PAREXEL
* Trento
* October 16
* remote work

Support worldwide post-approval regulatory activities focused on CMC for vaccines or biological products. Develop submission strategies, assess quality changes, and coordinate cross-functional input for regulatory dossiers. Requires Life Sciences education and experience in technical/CMC/quality regulatory affairs.

report problem

[### Regulatory Affairs Consultant - CMC vax/bio](/clickout/4a50ec5215835cd6?ql=l&sig=034d625031b01f4c8be278dcdf9ed1c94fb12e46&e=lItGjj3gj21HDaCkgLYnGuHW53gk63nE112_BSeA2-GqxVHfKlvy0vbNnHtV9nTSfndAmPCf62PxtVvyLeCSfP1fXCByyrVpoL5Zy37YEVwq4BwQgv38gPXsplbrfPht-4AHQYjn1tQPq-404JtSiYGE7O9i6V4NblTcOrkJ5yqx2L2VSFAPp07qII6Rtn_DYGxrUmG054rj5r1FF-zul6zXX8-txv7VvrSPveoOaf9mRdYxufCtaHJl7h4VBO_FAK_JI0MC3PPboz4eF9nwZrORtG8WEkXSKVlTgxJLPfBiEgf29h7q-D7m2B71vm0eMgwZqoPdAPKrykPIAUJbem9FPiE_RvLuUFDiUnCZ3GbahQEEtDjVLpittnYMUNLAG_k8fRDeJbq9Pwwb78_bYQKzOnEVL7u2wXHv2h5Cl4lode7y1MJQqIb2hWZbeXim0LyfOQ7-D-M-C654j9iAkrETzTdoab9mbJM_mgj5LB9329DFqZZ_hGcnk7mSODWZrIOQ3PXldVyTuq5VQGJb59L2L6TV9n-v-up2SNf9ALvHpOwFCaRN5ZVVoohRjzz-kEVD5TS2Mk6btep0sC6RFPAz284ink_7suOlh6VbxEUOgFVvI7CfhChsnw1vIigbPFy2ZXU9KlBgc3WLEx-z3irv_YuUzqVYR0C7IRRcFlqh-PDZCtNZg1B_jeqQDDoDxIo6LYUQ9i7oyqrgtS-SFQQ34xHPIxS2dRsgUc6li-afDNsX1_EkjVEkwH1ijXlmr1JMF-Ztx1IjuZE7Gaj-lyA0uKlgnNjo6WEnMhpDYumviT7vVE_MK4qKdo7RQQL0_ENMScttF96EfYPxpCNWZf37j7Iw1ofvx6oLmPLsfWlKTT4kY1hOK0MCEZ_5wWZDt5YcMeWQ_c5g647jUk9CZJcn4Dgpgpn_7zea7JwzhuTH1kUUaO_XKLhA8kZCOZay2X4Cr8zKEqGOSqPRyRVVdxq1LbgiroDkF-btnD4kp_V4ex6O3yGhce6MYOWuMwtPVesjv68YABpfcA_B7HsmiOGkNu6pjdfOQcmccyoOuQcXt2wCkR96-vdbuKeNqsfxecjGTM3nUzTpsRVB7orMZmBVWQA2JJWAe1kpaBsrhRA6X_no_nx_4Y-yEJh8RqglQWjWl72-rtybA1q1T4YYur0zRmlTlx7PJHcAcYhdNHUKsPqGvtvFzYDwvPx71N7zLi8_RQeTAbY8wg28Yuu7Ue96sp8W2JPU8EdwH2ZA7S_lgzNraAacYa1HX236Do4FFzoxUAK0Ehpi8JXHCX1bWZpUs3d9G1TGniU1MoVvV-URPBPaps30ag7tD1gS9iYj3I6Pj-pntaBeZDXgy7EhgXPYdSXtl62JTM3SEBgKc54aEomp9DLbc8ilt3tv6v4ZhNtVQ9mHlvbTo2qbwvjWIMLH6Ve5DHdh21q8t7Rm9OU2VY9R5JK5Jp-psg_3MxY-CcXhLm41fHQ1CV4&prev=RQ1C1BBE42909B1C&p=14&pg=317)

* Italy
* PAREXEL
* Mantua
* October 16
* remote work

Support worldwide post-approval regulatory activities focused on CMC for vaccines or biological products. Develop submission strategies, assess quality changes, and coordinate cross-functional input for regulatory dossiers. Requires Life Sciences education and experience in technical/CMC/quality regulatory affairs.

report problem

[### Regulatory Affairs Consultant - CMC vax/bio](/clickout/0e2840ec50d7359f?ql=l&sig=d42a703a1cc2cec45281c9308da103f26497054c&e=pNife1qCriO2mNc90nKi5zlgiB1mUjlgWekAY5SbOkkdxlCMSFEvSaocChrAdf6g0ZGR46FEZ0oL2OBx-T9JAj1JFTee2sb6miY0YmRgCgBpve47k7se18Qna4nSt2TdLECCO3lYfK8Ioj1R1fR-aiDaTpo_lYdoig72Szi3veSmrgX7ALejFjbl9g_2ytvHjzugcj7Pstsz4KBusWJSmWSIDybYLVPiGZAA4Jvpm1yPAcnRJuXXfcvBRc9Ysl1yPNoDuzSIWR5J1E6qYi_5WKYxUZs1wPCJGUyWYT04ju8NlO4RTMx_WX9eZhGj5pNp_Quy7WGXWiheoBpEjjLMJFlLg3LYzRub5ZGNWCbxEI9itw1oLJZhPLuWMX-r6Ea2aycBh_x3UJY2l7P-Ck_atnGpc5mfgLECXxi7Ebc_wfezIeLwSDY3wwO-Xh1BVkNygqFHGlUwVm1pOy2i-DmAkTNeAabCM1_qeniit-wXcrww7lSkV95ZS8dH1D1NEVuxs9Wbx960yuWyh9gMpLg0StULrMlVwXhV0pzg2-9RVfSauhx6jNOxpBHpOUY86YwciW-pOOHujuVI4wzX7csbrYPLwbZaTlkNWpDcveuCM0o3qTBigvET5olEgSbQMN8OMxA1sk0736FdlMa25OQiQzpffCd93DIkt0juG-RSS6rTCnmITb7ebESPABL29p-2OLj27sRGdsGEV1eIcFYwHRQo3BZsP7X4DWC-PwfAYi_Y--63ELC_7PvdkxhQOi66A7Bnh6QKlKxTjkshttLB8S6dCx2iyprsQchwfLYRjH_nG4Sw9a1ZqTdUuJY_dyHFjouJCUWispsRc0ZNBLJLabERizVDtQ9i30P-dhkEHLGkRh2cKE85Zfu5Hzfo9aHqESxTLGXGei5M6Mey0vMG6EMnSnTWjj-V7nSyUhne-rXfdQ5C6bDSCTpVwHfGs_sjL6r9DF7Yfp2aTJsxfHe_jvZdHeVHaQfv62FqS5dPS3f4JlgAUwnV43-jQNymwfAJh2A3EUxyGKqVHHCu722teQWO12uL3Ju8O4UiCBnPpHSOGp8soZkKO0k59IwjvINdE_cf-sOMWsXjUj3kOPyjaKTQ98tNrHkCJrun7EMvbNezdeSutFhbE1Kc3U6NC-xq8VntLZ3w3Um85juGmY5miPNRcVgP4z180NBkT1ttBUX7MDGquKu6WU00uaLuVSk1QXsG4gErougfIHYHw5eC-a1RrcXgDljwnSjeXLFxTwb2vRnU1SoosYcNTXOWavbnwqheKzS-2yt0Sq2JRK-XFIBGRLFe0POB4g6OUcmqfAWWmrMycVwIYF1Zgb9MIQZsWnvcjuXVlA9M5lgQgs2OPu7LP64K1QdKkkzRQi1ilr2t0rJsVeYdkjMlwEu-hudr0UpVYVq2reJOJs-2gXQ8JJ1Re2pmWfV70DbnfNe3cE4o9XMHZWVnPXNPDlYTzGPgX64VmPc4f62k5R8&prev=RQ1C1BBE42909B1C&p=15&pg=317)

* Italy
* PAREXEL
* Ravenna
* October 16
* remote work

Support worldwide post-approval regulatory activities focused on CMC for vaccines or biological products. Develop submission strategies, assess quality changes, and coordinate cross-functional input for regulatory dossiers. Requires Life Sciences education and experience in technical/CMC/quality regulatory affairs.

report problem

[### Regulatory Affairs Consultant - CMC vax/bio](/clickout/c77f61f1910a0645?ql=l&sig=6ef3be12479f691c83d6b49db78ccd677294abc7&e=zZVzycm1K2orfFUOr5WAvZ6mTURMYCVuzig8CSoeO8CEVXQfExn7XwB4xjAwuj8-BFlv-PX0cSlwkHubEj8pe6S7er4D5LQ3YUG5vyH0W9IWLdVlWRZBGOCOQwZNqW4e7phG7iEXJiLW9U2R5fU42jLYNapyhw3M1Uer1kIBBuAKyBNdRFk5BzYzikHbpbQN05OA0BYtKMS24LfQITUjS6YS1V3vqx03l4p6zTd9fCs89Pu_RBgpr_Ft4THYIsVsyyUJpn5GfO_WRhawAhf4yJVyGXxcRYSTZyaT1l5vz2B-E8dKNbZmtC0zkfXRPOT63uRE_zn-ZHPqvH3jQziKL1tCvaQe52NftpoYhcu8JFrNGd3SGBcIXjU_IZ2EAngK3D7Dhh_zX7a7OdDQgNbZ1i0JCeX4Z6OFiiZ8ANwGW-dTP1n4pVT5dh8hL6aRGdtIOHvgBTEhZfwVN9mW61JuZiDaHZktvOlIZgBNqmYX-SR5lY0uZ2zgvgx21wBitW_amgsKEua0n2-QMh3UnFUPodlIAfq9AQtM0nHKpsOkceUVv3NG3aLsTrbPYaTPeHkJriRchcDJ-tEQiLJ3_q0ghSSBJHWsCGhQ9AXN-IxE-C2FNKvOaSbzGcS6bdPhM1jWNRHfJtFhVewQhw7f676ZpLRV06FcDxGJSrWaRvISEZg1RVA1hmLtg9Y4T4XMwmJMgw4kbUdGgFH0jPBGQab0mmskR1MM3ndK-DMKn0q80kIdb6nrUlBxNmMDrRXpcMPPRWsR0Ru_gQLUwoGSEBmze5SZSijeDPRl-5GGGELL19eUu3bESioYvS61SZBNtaZ6HUJSbV85B8b_CaWgr1Ajbo3gsDyrc5sB5uP8y99LMb7u6qeH0bhdFjDBacz97wpbkBfBW1Fq8vMMBXZNK2TySH-Nrbn7vNqklktE2HLGz6DpHL4_0fgmBOiptkvNFE4NycYnsyKjbulqmzvbZyj10K2F1TNLHHbBgZ9w71us0ie5bN-Tqodqqdzb2Wh1vWGiPi-T1yVzdO0X9AkKWcxiHpq1DyDSLXfUO3XGbMCah8f3c64qxck03UiouE9nDrX43gndH-awAuWl6LZpTzfFNKjIE65p9DxU7inJgovB76xORFx4V5FSwA4ap1AnPGudUmzz36_S1Gc7AFPYSATcY7ITF2khhtuzPDOxVKieOm2V41gCex4CGxpAS66pYGyCkhAnI5u8par5ZmWUg3D2JmyfDzeXI3P373uoPAhLypFGzzImAFewYGO7XMbSbOOrlX8yqarlWGcsc0rKjp_nbolSBV6hd8OQ5eaB0nSKGPc2GQZ8tb8OWG_NWGBJN-KQ7RapWu174anVd_YgOljXp7w5GChRf2OwjfBVt6fPJ2y2pBKmI28atA8Y0VBjwbzBUpoY7dF9MEtwKGKUsPNgz06Uv7y2Gby_-lA8t47_xOycYrzjVvBnfdpxATPOg2WGfBmdxDAHHI98&prev=RQ1C1BBE42909B1C&p=16&pg=317)

* Italy
* PAREXEL
* Como
* October 16
* remote work

Support worldwide post-approval regulatory activities focused on CMC for vaccines or biological products. Develop submission strategies, assess quality changes, and coordinate cross-functional input for regulatory dossiers. Requires Life Sciences education and experience in technical/CMC/quality regulatory affairs.

report problem

[### Regulatory Affairs Consultant - CMC vax/bio](/clickout/3365b9677a895db6?ql=l&sig=3c3aa2b8b5d79a3bdd56cd1337fd49b14129a474&e=YnQwxv4hFiuw9S9wrVnGrBOW032B4xa0Ty-u-aH9XpLzxegzPr7p7flub8MsEXyDbBD7SB4hbYh9xJ2IvJGXXzGXLqey1PN9wh0E6f7IHAb0b1qUGN8IhAO2_GHUYJ4IHt5PkacRPXNCibv54cCT0ard15uH6xPBsAmlw0oUbvQKzPe4-PET4Up4xveoevW7ki0XeecmRl_2bag-9GPBt_a2enH_42S4KsPjzP7ruMFGeMmy-ZBWl7k8OhWUlfQDDMGu_q274ooiq6deafCrOt8lz-LDEg-h5_uVeeHremvWd35YB9tIo3cjZHy4Cu3gWQtVa_nzRFs8W-0QGVUtQ5WV_HquTTMa7bF--bToYJofdK81zTUa99pJtTGC60eWTjkCSslehZ09OSYYCKAUZWdCyrTAUp7ewLhVdDxkYgDvW3nVh6q-WeS5jDO00lpxgNy1jBvfwuT6NH0gCWm-V66C1altIp-KJeSKXsjLoojqc9VWj07zQvoSQOpRDn63Z-EzFdGM9yK4idZMK7xxEHYVrSTvgSU1WLSQB4_KWUcfVs_b7urZeYLwqY_4rwd314H96tvrDi7Zvla5Dd3W6yxHSFnc6zZi9vYMX3m_wvI3crjlwMQIE6B_vh_VB0U88f9zTrXt3fDVlL1dCk3bNe4BIxlBv8ptgCJ6cy9VhBby17UTagcVeSp2u3G_W0eYUZopRHWdfP9zG4Ts5ZiCC1tWUO2pAFcjs2YNzj80UHPnIuFXO513-UEc6XFT_tbHqLzIFWXViJ9G9z-JRl4mx9mCjqKKq6PemNqLMyg34YsJRsUOBYobGXLkHf8KGN-0DRrWsjnE8MK5sMLCIaHKe4_DqM7LXSdQprm2fOVa37QKCbQIPnV5Kyc1_ndwmcWlOdpxJn8wjz9DuQfw3jzfVNHVLy7_m8jQNV5tc1nxHOXUw2cINNvjmiupseqQcdBP5RxWCSuV7xxdipGvWJJDzIbsnENOjyXLqQOdCS5O0uDmymkWVWeo_Tou2cXOgXe3yQqN6J4ke9SKMf0mqnVacsqoPtQdzgFFSkB80gVJoCLeiaKx2rYswreovj_kZQltdcjgrxiIIsNpQV6EKZ1-lpUAWsqZSIc7Z9BPHyzNvpkdDU5GqAmgBnHTieRfaEZJX2TeeWuAv8lFFn5yf83dnE--6A_AJtdMqOwFsq_sj0J0ZfmIDrMZ-WzkuZw-ahiyD50tx9JvXvhgEPxMSz803F8uk99d0qqbQbfRaU9ac7vTDj6E-G_RW45h2LAPZ3xwmRu0IM1lI_zX05N01inlEB9J74pImcoX15ESnk77SFNePkgYI_qQU1H4dPKtWWeyawoN1VZzwh-5_XQhtSgSwKOaZkRWykORt37oJiouZIw5aAJ8YbqxXsPllpC-eQJFVQCQHoxcbvrWc1FDuY_U0jNTLi8YniDSqdtekd9Rd5Ab0xhIv1VV3W18qhS7naKOOqzFqFhbxVutvKQ&prev=RQ1C1BBE42909B1C&p=17&pg=317)

* Italy
* PAREXEL
* Novara
* October 16
* remote work

Support worldwide post-approval regulatory activities focused on CMC for vaccines or biological products. Develop submission strategies, assess quality changes, and coordinate cross-functional input for regulatory dossiers. Requires Life Sciences education and experience in technical/CMC/quality regulatory affairs.

report problem

[### Regulatory Affairs Consultant - CMC vax/bio](/clickout/0a0e0b5ee05eb55d?ql=l&sig=fef26ea5bde71b9a4ff2f678cdb82bda008cdd06&e=GHuWRV7WrPWi21lmb3ua1DOxNi0uhBTr8OonE9k1VybooYpaVza_5uOFzvXPs5_eou6Hfzf336_hSL9i7WdPI1vbG2p-Lplywf36oEo_YWn5-6NOaj2FsACbTnumzS9TvLWeWw5iTuNP6OuMjUW2nbiIq0Yp4iTLKQHosMMHWSlgkAoYwIKqM7052MBOLFKPlZTWymSUt8cjFtCEOLrsKoXnjmWrsjcBs_myU8ZZeAzj4tu4WSiB7GUcFENiHDTxE3o5DQwu7_1eNxYdbJ1wdTYlJeNywit5bLD4fkCMbrTalSJxTnPWNDIQrdM8N--ex02B1myxdzyxGOeCMmWNGLns1HN3pSadbnf5Mf1rxRiaVpzecqMOtHoPXl5tHstxLLZcS3YdkEo2LkHIZpYEsBmRPAhmEYRZqYq9nMgDP7U4VNY5Dso1IhnDuO7QoABO_BU3sKY7pX2F0vDNj4pfSl1jGW9cfbP8qAFVYcGFugUH_DfJVwFUKqwr0M5hLE2CkiQ9sDNJAO9BYAYHlvgtHgPx1q_BJUqfyflVTxzhvulo918WtowWk7OSWQ1j_nTStevDKYqQIWalu__fOeM3DA2JxGReh-dWIBMYOVUbdtkgNraZzb1GjZke9NytAX680JH9JHeiuhMyA3HMk4UTUYDdgALE6e5LbGkJWa0P0N13PZdHc61BtbYjMtXYKqy4wdGcRxstlimulMr5EG1zdb_K1IH6hJXfquDejg8vDsbaPDFsmMJElz1F4ycEdFPgXFSc8odwpfLggzCTFLC0Xjuotljx6xYDFnlck4o0vHWw3OyXKU6AFdEzaa_ahpoH8r1fTVdp5liRgQEsMXyXqALUkPRfp2oJu9J4HqHPUNUhBOOX0LKbzK1Qg2xsSCI1aKHwwSHbmdnqi2DFtS1QhEGVsxz2nyb5xB-zFE0c2_1tFyq4XUxbuHJQ9bdaGjdWA5M58B--C0q4NNwG1XnFEOF8ITN4ZD_Si0qFOIhTp_OgUOR5ychIQV_Nmawtyhq6mmWMHFmjMinQPM2xxwvV6T9cuqANCMmXC_e-RaXCibuBOa4ilXR2vWkGIet048mXXKxehtZYwSS5iUVecON_SalKon5nJM52bPUkvR96igMp4K6GPvgs7Y8sz5QhN1nDIMj2Y-OhxwU-5rzjtw6KfbKYd66lzmKY-laK9fBDpsZYyHvXHkFMNYa4ZA1x3ElTyI5oieeWu6dQbMKPyMcuTNjPs7MQBJv1LUlAZI1Pv9_9gzGv-_iuJWd6R_KpQclngz-ydRh8IT0jldDNuUuN_9IQAPdGb5p0LVkW7JD9Q3JNY98i9Gr33PvTzq04X0AHs8REnSREly1ZFD0_LqqCriSWFeZgMxHhB0ly4JfCP0tEESlpXr4ydvkdGIdPNCnOe6bDgww5WZdzA5OBJzcNdX5TaLxlcFIWzEFvwYVKU3Mh7rdgoq64Kn8FjX4KQDsoGlZeaW2X4QK1rQ&prev=RQ1C1BBE42909B1C&p=18&pg=317)

* Italy
* PAREXEL
* Cuneo
* October 16
* remote work

Support worldwide post-approval regulatory activities focused on CMC for vaccines or biological products. Develop submission strategies, assess quality changes, and coordinate cross-functional input for regulatory dossiers. Requires Life Sciences education and experience in technical/CMC/quality regulatory affairs.

report problem

[### Regulatory Affairs Consultant - CMC vax/bio](/clickout/57cd24ae18263139?ql=l&sig=49a0128e229b05c011e796e23eb3c6b05be20ca6&e=b7xLcHs1ioJuVIuyAGS-KPEEJR4HYl8j2IXM--fP46pCK_qLUu9UT_vFDobnmMUyGF9gBtBpP78yry4HMkfJEXqw2a7PqUsK3cU8BOdmi8giUuXktFRKAq3t-cFZBLoDvldYADp-p_WdXCLeswebb3r-XPNShbg3dDBO3Wsg94yCwx3aaKrPO08Bwp2ufjGo0M35FwqyYbLqBNZXsvRXMv9ElIQhhA8UP2B1DqjUeUtZwA4_-2inCdy0s_c7ZLHoj91CPBunl961AysiAjCpjuIhzul85TndziyfDmVqLMOcQpezLQ3FkF3Q0HoVMd7QU851oReFT37T6XOv45p0wLADuGqiHtU7LNbuHN2_Imj5DJYLVkZADqsL-Gt8qyzLZYaY48ziE1jM7Btk9_696UwQDoAYd_9RW-HSL4o3x0qS9l5I2v0UVIgMlUvUUFV7zVv61IwJXMa9Jlb7S1gdN3yECvg0mNjTfdH1GjJOVNygUevXlZC1yxx1vaz7zkMc_zHcsRG6dBveJUiaZuVpEzxm68ELQuhNhVo3lQKzGkR8zP4HMsaoQGtomDyRPfC64EVOPFgjTwD57NfOmy1pnYR9Ot41LEyxXZ1CjrXcJdXzw5HSLdp-gGSmPHkabkioDP31o4uFoaoKQ8BsGM8SHGuYoAWCL692N24DIfJ4Rb3E2DxttYLTBACd_pS6ugOgWj-W7S_QUV_F8ZR3OoK7AB18IBirIBSTEmoEO2IvfsL1EGEeyv3RhCPMEMvnW8F-E8AmyGHa3hpmuw-rkzqva2W-LpgjhKCKSt8vstfyd2o-pKCW3nKbrHR5uNhADteIFMa6uplMC7IfPTgRt9T4KJGZTVDzdDs4H3rOuOLfRof91vv1lE8_9CqYCUWgeUR9FIzU5mYhpWg-z6iFiMt3s2fk9Q-NVrukfk4wQ0Syq7atBKVUxxvGNrYiE9s4dqT1Fboq08cCkbPWvSTHrKdZH72EmNiXvM9kSnCCYREMHr9TuMakCMk-__cmihbOp9kaBuvUUeodCK5WVTAEx5ISsAJyIAK6Se7PkvPoodQ-ABq42a5xIruhS8WjG37vE5pIqX0I-cnZbL-XPC-o3JLODV5BxY11QoNcgVHqKxgQAUFarsS4O4cuPCghYgPxaXBJI1oDj_MexQj2x7qQB0j78eEd8vNBIiWqYhuLor1SuirsfvmdhleBHspRkn3bsC1dOimM67hMRtGeQLUkaKcUdJpRAzuAbw5e5k4U24SvaDP_LHr8_2dczpJCUZYPeZMzNHF0QLnB-wi_5JsDIsDcwuykCx3U4zvG6UNPkkZZojwSe67MrYqSHiQVtD5IBlL8EW--8Cq42HMeln-yTC_w8kw2aYhf3mkCMWYfAGfspRnimD3LrLYaPvc15HE3vPhqmNPJ1ioC4OXigVkvk_LsTsQXEvyUvLQpM9w11TD04RsT4NVjnpb7HHfdzSDeCu63mgpesWWQo4xuFG2y&prev=RQ1C1BBE42909B1C&p=19&pg=317)

* Italy
* PAREXEL
* Trieste
* October 16
* remote work

Support worldwide post-approval regulatory activities focused on CMC for vaccines or biological products. Develop submission strategies, assess quality changes, and coordinate cross-functional input for regulatory dossiers. Requires Life Sciences education and experience in technical/CMC/quality regulatory affairs.

report problem

[### Regulatory Affairs Consultant - CMC vax/bio](/clickout/f7e65631009811d9?ql=l&sig=b837d9f46988781295ebfc15e4fdb256d1c08d93&e=fhgBp268cEJg6P-MLa-P4lKZazMKHZLjeaOARgQCnQ2mwJNE_7U56E53531Ps-fabLmOsWLx4FIzfFiGz1SJTMFw30X9IyKavJQZbd-IEwCJFpsaE6eAuDSUANjcmZEK5zk6QrktMx9nb3VTp5LOHNbfe13K9SMqzqx4sgO1dc_6c1mBba1wDea6E-1UDTp9k1oBiELNGLolNdAH5I0pesbM3zSOC9scB90XkfaLL-sz6oJ39GaG__0E9LTmoGWFqp_5Q6-jogzR50_YB0QJ2Jck5zflHQL3QXAkqJfJYXl1ppRUQLEeUPG1zFB6Mlh0ybeXILYIdAbjJJTdl6MOA8ZO-HBmoh8P77RKh7Bfy-cyeHZNYXvC7PEXxFNKms9_TsL-PyHzPm_sa70J_Uxdgd0MHOvglD2zNe5OdplTepwL892SlTZygVCb338FfWzj8Zt5g3CsIRh83m82ZCo-8sfisem_OhlnR7OE3VPL9ygKfi2id9atCqjYQcJtuHmTfJ3vrQacPlPGEV3-S_Su97XXxLRPsaFZ3h0IkEmEpBJjGa3II0yyB507-F107Ho-nxaXLCq7-Tps8fYoAt4kIYoaSH5gldjAiNM7_l656liQ2z1uCR2psSutNBxrUQMW4qSNGe6urK5WJ5WpYqKDLQA-XYIREkJYhWAfUJSM938Iq-8C7PMhApaZU80adt2WWHGxiTunrk_bWWFMwjJZ7CGmozAMpKXoaGdadW97vbe2j6nP7HjKWrpCicoMkNQEXqMZX5XGSIevEBzVBI0LP-O3LePEk39uCyu1ERld_ihR090D-QnS1okHqsZDtvLXQgJfaMyeYhmGSos6D7GRvGuIGccBKqP52vHS-hWR5mH2-FEBdX7xZjYCaExA9wYt2TUsLwZeDIcsMudr7ffBZpKU1nWUkRHxzID3D01e3htHitgSlPVSGRKymPjO7XXwCIw30_sm31BlnsX2N_-RetCCHS7MAqEk6T9WeQuHgqd_8JpdW4diZFEPGe9L1KWa48i-G43x7vUcqsYEktqj1N6vUIh6JTJC6zJ93Dfpf7xQWWFD-jDa76CfhfgK2YzW-lbR4NHJwqN_xsAdH4jOZ66PryUBRDK40uFJHb_N55uo-tHrhKW9AofGoFUyzqttsvBcDaEzBhD-DBsZCy5eRxBkL3-3KC3r8ltpC_YArpp8H8kJ59E-BV3qiQhTko3D6GAqg1cK5kx8T8Wh9lDT4EhzdxXSkdkTL3p3eJzpOegvSYc0jrtsl_ibj_a9l291saXMYYpQjgLr7PRj4CCUrcLyUD9ZF3PRZyjchHykXvQuZD44yPsDSvhfgrM7Hqm3pbNIEOqHXbSGAQmjH9NpkRD-ZZZYwDMDUopNsyqe5YT_hbK_Afeb1AIZfmRysYqCLHcBDkCXWxB6z7vS6sFTeOQSSdbudXhnxQJVmSS2OnPfENaY4y0EuFotpQWR0JMIy-juUPYHJR5KnnA&prev=RQ1C1BBE42909B1C&p=20&pg=317)

* Italy
* PAREXEL
* Rimini
* October 16
* remote work

Support worldwide post-approval regulatory activities focused on CMC for vaccines or biological products. Develop submission strategies, assess quality changes, and coordinate cross-functional input for regulatory dossiers. Requires Life Sciences education and experience in technical/CMC/quality regulatory affairs.

report problem

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