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# 6745 Remote jobs for English speakers in Europe

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[### Regulatory Affairs Consultant - CMC vax/bio](/clickout/c1855b5b0fdf2e47?ql=l&sig=0e201356eedb3eece0f99011f9f25f78aff0eca2&e=Ev__D-blNSbtMH7VSWJ2hEaYyZZ-j6Rl-Q0ZchHLFPYxvP53GbOTCl0nGWBwzRY6Vx2wuUV5fXErmolUvGfLpS6RXP2vlYJGJdGq_L3-mPvU3b8zjt5WAFXxXbQLOrFhAQAtw60j7Kc2QbBWOo5lu-aGUGjioQtvCpO-hD_zyj1dpDQorD7kxwK0jI9oQt-qOtLucfw77CV6Y5kpb0oZ1uULjddW60MmvLBim684g6pAu9GYWAH8YfWPUhcYNleJjHOe-yOq23qROdab2uCvxDz-X4HUk4ni8kJ3wW3m59FQxPwGCj5LvXLiqLCxizZ80I9iz0VHy4T6tD_wTaZqzhpbsxMfdomN7KMwPEEk90tjCQEVH3QYRVXHYUcD74_TUmx6tW9WeG-jADcA4lhW1HakZuOGGPyvZhtnp9u20BP67rlwyLdaoQ-inm3Rutlin7oja0NQINIXdZq6D90ppb_kXtvulVEcCthaXDRUmm6wlEC1WYiSrDfHYrGaM-O3keP8Kcm0L6Nq76j02fdjfUDjK46GgRWFvkhqgKh7gWZY2D0S-YH6SgnrG3at5-BdKdDtGvAutIUAyNvQw18DHBNvnP8bFusDKOlqO6UDM_QmEt1hfxT2-YuIXLIZc1OpxmbCOd7oONs4PM5Dc95Itq2V-3iv9yVTSwKvazlcksdkmKFeKQSWGUedQNjQBdWn7j7IpROJNMWTo0pSC-D9ZKx1gaeG8DOpGeofyXSVNQOSqrt_MGtWFTliPnhwdrsCO_Dc3dtDjFU2H3O4aZn79JgB2wU-rb-FiRgWevnAvXEz8OLWxfkdfjAhh0Wzleu23bwgo0LcLj8cjIAe1hbU5xqfkpR3XYTwMXy05nqZMq0cw97hJWQ8iKNP8sfULGNiIcWKcNMtLMrsN405TMZdaghkTuncF_vGa-6ONRdazBhB51Xaq0ZV61OhFZZJxWJzB6DLH9STLM9_HAh9Fgw0ndfRiUBUXVOC4miNxEfRBlhX8Lxmtrg5H5yjxgZbr7HwZZH7Or6tqQLXMm8EUvuRkTaXmeTZA7HnAWS_bmz35FTaA6rKWIHbCGI3j5WNRbbZe4KcRmynUo3EIa1bBWRes8M-OJcmkJru0fXQePz521MPrHf6LG6MnOpwBzVqDr6fj7FIJJ_n72OB4vP76tst8AdH688kX_lLTOE4E3TW2cq9zJyvmH2rXfb9TGLuJOraJumyxBWRyFSvQMN2vOdNXlBpLNDR4hPMVwpfBmtxt6z9ZDTsNNeFN21lNudyUMkTeCzZbBv4lnMPoZTG9Kwr8_K2qcFcY2lkrLkIdTmjuCTs8sA26SPSmIl_f0VP44T1DMxXQV9_yQ8nEPwS5cx6eMErWyRFBxlEa7PfwPYdH-eJ6d0vdxABiXBcNMpyBqO_W0beaB5vaut08-wu9e6849IQQ3IwYOMuVUjt6vdpcree5o4Bm64h_Px_GsCaO7Zg6JGE6znHxHF_9n4&prev=RQEA3F51628E925B&p=1&pg=217)

* 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.

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[### Regulatory Affairs Consultant - CMC vax/bio](/clickout/096673c3fde12f29?ql=l&sig=049a2445853fde68f3936728322fed37cf6b49a5&e=9y4dN9_dRsaAze9ljSJQ3qNCVDrhhg_AEAeO0nqu0FuyPP-UYrbdiqQi_YzAu2jwQ0tI2uNUp0JrRMXI0nhQ1NA0hIY3X5T93lSdAggrwaEAbXiszuvrZTMbmGZ0vz8y569Q77-rp4ngh_TDsyzBw43ccLbgu3VcDe7lBQYRmxn2DJ_NEDig9M4jgZSN82-fv4OfXYEBm54i9i7p2k8ltb9ecNK8DzGBbJUFfwnZMMRivcjifuS7-petFfHTgmZx-UH7DeV62Dcfhp-JkPgxFm2ADTf1da-qVM4ntd06G3MhbmXJ2Y8g9152zxF5vKsifm8B9Bkpzs1hWQi_CA-qFbyNXFctyfNtuQ8jBfaHLxKX_oEhOAtMuKsAWCfB1v5yoYTlBywpi_fwMAkhkxzE_0vNqeee0rALojHtocl9EYvkGQAMYi0UCD4GybrWXko6rwkYngeLR0uIercAlPW95sr47d23M-OrBDY34vjCyR2x9GiO8j-wiTzsOjOq46g8jvzYmy3e3GIoiyefzVWbZlG9YC2iZEfTGsjWHsx8OK8NdWJpGqKTLTinwQRTVAarQbmYZfZbYjqj6YE20gOfY8Mw-nw3iFdQB3HxBdszBvylX_jM2CoPkS20AM0nG7iamEnkflitKG4muTXrGPpGDIjezsMkaBXfU2QejurInAHjwTWFhkKlHoZPnKO_qxrzt-HBbK3x8kIageF42Y1yvOpeaFh10ZVidmYxMknMBYJT9KUjDtWlGQ3isT2MLZ-sN-srqVGikuoarVFQdHiLB1AyV_opPK-w0wcdvhUVTUTIobu7ANA8homlmVtItcqOHSR0NWt-BfCb6IBYkk0v7DRGNkIA-DrSdSDCBG4PoP9CGY52f_bnA3vMCZBr47Aq8bSUi3ldPVByWrM5RmScFf92Xw-USmY9FnHUSxJ4h5Ybz2spjdQG0_Tls9ME89O3nI1zC1Ux6l0ADNYrRzoUuoQs6_i3RRIqeLEpHbgLLyW4czqX6mzFPx6LGBM_FDbd1oeb6dCNmHwvAA5jVxxryPkMjB_Rf-dBzhc-stu8dSFeX8LnnJBFf00olzb5zJNiZ0pREXJ0TkYV3vhHmlJQy8aXOgNIDWCfW6-obbp3xOESLVKOCJZWSs42Bj3g8IKF2WDrzeGIo6NkS9dH7Z6WNgMiWyZUbjUgzmlg-hE8EV6Ap0kHxfC3z5f6h7PcxdWITkLVcD9wTtWjsc4KhoxdHB3fp7_YDMaAM_Ip59b2t8XPWXq6Gnhddlpv3rXjST6JwC-2hs8Pr7Udsk_ZDMPNG2U5jo2R0RxWxcSFVx3ksLD9s5MrjiOUKH7ul4QpalDVoHRDsUoSoEDmUBcfFrhTXZOdNFrXAFMzz9AFMhbeWXH-u_BQ5x84JJC5S1jCur-2X50SQ8VZsinrGb-0_0i_aJfCZ9yGwKYdLl0xeg9jwA0569iXNyrXtK3vyVLuIQApz6tBuos46AnvHmaR&prev=RQEA3F51628E925B&p=2&pg=217)

* 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=aMHNtDbXPbSP7XKOdbY0UbEI33pbJ-IfGW7wrbcF2mmqoi6kYXhBbNY8Z0NdBT6zyJ1PmS3_Quy-IhhKXtTaeKTi8p4XPFF57y1Uk4NHk3qkSYQpRY-6oPoF_O7G_7Y7jqX5DV1VaR-sPIB2-bII19I2nGXIVPZclXX6TZyUcCQFXFXtou5JTFCYQRWqc2mZpY4X_m9qZ8-g0j2EGmDioJzBHPRR7nRmSsGtUULUyY6ag9GGIpqtvESgJewyxwjHnpiSFe4d7wZxmUmotDd38cN8NUFOZI_ZWESFpkNk1O6BV0Nkd4QoByfv-yvMVl2R8UErPjkk9BWMtsRJMHZjDztlTENlSjl7v-1FXHWQtVCOo-nKHrp0z_RpdwzY1tFchuEqOcDL5RUvk-Y8tPMZbUX7AYg6eN-mZdOriW38tuF4zsYfOlgPef1v1CcP776EAjQ0OTZXTIq2JIjj6ThsWka4SSoVmsAhzbyrUqC8A3ZNRNwyPaPVfu54YNVZFDGlGWtbWN5y-i03L2tYK0QAu_3YWRnilcpxkaqZHAl9IEPaKWdEuR3b-EkeQcD0FvNWDBFV1XCnD81lImwyKElRPrqYMeKDZrc6ocraxl7J4iDkgQecV1ipdO4hhX0SA0z3IVO48vsFjLaFc8juEQS4KNKhRiqfa_eEjdMMHLILlkv0fJgYNDRnbIPU2R0QmDdLkZpdBxw-oQLYUQSk8puPNfMzTMBTVsmY-NvbzV-YZMJlybN9vmsm8JdYPa_5RTJzm255bm1tqjHUlxe3ofu8yLeZlsZuccc8PYHrGMj3OvxHU9d0jExyaCUi92DmMQD0KmDZfoLQvw3eIsO7RQaPvu0-AzNznoozakP85eHUIHLKGeqKKKQ4oSlHsNbWDijgtQSAySWJu0tB0nesTozi9TxQqJSo2komVRuaioLKvxHSdhKedTtO3ta6VH5KYnidBIwwzl1sy1tDsKDoorZgWMedfAaAw9-wxx-rz3A3Jt24aWCPGbTh6QAkcteSwRPD7cusDNqH3zNG57XTn1MngKmOJCJhF7uH3tmz00a5NRMJ2tdOr8_2QYQF2R9dNEV8Oay63ye6liaKUXznFdjhYgRpgopqREulEwtPotEjxcnxJ7TYlosdG9Jl4Ddd_AscodnQv493h6iSaaSOxM3NjWj8tvGP50RuUQO6AebIg6jruGhtf6c12oBFIHYKKbK6J1DN1z6D11i8PUP6ybWrvzWWiBHWSfaSvk4yObZ5dZI1c8m-bL0K0qRTa6ycMscvMWXZ2-FxC_9Q3l6Eo99m0gfWlBpx0zYKoLJVJnQvHSe4snwA3EFKuYXHr-uzmBwXbB5rujoENKbwoQuPFuiRsGogH5ZiH7XfN8OB-Qegv9hY9F7fzTNNFP4Tf1b6VnGDJ8VwRAlej6l-fGUqUu_64eR7dhELOURuiGGL5o4svE-UddaXfHHldhzsdn4qqdifleGLLr4ZM8iD5g&prev=RQEA3F51628E925B&p=3&pg=217)

* 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=nJMdCbc3wnDg51-L5hZI_Gjc3H8gS3Yl9ldPEEN2QfOQcDjUrD4QgcOKto5SQvqQqj9w2Ax_2zfoxAnpcWQGNNvjMCMPa1hTsD18WT2iT4zQULJsi0Et76SKWB7H_RpkRJzq_PW2QgzwvHoz11Nosmzc6J2xg5acqP6HKfNSxq7qifYQU5nedpJTgU69ArNFuc2xFCYI2iDaOX72wQzDiena2QqsNNCq4_FfvIdqhyLUFncAc820y0dhEHlA10XuY1b2ZlCM7h2Jb5_VSy6GKNx3ZkaQPALW9Nr42Mn944eJATFjTMYqdUrF06DmkVqANwgwgKWyzEvCDo6Q2vxXBtDlqpHfP-M4J9cJ9boPlPUgLoJgVWz_glM528D30F66h1tAcShfOOV0HHb-vhzqxvJGu08NQZlBB3EKkTU4o8mAPCq-ag1IdYbXtLSoF-9PQP5e_HJjzNnHUWaAA1kDHwSGMRfn3Zyf-9QfWe0A0IJI7-i73qYDfkBinpdErsAaFQETWVQq__KGik7BKhSAznR4eeK-3UtzpX7T90Hw6u2WsMHaw6MSKpXGVp7ggwM_Aw3_odmbNU8Y_-GCIEAdU_jA51xZUbh6UPpuUMCUZReuLsalKX0nFFrsalDubQRij7Lg_cNvAxOz2xAG98nZTGbvtMypOB1S4yWaJER_mqrSv0S8_vTPMVXT6w8SBllevv0smiMT66zWxBeT13hyG5h0M2qPMEzrpYTC6q1UqVSTxFQLOiSuAc_iImjq3gAqhgb6tyhwozeMqZvS108qej9Ut7cBYX4NTJyonyp1NtiUD7RJG3vv5TfY6exdTesDNGb1gsbOYXQ2jZ_4dtddv9598_wlOVwP98v25-Vo9XHWtFqwJ7APSroxnUM-NuRtO6jhJrRrAtPpnuBbH9HBqL3VMyqSeVdkcQMONySgCXIIy_bJJXDoz0EBeAVsuVItUmPIzsM-z52AFY6IC1i389itH09t21FQahI1Sc27TQS4TN8_MRp4vl7yILVjr7hNd8dm-yoX8_muTIcPRPJSjIXOduOT72APJBoqcJ0GjXaGEHl8cdTvOh6nLfyC0UST6MjGKn1Dlm2zHRhrBG8FKYVS1WlX1iZ3YpL7gZv22uxthxA1Tp0inuldCj15JCx6EWHF1d_Xd6x6wAoyY7IhvjJLw-gJCOc-PVZioaK1Py6EGadUMLMfqQpKTfJws1jRYohnM6mPinxqrIkE7rFkV-UU4LPGi79-oDk-0VGY1S8IlkefSNwb-9swdqI26bF4ANaOYychSBd-8kePjLkyKPKIUjf_KzPUNBCEzAw22PhU4F5Zn9M1VJTGZjNi9nlcfK25l6O9lpEl_BxI1uAdBeCt_WjpMqxEyC2v7iL00NPLTuBUFP5skgWWkB56-mrMVUYMcBZx9h16maHsUD1TIcavev6dGXxu-Gc0adxskox55OqV6JWmF9rstCVq3oee2HITHZyBBm5HdLbe&prev=RQEA3F51628E925B&p=4&pg=217)

* 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=YXcMjADUwWG20YcsnyUgaFoVmb5L6dTKMS5Fgvjo1qRhU-5pdaI6gVshIDQNZXB7LSIlrsxcbd8Q14vK3ElhwUIOcw-k9XZp08bmkgk5qU-H14Z_Qo96z29PkLYNgfMLs6Kc40jg9pgxA94F7GMzLuS4BLDCXmejcRX_Z-Mb5UtvAIjVVz9qD1l3xRuYwBSy8gNwQSOOvS5Gsc4TfiW8p84tbsDI8d_krV00704B8A5hFIjjRm9zjIeexpYDvxbbJ3aYUu0mzybIcYHYxIDuqkDgMhWokNHEWDzqUCPSLo9_LCPw9QVszTvDSR_Od0kdZmbHybZJZ4RHrJpVrw8uxwq29tbiD4Vf0b4xJLQnhxnWRTJqKZr9NXVdrO8hKwFp0whQqPmGWDvQuBh5bRtOV3masP2zMnLgnHaZwJdI1Fl-FhbAqtoLVnlu4DVYxgBifjMKmM4hVmo5a50t1Wk4sD7SZ61eDaUg52Rkqy6xPbP-Vn4L1_UF6zL8tTkc-7tjuYX8viiCDR9DpcACQq78ODmNmnFvLo1UzPvM99fOng6wdUmfYudlQj2Xv1Bc9JNX9GmB2V6Qh4Ac3M6zb-ND7ztxYFookX8AZyRqw7wVvBFXs1TJ7pdCAsnN_AK7b9FGcOc_8I8rjBZzOtZYtzd6fJR5sLb1o4dBY8ra4aVn_QENAfezxAWRhX6E_JLjiH-Lkkz0LMCHb54oqzLs0WCkryrQDJHyZIxFNEu7O1rb1DwkdccIMCUynurhgRvQU1glVZzqzk8gcMmKY5rBjtUCHcSC0B0G0AssjHwE5W8fEcZ0FMMrPfz5kMEOCgb4T0mgibhDZPHPEnZXGelKh30pYxAQ4XCD9MDuUru3GSA4FnJZ2ZBScm2V5fRZI9qaywGN2frK1pLskBkc5J96w4lFm7r8jvV1Bxho-FoIwXTYxm8k5sclb9BzbwkYI2RRer24sdemj6dGsoHD-z2xUPJJZp8f8eLaZomnHjSFOcAR0rpSdtJjcRwoeP3POJc4b9mxq80S5HLaMpKBEl_Yu8fKBtsABT6qPIkSc063bwCplsIc-6c96tos3jer2A9JxZlBa7yXg1PQ6Ir753zm3M7tiPtJgE_dM_2GkCqEQf0MCHTmqCeKV7P2YT2eYljr4X_81yx1TgxkYdoEUvBDWCCQ359FeaBzUdilenECE5IJmzbbM-CtX3Dy8T60bcVXmB3ld81b4u0BvhfPJV22j4v6Xh1-vp1X9T1OncAzym3QAcQ7gYTU-O8R9v41heLK2AXoHrtM6hcCtuTYFXj_B1XOs6Gy90Smfbipn9-zEwsx28kvm1_9uHbf9NVGD0icIfmfS9Ki3k_HqyLezvUkEvNgBcGsGkbMlp3VlhzMeonEY-QUfYFoyl_ZTWFFoY8vwTYHiGbHnOMyz_-9j0Gg_twW5h2fmFR7sFIJlUOWdOJH24QArDHgSsqNcO2tWZsRvPjVgnOTGe3fETLMURdNTjGvDfU&prev=RQEA3F51628E925B&p=5&pg=217)

* 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=1BvWmtH5muSKycAE3Hc9Ni3Vbu965Q5RrubSQ1RQKok1Y6hi99FfU2QBp_UloFn_AcbG8rVJxOr7vQ8g6XAvFPIjEWp3ODgfuQ_YPAE63KlrhN6xPWQwLd5tdvaR0udj3hdPuo1iHF1b3Th1VE5msoWvgy0hc8wRetNgaSpq_QixwsN5mhTAMwuhg1bD9P64tQ_d9RrlZMIEh29yqcHrRrZJuZzWT3PfQ6RFtgXj40rAH9DSUTB2DMIAeihDD8Trwgvdap00Xb6_XogAiPbgggL4NwuMPs_kKHMuHauWTqjNcc9FAe697cJhiy46i7K4BXFxwhflQe7phnjH_bm3rBfMxSKPTkz83TWotqIjXg7_CI3r5wPD5nS1UjsYrwoNRZJ0TjQ45LjvDpAkB5Embd2uEEI3uGlL95r9dHDcDluXdPpC_xebV0P3INQ0xDhs7i-O74xX4ZLZfI1J6j59blYGU6_KuCMRke3aGk8LF22QPWknS3oeUxSY85icdBavwjXjOIuin6E2Ie9BzVMrRaiig1fFE97D--k1Egh4ERVvv1OQgJL5YZD_mTmwGOSffEQB61bTz5i-ZpAZOA5HeAchZ_-JJxNyTSUvQuMZXY8tahMV1tGaq4XKbNahixPbhVRUbK1A4Px-Z7WWHcT5v4uRPMkR2t5WETeth2BX-zCkhysxDq4_SZ7pYCyGZWqhy3sxvPrzL3cA_AzjJKj89r5nmcXeQ0eJyebnM0VGsPWiMwlth5HEzWf0d3z0ahsDOWpaDupvPZJzE5Z6Lfcvv_fxPb1RJcJQJ_NLTxyStc9r2GXwLP7QPe2a2W7nK5f7d7dDoq2CXBbBgWyMQ-DeNFsZB6PbD5hH5WPctRaE5gbXgUag0DAzVRUCCi_D4JxgUmAFTqxmJ83lwCf7r9_Vcuz9Sm1-Lro_Izg_FnhpEuyejbAbYde4mHzIcB-rG_qwoD5qgKL9v_gr-94Lqu-qhljbFNacZc9Huk2gMmBX6xpkt-npbFfR6w6gGOuEXPgEZOCOyqUGludbpPvcYIbVn931Zwi4_1FTbriY79tHM093PZVd9kFtNOPd5qfTk8wDuopPD6oGvmIi25mEZGSfSgAdq01hN8SdAAw9NHq1UKM_iH-y6Bg9uGciw5Ii24A_U_MRoF3wZyzX3vkjTqlwVZL_UJzLLXgtGoegHWEJM5iNXj0i2f6MoIIwBpHmcRkaSglLy2nqgHq6Jm_lnd59QOYmzXCsvfH7jjlRAKDfTxBwA-GKT6kopRyNA_OXOZeJXzZU2oI2ML6h_s0rvMfawwkg23yuS1__PGe753jbXyo1hseZlaUKANYHnpremOnGFWfwMG0WbCNBfXWzli_UFPv_Xp9vD5NyCslvPS5vcilt6Q7xQZEcOz3Y2gpaZvylzEjn-94Cjrk1yXxW5yUrAG7RISzGdtXDDh7w9K0DgAD_8OaWd4ETR4LmG4ghLWe3DT6ji6nm5z0h&prev=RQEA3F51628E925B&p=6&pg=217)

* 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=H4t95a5ub0uhNXS5reYB8xxYTGF1q1nZlb8-cnsEluLaT-l2PV5K46IKSIx2SjP7RpbNC6fSxRryVmVD-7mUTD_TLTRnfxT_a1Y2F-9k2gqZWBG3U9Aw5iK6JPKgjZcwqP8cAQYBXON6zlBBEaA2LisiGJlNwJ3jGAIgACXVvPxUOLWWVeQ2Qpinc0j8fJEREtBpsOtI-rCImKKZ4sZwigc7thlf56pQJB07TEb1SpuuFcHX61am_wVnRS3Dosb_Ihx2NTu2IwdVdfWsigY8JEZB-DvID7i_s2VX0pFm-ZV9b4-fYzquBhmbhvwSkMKfubNiKx6CDzHGtGREzD1sCTHrhJwRrO9J9giea_kn6P7VfxawmHDgosGi9py7wg-fWIusrlCcGearmSpzDgBOmmGiVH_NPOBiWqBAJAb5CgDmU5Uf9gql9nPLYQZ0MxUeqDcrnhyzeV2s-aCbSV92vLdt-XUtPQSV2vNAAk6P1-d3AmzM5hoNxhWTTyDfgmyzcRjeL3AVSPrB1VmjpN0u9FyuKixlkMa9X-8ofqz-Uo8Cd6gk8wzUVkPrXCmOR4A-9iu_6_jqZjFR7Vx2NKBjffEWH8ut62lvGa2rlnEWlxuVVkkeBHpRlfpRc6vmETQzSprcyC42C00mCYqKlYK8GaoEJD8QQw1f3ZTw8Nav9Jr8qD5Iy8MfP8j38GLDThdN2Bs7V1_F8f0Swi8d7lgZY0CuOXJnQj4aVal7I5uEjwlUBNgJVHmoaZig-OQEZ7Ohb75xzn7b1yYGgvYpX171QRdUo0BrHB_lLRPw8zJwimjLEwgi-cJLFwENS0ps-dmWhiAWmGRdbSxILwTnbSMErFF1flH6tQmy5NYBghkkqkleaQEU8YFKsoxJv7--iM6yJIQOPgsppOFEpYb88JVEb6o8B8m9cXsIyr4cQul8odI2i-YR8T3BD3CL90Eiv9J_a4moItz0RP4l7-xtURugjhRRaSDypg8FOzVHMrd_pGX4BlmMZogOQUqnC2J2q4YxpiTvKTLvIVgNt33LByVWhtYS8QnviyWYgPZD4VUNjzu1UTjbYfH50uogKq-TPRxtQbqZ4ZzpSu-6Jp0BQqd75GiwjBVpFyUaImmeQ-pvfDcVDngb2NwPDlIIvq0J-5PcRHx1O01vzeTZtnXGtR86KF9fr7MATzW7J-0o6MYBHYVS9wL_LASIPSiQeySDcTNd77Cfq-1D0HmddAm-ewDSX2StvbQk8G-FURVKuuVbQZcvN4OJ0OsJDgJRiWujb2zDesoQom5UKraWpgcdHrJAxDVoJbSRUuZv3_KXORDANMSvjvFEM8qUIO3916J1NSvMkI-uvHhKVrGboPIC55y4CfPEjaGoimOZI0H4vwfaQHdOVRhdl_ETfJ1vUHIBCSZRtRT9PyvgpoulumMipm5_15m_mrulbLSyaMYVN9HXZJTa6DtaS4KyTOKX4tZf3ll5va_ysGqjOS1S3A&prev=RQEA3F51628E925B&p=7&pg=217)

* 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=Uz5-9l2HT3ScOPRsBl0-S17rdGV2TkKEbdQP1sgW7ZhtqPUEhVGeggBLyvkWyBIWzvGgRbVZ4BhpQPbS84oW4czlbBwNHKkt4HtFhzLPvceDZdNsWCI5U_zrHmn3QEIAVNM782cfvs9kPRxjfwiEPQ5Qb-JF_DxN68SxWPFs6fqfHK3p7lmpjmQKJTur3SnYiZr9wKYbiScYMcO5UaTX1C7VohN-vyLYRWPwilvXLoST5k6NogNwcvZUzz72V07Vfn7xtPIQw1rfUDM_3-wr65cE4Va5YnUT-vl5j-hH2MVZzpJDNCBZSfYIfOVeZ9gG61yW4TPBo-9F08WAtM0m5K-br1uwDzqMJPYAc4JaJPRn5tgTB-C4lHdtTCF79yaIvbYtb6hXMGML-BLUzbqImMUnM_jDnyxoi7cKAcmwWma9K5ayGL1z5UmQRICL97Ldig0c_qFevm9vx6mxTuBuQKBGBgbgm0zbyCyEtqLh6jJp-vgd6cO5ueKOsoQRYDM-ifbbuYmLn4lrv4qc9rVY4KLBamX4CUv0FGpUzEIwfpdAq8PKXNXhEf5HdHglYcBoYpqbReRouFZ8s5aUtM09iMnyY1l2WTpCshUKWknQis8pZC71jmnf4SWbe_ulwmibUGqNzmB2aud4KgWAFQR551VH8Veo-bSy51hKNnipGFpIJNIMZlDqKOnSzi1kIYoiw61voPs9sQbBsVTmUyy6SromyajrJFcHlaeR7SKjLyp1idbvJ9JyCJ-8GS03rARR4wQrWdClxFFJgDTDEqs1UW99BwhHPrXcnHKiqfHnUta1BrO0V1nhPU7Kf6bLsKwOg-s0xxO30aLARvtx9UKhb49tsAcJTsbadXbJdIA0m1bxuhpbI_7fNXyAgpzbqJ5IqIVMAoDvi1bW_7blV9B9wzlWco8nSRmEalT_mV1MJl2wzeWamc9fz9SDfx5f9c0r43PHxUNQgg93hLZCuPgNeVFwuS1ZS_7inBQ_NkNzHomDR9p1txq53V5tOasVtTU4L-PkNbauMVtrrKMOSptcLoceQ0StZZDHhFEBM4Co84rqcUrIFsGG5pi6L8FfGIHyrKpJFm55Wt-kbylDf_4hKx5MvPh6Eg_urdRmNUvdQri8IsnqIyUlzQMF_uUL2mXO88DGsY-2eQpUIUxxUfu7b4dvw51BCx_3G1B_u9_xnr2fxVqIUYjTV3nawrqL8zEKJNXqmPUPUkDp90IpumvzoJbDQfkGI36FodPJ1m4dp3kg4I8wSVgGjB164HuChCnHV6ESeAbyX0NBjrvmVd7rxAs9qWD6ysExMtwkIGlfJWeUuEWEVK7wknpXX7tXzbrCtZtCBuWYfIpVWcbKGXGREZmnd_yvCLepsMf_Uplpp1ut23cney0tdKFqVKDy30eGg-Tqdx46nnrzoEMq61M7BucY_STaJHlgdzKO3LzCflnVnsTQTug_9yQsNIyAu3PA_bsZeRQI4pmIFg&prev=RQEA3F51628E925B&p=8&pg=217)

* 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=P7gOGpq4fn7ilEiflCOZvf6HGGN3rdDsW5mZv2fX44x4vIHZ6jcTAkz09qlhmTq17Vi0uuHBvrwxR48qHBdmODJbH_xeGVaP92E6IfldQs1OOlc4ppzyhqp1JLd98LDHs81wdnKo-8ipu4kc_wlsiixzeVHb1noJyCONgX_dKbOFKbn9YFCcTjNpBa39EANqnkYsbQ31AEBYMpAl2jYUgL5fhCNxbO7pVP8pji_qluN1QtEavW9kzmYUMClCbNEJtP3zXpZ2mz8Rngqjrf-q8XToBMvoY0gQj3nwxXpHDoE3Y5BRkh7pLgWqqclR7LIjhR4wm-n4k0bURl8oEbWAOaGwJdQwqSDGkL-FF-j42SI-DYukEu-8O5U6nj-LJGZpylK7GFHNWF3vFfYLI5E_QWF74UzT6hTKkbaawF1jNmxfamu5DUp_F-9z9MbddrVgnJUygj6Bb5svLfkGEaYrtforOb8g0be9UFw9WreUBTYh7_p2aiF0ZWsBqbbEOEdYEIKm5oBhXdCfa881VzEDFy8hvAHxaIihwQT7M0aIzGw-FVNe3z_lU-VaYYzEYWmV0kNyZyFEQ7yd0oTYGL4_3quBTbAZzpaFo2_Zeyvb3mdHPeLvdWs8qMnvfHae6GPQ9sz3gLJptzPN1TC0jYMqL84PsxPoo380WbWvD83bFNMtrbVQLYxctPmJ5iNv-EuNEiJJmDA3nD7cez7K4AhQyPezNe8pbi8KbcbzoFrTYFfO0ZGN9NoeobJdFb9hOAiuWrGLmRl6meMFC3XxzSGBMWtLnbIei8_1IRZAGhTRiyDRqU41E_PGUU3R8Imw6zlqQFnQzmNfidgaX7irPTto3Pd095QdHH0wtiwUb-GzYHFvJa_ZipJcbYhBCgOpOcSwNBF4UEAl5NPs-Fy1sJiRYOpz92lO7YI8Ub7cglnVtDjgUmmR5exub--2ygCsVtUnztO0sd7cGg74IRxZzDQgwB5Pj_Z1tNGNkB51dlv1vTViIKX_eDrMDH7GxpPjKRoT5SJta5D0JIvVeoDHBdOwPVS6RiqD4my2tpWkznxmNvvtP-rI41WT4PAVBPJaxlYHnQMl_FDC8uAjKY5ZepSX2H0YOsNpDGBZgsOd_-sHHViH5SJj6XmjQueqqsfC9vc6hJNqTtycKFcx0J4kLe3EEb2iXg1Gh4Lhv7j2c8enenViUo_357JE11-YmG1sDc9t5T5AlaZHYGVRqmWXD2-iTTGRUlFQliVQM_uj5YfXnmc99hUNBqI1IA4-TzYb_HOeljPz3QqBub5DaXj_YIfQ1o8jXkOs7X6r8PNV8M_QhrX-XGj0NF4PlP4JLvDcQASE5mM5F1RoWigtqbBzJQKATmiH-5uoFFYxkk2y7ICOpAD9nsXJyp0ul-JGhUBmgU7x9v8AzfTLny5k1ynvZi3mK0B1N7b1BqCV0PlPxlgQIn4sVp0J-XqVJS-m13keZI3-4au35dVaCv_PIIUS&prev=RQEA3F51628E925B&p=9&pg=217)

* 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=ceh0Gb9s9dK-8_-dLEhsSNzzha6x3ZCv6M70QYW5-wMn3NWuHJx6iLoBcIZhwXxPBm-1uvTD2e8rZW14i5BJqB0kpU7Z9GivHvYNL0n9cU01FY-57mZusXaFetakEBQuQdn9zNSECwCTANtNXWSYEP82SNfdNr6fe-svZFJ0UIxRi45QJojSJY7SRV4sZAxgCZmmUx07VbV73JczcmRaYJA2fUhN1ZpMgFPeYqgEIyhOZrEBkVhLaGXyzTyXxDgOY265B7jrCB5tKGVDbUPsGywFD73Wf7Bs_mlmTqLm9FNmba4kbOHVwGavTsfdLTrKue86gcAVCK1vnRVVe-YBhk3lJKmfd9BjYqROIESnUX2s1UtCSzw_7czocX0UCU2xE95cl6Xn0qPnI374KcJQELw0dg5-jDmZCwQLCITBG2iu7bwb7ehv4qFRJplCiSEuoD-8e5-AldZcfxTK9HHor6498oWGbsC1c91D8rkHh5o6IvfSv76EAEGMQYl7fS0rdOcMjF6peQUuyMqgdjxYoR0QrUmTdxAWnAnZsw2cgfaKEdmi_2MiA6wTbwMl8pHH4Z4XW9Kubcdr-B950Y4RoDEd0C4XXZOy3fcuUnL-11nueZYZ6A2Cw8sFPFhU5VTN4DNtbw2gyH11F1SlnHnFwH9qxv0lYCVC-rXoDhdj3N09Ad2KQmbWVZwcY4McQHwrkBVjPgBGUudeiwkGNR2p6Pqd9Mge8vIP-dwPLsvxWJkMwJSG9k2ZPi0U5_lAXKQbxYHgQcLmNgXueKIXVXBF5cTDWyPtwBUf9rco-IBqecezOH7unZ036GU1iajKB-6AkHsykMPLCsHySZIkZIgyASQiIsLQLWUWmyM5V2mZTQc158UIMYZ58v_ar2lS3NapN4TZSu_NRgliwm6JwLXXy7wpI4CUhTZuDAE2lzyYURY9qMHINXuWuEPrGosAZ7nvWBJEWCdPWNsg0sh8TWJecguaDutXodM9D45grF9Faj7cmsldRP0vMs6ahPv5MJKJwOAje_C3vVGwuEH6sKkrnJ3QUXLq_5btH3l79z6JXt6hiCfbecFDIP-u2m6nKNztbeQx7NXHBNLckrqO8aQ0W6Cz9C0NPO7kLP7BZRAD_fu40q6xi7jqVWZjzcbid9TUlt67AHDteh1QvWVxI6AzSSQY0QlyplYAzxx_-BQTV3-9dNbu7phRNu6hCayvqWrlIxGNbZmSvaVrrFVnd8a-Z6w9WNhIZY-RCagjtrpARhzxnd1_FUr-fw-ZhHt95-GnGbfoBUUb4Ws2y6Hepchjg-qizKU6ZS5BbkoYN2UXqZcGMzJAzBtm-BTnvlXtu0CSYwoP-qC7Wsh6IZzeOf1A0FDDku271huVgGZwAL63w4zHlXti1yZcWKek9RfG8pcIwRUtXhFP8WLaIDuO7FHRCDjIYt60ot8UCDs2ee9l6pSxukjs3Jzejyq-G1q0P_77AL0hL8RVkhfAw-g&prev=RQEA3F51628E925B&p=10&pg=217)

* 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=7ZdnVVxtq-pvtil9TDXog0AOT2zJ1F57z9DAoq0uk-fenuLqH9PRy_53PEvONJTtME667KokV-4ZXzNNVSPDWctVuI8C3E60eSr7yrOWu9UB_k0gz_qUV3Er2rNsVTF-UXd7z9HIFPYxgr_UxLKPADo9kO_OpznWhPLRxq3ePiJ8jAnJP_Skz7Z72t4v5rWsqySD2PV8RLgxZXnxMzkjempfkd-IiNFa8L7zu7VpeG5hLYRgQxipVKFZIWt30mM-Mm56eJnUStqBs1ODmujXlnPmx9z-HeM2AbClf5QlQgK-NQOj9V1jUQnvHooBOie7bagXKJj7XcAoQTMpB-9IO5h4xx69WHoaovHF8whjcLGs3FhUFmBIKEDoxNOrmBGVugb7qk3Zud9xh17xUVxXMNjZ99u7mlOaf-5rh8b0fq-dUqo53B20pRmJkEpUHBsp4Q0wR_tgM0LM_qVJsC2PDxnoB-_UxxDaSH82K1y3cx5yDE_1XB67Kt4urIYewtOeT1OrYTXtAh7bsBuhsoVVCYMZuKVhLrAk6iWTaXRuQ3KITblePzpNrNgkjpavLvQoUBCOaif9qVv5PGzg5QyfYDWPmRnQmAaiAeY221gQfQMJmVHvUEKE5L4O-r7DY08YiLMZRrtEV4DIXUFWZ4qoB--Y1e7dt6qJUIUgUm1Jck7FdR6kCkvpLv0-C3YoiS7wUw-5sSgZhw3mlZRYBJMos04WhdGdOuL-KAHMzM5xUynsitXnFwCu6JY3ZY9rWTnhrI70XTKvFJR3tYJFf892OVSZEiy3kjsKwpRg38aLd_Udy60HW9nzssnBwBvIKCpXeGRkkt-14lFRIh_WHXALXlVV1gLmC5nmowQTxJfxPo5c9m7LLpbGsNIQBcc4Bmd6MNTX8JMa4-mwqcZJbhaJhM7P97Zlgg8J1Ir60femKG0xyVoB8-6ObWyCQ5tTzTRTfe4cQVN5x8Ma4qZC9NzHClHrfAJGRLGqVtGG3SJx_81UC4KY6tsz4nKEbGX7ANZ73H5A3r7Cu1u6K4Hs77Oc2efxexui3_ht1a_AQWA2HpJeX9PFDJiEkW_T7I8O7kX2ug0jk1yhXpOYgC3bA1xKGRC61nmCG3Pey2tEtD9YhSJlWbcbCfDdOMZgEA_qaLhdAZ0e9PdtzleBTKUa8G6kr0TEmEF91hLzYhURo6GOqDngjqJSjwCGS4MKd1d9fMrgFyrh3CG-iiz_gupkj4EfzEpWP0XxHUG7QPuI2s6RTC5Uo9TCDRyWDXJ0RG0Qvd5Gk_KEeRh1-afRdc1LJO6--HN-zaSqqlSbVKAlNnU8NuWvDshCt37iWFk2PXn_66_NGi-hpsbPsRfTBU25w2rIolGmAKoGiT_FrHvVcFKNwAhEQG954cf8LbrOhhMPWP6O64JM5Y99RewQlL3RHgr6MrwCtVINQESQgc3DjqQIeq_yuyqPu6scrfWEfZz5A5pQYAN1MRxo66Ik3yc&prev=RQEA3F51628E925B&p=11&pg=217)

* 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=wt6X3pmbDGOWJO_zimD8od2KavTyPLRYNH_bm8tr2IxaalhObNapA5DY5dXFsCIx5rLU6cU_YzJx1XmS7DUUIpIs5o68C72iGvT3oz3c-oIM2Qd5V-AmdaixK8zQ5CITcsy9qtD04JxIThXjP7jhLxI19YOYQn9IGTjiCkNz9-7C6-MWRuvl79Dp1Ni2je_QgbjMQD2YuD6HBMQ0uPElOFoY1LK7yc_lEv1o1YW8Vo27e6L6uSiCnWkVkOC6pZPZVK5huBBy7TynHw7h-i_S4z408mwE8j-btYwkROjyCheMyXV7pRgndGQ5F2LOo-V1koo2l5QRXW5fkrIjS3Nl3L7dCO_RSGlcctOTky3EIUAqeyTQMrF_62tH_Mr2X_C9kUjzgrTcCV9xPOQqvS587F2yiQqi3klsJ4x9FDdMjgzH8ai-gWAVvpoFTysIK9UF5S_a-URiF8QvYS8GayvBkEKwLca3A_Bu4RMO1TGHif6NvVjBtui02hg7WU9xxTeIE3kZboBLFzcG6JhdYqgRmimQkj6NzpldV0PaItzHgN2bRjhfCUi0ViQWg0K_eBz3JqEl4gVRTMwZfSlVaQLcyQW0X2cfMXiARoPiLUZWYcX9aSz_4epn1yTcgxT0sdIy1PoTXu4ROtwHHMxzSmap3TUoAlRc4Kxe7O1NRmuSO1WGILtZAz35sPdg8JkTi3rVWp68-cAB6_P9wJc2dTPZOjIOLnNadXw2hBmStekKFocsYrqWtNXRNsIPbnZi3vdgb-IZwvDSCkIRliIFb3iPAVafYWs6aFsIqNz3_Djx287xbgNMk3Am-zes65lmwkcv5n5eMzuOb3CZIkSNA0YPWJd3wW2e00F0eG5bbVvelu9pA98S7_dDAI4sPBUjcX15IGWe2K5cgeS4hap0tzKKMYJd4wr_mRJD3vB2Z1g5AJrLqNeP4R78HyzXZbtyGfJRH_TOd1SV4WIZ5YccFKEpMbxPmmrDEelCechmscz4Wt2q4-3RDA9r5GeLxg5tbQM3FWTxOglr7qlPEeT8uQXr16nrCcZaSQI91FiJtlbf2R5074-cL6Y7rc-Ki_PXNRIQG9jJxDgZEpteJcTQk3iRSle-wrOwpLWxhMFy5t1JSGNgjP0naqsQRv13kQKeM4YT0FpsN889djq4PbzXS1YeAO_SVojcre0M9qH-fHBwp0NSF2I4qcnG6QUnB6hKuMa3e4THD63VCFLXgnX8RmQKFKlennRBceTYNRQ3hTNVf5F4ieIHWVn8P94RVk3PZFiSSXTK3Jp_BRj30R3ikxNIL8mWlxZ3Nwvf-I8hsl6vkzKkxCPhRB2dQNCUn48FPbcjzHa09yRRI418KJaf72K1mW0biXA1VAzD-BY7Ae80-cexj1A52ttZOZ5Vx-eCtvL8I3kYkcmNb62T7B8R8TNvJgDbYQV9Sh02yC8UKAwqxWqvhHG31M29_un5VhHR4EtXfpvP-NLqunBF&prev=RQEA3F51628E925B&p=12&pg=217)

* 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=XCCce2G5D3acOMnr0UTUs0zZTljNebIugbXov6F6meU7Uf8RMvEZ7MX-bwp45ZWZB3XdyJScIjQfNHhKBwALyUGu_Tn0rQJSN6CdTduWUJ4VIjZvxyS-Ypw8eozMygSMsXvUSGj0lpE4iHOzV7K2xuxa8O-teN-Ug9wp_obPy5KYJAP0fV6tgRzQLA_yUSDLCLAcvKh_FEqsAZlOjFnKP5P3Y0-dDAOgHMzpFS7QKZLpwBEE1M2ExiR2y5uLRMuIhCXOZmZzgPoJE_tvmFMk7BDE2E0ZVPfe7IrSwl4fmiTy4rsyd5MZEj46ksjYY7JrDKqprUKJG8J-WFF2s0gW7satgLVBazoC5sx5uH_XxAd8w_qQmHDyPhA7TUV7Faj9CaMZeNKsr-b7w3ghF8U4TQ7HyUaq64ZMYDL23i2ygrRb-o6eOMj-J5z9asPChEJl3xxRTb8TtIjxPw15a19xcVAuGYiytu0ZmnrhsG2i4hyvcifz9DjPWPfabknpJrpZYwM6ROH4SQVFFQ3jggKuPf7YLrmRNzD6BX7suY8F41Xr7x-PWwNqLPQu4_bzEcxMCRbQNCyFFN_TZYMxQKUCps0YIJ-6j1M9G8TIUF4DbmiC_2KnCnoyJ-Ny495kV8x-ABvX45Tk8-WdgnF4_4fJRd4Iu7wZG9192BY9Yfu95grAx_dxan88eQHHX8DzzC0NsiGnYwJgqBGXcnUklTXNCfrUDxJCISEVYTtf02w2Bv2TyoxEieqC3mg_oyIHCUZHZo2s-yPijV_v4jX0Tv9XZLpM_ONcatxNj2ivGaRjrczXIWDe21PHLU-9VbHLTCjNlvSwxTTW_I89GS4TPreGxpIbMcWZ2RTlxOLwRKdLozL3jT5tQgPphWjuqeVnhpZTGjS1xF6rAkn-2zA1eeVRFdiKnUfQRZ6BWQ_lCi683dPEwNlM0jr3boqHJZzd4L3YgUpiZEJ_OYq9hbPUPhgv2AB05boM_kQ1fFD8dYpQ87sayeNU_4MLx0i2cF6UedGdt9HsfdqriMfW8APK_XQ89sQyYg9xSk6bmH8xjf2Bx013vT9ENN0s2boS_GoOCkujhwzgT6-FnZcTCSSfDjZBbPAJS5X0Zfbg2RLKjzI3DIXKDQbZAYiKHKalnmfO3oMxd7mHYMHaLIfaR4p4IuWDILCGPgeWmU-FdVysOEu0AxpHCjRZ-Pqlp_mOxD5BE_zD3CdeH6CaQiWdNcD90IRdM0XT_sfWCJ3Z8nf8dTtGHl4otcPUuMlkmt2BW_AIEHqqwSrpcIDIea63JqGcZtloUvGp5b3DCqlzAFxAOr6i1vyCuPtV67PGy873tjgWa_kifbXGsbfo3x0-Ncz2kagqgZWKLGqosT0glqxLEsTDChiCZQGKQ0J8HE2udlta9BV5PwztYy3H-0ji3od4379pq6yds7EvXMPi1oKxdaUHMOp3BLuHWfCE-X-93Ya6NOU0vLem68M_QWhLEoOP&prev=RQEA3F51628E925B&p=13&pg=217)

* 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=s5CKzj4CW3ydTiCWi8ok8kKPt2SdMMgUyoENVHkYDsEFxvTAnBHgcOAd46XLmKz43hEh0dHw0T-YFahNmPicqMupy7exkL019eKrgrm8D-mnqmFBTJGQSQkicyVIMMMxNEFrbIcWK8X3Kpavf-ESAFpY86kTU_2uvFEdl4ehcLVYEqXYWjW7sgaEmywu-Mnv8zO9ZAGjjiJlv5dCZIfO0HChJmv371lWIhCNbdA1k4KYWt2IBVo3OICQ22Mf6bTLemGtBc2IvzuCp7PrjpKSQc6d4F-Ox-1tt_NU_HSDqoWUJoLG58hMJVXsQAvRKxnZgqThXkm2iifqxBsVVMxCBWkoM38y5eJ6uWCYg7Cs1ch8B5nU32k7VUQ7Lx4SxM9Ha7dl2jirOl6lq-QwJIXwd3q3Sk_dwYY1-d6zibx4XJ2v_8MCPCeLI1t9yszTl_iL1hUvMMdVBviv9AtIjTWSmPLel7Vpm56mCzSr-Q5NRHI30QsU6LoV1myvA160pgFCAypt8OSbndN3dlWsUiOT1q6Uvo2UZ7KfteuqXzgQtI62-r0wSi8ny82tjhQD97zPPDEzNDJPwV-oZyPmoYVrDpO5vm-liG5sipoTFPasFb48QndMPvcNdkE9BM-PWnhXCfP0sX6h3ZsEGDfLpL84hxws3F88cDiD7AekQLMZebsAYzyUif5eJSn2DUWKVcw4Z73xDcy3ys5XyGqBGiJbbr_7k9jJeD0cuAQrfTeFMVH7PSnI5HVZJsGNqhR618ioqW4ID-r-j6mJfcswRLSuZffri5gVzep38XRayWXHqv5PusZgAY99-82cxhcho0r9n_Cc_16v5jSsARObrMcHFYxl7Sufflc9SF6Fw93f4l4PY7oixTWiDK_JPYtp56DHoGKJBew-8NBdGZEN7FLp6sPQB8wrHt26SnH7km2PvBLFKbPJEks7WVb0xMACsgo4fXerJy1XXcH8kwAjf3kVxoJBBSo-oTSpMZNpovgHOunj9V1zrQ_xNMxGOcR-T6B7SYzfQJw9AlaeUEkoMeHHWmECw16gV_KU1WIaMMgJ88omOmaIE5G5pRLziW4kgvBPbY0crPIIKT_wFX1Bliu17zhusNY0BjHgHFeue2a4fjspuplBJx-Z9vaYRMll1K2P38Xdm1MDAvxF2pbsjGoSQsTNp9n2YOFh-MJctAZH8vAfhKaVH1awhxfWDqm01Tu68i0YEGFl2hazlirOx5Z132cwDo_84PcG9hkUGIcoQZmxsMeKPsdc3GsZWyX2AYE06kPNloufxyEfS_adQRq-1PeVMFsHR6lEN1pKCgF04DJrNoiKyuKuEDR0d8Fj27mgKCZrZplpqvHeJj9Jr1JKQoDWFS-cZ2LRbdZ9xan87JDBZ9r9KEwcXW8eAxnwR_wnxrgdOJeciDJJ3kK-DQVSwnVAtl5vlGnDEdkqBcoCwu7lVUjyCAee35ebHx0LySKorq6Trh5qALbt&prev=RQEA3F51628E925B&p=14&pg=217)

* 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=0HcmWINPzY89Kn40cEG3BEzAYwxCfGiaXdxvokdd9jOnBKXE2AA0yKG7yhEDt8AqLOthjpz-N1_NirINZbIRIgYCx5uMot49y60EJigYiRcbebtiMyQIdRoB4I1lYET_knYVTN2I5uXMRW2UaYVpAyrc_mWtwfoAU8g77gxWw8efhYX1me8bdmvxfFagfyNrt6jH-fvdOdr9tU_mCmKcr5KoUCQ42zCIHfFVuFeBocwgMaF9X1Ab_d3m0HU60zsdma9vKAzGfYBh3JhGvtKfkPbmVMhzwiGz6E4yrWw1ghg6whs_5gJgP4bYEL9hXdn_W7WKEYaQS7zVCQFAjZNkbBTt1iw4yyuWq97M9NTrFJ_g-iLlcTTQ489FEPoYs3DAxuZOgCf0pOYeFeS-PuZH7cDSo7bDuttufa_TcJT9zJMZAhBvHrMYqycq3fXRTte2tKvFnddIAp3BZRXosauMTWbRny2kc5CxmYD4bnwuaRMhzcWcBi7UWuecMsuhKgDGZyAoRZbHAnsGCiUIbgJCSBJrvVms_a1J-v18Hr_oiat4i3H5aJQxtnwu0Vamh9VAdRlyoloCpwqN6YaNWr3KSV9ylpg9oZAYkagtjaCAAiTx-naqEUFnRlhgITZPsFQM1RekOZNwe5MpWEWInmPs59SxCBeIUMQ-0UAVuEfE1viIXtYjksnr2vLwL4cB9-VTZwTFDONeNk40qPj1yzeemZCl_Ro9jtoq_9wNRUgT78EK4Afu3GCisOYwqIG-lTM5ddzPfc9MeGtq47po9n5sJ1XfzIF829WXyZJGjSqqrMeDxp5s2JZnYbHspw_XJYtXM3NNwRtaop66Te2WLCiJ4146F4wtwlRd4AGIAQwmgYXq0f87NhQQpxIZh9jQIG3bBGuz7VwpgvOxWxAB2z8ywKwIZcPepSX2Isbvey1c4RzQw--PpymMQPrjdwE0aOJ55uJ4VA1dfSCSHPPxSdopqKR0TSx196EJPqBvmY8F9lkZ2IqwCrOeTqp53vLa5eovHfM-nPXE-sLbAeNfOmx2jGAr9zDThOcKc8_vCpa1qMjmVIXf3LbB_p_WCsiKI1cMJNrzx7_6vrhkqamvO_buiZlw4WLNsp5lrY4fJsWVLLxlmtH62g6wWHQDeBaWS52DB_wHhNRsx4MsWHfhJHfBEh1XvKpTa6vzdqvT9bm1bpB6XQ3W0ke9kIVIHOlM7TU6jzbd4WVROZDaCJ-utg73F89I8ZFsjIHCMaWB4SzpgLtN1BJwOVl8asHE-Q9AG6PipenB7aR6VtnvxooZcNiX3bvlaO2NVA547tYpzuFUzo0vHlOIaGKl_T2-0hRHIKQuy2gU0IF7ImGeUB8mGYhdLh5-uHzfvao3nv2wXvT0N0az0aEjmb06d6DrW8ZrlsPlSlmnzPL86cDCAlOesfWkbjrlV91giYvSjJywvzDJftPUsWRcrhg5ggjtqGWrfjBaFM60jzgU2mNiKg0&prev=RQEA3F51628E925B&p=15&pg=217)

* 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=iWRe_tRKnRN9HuCkDtg3H_moQlG3g4sifXkFWRHnmJb9wor1RVUwCh-5DGAI4_s2_7DqenldWRuP5hGRg9MEJCWUtLxUTgwvPspWDoAREqYuoHB2oD6we4eOPm27w-S3s6Tk1z2Sl5Um39QRrH4tjMdhKcyiyTahHvvv10HFDEQykL-bDnRg_2ZBfLgD9ttBHJjNFk8zlXrabetavJM2oamOOlvr6Zg1a7aw0c-G7oWGCtHdOykVek_1HMi-ewSZLeWdlX73dQHE0o_MU5EJQPoUlXjEYjiGYts8WOFuwQtIJbSzXsqqOea8klQ73v9ycvKuxCaehM66i0lmXXS2U1RfeUPwo3IHm-1yTHDkkQ57L_gutZu2URiazq17yOGRI7XdDkQQ2PkLUj27E7X3_byoFVS8eZrSBwe2aibQLwxs1vL3qSP5m5A5ODyA1_Qa2yDtoaqTnFDKfNbuQbU9ujGGpJ5bURFMBvG9ZTajXba7y_xjrr6Z-bAoAk0WQHn4u0viDr7vShKGfAzHI0vx4IhgChR6QnmqCkso_qCvppNqviqBJWdNmEZ4kJAyNyQqzw08IpEFfgM1L7ACeiX8klXdX1UXu6R4cRwMr7lZQXb-juklt_FiPkdCMsRN7n6uyXcR179aFfLmEdocyMh0IeqSiR7FWDwllxuULxidgbYxbblyCs_tnCPLJ3HtF6KFg8c90WCeh2Yc1lno1Qclx1J169BELv0bOQR8wtgnc1LIXORO-rTRo1lNyW6iTqk2YtQSAPvVLaHE-83-xhJAm0-4JJorEuoTduh8gxn5RYnwkhEdiAi2T2uOY6Nkggb2UmSqmS1gZZx3JSpagILTGi365HxCRR_w6XXMu6yW3NdJIIDnx1DXeSTAvbnn_vBManDPgnlWb44yeYIl_8Pf_VgLGm4HSIljiChPSRp8FA9qkraw4By4MrM14FQCuvz2cGYHGgwpy5qYfu9puVSP0iwTgN_3OhIPsIxK3HSLqTfQ8A3STgawVgg33XaRZA8xt2eeVr-aTuUjs7Wrtc-7mkiv8gDinhEs9Zr0f9-ZUD9pXkEtHGR2BEaqogHcRyJI3kkorBKlkTScOid9PGsa9zIVOOjvb4fk_P2OQKaPyQkSjIu733-COBg-F4AvyBUGJUo453whr6u1TbbxHiRRVR0iQTrf-Yt1t_wGl5TIsbI5cTEgGgfTkDzKwPur02OItfM2GxOCa3VZy_47n-yntmmJLlVlB7Oa1BcSA8wAfR5yQQrs92LWNyrTrzXxNgMnWvF1IfXIYdNPEnZy_Otc1B5fmHFc_iQmc5DL7G--m1omIlDzHxY9OsEJrgu1MFhIP3OJHjdHwGtWdRQrH4ebx7DID99ROcqOYXrtrpF6da9uPa-njpFKgkOoSGzydrOJkv4Z96WjNccI0dFQB29QR_mEHrv3rND4S-maP4mrPmRY84WiXhPiakX7Vthk2TIpZV3_ZLbtWE8TbA&prev=RQEA3F51628E925B&p=16&pg=217)

* 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=RTQPdkbxWTjqO6qIt1kJ8qWnmbH1Lla519-71BvqEWrNM-sNEgCkyvR-8QLoeEoVuVxbUbD3bfcIa6QESMoD3qPaAHTjePztxFOdccJLPLj1Badq7U0x-yttnZJB2A-Z00LYk7QxezlnBI0FHMenMblp9TUjILagMhQQGIbFC9T-i962aRL0alqEmEGSBdtwLCazxSu_IWEufI3NdjVOEHzOEloTnnEdNy8qIj1OJvk-_YDbCEISZVWz1crJ4KRy1G1yd8FaT_besnvbu4cchfxP1ooffci6OwxP9_DCVvD7jTkTEdlnSQEXUrqJlijK9U0Xnlt32dDIuY1pxUy9orrya-qMZb5KSICkFJPFRelrQB6jkMZ9I4Jc01OPBQGAf0WdHAwYBZYH5I38Q1yh3NDczlylfusYAG-r-g5zUZmV2UzOtVWnkNWa_tBHk2z6XgfjDnkV0AfRSUeb3l-IPeY2X69xPiOK_eIUTvtz-bmdcdQ8DGZekAppyoZmf0hPyrdI4WTg5OWEYh0asVGpVYh9E4blLBuW9PGN4jXwat8TpdJv0d0EezBzfmRijxJbo9ox0niBeC-eWDiwg2efgJzEnG-ULK11snWg3sQ6jAl-F3FBLD-VIKen1CDaJsLs4rWEUTeQrk-ZO6g8CXBkxTVgX8JxXluXbRI8mIaoe35uxXDc9ZLIh4RUCm9XpEryi5ej1iSDSvf3fKGrV01gIN-YqbW-PrDOcJByMW7iHVchqIXO3Yy9vT-Mk_cxXLZlUKm6W8WzXN8LCticFe7VyrSC9aAyL6IrmHzG4lMVVKPkKzk9P0CmkTnkssynQR0gOWju5xZFhLkykDhNN-RK4OkNoEUt9d_l_ut33m3NBz42gay6EdhgEUNPxmGBsDCXNK3XEnbGwOg-0wiBGBcVUSP3GGP1oJaBA2VABIn4cV1sVEri81l9UAgat2kEc7NgkTLptlxld7bMElEA5LSKGlnJisj-BR8uD6eFrzaXKIWC2cy1L66trZxipnThr0sKQtCcYpHR9HuLvWGUguWMVa6P7Z5rT85xViIvTitiJHC2Z6IuQLAnnvLDIhrmuAfJfqEDWNyioUw6GBPaV5fZfMPtgpZh7rwwSGOfWzBKTISRNk9zqJ7_VU6eNE1eqouMduvgwC5YfoV8rI8RAgDTxXfHS2yhZ8Gn4G12uoF2kh_vYW6US4Ib5L0M7MVT_MGsFiOW4rdd60Yj-tj--_3Byg57r9RCGTE6hNZ8Hl2KcCHgfY_5nypxyysE8KVwQrQTkWZ8VC0hNwe290WGMo6hTKB-54qKHbHeuT5zOKBEhrzWWi69Bc7i8YE3j9yVPeSbrdDx5PtXmaLNHl8r5dITa-DckCqtDVJktdoDJ0RNXbNYX-ZhlU_SDcVe1j8wKcvFfxMcXqQC4fFCsQnr-xsf4BI13wsvkzo_i0OxFbsEjg0xLO2OR0nPBVPzJXf4JTPlWS8WuleRYs0vYx-N&prev=RQEA3F51628E925B&p=17&pg=217)

* 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=cJ1bQ7ejRF40FTUC9q5YC3ySxGtuP7143GZqO9pU3v_b3ubi_P0Aa7TD85RShXVEhqjoDpD8Kc3Is1XvBRFOf77q4vDEfhJsHJ_HdMB_AW_B7B1s0Xjb5lrXjsp6XiQVDP2u2RUfYgACXVIsy6Y9NI7ISfBESM54GC119qrR818ew2BT_7WCwny4jhSoVB-myLr218wYeTa0xo5F12RY24PibfgdqD8dtp-wx7zsCR7P5Gh-ebk42zJUxTjYbVNWx6BC_eKqAaMN9J6CX22GqW5kAtNUOYBEaVoq5HA_P9vF63Shkp1lGwE-n3nE1ZZZHYlMOpln-rY1w3fSeHBK0JLUYuHIBHqepXysd-NISA16xxF2-LrcJqA2B6oaf9_ldJaDxrDtW3Qw3E3fMhVpHriXRp1iEPwy4JxfiNBsnHMimRMpXa91UklcWeks8F5XeYh7xzTPMZx_jqhVApq1O8gaarTUemgVkoEerdXbzsBFl3x_QL08gz1biBkB3Mu5jXNY2TqTRe5w63V4Poe1oFKdg-zX8u2mXXUVglPKYm8Q57SomhJsNFcqeMrjqOpCs9q98fp8SK1qVaf1tLPDDlwbJyE9QCybEi4KRuIUO9iBSSCPo_7zlqG8ZegG_bQI0FpjyucE_BF313k8QLwCSIA3dlqJYV80MvdFTvKQmdZ0uytbP4RnR9JzZnrDakEIPikLMJV72kwMLJgm-uFzlLW7qRJefb1BvM-vv1UaCSWOlW6vWzIPewxYHI-pKnbF4m5mWQ6Oa5A6C6PHXOOd_jqzK9LefqJ-F8oA-LpzEiYYcFxIsuKOK36X6EDoURBwgPTCNcrdyDJ9ihKks4HYSBfL2gm3N3TvVDgyNMi_XZXDPJJH5V9xrEnwsPoVTL5yhJMPKY1gTKjeCbtDyLVDISx5CfIdBPz3JA_ZjfYnklr8iv5TJEff8kSHATVmFxRd7eyRi-k0iuSmGNqCH1fgwA6f8R19Ia4fCC2E3sdRDUWHOdIGNYugwkqjv9_aRUYNgVR3OYy1RkMmkBmblDDiWMSfZ_h0J-_gYgcEcL9_Q-baqe08kNE8q6hWMshz0oZPwNiIryzBBtdfmIFhuaOVpxfmFu6yf2FY11dmJwihodC9f-ql2xvDNrPxgz13Jr_ntk1utMk2Y9r076r7FulzDWjvgkTbPbqKbTWgdM5EYbhkdR1yyPobqjPkGZZ4HLn4wnn-HB1c7s33LkikfxfZrXmeX5MQzpBSnFeNysNcX6wbQuWjSj-geK_N7kgZ7GFUJ_ce-7hqZkO5u6o90u41myv4VrCmhvHrg7dWPbsp2VurJJhD691XSM_S-MiEOurPHztk_NxQ1CzT9xpM_OJaiYEDFEKu3_qGB2dQnEjnsrte7XZ-CzZb6jlSmbXFeEdlJwLoc6otRTECo_RTcWuBMGUZrbtuFfyrGNg_yLDOsYP1wDD_6rSYY6kNqFFNy4PCI4LL0K-ndbzZe7s&prev=RQEA3F51628E925B&p=18&pg=217)

* 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

[### Regulatory Affairs Consultant - CMC vax/bio](/clickout/73511f84bcda66f3?ql=l&sig=a144cadf4e85fd2cec8a1c79eff2d372a27e330f&e=xN7dPjgVcHFtLhxUH4X3GytmJ7sCL2Rhz7Tyb8NnCKsAGQrlVJVObO8L3QN-NmMd_C1s9B5sk8IxT1sAxWP6ZngE_Nm0GBT5_HHG4NLzu0CbYFlFvnEezK02b9n4vt7Nuad3dp8XmJN700pMh4Zx9Foy_u96n8nk6ljFM7JO5tD-BZqp4vVHSdTHRW8JnkmjmhFTUmnSe2_PYdpvOedjTWVP642wTT4nMUV40Aro1dCNoDEX9f2nlcdPotfllOW6mp_Egn_CyQCz8um1feIdpNLSGqM6bo8ltVBfrWJbRGuqx8wjYuqN6pnevm6vod2DpUK-FlQd0PU5G81k7EPipUMXTDeTPJTKh1OimGAEwBUREC_G8TfsY_gszNxZGPA58s5L_xVl2hSn7aXE8G8_U9x1FC4UUqBny1Wl6PaqoGcOTAP1iLyyqLJaTFByjccsPTp1Z69PaTntWVU0uUcN9Ercj9syti2PjrwN97hxskpoSP238dU3w4ciif_rOliyIWayDUt6HGEr8f-2vs0NHpLwjhQ1x2O4xo1Prtfq1oIf8JJo1xgdGkajaCbqd5KyY9FCoSFpEtBlGPsRsdgFveT9F1yWXW2oIrHq_Y0VdZ_4FLeKOQm75-9DnzZvYrcvedQHj35OJhAX4Kr5Q7Fh_NxUgY4cXO2Mh2SZKBGjCsMRhyOreNFryWGuRzdtEYCLu4_gVmoxyeK-4LnEDBT0C7L5jNGwL7ctAbVhZgYeQYtw_en_tOGVpbUVTg2Xgm2gU0oz8QFNfB8-nl31pgyBkLfo9iRaUeWIBKxLn680kAUYzi54174lgA9mvUEp9p2OxJxc2euOkfL8VJj08nlbohORAooyaTZ02lZOixPGS_87bEVfW51-0TRqRb1BLyXRBymSc5SOvJRec4Hosj2K9Hn0RhVmDWomMthsYZGo6xfcS1RVmsq_mCxQGWRcHqjFAph91J82lxmP-sNOqbrK7LU7Eb9ZMLOiClfSgFpFTe7KEzsCJyprXM_GAeIH1Y91FIWB3KiNNfK-YqGuF6B_gnu8fu0neqiA12L55T1gtmh5QsPw3RQJE_w6WN349pVxVKay3JY14kqlWxEBEqwbF6fD215iiz1Ap7x7_Zd58cAc_baLKi6Lfq5RCRwdgTm4bNtcnHbJnBm8-eWEjxgcBO6yejT20-sOg6CWFZep_aSvpe_Rc3qUKoKYv4vq9sQ-_5wJ0VcrypozQ2ihBZLTUOhOQOVnv7uGeiXR7DvA_0MbRVsRHOVeY02b4p9rw7CShLqKBFj5a3MVK9y4LBn9mr64yVkBBMaKLcW_-RepjWvSn5vuVDMy64Oc-BlcVf2bFCGFdfnMmBEdANIRdS3UImXvD_PObc1iCBP1mwP_XSpu8M9-ZrHPojP_M4mtrl6JEHHj6TPC7QYcOAbuRLC3PQbWnJx5H2g_Qs3XgtWtafOIJ96nfO4hzrZuWDPdoJ8yGYhFNZyFy8EkYQ&prev=RQEA3F51628E925B&p=19&pg=217)

* Italy
* PAREXEL
* Ancona
* 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/d25b7bd41f81168b?ql=l&sig=be30b9d4af7d4678260da0a78339886515c811f6&e=fK5rilHQRPJaCX2yZB4EhOT8boCBbJ5UM4jMgEzrMv9xlJtvFXqtFyDKrzA8ET8sjoNm5dWhB9tMruZIu8TfAtHWCi2R2R9ouXmDmNf_9mm0zurF9WeWThYYiZnQPNTHwM4Plv8Qw05KNqbJogaI93WW8F-_zQ_okwozgNEJJJVkalBhYBq17s-rw_KO9q21NIhFxcjiR1HdRkJD64ZqxPj19DhUQn1B8FvnJDGH1mxPb1QTCw80zP6QGOLkNl5EEB4j5BgFBImMdPo3tkzCWtLAwpwmsrcXT57gIbnt-LnScB1zN06_3njwe_1DcJkNhPAqjPE5alTRyunBNu-e0GF-4QnioTulFvSQhfrvhYHKN87D2GCZoPnX8GhTKWXeZO_GJNlc7V_kTzg7DXAkykzmhJTENlyuvVptFKykLcKUelfILXbuR780TfzylNa11hbMcRjYD7UWkVtlLTt_JEkPPfz1Yfq7hfT9ug-mm1uTBW6mbBx23RMQ4lPtwKJVdh7nWG6BwBKVvz_DdCL1-FEAkic1dUGI9Q-potKRqTM3M0FqI1bhsE7qniINf-89BR9WdqKBfi3iNyWdjdnlpX8PXE39Ksr0HzRD0W5hndqos3pA6XfKa9mZTjl2zecoyzmcPJgc8wpcCYgptI9WTqfDWRgIZKtDd7szS_PlrYN0zY6U3g9_-WAAAwZkpT6kIv5lnOFr9BRo2C7Dsye3jL2VqF5-_08QWGsd0UdS4ZUW5vOU7JHS6PRvcyt-nootBvT6odXQd6AOPMzwsmBSxWQ5Nplqiic8Xo5-WE6aeuj3knANBCfvkwvqXIQINKutNqNH0XrrILs2oojeDdzFcVfJ7tHv4IhVxJRL5UQx7hfShc-rHfsIncBU32fizOj5-h1YPDhcHfVPH51DyeUgXS6vseMezx3SE7dSbjsmGGfRWRO3KcvfQuwu9KUvqAlnAThzBrbjFjAE3F3CEFLUbUKwQs6KrKVOMuQYFzBm1AVP4sofLYQ3WlEUlba9dCZrFXsnfJG1T8Krrcgt5ABkJXIGSVaVK3kfSQMGFaZvPW6PF-1aknPZ3xXIszAOxub6ssn5cQzvL8nktN73J4nybFCbScRnRMlP1R4bcc0RRMmNB6ocN-WMdx51i-dvYY8ouLI7osIEpN-UQ_6j0JUR1i_d4BhPSYVOzy3Eb2uj10AlUCFbCsYL7GdWq6oMs37-gXrUX4xDrG9KxMV7rMohldoXK6YOMpwq-xgW6JpDXoYimRBLUpCMy4gYjcY-8OtWZVIx3uoGkydDs2UmEvYKMxO3csC7kzJ2DI5JnQsBkjDa0zut05TO4BoOWdAgNRyEHLmleAPpCRbIubrl6r9bJKGB1gNtAtP517DbmHCBslMfZ--UDBAj6w00uyR-YrrA1C3VklU25a768kN90BwyoRB7kqvNzhEjW0mr-is5DBj_MRMAjsf868KQVHx182YFncBc1OvUgH-i3VLFag&prev=RQEA3F51628E925B&p=20&pg=217)

* Italy
* PAREXEL
* Piacenza
* 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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