16 ott - Monza
Experteer Italy
pIn this role you support the Process Engineering Team to introduce new manufacturing processes for sterile injectable medicines, ensuring GMP and regulatory alignment. You collaborate on technical documentation, support tech transfer activities, and help prepare trial reports. You review shopfloor data and ensure analyses follow approved protocols and procedures. You participate in cross‑functional teams to shape the product introduction strategy for regulatory submission. This position offers hands‑on exposure to validation, documentation, and regulatory compliance within a global pharmaceutical environment.
/pulliIssue and draft engineering and technical documents for manufacturing processes under validation /liliSupport tech transfer activities and extraction of information for trial reports /liliParticipate in project teams to discuss new product introduction strategies for regulatory submissions /liliSupport operational activities from a technical perspective /li liReview shopfloor data and analyses in line with protocols and procedures /liliDegree in Pharmacy, Chemistry, Biotechnology, Biology, Engineering or similar scientific discipline or consolidated experience /li liPrevious experience in pharmaceutical companies or tech transfer/validation is helpful /li liProficient English (written and spoken) /li liExperience with company IT systems (PMX, LIMS, Trackwise, Minitab) and MS Office tools /li liExcellent interpersonal skills, proactivity, and team orientation /li /ul #J-18808-Ljbffr
16 ott - Italia
ElevenLabs
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Pizzeria MAMI
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GAM
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Gruppo Ethos