Industrial Chemist

12 ago - Milano
Tensive

ppAs an Industrial Chemist, you will be a key member of the Engineering department, reporting directly to the Engineering Director.
Your primary mission is to support the industrialization, validation and scale?up of chemical processes related to implantable medical devices, ensuring robust and compliant manufacturing processes in accordance with company and regulatory standards.
/p pYou will contribute to experimental activities, process validation, technical documentation and technology transfer activities, supporting the transition from laboratory?scale development to industrial manufacturing within a GMP?regulated environment.
/p h3Key Responsibilities /h3 pIn accordance with the company's Quality Management System, your main duties will include: /p ul liPerform hands?on laboratory and cleanroom activities related to chemical process development, manufacturing and process implementation.
/li liContribute to the scale?up of chemical formulations and manufacturing processes from laboratory to industrial production.
/li liAnalyze process and experimental data for process validation, monitoring and troubleshooting activities.
/li liPrepare technical documentation including validation protocols and reports, SOPs, risk assessments and process?related documentation.
/li liDraft User Requirement Specifications (URS) and technical documentation related to process equipment and manufacturing activities.
/li liInteract with external equipment suppliers, manufacturers and engineering companies involved in industrialization and process implementation activities.
/li liParticipate in investigations related to process deviations,



non?conformities and CAPA activities.
/li /ul h3Required Skills Qualifications /h3 h3Mandatory Requirements (Must Have) /h3 pWe are looking for hands?on and analytical individuals with strong scientific background and interest in process industrialization within regulated environments.
/p ul libEducation: /b Master's Degree in Chemistry, Industrial Chemistry, Chemical Engineering or related scientific disciplines.
/li libWork Experience: /b 3–5 years of experience in GMP?regulated environments.
/li libProcess Validation: /b Basic understanding of process validation principles and related technical documentation.
/li libScale?Up Exposure: /b Exposure to chemical process scale?up or industrial manufacturing processes.
/li libRegulatory Knowledge: /b Familiarity with ISO *****, FDA QSR and related regulatory standards.
/li libTechnical Writing: /b Good written and verbal communication skills for preparation of protocols, reports and technical documentation.
/li libLanguages: /b Good proficiency in English, both written and spoken.
/li /ul h3Preferred Requirements (Nice to have) /h3 ul liExperience in Medical Device or pharmaceutical environments.




/li liExperience with implantable medical devices manufacturing.
/li liFamiliarity with cleanroom operations and contamination control practices.
/li liExperience supporting Design Transfer or technology transfer activities.
/li liExperience with analytical techniques such as HPLC, FTIR, UV?Vis and Karl Fischer.
/li liKnowledge of statistical tools such as DOE, SPC or capability analysis.
/li liFamiliarity with risk management tools (e.g. FMEA).
/li liLean/Six Sigma or continuous improvement methodologies.
/li liAbility to work in fast?paced and evolving startup environments.
/li /ul h3Benefits /h3 pThe company offers a structured onboarding program, including a two?month period of induction, training, and close mentoring to support the successful integration of the selected candidate.
Depending on the candidate's profile and assessment, the company offers either an apprenticeship contract or a permanent employment contract, with a starting gross annual salary (RAL) of €28,000 under the Chemical Industry SME collective agreement (CCNL Chimico Confapi) which will be adjusted based on the candidate's knowledge and experience.
/p ul liAnnual company's performance premio of €2,300 gross /li li€1,000 annual welfare allowance /li li8 meal vouchers for each working day /li liHybrid work policy with one day of remote work per week /li liAccident and supplementary health insurance coverage /li /ul pIn accordance with current regulations, this position is open to candidates of all genders, without any form of discrimination.
/p /p #J-*****-Ljbffr

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