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Chiesi Group

Global Technical Leader – Product LCM

Chiesi Group

. act as the global technical reference for sterile biotech products .

Posted 4/21/2026full-timeParma • 🇮🇹 ItalySeniorWebsite

About the role

Key responsibilities & impact
  • act as the global technical reference for sterile biotech products
  • ensure technical robustness throughout the product lifecycle
  • deliver innovative, compliant solutions supporting the business and Quality organization
  • contribute to the definition and execution of the industrialization strategy for new products within the R&D Product Teams
  • structure, plan, and coordinate industrial process validation activities
  • provide technical leadership for lifecycle management projects concerning established products
  • oversee the technical assessment and implementation of modifications to critical components
  • lead and oversee Technology Transfer activities from R&D or external partners
  • coordinate Product Technical Teams and/or contribute to cross-functional workstreams
  • review and approve technical protocols and reports
  • support Program Managers in preparation of key deliverables and updates for governance bodies
  • collaborate with Virtual Plant Managers and Procurement
  • perform product Sustainability Assessments and define improvement plans

Requirements

What you’ll need
  • Bachelor’s degree in Pharmaceutical Sciences, Chemical Engineering, Biological Sciences or related field
  • 10+ pharmaceutical/biotech industry years in drug product manufacturing
  • experience in aseptic processing
  • fluency in written and verbal communication in English
  • willingness to travel up to 30%
  • experience working in multicultural and multinational environments preferred
  • experience working within a CRO or CMO environment preferred
  • demonstrated strength in project management, problem-solving, and interpersonal communication
  • solid understanding of the pharmaceutical industry and end-to-end Biotech sterile products manufacturing
  • experience in pharmaceutical or biotech MSAT process development and/or GMP manufacturing preferred
  • strong working knowledge of current regulations, quality expectations, and industry trends

Benefits

Comp & perks
  • comprehensive healthcare programs
  • work-life balance initiatives
  • robust relocation support
  • competitive salary package
  • performance bonuses
  • flexible working arrangements
  • remote work options
  • tax assistance services for foreign colleagues

ATS Keywords

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Hard Skills & Tools
aseptic processingdrug product manufacturingpharmaceutical MSAT process developmentGMP manufacturingindustrial process validationtechnology transferproduct sustainability assessmentstechnical protocol reviewlifecycle managementcompliance solutions
Soft Skills
project managementproblem-solvinginterpersonal communicationtechnical leadershipcollaborationplanningcoordinationcommunicationcross-functional teamworkadaptability
Certifications
Bachelor’s degree in Pharmaceutical SciencesBachelor’s degree in Chemical EngineeringBachelor’s degree in Biological Sciences