Descrizione dell'offerta
Evotec is a leader in the discovery and development of novel small molecule drugs with operational sites in Europe and the US. The Company has built substantial drug discovery and development expertise and an industrialized platform that can drive new innovative small molecule compounds into the clinic. In addition, Evotec is building an integrated platform to deliver iPSC-based therapeutics to patients and an innovative off-the-shelf cell therapy project portfolio. Leveraging these skills and expertise the Company intends to develop best-in-class differentiated therapeutics and deliver superior science-driven discovery and development alliances with pharmaceutical and biotechnology companies.
For our cell therapy manufacturing site in Modena, we are looking for a highly motivated
GMP Quality Assurance, possibly experienced in aseptic manufacturing . This position will have a key role in Cell and Gene therapy team to guarantee company and intercompany ATMP manufacturing activities .
Essential Functions
manage a comprehensive documentation system for all Cell Factory operations
collaborating in risk analysis
collaborating in change management system
managing deviations and corrective/preventive actions
regularly inspect all departments and assess their GMP compliance status
support the development of appropriate training plans for new and existing staff
qualify external suppliers
handling complaints
distributing production batch records
execute the Batch Record Review
Document management
Required Skills & Abilities
Knowledge of current GxP guidelines
Positive, team player and problem-solving attitude
Accurate, with excellent prioritization and organization skills
Commitment to the assigned deadlines and ability to deliver them tightly
English intermediate level is required (written and spoken)
Good knowledge of Microsoft Office applications
Education
BS or MS Scientific Degree (e.g. Biotechnology, Biology, Pharmacy, CTF…)
Experience
Previous experience in Quality Assurance is mandatory (3+ years)
Previous experience with ATMPs is a plus
Previous experience with sterile products
Previous experience in environmental monitoring, safety methods and mediafill activities
FR : Dans le cadre de sa politique Diversité, Evotec étudie, à compétences égales, toutes les candidatures dont celles des personnes en situation de handicap.
EN: In the frame of our Diversity policy, Evotec considers, with equal competences, all applications including people with disabilities.
IT: In compliance with fundamental ethical and professional principles and with Legislative Decree 198/2006, Evotec is an Equal Opportunity Employer committed to fostering a safe, diverse, and inclusive workplace built on mutual respect. We provide equal employment opportunities to all qualified candidates and employees based on their skills, experience, and professional qualifications. In line with our ethical and professional principles, all employment-related decisions, including recruitment and selection processes, are made fairly and without any form of discrimination. All qualified candidates will be considered for employment regardless of race, color, sex, age, disability, genetic information, gender expression, gender identity, nationality, religion, sexual orientation, or any other characteristic protected under applicable law.
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For our cell therapy manufacturing site in Modena, we are looking for a highly motivated
GMP Quality Assurance, possibly experienced in aseptic manufacturing . This position will have a key role in Cell and Gene therapy team to guarantee company and intercompany ATMP manufacturing activities .
Essential Functions
manage a comprehensive documentation system for all Cell Factory operations
collaborating in risk analysis
collaborating in change management system
managing deviations and corrective/preventive actions
regularly inspect all departments and assess their GMP compliance status
support the development of appropriate training plans for new and existing staff
qualify external suppliers
handling complaints
distributing production batch records
execute the Batch Record Review
Document management
Required Skills & Abilities
Knowledge of current GxP guidelines
Positive, team player and problem-solving attitude
Accurate, with excellent prioritization and organization skills
Commitment to the assigned deadlines and ability to deliver them tightly
English intermediate level is required (written and spoken)
Good knowledge of Microsoft Office applications
Education
BS or MS Scientific Degree (e.g. Biotechnology, Biology, Pharmacy, CTF…)
Experience
Previous experience in Quality Assurance is mandatory (3+ years)
Previous experience with ATMPs is a plus
Previous experience with sterile products
Previous experience in environmental monitoring, safety methods and mediafill activities
FR : Dans le cadre de sa politique Diversité, Evotec étudie, à compétences égales, toutes les candidatures dont celles des personnes en situation de handicap.
EN: In the frame of our Diversity policy, Evotec considers, with equal competences, all applications including people with disabilities.
IT: In compliance with fundamental ethical and professional principles and with Legislative Decree 198/2006, Evotec is an Equal Opportunity Employer committed to fostering a safe, diverse, and inclusive workplace built on mutual respect. We provide equal employment opportunities to all qualified candidates and employees based on their skills, experience, and professional qualifications. In line with our ethical and professional principles, all employment-related decisions, including recruitment and selection processes, are made fairly and without any form of discrimination. All qualified candidates will be considered for employment regardless of race, color, sex, age, disability, genetic information, gender expression, gender identity, nationality, religion, sexual orientation, or any other characteristic protected under applicable law.
#J-18808-Ljbffr
Candidatura e Ritorno (in fondo)
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