Process Transfer Scientist

AGC Biologics, Inc.; Milano; In loco; EUR 40.000 - 70.000; Tempo pieno

Descrizione del lavoro

AGC Biologics is seeking a Process Transfer Scientist to enhance production processes in our Milano site. The successful candidate will evaluate new technologies, manage project introductions, and coordinate process transfers across production sites. Ideal applicants hold a Master's degree in Biotechnology or a related field with relevant experience in GMP processes and strong analytical skills, ready to contribute to life-changing therapies for patients globally.

Servizi

Highly competitive compensation package

Collaborative culture

Competenze

• Master's Degree in a relevant field required.
• 3+ years of experience in GMP processes.
• Experience in the Cell & Gene sector preferred.

Mansioni

• Evaluate new technologies for production processes.
• Manage activities related to project introduction.
• Coordinate the transfer of processes to other sites.

Conoscenze

Interpersonal Skills

Problem-Solving

Technical Analysis

Knowledge of GMP Processes

Independent Work

Formazione

Master's Degree in Biotechnology, Biology, or Chemistry and Pharmaceutical Technologies

Descrizione del lavoro

Process Transfer Scientist page is loaded

Process Transfer Scientist

Apply locations Bresso, Italy time type Full time posted on Posted Yesterday job requisition id JR102273

Our purpose is to bring hope to life by enabling life-changing therapies for patients around the globe, creating a healthier and happier tomorrow. Our mission is to work side by side with our customers in order to improve patients’ lives by bringing new biopharmaceuticals to market.

The successful candidate will be primarily responsible for:

• Evaluating new technologies to be implemented in production processes, working in close collaboration with the Development and Production departments.
• Managing activities related to the introduction of new projects at the production site, acting as the focal point for collecting technical information and writing transfer documentation.
• Coordinating the transfer of existing processes to other AGC Biologics production sites.
• Critically analyzing data generated by the Development and Production departments to assess process performance and identify areas for improvement.
• Providing technical support during investigations in the event of process deviations.

The main requirements are:

• Master's Degree in Biotechnology, Biology, or Chemistry and Pharmaceutical Technologies
• At least 3 years of experience in GMP processes
• Experience in the Cell & Gene sector (viral vectors and cells) is preferred
• Excellent knowledge of the English language
• Excellent interpersonal and problem-solving skills
• Ability to work independently

Our culture at AGC Biologics is defined by the six core values: Knowledge, Trust, Quality, Ingenuity, Accountability and Teamwork. Our core values stem from our team members and are embedded into our DNA. They provide a common language and understanding of how we as an organization are connected across three continents. Our core values serve as a compass and reminder of how we achieve our purpose of bringing hope to life for patients around the globe.

AGC Biologics is a leading global biopharmaceutical Contract Development and Manufacturing Organization (CDMO) with a strong commitment to delivering the highest standard of service as we work side-by-side with our clients and partners, every step of the way. We provide world-class development and manufacture of mammalian and microbial-based therapeutic proteins, plasmid DNA (pDNA), messenger RNA (mRNA), viral vectors, and genetically engineered cells. Our global network spans the U.S., Europe, and Asia, with cGMP-compliant facilities in Seattle, Washington; Boulder and Longmont, Colorado; Copenhagen, Denmark; Heidelberg, Germany; Milan, Italy; and Chiba, Japan. We currently employ more than 2,500 employees worldwide. Our commitment to continuous innovation fosters the technical creativity to solve our clients’ most complex challenges, including specialization in fast-track projects and rare diseases. AGC Biologics is the partner of choice. To learn more, visit www.agcbio.com. Want to keep posted about our growth and learn more about our company? Follow us on LinkedIn and give us a quick Like on Facebook !

AGC Biologics offers a highly competitive compensation package and a friendly, collaborative culture that values personal initiative and professional achievement. AGC Biologics is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to age, ancestry, color, family or medical care leave, gender identity or expression, genetic information, marital status, medical condition, national origin, physical or mental disability, political affiliation, protected veteran status, race, religion, sexual orientation, or any other characteristic protected by applicable laws, regulations and ordinances.

About AGC Biologics

AGC Biologics is a leading global biopharmaceutical Contract Developmentand Manufacturing Organization (CDMO) with a strong commitment to delivering the highest standard of service as we work side-by-side with our clients and partners, every step of the way. We provide world-class development and manufacture of mammalian and microbial-based therapeutic proteins, plasmid DNA (pDNA), messenger RNA (mRNA), viral vectors, and genetically engineered cells. Our global network spans the U.S., Europe, and Asia, with cGMP-compliant facilities in Seattle, Washington; Boulder and Longmont, Colorado; Copenhagen, Denmark; Heidelberg, Germany; Milan, Italy; and Chiba, Japan. We currently employ more than 2,500 employees worldwide. Our commitment to continuous innovation fosters the technical creativity to solve our clients’ most complex challenges, including specialization in fast-track projects and rare diseases. AGC Biologics is the partner of choice. To learn more, visit www.agcbio.com .