Manufacturing scientist

The Senior Material Excellence Engineer, Site MSAT is responsible for leading global implementation of dual sourcing of Lentivirus materials, specifically for Project S.U.R.G.E (Single Use Resiliency & Growth Evolution), that will drive reliability, innovation and sustainability in our processes and plants across the globe, both internally and externally. Execute deliverables required for identification of vendors, including but not limited to, identification of materials for dual-sourcing, creation of URS documents, technical review and approval of vendor drawings, performance of formal comparability assessment, determination of material quality attributes, change control creation and implementation.

Role: Senior Material Excellence Engineer, Site MSAT
Division: Innovative Medicine Supply Chain (IMSC)
Dept name: Manufacturing Science and Technology (MSAT)
Duration: 12 Months contract

Position Summary:
The Senior Material Excellence Engineer, Site MSAT is responsible for leading global implementation of dual sourcing of Lentivirus materials, specifically for Project S.U.R.G.E (Single Use Resiliency & Growth Evolution), that will drive reliability, innovation and sustainability in our processes and plants across the globe, both internally and externally. The capability to effectively facilitate change activities including the ability to navigate within a global network and collaborate effectively with internal and external partners will be key to drive critical programs to successful completion. This role will work in a cross functional setting and must have strong communication skills to foster collaboration and drive success across the organization. Up-to-date knowledge of industry standards, regulatory requirements and pharmaceutical manufacturing processes related to viral manufacturing and/or cellular therapies are highly desirable

General Responsibilities:
Key Responsibilities

• Identify and lead process improvements projects, specifically dual sourcing of materials utilized in lentivirus manufacturing, to deliver innovations and increase the reliability of our processes and plants.
• Manage detailed project plans for dual sourcing of LV materials under Project S.U.R.G.E and collaborate with cross-functional team members to track deliverables, ensuring the highest standards of quality and compliance.
• Execute deliverables required for identification of vendors, including but not limited to, identification of materials for dual-sourcing, creation of URS documents, technical review and approval of vendor drawings, performance of formal comparability assessment, determination of material quality attributes, change control creation and implementation.
• Implement standard processes for supply chain management, logistics, and distribution to enhance operational effectiveness.
• Work closely with the production and manufacturing teams to optimize resource utilization and reduce costs.
• Drive organizational change by implementing effective project management strategies and communication plans.
• Effectively delegate tasks and provide clear direction to ensure smooth and efficient project execution.
• Continuously monitor/analyze manufacturing performance and design projects/initiatives to enable manufacturing performance, cost reduction, and process robustness objectives
• Conduct risk analysis to identify mitigation opportunities.
• Generate custom visuals and analytics detailing critical path, key handoffs/transitions & high-level summary schedule.

Collaboration & Communication:

• Collaborate effectively with local and global stakeholders, including project teams, site and global Leadership teams, ensuring seamless integration and communication of project requirements.
• Represent the Site MSAT group at internal and external meetings, effectively communicating manufacturing requirements and insights.

Key Qualifications & Skills:
Experience:

• Around 5 years of experience in the pharmaceutical or biotechnology industry is required.
• Specific advanced therapies or lentiviral vector experience is considered a distinct advantage
• In depth working knowledge and conversant with cGMP guidelines and Health Authority regulations (EMA, FDA, etc.)
• Minimum of 3 years of project management experience

Technical Skills:

• Strong expertise in biological manufacturing processes, including upstream and downstream processing.
• Familiarity with material specifications, URSs, and change controls

Certifications and Software Proficiencies:

• Professional project management certification (i.e. PMP, CPM, etc.) is preferred
• Demonstrated expertise in MS project is required.
• Proficiency with technology enabling tools including Powerpoint, Excel, required.

Interpersonal Skills:

• Excellent communication and interpersonal skills, with the ability to build strong relationships with team members and stakeholders.
• Experience working in a global matrix organization is preferred.
• Demonstrated ability to solve complex technical challenges independently and within a team setting.

Degree:

• A minimum of a bachelor’s degree is required. A Bachelor’s in Biochemistry, Biotechnology, Chemical Engineering, or a related field is preferred.