Are you a scientific professional with a strong background in biotherapeutics and vaccine production? My client is seeking a Sr. Associate Scientist/Scientist to join their Manufacturing Science and Technology (MSAT) team in Leiden. This role is pivotal in driving innovation, ensuring compliance, and advancing the lifecycle of commercial production processes.
About the Role
As a member of the MSAT team, you will focus on:
New Product Introduction (NPI) and Life Cycle Management (LCM)
Process Validation
Process Improvements
Deployment of standards and new technologies
You will work cross-functionally to lead and support key initiatives, collaborating closely with internal and global stakeholders to ensure the successful implementation of innovative processes and technologies.
Key Responsibilities New Product Introduction & Life Cycle Management:
Lead or support LCM projects and the introduction of new technologies, including digitalization efforts.
Act as a Subject Matter Expert (SME) in upstream and/or downstream processes for pharmaceutical proteins and vaccines.
Process Validation:
Define validation strategies and author/review protocols and reports.
Ensure validation activities comply with site standards, guidelines, and quality requirements.
Integrate global standards into local production processes.
Collaboration & Leadership:
Serve as the primary interface between Operations, Quality, and MSAT teams.
Represent Leiden MSAT in global project teams.
Provide expertise during internal and external audits and inspections.
Lead and support complex investigations and facilitate risk assessments.
Continuous Improvement & Technical Expertise:
Drive process improvements and the adoption of new technologies.
Coach and train team members.
Troubleshoot complex issues and deliver effective resolutions.
What We Are Looking For
Education & Experience:
Bachelor's degree with 7+ years of relevant experience or an advanced degree (MS/MBA/Ph.D.) with 4+ years of experience.
Technical Expertise:
Strong knowledge in scientific or technical core areas, particularly in biotherapeutics and vaccine manufacturing.
Proven ability to manage multiple moderate-sized projects effectively.
Leadership & Collaboration:
Demonstrated skills in coaching, training, and leading cross-functional teams.
Experience representing teams during audits and inspections.
Problem-Solving:
Skilled in troubleshooting and implementing innovative solutions.
Communication:
Strong ability to communicate complex technical and business issues effectively.
Additional Information
Location: Leiden, Netherlands
Contract: 1 year (with the potential for extension)
Start Date: ASAP
Interested?
Send your CV to Khanyi Mabena at k.mabena@panda-int.com or contact her directly at +31 2020 44502 for more information.
Join us and contribute to pioneering advancements in the production of life-saving biotherapeutics and vaccines.