MS&T Validation Specialist with experience in regulated industry.
Duties:
- Lead projects focused on technology transfer process optimization and scaleup activities to support manufacturing operations.
- Oversee activities related to process validation troubleshooting and the introduction of new products or processes.
- Serve as a key liaison between R&D manufacturing and quality teams to ensure seamless integration of technical solutions into production environments.
- Develop detailed project plans timelines and budgets.
- Ensure effective communication and coordination across stakeholders and crossfunctional teams.
- Identify and mitigating risks.
WILLING TO WORK IN USEAST COAST
Requirements
- Bachelor in Sciences with a minimum of 5 years of experience as a validation specialist in pharmaceutical life sciences or GMP industry.
- Experience working with digital applications and systems and driving their implementation.
- Strong leadership communication and stakeholder management skills.
- Experience working in a crossfunctional global environment.
- Proficiency in project management tools (e.g. MS Project Smartsheet etc.).
- WILLING TO WORK IN USEAST COAST