My client are looking for a dynamic Project manager with over 5 years of experience in FDA-regulated biotech or pharmaceutical settings, for a pivotal hybrid role overseeing project coordination, implementation, and quality assurance in New Jersey.

Responsibilities:
- Efficiently plan and implement projects.
- Define project scope, goals, and resources.
- Manage project budgets and timelines.
- Lead quality assurance and ensure compliance.
- Evaluate project results for improvement.
Qualifications:
- Scientific degree (e.g., pharmaceutical sciences, engineering).
- Project Management qualification or equivalent experience.
- Strong communication and analytical skills.
- Proven track record in validation and quality control.

Why Join the client?
- Contribute to cutting-edge projects in New Jersey.
- Collaborate with industry experts.
- Opportunities for learning and development.
- Strong IT skills (Microsoft Office, SAP QM module).

Apply now for more details and to have the opportunity to be part of their dynamic team!