
Senior Validation Specialist
1 week ago
We are seeking a CSV Engineer to join our organization.
As a CSV Engineer, you will be responsible for supporting the validation and compliance of computerized equipment and systems in a sterile pharmaceutical manufacturing environment. This role involves hands-on validation activities, ensuring adherence to regulatory and quality standards, and collaborating with cross-functional teams to maintain compliance.
Required Skills and Qualifications:- Bachelor's degree in Science or Engineering, such as Chemistry, Microbiology, Pharmacy, Chemical, Mechanical, or Electrical engineering.
- Strong understanding of GAMP and ISPE Baseline Guides, as well as quality management systems.
- Hands-on experience in validation activities within a healthcare or pharmaceutical manufacturing environment.
- Knowledge of cGMP regulations and compliance requirements.
- Effective communication and facilitation skills across teams and organizational levels.
- Ability to manage projects effectively and meet key performance indicators (KPIs).
- Problem-solving mindset with adaptability and resilience.
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