What are the responsibilities and job description for the Validation Engineer position at Validation Professionals, Inc.?
Company Description
Validation Professionals, Inc. is a biotechnology, mefical device, and pharmaceutical consulting company headquartered in San Diego, California. Known for its expertise and commitment to quality, the company focuses on providing specialized solutions across various sectors. Validation Professionals, Inc. leverages cutting-edge expertise and innovative practices to advance the industry. Its central mission is to support clients in achieving their compliance and operational goals efficiently.
Role Description
This is a contract role for a Validation Engineer, based out of San Diego, CA, with a hybrid work model allowing for partial remote work. The Validation Engineer will be responsible for tasks such as performing medical device equipment validation, ensuring compliance with industry standards, writing and summaring validation protocols, and supporting automation validation processes. Additional responsibilities include ensuring adherence to Good Manufacturing Practice (GMP) and collaborating with team members to meet project objectives.
Qualifications
- Experience with any or all of the following: equipment, software and automatiion validation.
- Strong skills in issue resolution
- Knowledge of Validation methodologies and processes
- Familiarity with Good Manufacturing Practice (GMP) standards
- Ability to work in a hybrid model, balancing on-site and remote tasks efficiently
- Strong analytical skills and attention to detail
- Effective communication and teamwork abilities
- Bachelor's degree in Engineering, Biotechnology, or a related field is preferred