What are the responsibilities and job description for the Process Quality/ Validation Engineer position at Vetforce Solutions?
Company Description
VetForce Solutions LLC is a leading provider of IT services, clinical research solutions, and specialized staffing. As a Clinical Research Organization (CRO) and staffing firm, we deliver top-tier talent and innovative solutions across IT, healthcare, and life sciences. Our expertise ensures seamless workforce solutions, regulatory compliance, and operational efficiency for our clients. Partner with us for strategic hiring, IT consulting, and clinical research support to drive success together.
Role Description
This is a contract role for a Process Quality/Validation Engineer. The day-to-day tasks include ensuring compliance with Good Manufacturing Practice (GMP), performing validation and functional verification, and troubleshooting or debugging issues as they arise. The engineer will work on RTL design and validation processes. This role is on-site and is located in Boston, MA.
Qualifications
- Experience in RTL Design and Debugging
- 5-10 year's of experience required
- Knowledge of Good Manufacturing Practice (GMP) and Validation
- Skills in Functional Verification
- Strong analytical and problem-solving skills
- Excellent communication and teamwork abilities
- Ability to work independently and on-site in Boston, MA
- Bachelor's degree in Engineering or related field is preferred
- Experience in the clinical research or IT industry is a plus