CQV Engineer
Are you ready to make a meaningful impact in the life sciences industry? We're looking for a CQV Engineer to support high-profile pharmaceutical and biotech projects in Boston, Massachusetts. This role offers the opportunity to work on-site with leading clients, contributing to the delivery of safe, compliant, and efficient manufacturing systems.
Key Responsibilities
- Execute commissioning, qualification, and validation activities for GMP equipment, utilities, and facilities.
- Prepare and implement protocols (IQ/OQ/PQ) in accordance with regulatory and client standards.
- Collaborate with multidisciplinary teams to ensure timely and compliant project delivery.
- Develop and review technical documentation including validation plans, risk assessments, and summary reports.
- Ensure alignment with FDA, EMA, and ICH guidelines throughout all phases of the project.
- Provide hands-on support during system start-up, troubleshooting, and performance testing.
Ideal Candidate Profile
- Bachelor's degree in engineering, life sciences, or a related discipline.
- Minimum of 3 years' experience in CQV within the pharmaceutical or biotech sector.
- Strong working knowledge of GMP regulations and validation methodologies.
- Excellent communication and problem-solving skills.
- Ability to work independently and travel to client sites within New Jersey as needed.
- Must be legally authorized to work in the United States without the need for current or future sponsorship.
What You'll Gain
Join a team that thrives on technical excellence, collaboration, and continuous growth. You'll be part of a fast-paced environment where your contributions directly support the development and delivery of life-changing therapies.
FAQs
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