Validation Engineer Opportunity
Seeking a highly skilled Validation Engineer to support the development and implementation of validation protocols for computerized equipment and control systems in a sterile pharmaceutical manufacturing environment.
Key Responsibilities:
* Develop, execute, and manage validation protocols (DQ, IQ, OQ, PQ) to ensure compliance with regulatory requirements.
* Generate and review validation documentation, including protocols, reports, and revalidation plans.
* Provide technical expertise on current FDA and EU validation regulations and guidelines.
* Collaborate with cross-functional teams to ensure project timelines and quality standards are met.
* Conduct risk assessments and implement mitigation strategies to minimize validation risks.
Required Skills and Qualifications:
* Degree in Science (e.g., Chemistry, Microbiology, Pharmacy) or Engineering (e.g., Chemical, Mechanical, Electrical).
* Strong understanding of GAMP, ISPE Baseline Guides, and 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.
Benefits of This Role:
* Contribute to the development of innovative products that improve patient outcomes.
* Work collaboratively with a skilled team of professionals.
* Gain valuable experience in the field of validation and compliance.
Why This Is a Great Opportunity:
* Opportunity to work in a dynamic and growing industry.
* Chance to develop your career in a reputable organization.
* Join a team of experienced professionals who share your passion for innovation and excellence.