What are the responsibilities and job description for the Senior Validation Engineer position at Techever Ventures?
Company Description Techever Ventures is a technology-focused organization dedicated to delivering high-quality engineering and validation solutions for clients in highly regulated industries. The company emphasizes rigorous standards, robust processes, and measurable performance to support complex projects from design through implementation. Techever Ventures values collaboration, clear communication, and practical problem-solving to help clients meet regulatory and operational goals. Team members are encouraged to bring forward new ideas, continuously improve, and contribute to a culture of accountability and integrity.
Role Description The Senior Validation Engineer at Techever Ventures will be responsible for leading validation activities for equipment, systems, and processes in a regulated environment. This is a contract, on-site role based in Thousand Oaks, CA. Day-to-day responsibilities include developing and executing validation protocols (IQ/OQ/PQ), preparing validation plans and reports, and ensuring that all validation documentation meets internal procedures and regulatory requirements. The role involves collaborating with cross-functional teams such as engineering, quality, manufacturing, and operations to define validation scope, establish acceptance criteria, and support change control. The Senior Validation Engineer will also participate in risk assessments, deviations, and CAPA activities, provide subject matter expertise during audits and inspections, and mentor junior team members in validation best practices.
Qualifications
Role Description The Senior Validation Engineer at Techever Ventures will be responsible for leading validation activities for equipment, systems, and processes in a regulated environment. This is a contract, on-site role based in Thousand Oaks, CA. Day-to-day responsibilities include developing and executing validation protocols (IQ/OQ/PQ), preparing validation plans and reports, and ensuring that all validation documentation meets internal procedures and regulatory requirements. The role involves collaborating with cross-functional teams such as engineering, quality, manufacturing, and operations to define validation scope, establish acceptance criteria, and support change control. The Senior Validation Engineer will also participate in risk assessments, deviations, and CAPA activities, provide subject matter expertise during audits and inspections, and mentor junior team members in validation best practices.
Qualifications
- Strong experience in validation engineering within a regulated industry (e.g., pharmaceutical, biotechnology, medical devices, or related).
- Proficiency in developing and executing IQ/OQ/PQ protocols, validation plans, and technical reports.
- Solid understanding of applicable regulatory guidelines and standards (such as FDA, cGMP, GAMP, or ISO) and how they apply to validation.
- Demonstrated ability to manage multiple validation projects, prioritize tasks, and meet deadlines in a fast-paced environment.
- Experience collaborating with cross-functional teams, supporting audits and inspections, and contributing to risk assessments, deviations, and CAPA.
- Excellent analytical, documentation, and problem-solving skills, with strong attention to detail and accuracy.
- Effective written and verbal communication skills suitable for technical and non-technical stakeholders.
- Bachelor’s degree in Engineering, Life Sciences, or a related technical field; an advanced degree or relevant certifications (e.g., CQE, validation certifications) are a plus.
- Prior experience in on-site roles within large-scale manufacturing or laboratory facilities is preferred.
- Ability to work on-site in Thousand Oaks, CA, and comply with all site safety and quality procedures.