Validation Engineer II

The Validation Engineer II will be responsible for leading the commissioning, qualification, and validation (CQV) to support the commissioning, qualification, and validation of new and modified equipment, utilities, facilities, products, and processes in support of the project, operations, and quality objectives. Working closely with system owners and related stakeholders (Operations, Engineering, Laboratories, IT, and Quality Assurance). This role will guide CQV activities to a compliant state throughout their lifecycle. This includes authoring, reviewing, and executing related CQV documentation as well as related documents for the role (eg, procedures and change control records). Serves as subject matter expert for CQV activities.

Essential Duties and Responsibilities :

Lead the development and execution of commissioning, qualification, and validation protocols for various equipment and systems.

Responsible for all phases of the CQV activity, including gathering requirements, validation planning, protocol generation, test execution, configuration documentation, and system release.

Executes validation activity in a timely manner, planning and proactively pursuing details to ensure project completion without avoidable delays.

Evaluate System Change Controls for Validation Impact. Support Change Qualification through the creation of relevant Change Actions.

Support the development of Standard Operating Procedures for new processes and equipment.

Interpersonal skills to manage interactions and achieve results across a range of functions within the site. It may also extend to external communication with system vendors.

Serve as Principal Investigator for validation-related excursions.

Contribute to the continuous improvement of validation processes and procedures.

Basic Qualifications and Capabilities :

Bachelor's degree in engineering or relevant sciences and 8+ years of CQV experience.

8 years' experience with sterile injectables, combo-devices, or biologics.

Advanced degrees or certifications relevant to the role is a plus.

Knowledge of regulatory requirements (cGMP, FDA, etc.).

Experience authoring, approving, and executing validation protocols for major pharmaceutical manufacturing facilities, utilities, and equipment.

Self-directed with problem-solving, analytical, and technical skills.

Ability to think strategically and tactically (detail-oriented).

Strong collaborative and influencing skills and ability to work well in a cross-functional, matrixed environment.

Ability to lead, take ownership, and follow through on assigned projects.

Demonstrated ability to work in a fast-paced team environment, meet deadlines, and prioritize work.

Experience in a process improvement environment, including change management and participating in Lean / Six Sigma project teams.

• Ability to work independently within established guidelines, procedures, and practices.

Preferred Qualifications :

Experience in a sterile fill-finish facility.

Experience with single-use components in drug product formulation, sterile filtration, and aseptic filling applications.

Start-up experience preferred.

Experience with validation tools and processes, including temperature mapping and use of Kaye Validator.