Position SummaryWe have an opportunity for a Senior Engineer, Validation to join our team. This role leads the planning, execution, and documentation of validation projects to ensure compliance with regulatory requirements and internal quality standards. The position provides technical expertise and oversight for the qualification of equipment, utilities, facilities, and computerized systems across the product lifecycle. The Senior Engineer, Validation acts as a subject matter expert and key contributor in cross-functional teams, ensuring GMP compliance, inspection readiness, and operational excellence while mentoring junior staff and supporting continuous improvement initiatives.
Shift: M-F 8am-5pm
Location: Harmans, MD - BWI
100% Onsite
The Role- Lead and execute validation projects for equipment, utilities, facilities, and computerized systems.
- Write, review, and approve validation documents including Installation Qualification, Operational Qualification, and Performance Qualification protocols, reports, risk assessments, and traceability matrices.
- Manage Computerized System Validation activities to ensure regulatory compliance.
- Review change controls, deviations, and Corrective and Preventive Actions, and perform validation impact assessments.
- Coordinate with Engineering, Quality, Manufacturing, Metrology, and external vendors.
- Support equipment requalification and periodic review programs.
- Participate in audits and regulatory inspections and provide validation documentation.
- Troubleshoot validation issues and develop risk-based solutions.
- Mentor junior validation engineers and provide technical guidance.
- Drive continuous improvement initiatives within the site validation program.
The CandidateMinimum Requirements- Bachelor's degree in Engineering, Life Sciences, or related scientific field plus 5+ years of validation experience; or Master’s degree in Engineering or Science plus 3+ years of validation experience.
- Direct hands-on validation experience in a pharmaceutical, biotech, or other Good Manufacturing Practice-regulated environment.
- Experience with equipment, utilities, and facilities qualification.
- Experience authoring and executing validation documents such as Installation Qualification, Operational Qualification, Performance Qualification, protocols, reports, risk assessments, and traceability matrices.
- Knowledge of current Good Manufacturing Practice, Food and Drug Administration regulations, Good Automated Manufacturing Practice 5, 21 Code of Federal Regulations Part 11, and Annex 11.
- Experience with Computerized System Validation.
- Strong technical writing, problem-solving, and cross-functional communication skills.
- Ability to work on-site and support cleanroom and Good Manufacturing Practice operations as needed.
Preferred Skills & Background- Blue Mountain experience.
- TrackWise experience.
- Audit and inspection support.
- Mentoring or lead-level experience.
PayThe anticipated salary range for this position in MD is $120,000 – $140,000 Plus Bonus. The final salary offered to a successful candidate may vary, and will be dependent on several factors that may include but are not limited to: the type and length of experience within the job, type and length of experience within the industry, skillset, education, business needs, etc. Catalent is a multi-state employer, and this salary range may not reflect positions that work in other states.
Why You Should Join Catalent- Defined career path and annual performance review and feedback process.
- Diverse, inclusive culture.
- Potential for career growth on an expanding team within an organization dedicated to preserving and bettering lives.
- Competitive paid time off plus 8 paid holidays.
- Community engagement and green initiatives.
- Medical, dental, and vision benefits effective day one of employment.
- Tuition Reimbursement.
