About this opportunity
Hikma Pharmaceuticals lists this Validation Engineer opportunity in bedford, Ohio. Review the employer’s description below for duties, qualifications and application requirements.
Job description
Job Title: Equipment Validation Engineer III
Location: Bedford, Ohio
Job Type: Full-Time
Req ID: 11964
If you want to know about the requirements for this role, read on for all the relevant information.
Summary
The Equipment Validation Engineer III plays a key role in supporting a sterile pharmaceutical manufacturing facility through the qualification and lifecycle management of manufacturing equipment, utilities, and associated systems. This position leads equipment qualification and change-based revalidation activities, supports manufacturing investigations, and collaborates with Operations, Engineering, Maintenance, Quality, and Regulatory functions to ensure compliance with cGMP requirements.
The successful candidate will serve as a technical lead for validation projects of moderate to high complexity, providing expertise in risk-based validation strategies, equipment qualification, and continuous process improvement. This role offers significant exposure to new equipment implementation, regulatory inspections, and cross-functional project teams supporting commercial pharmaceutical manufacturing.
Why Join Our Team?
Opportunity to lead high-impact validation projects in a sterile pharmaceutical manufacturing environment.
Exposure to equipment implementation, capital projects, and advanced manufacturing technologies.
Collaborative cross-functional environment with Operations, Engineering, Quality, and Regulatory organizations.
Opportunity to mentor developing engineers and influence site validation strategy.
Direct contribution to the manufacture of critical pharmaceutical products that impact patient health.
Essential Duties and Responsibilities
Equipment Qualification & Validation
Lead equipment qualification activities, including Installation Qualification (IQ), Operational Qualification (OQ), and Performance Qualification (PQ) for new and existing manufacturing equipment.
Perform change assessments and lead requalification activities in support of equipment modifications, process changes, and lifecycle management.
Author, execute, and review validation impact assessments, protocols, test scripts, summary reports, periodic review reports and supporting documentation.
Ensure validation activities are executed in accordance with applicable cGMP regulations, company procedures, and industry best practices.
Project Leadership
Serve as validation lead for capital projects, equipment implementation efforts, and cross-functional initiatives.
Partner with Engineering during equipment design, installation, commissioning, startup, and qualification phases.
Coordinate qualification activities across Operations, Quality Control, Quality Assurance, Engineering, Maintenance, and Manufacturing Science teams.
Manage multiple validation projects simultaneously while maintaining project timelines and priorities.
Technical Support & Continuous Improvement
Support manufacturing investigations, deviation assessments, root cause analyses, and CAPA implementation activities related to validated systems.
Participate in risk assessments and develop scientifically sound validation approaches.
Identify opportunities to improve validation processes, documentation practices, and operational efficiency.
Provide technical guidance and support for equipment lifecycle management activities.
Compliance & Regulatory Support
Maintain validation documentation in a state of audit readiness.
Support internal audits, client/customer audits, and regulatory inspections, including FDA and other global regulatory agencies.
Contribute validation documentation and technical justifications for regulatory submissions when required.
Leadership & Mentoring
Mentor junior validation engineers and provide guidance on validation methodologies, documentation practices, and compliance expectations.
Serve as a technical resource within the Validation organization and across site functions.
Required Qualifications
Bachelor's degree in Engineering, Life Sciences, Chemistry, Biology, Pharmaceutical Sciences, Mathematics, or related technical discipline.
Minimum of 4 years of validation, engineering, pharmaceutical manufacturing, or related industry experience.
Working knowledge of cGMP regulations and validation principles within regulated manufacturing environments.
Strong technical writing skills with experience authoring validation protocols and reports.
Demonstrated ability to independently manage technical projects and collaborate with cross-functional teams.
Strong verbal and written communication skills.
Preferred Qualifications
6+ years of validation experience within pharmaceutical, biotechnology, medical device, or other regulated industries.
Experience performing equipment qualification activities (IQ/OQ/PQ).
Experience supporting sterile, aseptic, or parenteral manufacturing operations.
Familiarity with GAMP 5 (for computerized systems).
Experience with risk assessments, change controls, deviations, investigations, and CAPA systems.
Experience supporting regulatory inspections and customer audits.
Experience with commissioning and qualification (C&Q) activities for new equipment and facility projects.
Demonstrated leadership experience in cross-functional project teams.
Preferred Technical Experience
Experience with one or more of the following is highly desirable:
Compounding and formulation equipment
Filling equipment
Lyophilizers
Autoclaves and sterilization systems
Clean utilities
CIP/SIP systems
Environmental control or HVAC systems
RABS and Isolators
Inspection packaging systems
Physical Requirements
Ability to routinely work in manufacturing and laboratory environments.
Ability to walk throughout the facility and stand for extended periods during qualification and project activities.
Ability to lift up to 40 lbs occasionally.
Ability to utilize appropriate personal protective equipment (PPE) as required.
Work Schedule
This position is primarily a first-shift role. xhqgsiq Occasional off-shift, weekend, or holiday support may be required to support equipment implementation, qualification activities, manufacturing schedules, and project milestones.
Worksite address
bedford, OH, 44146, US
Who can apply
Review the original listing for work authorization, qualifications and employer requirements.