Validation Engineer (CSV)

Validation Engineer (CSV)

Job Location

Summit, NJ

Workspace

Hybrid

Target Hiring Date

May 2025

Work Authorization

Applicants must have the legal right to work in the United States without requiring sponsorship. Corp-to-Corp (C2C) arrangements are not accepted

Requirements

KNOWLEDGE, SKILLS & ABILITIES

Strong working knowledge of MS Windows client and server technologies.

Working knowledge of standard networking principles and technologies.

Excellent understanding of cGXP requirements and good documentation practices relating to systems, equipment and instrumentation within the Pharmaceutical Industry .

Strong working knowledge of ISPE guidance and 21 CFR Part 11 Compliance.

Ability to work with the end user to identify and document User and Functional Requirements.

Knowledge of pharmaceutical laboratory and manufacturing systems.

Experience executing equipment qualification documents.

Ability to interact effectively with laboratory, QA, and Facilities groups.

Strong ability to organize assigned tasks in a high-paced environment and concurrently monitor tasks/assignments with others that may impact timely completion. Ability to effectively manage multiple tasks and activities simultaneously.

Strong written and verbal communication skills along with solid presentation skills. Proficient at writing well-formulated emails and reports. Ability to follow oral and written instructions, read and interpret engineering manuals/drawings relevant to the assigned task. Ability to effectively communicate with employees, contractors, and vendors. Experience with technical writing and document development/generation.

Strong computer skills in Microsoft Office Suite – Word, Excel, Visio, and Outlook, and the ability to learn new software as required for equipment qualification.

COMPETENCIES:

Technical / Professional Knowledge.

Problem Solving / Troubleshooting.

Action Oriented.

Attention to Detail.

Multi-tasking.

Building Relationships.

EDUCATION & EXPERIENCE:

Required B. S. in Engineering / Computer Science or any related field.

Minimum 5 years of experience in FDA-regulated industry, with 5 years experience in CSV.

WORKING CONDITIONS:

Environment may include working in office or in a laboratory / manufacturing area.

Ability to work safely in an environment with hazardous, radioactive, and infectious materials and waste.

Ability to work safely when working alone, or working with others.

About the Role

The CSV Engineer supports the successful implementation of manufacturing and laboratory equipment and computerized systems at multi-use sites through interaction with internal customers and external service providers. The incumbent in this role, contributes to the completion of milestones associated with equipment qualification and systems validation. With minimum supervision and given general instructions, this individual carries out routine tasks and functions, and uses basic analytical skills to recognize and solve common problems of limited scope. As a developing team player, the incumbent interacts with their immediate supervisor and personnel within their own work group to achieve team goals while building trust and collaborative relationships outside the immediate organization.

DUTIES AND RESPONSIBILITIES:

• Maintains all qualified and validated equipment and systems in compliance with policies, guidelines and procedures.

• Develops protocols, and associated reports while adhering to a change management process.

• Supports the execution of equipment qualifications and validation protocols

• Supervises vendors for qualification functions.

• Supports equipment qualification and systems validation activities.

• Configures and documents the configuration of computerized systems

• Develops validation/qualification deliverables such as Validation Plans, Requirements Specifications, Traceability Matrices, Summary Reports, Change Controls.

• Manages projects of varying scope and complexity.

• Supports laboratory and manufacturing equipment implementation projects including scheduling, procurement, site prep, installation, qualification, and turn over to business area.

• Independent ownership of all lifecycle deliverables in the Qualification of equipment and full CSV for single and multi-user Computerized Systems

• Supports internal customer groups in the procurement, operation, calibration, and preventive maintenance of equipment to meet business needs in accordance with required schedules or dates.

• Completes all qualification and validation documentation with accuracy, completeness and compliance to Company standards.

• Provides excellent customer service and support.

• Regularly reviews, prioritizes and promptly responds to customer equipment qualification and support requests.

• Provides technical support and guidance on calibration and equipment qualification issues. Interfaces with customers to ensure all expectations are being met.

• Maintains a positive relationship with all team members and site customers while promoting a positive team environment.

About the Company

Join Sokol GxP Services – Where Innovation Meets Integrity!

Join Sokol GxP Services, where we partner with leading pharmaceutical and biotech companies to provide exceptional Commissioning, Qualification, and Validation (CQV) services. We are committed to fostering diversity, empowering local talent, and building strong community connections to bring the best-qualified candidates to our clients in the Summit, NJ area. Our inclusive and collaborative culture promotes growth and innovation.

Let’s shape the future of life sciences together!

All applicants will receive an acknowledgement that their application has been received within 2-3 weeks from the from the date of receipt.

Equal Opportunity Employer Statement:

Sokol GxP Services is an equal opportunity employer, and all qualified applicants will receive consideration for employment without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state or local laws.

By submitting your application and resume, you consent to have your information retained in our repository for six months. This allows us to consider you for future opportunities that may align more closely with your skills and qualifications. If a suitable position becomes available, we will contact you directly.