
Validation & Engineering Group, Inc. (V&EG) a Pinnaql company is a leading services supplier who provides solutions for the Pharmaceutical, Biotechnology, Chemical, Food, and Medical Devices industries in the following areas: Laboratory, Compliance, Computer, Engineering, Project Management, Validation, and other services.
We are seeking a talented, dedicated individual committed to work under the highest ethics standards for the following position:
We are seeking two experienced Validation Engineers (mid-level to senior) with strong expertise in utilities and facilities systems to support commissioning, qualification, and validation activities within a regulated environment. The ideal candidates will have hands-on experience with critical utility systems and a proven ability to develop and execute qualification documentation while troubleshooting and resolving complex technical issues.
Key Responsibilities:
Develop, review, and execute commissioning and qualification (CQV) documentation, including protocols and reports (IQ/OQ/PQ).
Lead and support qualification activities for utility and facility systems such as steam, HVAC, purified water, process utilities, electrical distribution, and compressed air.
Coordinate with cross-functional teams including Engineering, Quality, and Operations to ensure project milestones are met.
Perform field execution of protocols, ensuring compliance with GMP and company procedures.
Identify, investigate, and resolve complex technical issues during qualification and startup activities.
Ensure all documentation is accurate, complete, and aligned with regulatory and client standards.
Support deviation investigations, CAPAs, and change control processes as needed.
Qualifications:
Bachelor’s degree in Engineering or related technical field.
Mid-Level: 3–5+ years of CQV experience in regulated industries (pharma, biotech, medical devices).
Senior Level: 6+ years of CQV experience with demonstrated leadership in qualification activities.
Strong hands-on experience with utilities and facility systems (steam, HVAC, purified water, electrical distribution, compressed air, etc.).
In-depth knowledge of GMP, FDA regulations, and industry standards.
Experience writing and executing qualification protocols.
Excellent problem-solving and troubleshooting skills.
Strong communication and collaboration abilities.
Preferred Qualifications:
Experience working in capital projects or startup environments.
Familiarity with validation lifecycle and risk-based approaches.
Prior client-facing experience is a plus.
At Validation & Engineering Group, people always come first. We believe that when you're empowered to do your best work, bold ideas thrive and real progress happens. This isn't just a job - it's an opportunity to make a meaningful difference by shaping the future of healthcare and technology alongside a purpose-driven, supportive team.
Excited to build something meaningful together? We look forward to hearing from you.
Validation & Engineering Group is an equal opportunity employer. All applicants will be considered for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran status, or disability status.

Validation & Engineering Group, Proudly serving our clients since 1997.
Our Mission states in part: "provide our clients with the best resources to meet their needs". In our search for the best talent, we are inclusive and do not discriminate. V&EG is proud to be an equal opportunity workplace and is an affirmative action employer.
Validation & Engineering Group provides world-class service and expertise to the pharmaceutical, medical device and biotechnology industries. We offer our clients: Validation, Control System Solutions, Instrumentation, Training, Equipment Rentals, and Regulatory Compliance Services to ensure adherence to Federal and European regulatory agencies. Our group had serve in solid dosages, liquids, creams, lyophilizers, and parenteral dosage.
Our agility in responding to our clients’ needs, access to the best pool of talent, and the combined experience and technical expertise of our resources make Validation & Engineering Group a leader in the pharmaceutical, medical devices, and biotechnology industries.
At Validation & Engineering Group we provide professional expertise in the areas of:
•Audit and Assessment
•Automated Process Control System Qualification
•Equipment and Facilities Qualification
•Facilities Start-Up and Commissioning
•GAP Analysis
•Information Systems Computer Validation
•Packaging and Process Analysis
•Process & Cleaning Validation
•Project Management
•Quality Systems
•Risk Based Approach
•Regulatory Compliance
•Standard Operating and Maintenance Procedures
•Training
•Utilities Support and Qualification
In addition we offer Equipment Rentals and training to your workforce such as: Temperature & Relative Humidity, Electrical, Process, Environmental, and. Analytical.
Our Offices:
Puerto Rico:
Centro Internacional de Mercadeo I 100 Carr. 165 Ste 703, Guaynabo, 00968 Puerto Rico
Phone: (787) 622-0996
United States:
2180 Satellite Blvd, Suite 400Duluth, Georgia 30097 United States
Phone: (770) 403-5802