ZipRecruiter

Log In

Validation Engineering Group

60 Validation Engineering Group Program Management Jobs Hiring Near You

ECS Ltd

Engineering Group Manager

West Valley City, UT

$111K - $111K/yr

Position & Office Overview As an Engineering Branch Manager, you are the type who is driven to ... About Us ECS Group of Companies (ECS) was founded in 1988 with the goal to raise the standards of ...

McKim & Creed

Electrical Engineering Group Manager

Orlando, FL · On-site

$106K - $137K/yr

The Electrical Engineering Group Manager leads and oversees the technical and design services for ... Tuition reimbursement, early career professional program, online courses & more * Work that makes a ...

Pinnaql

EHSS Coordinator

Punta Santiago, PR · On-site

Validation & Engineering Group, Inc. (V&EG) a Pinnaql company is a leading services supplier who ... Laboratory, Compliance, Computer, Engineering, Project Management, Validation, and other services.

McKim & Creed

Electrical Engineering Group Manager

Orlando, FL · On-site

$106K - $137K/yr

The Electrical Engineering Group Manager leads and oversees the technical and design services for ... Tuition reimbursement, early career professional program, online courses & more * Work that makes a ...

previous page

Showing results 41-60

All JobsValidation Engineering Group Program Management Jobs

Validation Engineering Group Jobs Information

What are the most popular jobs at Validation Engineering Group?
What are the most popular categories at Validation Engineering Group?
Infographic showing various Program Management job openings at Validation Engineering Group in the United States as of August 2026, with employment types broken down into 100% Full Time. Highlights an 100% Physical job distribution.

CQV Specialist - Packaging Equipment

Pinnaql

New Albany, OH • On-site

Full-time

Re-posted 25 days ago

Job description

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 CQV Specialist - Packaging Equipment whowill support commissioning, qualification, and validation activities for packaging equipment and systems in a biotechnology manufacturing environment. The role ensures that packaging lines are installed, tested, and documented in compliance with GMP, FDA, and internal quality requirements while supporting project schedules and startup activities. This is an onsite opportunity in New Albany, OH.
Key Responsibilities
  • Support commissioning, qualification, and validation (CQV) activities for primary and secondary packaging equipment and systems.
  • Develop, review, and execute commissioning and qualification documentation including protocols such as IQ, OQ, and PQ.
  • Verify installation and operational readiness of packaging equipment including labelers, cartoners, serialization systems, inspection systems, and associated utilities.
  • Coordinate activities with engineering, quality assurance, validation, manufacturing, and vendors to ensure proper startup and qualification of packaging lines.
  • Support protocol deviations, discrepancy resolution, and documentation updates as required.
  • Assist with risk assessments, test planning, and validation strategies in accordance with project and regulatory requirements.
  • Ensure compliance with cGMP, FDA regulations, and company validation procedures.
  • Support FAT/SAT activities, startup, and troubleshooting during commissioning phases.
  • Maintain accurate documentation and support turnover packages for validated systems.

Qualifications
  • Bachelor's degree in Engineering, Life Sciences, or related technical discipline.
  • 5+ years of experience in CQV, validation, or commissioning within pharmaceutical or biotechnology manufacturing environments.
  • 2+ years of experience qualifying packaging line equipment such as fillers, labelers, cartoners, serialization/aggregation systems, vision inspection systems, and case packers.
  • Strong knowledge of cGMP regulations, FDA requirements, and validation lifecycle practices.
  • Experience writing and executing validation documentation (IQ/OQ/PQ, protocols, reports, discrepancies).
  • Ability to work cross-functionally with engineering, quality, operations, and project management teams.
  • Strong technical writing and documentation skills.
  • Experience supporting equipment startup, FAT/SAT, and commissioning activities in a regulated environment.
  • Available to work extended hours, possibility of weekends and holidays.

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.

Apply