Don’t send a generic resume — generate a resume and cover letter tailored to this exact role.
Validation & Engineering Group, Inc. is seeking a Junior Validation Specialist to support GMP-regulated validation activities. You will assist with IQ/OQ/PQ protocols, data collection, documentation, and field verification under supervision.
Ideal candidates hold a bachelor’s in Engineering or Life Sciences and have 1–3 years of experience in validation or CQV in pharma, biotech, or medical devices. Strong attention to detail and teamwork are essential.
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:
Position Overview:
We are seeking a Junior Validation Specialist with 1–3 years of experience to support validation and qualification activities in a regulated environment. This role is ideal for a detail-oriented professional looking to grow their career in validation, with hands-on involvement in testing, documentation, and field execution under supervision.
Key Responsibilities:
Qualifications:
Preferred:
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.
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.