Validation Engineering

Stark Pharma Solutions Inc. is a global consulting and staffing partner established in 2014, serving the Pharmaceutical, Medical Device, Biotech, and IT industries across the USA, Canada, and India.
We provide specialized consulting and staffing solutions across Quality & Validation, Regulatory Affairs, R&D, Manufacturing, Supply Chain, Project Management, and IT, with a focus on delivering tailored solutions that drive growth, operational excellence, and long-term client success.

Validation Engineer

We are seeking an experienced Validation Engineer to support Oral Solid Dosage (OSD) manufacturing operations within a cGMP pharmaceutical environment.
The role will focus on Process Validation, Cleaning Validation, and CQV activities for pharmaceutical manufacturing equipment, facilities, utilities, and processes.
Support qualification of manufacturing equipment, facilities, and utilities.
Support equipment installation, process improvements, and technology transfers.
Work with Manufacturing, Quality Assurance, Engineering, MS&T, and Regulatory teams.
Support OSD manufacturing processes including blending, granulation, compression, encapsulation, coating, and packaging.
Bachelor's degree in Engineering, Life Sciences, or a related field.
Experience as a Validation Engineer in a pharmaceutical manufacturing environment.
Experience with OSD manufacturing processes.
Experience with CQV and equipment qualification.
Strong technical writing, communication, and problem-solving skills.
Apply Now: Submit your updated resume to Stark Pharma Solutions Inc. for consideration.
Stark Pharma is an Equal Opportunity Employer and welcomes qualified candidates from diverse backgrounds.