Overview
Skills
Job Details
referred Qualifications
Bachelor s degree in Engineering (Mechanical, Chemical, Electrical, Industrial, or related field).
8 years of experience in CQV within biotechnology and/or pharmaceutical aseptic manufacturing and packaging environments.
Proven knowledge of validation methodologies, cGMPs, and regulatory guidelines.
Experience with packaging systems such as bottling lines, blister packaging, labelers, serialization/aggregation systems, and inspection equipment.
Proficiency in CQV documentation and change control processes.
Strong organizational, analytical, and communication skills.
Ability to collaborate effectively with multidisciplinary teams and external vendors.
Comfortable working in a fast-paced, regulated environment with shifting priorities.