Bachelors degree in life sciences, engineering, or equivalent training and/or experience.
Entry-level experience (03 years) in pharmaceutical manufacturing.
Experience or strong understanding of GMP manufacturing operations.
Proficiency in quality assurance and quality control principles in a pharmaceutical or GMP environment.
Strong technical writing skills for documenting investigations, CAPAs, and quality records.
Proficient computer skills in Microsoft Word, Excel, and Outlook.
Familiarity with the pharmaceutical industry and applicable regulatory expectations, including FDA-related requirements.
Strong aptitude in root cause analysis and CAPA execution within a GMP environment.
Must be able to work an on-call schedule