Veranova L P is seeking a detail-oriented QA Document Control Associate for a 12-week assignment. The role involves digitizing GMP records, ensuring accuracy, and maintaining electronic document systems. You will scan, verify, index, and file controlled documents while adhering to GDP, ALCOA+ and company procedures.
The position requires strong organizational skills and the ability to work under supervision, with a focus on data integrity and compliance within a professional office setting.
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Temporary QA Document Control Specialist (GMP/ALCOA+) employer: Veranova, L.P
At Veranova, we pride ourselves on fostering an inclusive and dynamic work environment where every employee is valued as our most important asset. Located in a vibrant area, our hybrid work model allows for flexibility while ensuring collaboration and innovation thrive. With a strong focus on professional development, competitive compensation, and comprehensive health benefits, we empower our Finance Assistants to grow their careers while making a meaningful impact in the pharmaceutical industry.
