Quality Assurance Officer

QA Documentation OfficerOn-site – 6-month contract (high potential for extension)Job DescriptionYou will join the Quality Assurance (QA) team within a GMP manufacturing environment, supporting the documentation and training processes that keep operations compliant and inspection-ready. This is an excellent opportunity for someone who wants to build a QA career in pharma/biotech.In this role, you will focus on managing and archiving logbooks, supporting document control activities in Veeva, and coordinating training related to documentation processes. You will work closely with experienced QA colleagues, gaining hands-on exposure to GxP documentation, electronic systems, and daily QA operations.Essential Requirements• Bachelor’s degree in Life Sciences, Pharmacy, Biotechnology, or a related field (or equivalent by experience)• 2 years’ experience in a GMP manufacturing or GxP-regulated environment• Proven hands-on experience with GxP documentation (e.g. logbooks, batch records, QA forms)• Understanding of basic GMP/GDP principles and QA processesPreferred Requirements• Prior experience supporting QA documentation or document control activities• Familiarity with Veeva or similar electronic document management systems• Experience with electronic document processing, archiving, and training coordination• Exposure to pharma/biotech or other highly regulated manufacturing environments• Good communication skills and a proactive, collaborative mindsetPracticalities• Start Date: 15th January• Contract Duration: 6 months (with potential extension)• Location: Full-time on-siteInterested?Interviews and offers can move quickly. Feel free to reach out to me at k.vongeusau@panda-int.com!