Join our Document Control team at Almac Pharma Services, where you'll play a vital role in maintaining the integrity of our GxP documentation and supporting our robust Quality System. This position offers the opportunity to work hands-on with critical documents such as Master Batch Records and SOPs, ensuring they are accurately controlled, issued, and archived in line with internal procedures. You'll be instrumental in supporting operations by issuing batch records, managing variable data in TROPOS, and circulating quality-related documentation across departments. As a key contributor to our quality-driven environment, you'll also assist in preparing for client and regulatory audits, maintain electronic tracking systems like WOLF, LiveLink and TrackWise, and support investigations and QA reporting. This role is ideal for someone who thrives in a structured, compliance-focused setting and is eager to contribute to the continuous improvement of pharmaceutical quality standards. If you're detail-oriented and passionate about documentation excellence, we’d love to hear from you.
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Job Type
Full-time
Career Level
Mid Level
Education Level
High school or GED