About this role
Validation Associate at Accupac. Location: Pennsylvania, United States. Role: reviewing documentation, writing protocols, performing testing Requirements: Perform validation activities including reviewing documentation, writing/executing protocols (IQ/OQ), maintaining validation and calibration records, supporting GMP compliance; 1–4 years cGMP experience or bachelor’s degree preferred; proficiency with Microsoft Word/Excel/PowerPoint. Category: Quality Assurance Seniority: Entry Level Tools: Microsoft Word, Microsoft Excel, Microsoft PowerPoint, Calibration Management database Commitment: Full Time Workplace: Onsite Languages: English