Our Client, a Fortune 500 leader, is hiring for Quality Assurance Associate. Be part of a team setting science in motion across the biopharma, healthcare and advanced technologies industries. Are you ready to make a global impact? Join us now!
Responsibilities
Issuance of controlled manufacturing and testing documents to Manufacturing and Quality Control as per the production schedule.
Issuance of controlled labels used for labelling finished goods and other related samples.
Monitor the equipment program including calibration and preventative maintenance timelines and complete quality assurance sign-off for equipment workorders.
Coordinate the release of raw materials after completion of review and approval of supporting documentation including supplier and quality control testing records.
Conduct reconciliation, filing and archiving all quality-controlled records. The store completed documents in the appropriate data files and coordinated off-site document storage with third party as necessary.
May provide batch record review support.
Writing and revising SOPs as part of process improvement initiatives or as needed to support the department.
Coordination of document control activities and delegating with other quality coordinators to drive workload completion in the direction of quality management.
Requirements
BA/BS in chemistry or science-related field preferred, or equivalent from two-year college or technical school.
A minimum of 2 years of experience in Quality including cGMP and ISO standard.
Experience of cGMP and MS Word, PowerPoint and Excel.