Are you driven to uphold the highest standards in pharmaceutical compliance? Step into this role where your expertise ensures integrity and supports the delivery of safe, effective treatments worldwide.
R&D Partners is seeking an IPQA Associate to provide quality support for production and warehouse activities. This role involves ensuring that manufacturing processes comply with regulatory standards, company policies, and procedures. You will play a key role in monitoring operations, reviewing documentation, and supporting audits and training activities.
You must have the right to work in Ireland.
Responsibilities
Ensure production lines are ready before starting batch manufacturing.
Perform checks during manufacturing to ensure processes meet standards.
Review documents like batch records, forms, and reports for accuracy and compliance.
Monitor manufacturing, packing, and cleaning processes to ensure they follow guidelines.
Assist in investigations related to production issues.
Prepare and review standard operating procedures (SOPs) and reports.
Conduct sampling and inspections during production.
Identify and correct documentation errors while helping prevent future issues.
Manage retained samples and support warehouse activities.
Assist in training preparation and on-the-job training sessions.
Support audits by regulatory bodies, customers, or corporate teams.
Key Skills and Requirements
Proven working years of experience in Pharmaceutical GMP environment.
Bachelors or Masters in a scientific or related function.
Familiarity with Good Manufacturing Practices (GMP).
Strong communication and problem-solving skills.
Attention to detail and excellent documentation abilities.
Eligibility to work in Ireland.
For more information, please contact Billy O’Brien.
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