QA Manufacturing Compliance Specialist (Biologics) Rotating Day and Evening Shift.
We are actively seeking to recruit a QA Compliance Specialist to become a key member of the Quality Team within a West of Ireland based Pharma manufacturer.
This is an on site role with a rotating day and evening shift pattern.
Responsibilities • Ensure that all products leaving the site meet the standards required for marketed and investigational drug products.
• Ensure that products and aseptic process simulations manufactured on site meet the requirements of the end users, regulatory authorities and of the company.
• Providing quality and compliance oversight and assistance to the Operations function of the company to manufacture products in compliance with all site policies and procedures.
• Provide quality oversight during the aseptic processing of products, including aseptic intervention observation.
• Leading / Assisting in investigations arising out of product or manufacturing processes non-compliance.
• Review/Audit of completed Batch Records.
• Review of Manufacturing Logs as required.
• Completion of quality review of operations documentation (SOPs, JSTMs, Risk Assessments) • Completion of Line Clearance activities.
• Completion of Incoming Raw Material checks, including product status maintenance (as required).
• Provide Stability Program Support, e.g.
sample pulls, weekly checks, protocol generation (as required).
Requirements • Third level degree in a science, quality or engineering discipline.
• Ideally previous experience in a quality role • A minimum of three years' experience in a quality/operations role in a highly regulated GMP environment.
Experience in biologics manufacturing is highly desirable.
• Experience in aseptic processing gained within either a quality or operations role is highly desirable.
• A strong knowledge of regulatory requirements is required