Technical Recruiter at NIRAS Ireland - NRF CERT RP
QA Manufacturing Compliance Specialist (Biologics)
* 12 mth contract - 100% onsite.
* Rotating day and evening shift weekly.
* Days: 07:00 - 15:00 Evenings: 15:00 - 23:00.
Responsibilities:
* Ensure that all products leaving the manufacturing meet the standards required for marketed and investigational drug products.
* Ensure that products and aseptic process simulations manufactured 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).
* Administration of Quality Logs, e.g. QA Hold, Sample Request.
* Lead operations floor daily walk around of manufacturing areas.
* Drive continuous improvements and simplify site processes and procedures, specifically relating to the Operations function to ensure compliance is maintained at all times.
* Other support as deemed necessary.
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.
Seniority level
Mid-Senior level
Employment type
Contract
Job function
Quality Assurance
Industries
Pharmaceutical Manufacturing, Medical Equipment Manufacturing, and Manufacturing
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