Company Description

GMP Healthcare Ltd is a consultancy and support service provider for the pharmaceutical, we are medical devices, and food supplements industries. Operating across all the GxP areas, we deliver end-to-end solutions across the product life cycle and manufacturing processes. Our team of over 30 professionals includes experts in Qualified Persons (QP), Responsible Persons (RP), pharmacovigilance, R&D, technology transfer, and quality assurance to name a few. Cumulatively, our team brings over 400 years of industry expertise, ensuring exceptional value and support for our clients.

Role Description

We are currently seeking Quality Control Analyst for one of our clients located in Kingston Upon Hull. The QC Analyst will play a crucial role in ensuring the quality and compliance of our products through meticulous testing, analysis, and reporting. This position requires an individual with a keen eye for detail, strong analytical skills, and the ability to work effectively in a team environment. The QC Analyst will work closely with cross-functional teams to maintain and improve our quality standards.

Key Responsibilities

· Quality Control Testing: Conduct testing of raw materials, intermediates, packaging components, and finished products in strict accordance with Good Control Laboratory Practices and specified methods.

· Timely Product Release: Support the timely release of products to customers, including internal customers, by working within agreed lead times.

· Health and Safety Compliance: Ensure that all job-related activities are carried out in full compliance with relevant Health and Safety legislation to maintain a safe and secure working environment.

· Documentation: Ensure all documentation is meticulously completed in accordance with the ALCOA Principles (Attributable, Legible, Contemporaneous, Original, and Accurate).

· Sampling Protocol: Ensure all sampling activities align with Good Manufacturing Practices (GMP) expectations.

· Out of Specification (OOS) Investigations: Actively participate in the timely progression of OOS investigations to maintain quality standards.

· Housekeeping: Maintain appropriate levels of housekeeping in all Quality Control (QC) areas to promote a clean and organized work environment.

· Quality Management System: Contribute to the creation and completion of all Quality Management System-related documents, such as Standard Operating Procedures (SOPs), Deviations, and Change Controls.

· Collaboration: Liaise with 3rd Party laboratories to ensure the timely sending of samples and reporting of results received.

Essential Skills

· A degree-level qualification in a relevant field.

· Minimum of one year of experience working in a pharmaceutical or other regulated QC environment.

· Strong teamwork and communication skills.

· Excellent organizational skills with the ability to multitask effectively.

· Proficiency in using a PC and good MS Office Skills.

Essential Skills

· A degree-level qualification in a relevant field.

· Minimum of one year of experience working in a pharmaceutical or other regulated QC environment.

· Strong teamwork and communication skills.

· Excellent organizational skills with the ability to multitask effectively.

· Proficiency in using a PC and good MS Office Skills.