Quality Co-Ordinator Supervisor - DIRFT, NN67GX

IMMEDIATE START Siamo Recruitment is currently recruiting for a new Quality Co-Ordinator Supervisor to work at our client's site in DIRFT, NN67GX
. As they are already leaders in this section, and have a well-trusted and respected brand, this is a fantastic opportunity for someone to work in a driven and experienced team in a fast paced, and growing business. Shift pattern Mon - Fri 37.5 hrs p/wk. (8:30 - 16:30 or 09:00 - 17:00) = 7.5hrs per day, 30 minutes lunch break unpaid Pay Rate:
Pay £16.34 per hour Role & Responsibilities Quality Co-Ordinator Supervisor:
Supporting the Quality & Compliance Manager/RP on site in their duties to ensure the site adheres to GDP/GMP and ISO guidelines. Advising the Operational team on Quality requirements to maintain regulatory compliance. Performing Quality related task to ensure that departmental processes are followed, and systems are maintained in compliance with regulatory (GDP & GMP) and customer expectations. Accountability areas:
To support the QA Manager/RP in ensuring that the guidelines on Good Distribution and Good Manufacturing Practices (GDP/GMP) are complied with. To support the QA Manager/RP in ensuring that the operations do not compromise the quality of medicinal products. To support the QA Manager/RP with training and development. To perform temperature monitoring activities ensuring deviations are identified immediately and escalated internally/externally if required in compliance with internal procedures and client's requirements (including temperature mapping of storage facilities).

Coordinate with the QA Manager and Operational teams regarding the management and segregation of recalls as instructed by clients. To perform QC related tasks, including inspection and release of incoming goods/materials, returns, recalls, samples management, temperature management, in-process control (Co-pack operations) as well as other QC activities highlighted by the quality management team to ensure full compliance with GMP, GDP and ISO 9001.

To support business strategies in order to achieve higher levels of compliance and quality of service as well as embedding a culture of quality. Comply with QA processes and requirements within the QC department (SOP writing, CAPA management, change control, training, internal audits, etc.) To monitor and report contractual QC KPIs as agreed with clients. Develop and maintain a good working relationship with their peers, colleagues and clients, ensuring communication channels are defined and maintained.

To ensure QC related documentation is archived in a controlled manner and retention/reference samples are also managed and stored accordingly and available immediately if requested. Co-host regulatory and client's audits in conjunction with the quality management team, aiming at eliminating risk of findings during audits and/or raising and closing appropriate CAPAs to address any audit observation. The above list of accountabilities is not exclusive or exhaustive and is not intended as a list of individual tasks.

The role holder will be required to undertake such tasks as may reasonably be expected commensurate with the scope and grading of the role. The Quality Co-Ordinator will also have knowledge of;
The Principles and Guidelines of GMP and how the principles of GDP maintain product quality throughout the distribution chain ISO
9001 regulations The role of the professional bodies and organizations that regulate those supplying medicinal products to the public Understanding of Deviations, CAPA, Change Control management, Risk Assessments and document control processes Take the first step toward an exciting new role! Submit your application today via the job board with CV and text Quality to  Don't delay secure your position now! INDCRI