surpass targets Cultivate a collaborative, safe, and quality-centric work culture Tackle production hurdles through cross-functional collaboration Ensure staff adhere to industry standards (GMP, GDP) through comprehensive training Strategically manage budget and pioneer cost-saving initiatives Champion NPI and NPD processes for ongoing enhancements Supervise quality assurance and compliance … Track record of managing third-party providers in regulated settings Skilled in manufacturing site management Extensive (5+ years) experience in formulated reagent manufacturing (preferably GMP) Proven project management skills and adept presentation abilities more »
its capabilities. This will include ensuring activities associated with manufacturing and lab equipment, facilities, utilities, laboratory, and computer systems are completed, in accordance with GMP requirements Responsibilities : Manage a team and ensure validation master plans (VMPs), protocols and procedures are established To prepare and maintain validation plans (VPs) and identifying … protocols for equipment, facilities and utilities Your Background: Degree (or equivalent) in a Science or related discipline Qualifications related to validation and quality compliance (GMP/ICH/FDA/USP/EP policies). Experience of validating manufacturing/laboratory equipment, facilities/utilities and processes, including the generation more »
implement software solutions for all aspects of the products. They will assist software development within the team, ensuring best practices to medical device and GMP standards where appropriate. The software engineer at MFX will be a key player in advancing the revolutionary bioprocessing platform for the Cell and Gene Therapy …/hardware interfaces, user interfaces, data logging and presentation. Work with the existing software development team. Follow all relevant medical device directives and EU GMP Annex 11 with regards to software. Keep relevant Quality Management System documentation up to date. Qualifications & Experience: 2+ years of experience creating software for a more »
Summary: The Head of Quality Assurance leads strategic QA efforts, ensuring compliance and driving improvement. They oversee operations, manage teams, and maintain high standards. Responsibilities: Define and drive QA strategy. Set and monitor quality standards. Ensure compliance with regulations. Lead more »
if required), considering safety, quality, integrity and legality. Ensure all procedures/process deviations are analysed and actioned in a safe & legal manner. Hygiene & GMP: Ensure that the company has up to date, consistent and appropriate cleaning and GMP procedures that meet the requirements of BRC/Customers. Ensure that more »
to provide high quality, synthetic DNA for use in gene therapy and gene editing platforms. The company is growing rapidly and is establishing a GMP gene synthesis hub at its site just north of Cambridge, UK to facilitate the scaling and optimisation of a proprietary DNA manufacturing process. As a … essential. Experience of working in cleanrooms and/or manufacturing environments is desirable. An understanding of Quality Control or concepts of GoodManufacturing Practices (GMP) Scrupulous attention to detail Comfortable working autonomously or collaboratively Methodical, organised, and able to prioritise work effectively Must hold the right to work in the more »
GMP Recruitment are proud to be partnered with an established telecommunications company serving Military, Government, Transport and Utility markets. The company is looking to appoint a Senior Technical Engineers to enhance an already strong and competent team with varying specialisms. The role is a full time, permanent position working … to theory, installations, testing, commissioning, power & H&S. If the above role sounds perfect for you, or you require more information, please click apply. GMP Recruitment are recruiting for this role on behalf of their client and are acting as an Employment Agency more »
division. You will be working on a variety of projects to assist schemes as they prepare for buy-out/buy in, assisting with GMP data preparedness and the future Pensions Dashboard. You will take an active role to guarantee client satisfaction for the duration of projects and have a … background * An interest in pension scheme de-risking exercises This is an excellent opportunity to join a team dedicated de-risking data team, where GMP projects will not be your sole focus. This team is still fairly in its infancy, allowing for fast progression organically. For further information on this more »
