out by all departments. ·Conduct shelf-life trials and record results accurately. ·To ensure equipment is calibrated and checked as per schedule. ·To complete GMP, glass and internal audits as required. ·To work closely with the intake team on raw material, packaging and label receipt and ensure any non-conformances more »
the team's size and operational scope. Key qualifications: Extensive experience in Quality Assurance across diverse responsibilities Preferably, a background in pharmaceuticals, though other GMP environments will be considered Bachelor's degree or equivalent in a relevant technical field Strong proficiency across various quality functions such as batch review, investigations … into a senior leadership role within a fast-paced pharmaceutical environment, apply now to become part of a dedicated team. Keywords: Quality, QA, assurance, GMP, manufacturing, distribution, packaging, CDMO, pharmaceutical, batch release, systems, compliance, regulatory, specialist, investigations, CAPA, deviation, change control, operations, senior, leader, supervisor, manager, coach, mentor. more »
Camelford, Cornwall, South West, United Kingdom Hybrid / WFH Options
Saputo Dairy UK
to demonstrate the ability to learn the technical aspects of processes. Able to show an understanding and willingness to comply with all food standards (GMP, health & safety etc.) consistent with working in a world class food manufacturing environment. WE SUPPORT AND CARE FOR OUR EMPLOYEES BY PROVIDING YOU WITH We more »
with our long standing client in Bristol at an exciting time in their business where they will be commissioning a new GoodManufacturingPractice (GMP) facility. This will be in a new building and be a blank canvas for the new Quality Assurance and Validation Engineer to work on! You … will be working with colleagues both internal and external on commissioning and qualification of this new GMP facility. This will include equipment IQ/OQ/PQ activities, as well as validation and qualification of the ISO 7 and ISO 8 cleanrooms. You will be responsible broadly for all systems … self motivated with a can-do approach. Your background: Bachelors Degree in science or engineering with experience in facilities and equipment validation. Experience of GMPmanufacturing, facilities, equipment qualifications and process validations, including cleanrooms. Knowledge of cGMP manufacturing regulations for the MHRA, FDA and other countries as required. Experience in more »
Manage own time to ensure quality actions, plans, targets, training, and objectives are delivered within agreed timelines Ensure own work follows GoodManufacturingPractice (GMP), Data Integrity and Good Documentation Practice (GDocP) Identify and drive Practical Process Improvement initiatives (PPI) including undertaking/supporting Self-inspections, GEMBA walks, Kaizen, and more »
QC Chemistry analytical documentation, logbooks, and analytical instrument electronic records. Responsibilities: To ensure cGMP is applied in all areas of the business and perform GMP data review quality control analytical testing of incoming goods, intermediates and/or finished products under c GMP conditions for QC release or stability studies. more »
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 »
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 »
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 »