51 to 75 of 130 GMP Jobs in England

safety assurance and business improvement processes for the site. This role is instrumental in driving our food safety agenda, leading quality standards and site GMP to drive down complaints and costs, as well as ensuring full compliance with relevant Legal, National, Corporate, and Retailer standards. To excel in this role more »

for a strong CDMO in Occitanie, France. The Role You will be responsible for: Carrying out cell cultures. Perform routine environmental checks. Application of GMP Standards. Work successfully as part of a team or individually. Preparation of documents, consumables, and equipment. Collaborate with other departments – QA & QC. Monitor & maintain equipment. more »

to our customers through timely response and effective communication. * Ensuring Engineering standards are maintained, compliant with all legal requirements and factory standards and procedures (GMP, HSE and Process, etc.) are adhered to. * Liaise with department streams through meetings, understanding issues and setting plans to resolve. * Drive PPM's completion to more »

and on into production phase 1 to 3 to ensure competent technology transfer of drug products Experience in completing manufacturing documentation in accordance with GMP Desirable Criteria (The following criteria may be applied if a large pool of applicants exist) Previous experience within a technical role in the pharmaceutical industry more »

fixed weekly rotation. Responsibilities: Perform routine quality control examinations. Conduct routine analysis of raw materials and products using various techniques. Ensure all work is GMP compliant. Use a variety of instrumental and wet chemistry techniques to ensure analysis is accurate. Ensure consistent production of high-quality self-care products. Key more »

probes, ph probes, etc.). Label verifications. Verify finished product labels and crate/case end labels to ensure correct Use By Dates. Complete GMP & Hygiene Audits. Completing of Daily/Monthly/Quarterly Glass & Hard Plastic Audits. Micro sampling to site schedule and manage an ongoing shelf-life library more »

interpretation, knowledge, and experience for project direction and delivery. Support process scale-up and material supply delivery in labs and pilot plant areas, including GMP clinical trial material production as per business needs. Responsible for ensuring and driving compliance in all safety and quality aspects of process development activities. If more »

corrective actions Collecting micro-samples as per schedule Traceability Investigations into complaints Daily auditing of CCPs Daily label checks Calibration Auditing of processing records GMP/fabric audits Temperature checks Quality checks The nature of this role requires a flexible approach to working hours. Core working hours are: Monday to more »

on a permanent basis. The Validation Manager will be leading the validation function to be able to execute report activities within the framework of GMP - Annex 11 & 15 in compliance with QMS requirements. In addition, they will be supporting multiple validation projects, liaising with the project departments and the associated more »

manner. Ensure all technical systems and documentation is up to date and maintained. Work closely with site QA team and where necessary do internal, GMP and Customer audits and visits. Maintain up to date technical risk assessments. Deputise and support others across the technical and quality function in all tasks more »

Manager in the Process Engineering department. You will ensure that operations are performed in accordance with the requirements of company standards, industry standards, and GMP/GDP guidelines. Whats on offer? Excellent Salary & Benefits: You will receive compelling salary DOE, along with an exceptional benefits package. Innovative Leadership in Automation more »

background and ideally Team Leading people working on similar projects as listed below:- Skills and experience:- - Pensions Data Transfer - Client Onboarding - Implementation - System Configuration - GMP - BIBO - Buy in - Buy out - Pension projects Unique culture, fully diverse and inclusive, very supportive, with ability to grow and become senior manager. Responsibilities: Takes more »

management: 3 Direct reports including a QA Supervisor and 2 QA Auditors, carrying out appraisals, training and one to ones Standards Compliance : Focus on GMP, BRCGS, ISO9001, ISO14001, and FSC/PEFC standards. Traceability & Recall : Conduct traceability exercises and mock product recalls. HACCP Engagement : Ensure HACCP improves product safety and more »

and provide corrective action Use root cause analysis to understand and deliver optimal cost maintenance Delivery of the required standards in relation to Engineering GMP and food safety standards Escalate potential consequences to line manager where work may impact on product quality or safety Key skills & experience: Strong engineering qualifications more »

Haematology wards Lead on and develop elements of the clinical pharmacy service to improve the patient experience. Provide release of chemotherapy products according to GMP Facilitate and promote rational and optimal medicines usage Provide assimilated and relevant medicines information to healthcare professionals and patients To participate in the out of more »

standards. Conduct regular audits and inspections of the production facility to identify areas of improvement and address any non-compliance issues. Implement and overseeing GMP, HACCP, microbiological and QC checks. Experience: Experience in technical/quality management roles within fresh produce businesses. Excellent working knowledge of BRC standards. Specific experience more »

teams to clearly communicate the requirements for the Store and capture client requirements. The industries we serve have growing requirements for regulatory quality control (GMP, Medical Devices, ISO etc). The System Engineering role provides opportunity to develop the fully documented lifecycle to support adherence to these standards. Key responsibilities more »

skills in previous positions. Worked as an engineer or come from an analytical background carrying out on site support. Experience working in GLP/GMP environment. Be prepared to travel and stay away as required. Package: Salary up to £43,000 D.O.E Bonus Scheme (£6.5k) Company Car + Expenses Covered more »

this time. About The Role Working as a Multi-Skilled Engineer, preferably with an electrical bias you will primarily offer engineering support in the GMP area. You will also handle responsibilities related to site utilities and facilities as needed. Your duties will include completing both scheduled and unscheduled maintenance tasks more »

of swabs & water samples Quality checks and then collection of finished product and raw materials for microbiological & nutritional testing Conducting various daily audits (including GMP, Glass & Plastics audits, and ensuring corrective action with the shift manager Conducting internal quality assessment panels (QAS) throughout the shift & raising issues with the senior more »

and improvement of the Quality Management System (QMS). Assure the compliance of all activities with Good Distribution Practice (GDP) and Good Manufacturing practice (GMP) requirements. Responding to medical information enquiries from healthcare professionals, community pharmacies, patients, and wholesalers. Ensuring the completion of checks for new products; having the appropriate more »

co-ordinate the day to day workload, ensuring items are manufactured in a timely manner and colleagues are supported. To follow good manufacturing practice (GMP) at all times. To generate worksheets and labels, ensuring medicines are charged correctly using the pharmacy computer system. To in process check worksheets and labels more »

Lead best practice in the department and become a key contact for the mentoring and training of more junior members of staff. Act as GMP ambassador, take responsibility for ensuring GMP compliance and adoption of GMP principles e.g., right first time. Lead activities to ensure close working with Analytical development … understanding of cell biology and immunology (preferred) Strong verbal and written communication skills. Flexible, self-motivated, and focused on team outcomes. Strong understanding of GMP regulations. Excellent organisational skills with the ability to present results clearly and logically, working co-operatively as part of a team, as well as independently. more »

data feed. Due diligence on new business transactions. Requirements: Qualified Pensions actuary with experience within a top consultancy or relevant firm. Strong understanding of GMP equalisation, Longevity Swap or risk transfer. Excellent stakeholder skills and ability to lead/drive projects. A tenacity to 'get stuff done' and find ways more »

has a broad skillset and excellent oral and written communication skills. An individual who has a number of years of experience working in a GMP and QA environment is therefore essential for this post in order to provide the required support and guidance to our Production and QA departments and … Essential Educated to degree level in relevant scientific discipline or equivalent Postgraduate qualification Experience/Knowledge Essential Regulatory requirements pertaining to ATMPs manufacture Good Manufacturing Practice and Good Clinical Practice Thorough understanding of gene and cell-based therapies Thorough understanding of HTA Proven experience of line managing staff Experience of more »