76 to 100 of 133 GMP Jobs

out at all times. Perform sanitation on equipment as required. Sample product as required by Quality instructions and perform qualified testing as required. Follow GMP and other quality processes and procedures. Perform other duties as assigned. Jobs Supervised (by title): No direct reports Minimum Qualifications: A. Education and Experience: Ability more »

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 »

deploy software for new products, including software/hardware interfaces, user interfaces, data logging, and presentation. Follow all relevant medical device directives and EU GMP Annex 11. Technical skills needed include: 2 years in a regulated industry or similar, 2 years of experience with writing code in C/C++ more »

Overview The Scientist I will test and report cGMP test results for the Quality Control Microbiology Laboratory. First Shift, Monday - Friday Responsibilities • Follows current GMP requirements and complies with company safety and controlled substance handling policies. • Participates in repair and maintenance of lab equipment and lab housekeeping (disinfection and cleaning more »

the British nuclear Medicine Society Person Specification Other Essential Knowledge and understanding of the principals of Good Aseptic Dispensing Practice and Good Manufacturing Practice (GMP). Knowledge and understanding of current radiation leglisation Experience Essential Minimum 4 years( 5 years preferred) experience of working in a hospital pharmacy aseptic dispensing more »

analytical team to contribute to the overall group objectives and development of staff. Ensure that own work, and that of the team, complies with GMP, Good Documentation Practice (GDP) and GxP Data Integrity guidance's, and is undertaken in accordance with applicable procedures (e.g., SOP's, Protocols, etc). Requirements … Proven track record of managing a team within a cGMP QC analytical environment. Degree in a relevant scientific discipline or equivalent experience. Understanding of GMP requirements e.g. legislation, guidelines and requirements related to Gene Therapy, QC method qualification and validation, QC processes, equipment and systems, including Computer System e.g. of … EU GMP requirements for Advanced Therapy Medicinal Products, EU/FDA GMP guidelines, EU Annex 1, EU Annex 11 & CFR Part 11 and ICH guidelines Q1-Q10. Apply now If you are interested in learning more or applying to this exciting opportunity then please click "Apply" and upload a copy more »

Governance Team, you will contribute to the provision, continuous improvement, and delivery of a World Class service to the site, ensuring statutory, regulatory and GMP Compliance requirements are met. Accountabilities: As an Accountable Engineer, you will establish collaborative ways of working to build and manage strong internal customer & supplier relationships. more »

equipment. You can troubleshoot test processes. You can perform periodic equipment inspections and preventative maintenance work. Your Experience: Lab-based experience would be advantageous GMP or GDP experience You will have high attention to detail Able to work both on individual tasks and as part of a wider team IT more »

qualifications and experience: 5 years experience in an environment associated with the manufacture, testing, and dispensing of radiotracers. Relevant experience of Good Manufacturing Practice (GMP), typically 2 years post qualification. Experience of working in Radiotracer production facility, Aseptic service or similar environment. Experience supervising technical staff and management of resources. more »

always opportunities to learn and gain exposure. Experience: Previous experience in a QA position within a pharmaceutical, healthcare or food setting Working experience of GMP Operational Quality Assurance experience including batch review/release Exposure to handling complaints processes Lifecycle experience of deviations, CAPAs and change controls Strong stakeholder management … Mark Bux-Ryan for further information quality, assurance, QA, QC, control, analytical, chromatography, HPLC, laboratory, documentation, analyst, officer, specialist, executive, administrator, good, manufacturing, practice, GMP, GLP, audit, SOP, training, complaints, batch, review, release, CAPA, deviation, change, control more »

focused Extremely safety conscious Helpful and responsive and committed to delivering the very best Team playing whilst proactive and a self-starter Desirable Requirements: GMP manufacturing equipment Recognised formal qualification in secondary control discipline or equivalent experience in Control Systems Knowledge of high integrity PCS and PLC programming would be … Drug Discovery teams. In addition, a Formulation Development team was also recently established. The Hoddesdon site has state-of-the-art Good Manufacturing Practice (GMP) standard facilities for the development of Active Pharmaceutical Ingredients (API), Formulation Development (FD) and Process Chemistry (PC). We offer a competitive salary and a more »

for ATIMPs. coordination all clinical trial functions within aseptic services to meet the needs of the service. Ensure compliance to procedures and national standards (GMP, GCP and The Medicines for Human Use (Clinical Trials) Regulations 2004). About us Cardiff and Vale University Health Board is one of the largest … and interaction skills. NVQ L3/BTEC Pharmacy services Good working knowledge of safe dispensing and aseptic practices Knowledge and understanding of GCP/GMP legislation and QA and its application to aseptic processing Able to demonstrate excellent organisational skills Good attention to detail and responsible attitude to quality and … understanding & knowledge of operation of aseptic services, Good understanding & knowledge of safe handling prescribing and use of cytotoxic drugs Good understanding & knowledge of Good Manufacturing Practice Disclosure and Barring Service Check This post is subject to the Rehabilitation of Offenders Act (Exceptions Order) 1975 and as such it will be more »

RESPONSIBILITIES Develop and oversee a robust quality management system in line with pharmaceutical industry regulations, including Good Distribution Practices (GDP) and Good Manufacturing Practices (GMP). Establish quality policies, procedures, and guidelines to ensure the consistent and compliant handling, storage, and distribution of pharmaceutical products. Implement quality assurance programs, including … 8+ years) in quality management and loss prevention, preferably in the pharmaceutical or logistics industry. Strong understanding of pharmaceutical regulations and quality standards (GDP, GMP). Proven track record of successfully implementing quality management systems and loss prevention strategies. Excellent leadership, communication, and interpersonal skills. Analytical mindset with the ability more »

with our long standing client in Bristol at an exciting time in their business where they will be commissioning a new Good Manufacturing Practice (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 GMP manufacturing, 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 »

most understandable to technology professionals. Key Responsibilities: To maintain consistent and documented compliance with all relevant Safety, Health and Environmental (SHE), Good Manufacturing Practice (GMP), Data Integrity (DI), quality and best practice requirements. To be responsible for the product planning and execution throughout the product lifecycle in line with PMO more »

expert in manufacturing operations. Project management in technical transfer and validation of each new product Lead the product lifecycle management activities. Responsible for ensuring GMP documentation are assigned and logged. Management of change controls Requirements: Degree (or equivalent) in a related scientific subject Experience in an industrial Pharma/Biotech … GMP regulated environment. Knowledge of transferring pharmaceutical products from development into GMP manufacturing environment Excellent knowledge of ICH guidelines and cGMP If interested, please apply via the link. more »

ABOUT YOU Are you a Quality professional with experience in a GMP laboratory, looking for a role that will challenge you, and help you develop new skills? You will possess rigorous attention to detail and be hungry for a challenge out of the lab. We need you to have: BSc …/MSc/PhD in Chemistry (or related scientific discipline) A sound working knowledge of relevant quality standards; GMP, GLP, GCP and other analytical related quality standards Good working knowledge of Quality Assurance in the Chemical and Pharmaceutical Industry Quality Assurance background which includes some specialist knowledge within a defined … Excellent attention to detail Impressive written and verbal communication ABOUT THE OPPORTUNITY You will provide general support to Quality Assurance activities relating to GLP, GMP, GCP, and other similar Quality Systems established to ensure that the appropriate standards and effective working systems and relationships are maintained and where necessary improved. more »

with you. Main duties of the job To assemble and prepare pharmaceutical products in accordance with relevant Standard Operating ProceduresPrepare, in accordance with Good Manufacturing Practice, Aseptic injectables using isolator technologyTo accurately record and maintain all elements of paper-work related to the preparation of products and maintenance of the … Services and support the delivery of their trainingTo assist in the maintenance of the environment, ensuring that the cleanliness of the facility is to GMP standards About us North Bristol NHS Trust employs over 12,000 staff providing healthcare to the residents of Bristol, South Gloucestershire and North Somerset from … procedures Undertakes the physical and microbiological environmental monitoring associated with the facility. Undertakes the regular daily cleaning of the aseptic facility in accordance with GMP and departmental procedures Undertake the monthly and 3 monthly deep clean processes. Assemble non-sterile packs of emergency medication in line with departmental procedures and more »

trial design, to advise them on good practice in accordance with the International Conference on Harmonisation (ICH) guidelines on Good Clinical practice and Good Manufacturing Practice and on the regulatory status of the clinical trial drug. 5. To lead and finalise the set-up of cancer clinical trials, i.e. writing … years post-graduate training above original Masters level qualification) Vocational Masters degree in Pharmacy (4yrs) and 1 years pre-registration training and experience) GMP accredited Desirable Specialist qualification in cancer therapy or equivalent knowledge Qualified Independent Prescriber or willing to undertake training Experience Essential Substantial post registration experience in a more »

with regulatory standards and fostering a culture of continuous improvement. Key Responsibilities: Manage all site-related QA operations in accordance with Quality Agreements and GMP guidelines. Serve as the QA representative on the Site Leadership Team. Lead adherence to local or corporate Quality Management Systems (QMS). Collaborate in developing … for site use. Conduct external audits as necessary. Provide strategic input into decisions impacting the Quality Assurance department. Deliver QA-related training and basic GMP training as needed. Act as a subject matter expert on Quality-related processes. Lead or represent QA in related projects, identifying metrics, issues, and mitigation … and develop a team of QA professionals. Support quality-related activities across sites as required. Minimum Qualifications and Experience: Minimum 10 years' experience in GMP manufacturing, with a focus on QA/Quality roles. Experience in QA support for ATMP manufacture preferred. Demonstrated leadership of small QA teams. Proficient in more »

positions involve shift work, including nights, so flexibility is key. We welcome candidates from diverse backgrounds, whether you have experience in production and QC GMP settings or you're a fresh analytical graduate eager to kick-start your career. Key requirements: A degree in a Life Sciences discipline or equivalent … Previous QC chemistry or production experience is advantageous but not essential Familiarity with chromatography techniques such as HPLC and GC Understanding of GMP principles or willingness to adhere to regulated procedures Flexibility to work shifts If you're ready to join a supportive team and make your mark in the … pharmaceutical industry, apply below or contact Jolie Trahar for more information. Keywords: QC, quality control, analyst, analytical, laboratory, radiopharmaceutical, GMP, entry level, graduate, science, pharmaceutical, biotechnology, manufacturing, shift work. more »

naturally a flexible mindset is needed for this type of position. As such, I am interested in speaking with people from Production and QC GMP settings, as well as fresh graduates looking to get that key break. This team is very open to your background – it is all about your … experience would be advantageous but is not essential Experience and/or understanding of chromatography techniques including HPLC and GC. A solid understanding of GMP principles – or at least the ability to work to strict regulated procedures Flexible to work shifts Must have own transport to access the site due … to shift work QC, quality, control, analyst, analytical, laboratory, radiopharmaceutical, GMP, entry, graduate, science, pharmaceutical, biotechnology, manufacturing, shift more »

naturally a flexible mindset is needed for this type of position. As such, I am interested in speaking with people from Production and QC GMP settings, as well as fresh graduates looking to get that key break. This team is very open to your background – it is all about your … experience would be advantageous but is not essential Experience and/or understanding of chromatography techniques including HPLC and GC. A solid understanding of GMP principles – or at least the ability to work to strict regulated procedures Flexible to work shifts Must have own transport to access the site due … to shift work QC, quality, control, analyst, analytical, laboratory, radiopharmaceutical, GMP, entry, graduate, science, pharmaceutical, biotechnology, manufacturing, shift more »

values, promoting an ethical, positive company culture To maintain consistent and documented compliance with all relevant Safety, Health and Environmental (SHE), Good Manufacturing Practice (GMP), Data Integrity (DI), quality and best practice requirements To work collaboratively with Pharma and Health Tech leadership team to develop a Sustainability Roadmap that supports more »

Clinical Supply Quality projects with expertise and delivery. This may include all Quality aspects of projects including IT projects. Support Clinical Supply functions in GMP inspections and input to GCP inspections where required Approve Clinical Supply GMP documentation Contribute to release and other routine activities required in the clinical supply … lean culture that promotes standardisation, simplification and continuous improvement Essential Requirements – Education and Experience Functional & Business Knowledge Extensive experience of working within a pharmaceutical GMP environment, preferably within a pharmaceutical development organisation Extensive experience from working in a Quality Assurance function is essential; A broad and comprehensive understanding of Quality … Systems and GMP A comprehensive understanding of the pharmaceutical/drug development process Good knowledge and reputation in the QA arena and specifically in GMP matters Understanding of Project Management and Supply Chain processes Skills and Capabilities Excellent team working, networking skills and encouragement of team efficiency Demonstrates independent judgement more »