1 to 25 of 104 GMP Jobs in England

Analyst/Team Leader with extensive experience (3+ years) of using and troubleshooting the above types of Dissolution/Tablet Testing equipment in a GMP environment who is motivated to progress into an exciting Dissolution Field Service Engineer role?! If you said yes to the above, then this brand-new more »

their quality department. As a senior quality associate, you will play a key part of a team that is responsible for quality oversight of GMP and compliance within company operations, providing guidance on GMP, GDP and GLP ensuring compliance with internal and external requirements with both ISO 13485 and ISO more »

and vision systems integrated within packaging equipment including interfaces with enterprise systems. Responsible for providing cGMP compliant control systems as per GAMP5 and EU GMP Annex 11. Key Experience Essential - Practical experience working within manufacturing and packaging environments Experience of the automation project lifecycle including design, configuration, implementation, testing, commissioning more »

and updating risk assessments and risk mitigation procedures. Train necessary staff in relevant fields related to technical compliance. Implement and deliver site quality and GMP compliance metrics: tracking and investigating consumer complaints, internal and external audit outcomes, and customer compliance. Deliver successful customer and external audits: completion of a gap more »

and operational support OR 3+ years in a similar role with Manufacturing OT equipment, in Healthcare/Pharma. 3+ years working with GxP and GMP environments. If you're interested and would like to find out more, reach out on LinkedIn or send your CV to lauren.mckinley@skillsalliance.com. more »

Durham area. Salary and Benefits of QC Analyst Salary up to £28,000 Permeant Role Skills and Qualifications needed for QC Analyst Knowledge of GMP Standards Chemistry Degree 2 Years Experience in a relevant role Fine Chemistry/Pharmaceutical Experience HPCL and GC Experience Responsibilities of the QC Analyst The more »

regulatory compliance and consulting services to the global pharmaceutical industry. It operates across Good Clinical Practice (GCP), Good Pharmacovigilance Practice (GVP), Good Manufacturing Practice (GMP), Good Laboratory Practice (GLP) and Computer Systems Compliance (CSC) (together, GxP). Founded in 2007, ADAMAS has focused on ensuring that the highest standards of more »

including HPLC and GC. Candidates that have proven industrial experience of these techniques in a busy, fast-paced laboratory setting are encouraged to apply. GMP is desirable but not essential for this position. Benefits: 28 days holiday plus bank holidays. Monday – Friday, 9am-5pm (with flexibility). Role/Description … and consumables Requirements Degree in Chemistry (or similar) proven industrial experience of analysis including HPLC or GC in a busy, fast-paced laboratory setting GMP experience is desirable but not essential Positive, pro-active attitude Team player work a strong work ethic For more information please call Chris on … 1898. Keywords: quality control, laboratory, lab, pharmaceutical, QC, analytical, sample, chemical, GMP, science, QC inspection, testing, materials, ingredients, analysis, GC, wet chemistry, titrate, titration, HPLC, raw materials, intermediates, in-process, finished products, chromatography. 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 »

testing intermediates, products and raw materials in line with demand and business requirements. Job Summary: - Follow approved methods and procedures in accordance with cGLP & GMP requirements. - Report analytical results accurately and in a timely manner as dictated by internal and external customer requirements. - Ensure QC documents are complete, accurate and … subject) degree with experience as an analyst in a fine chemical or pharmaceutical industry role. HPLC and GC experience. - Experience of working in a GMP environment/method development experience/cleaning validation experience. To Apply: For more information, or to apply for this QC Analyst position please contact James more »

be accountable for all commercial elements of the Small Molecule and Protein Delivery strategy comprising of M&A, licensing, innovation product promotion and wider GMP manufacturing strategy to deliver double digit organic and inorganic growth in line with business expectations. Who we're looking for: Degree qualified (ideally MBA) with more »

focus: Actively participate in the implementation of site quality improvement projects, where necessary providing support to train operation teams and monitor project effectiveness. Complete GMP and Hygiene audits to required schedules. Assist in the investigation of consumer complaints and non-confirming items determining root cause and corrective action necessary to more »

to respond to change environments and high growth, high pressure environments. Experience in managing stakeholders. Ability to track and report issues. Experience & understanding of GMP, FDA & TGA Quality requirements. Culture & Benefits We are fuelled by our commitment to sustainability, quality, efficiency, and an unwavering passion for our customers. Championing solutions more »

monitoring good manufacturing practices, applying HACCP principles and preventing reoccurrence of non-conformance against these standards. To audit compliance against Quality Management Systems and GMP, raising all non-conformances against relevant standards with objective evidence enabling the operational teams to take the appropriate and necessary corrective action, to follow up more »

archiving and ensure document control. Assist the team with technical issue resolution and continuous development of food safety & quality Complete site internal audits (CCP, GMP, Glass and plastic, hygiene etc) Collect and coordinate samples for routine micro/analytical analysis Actively reinforce the company's good manufacturing practices and hygiene 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 »

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 »

policies. To be proactive in identifying and eliminating faulty processes by implementing long-term fixes. To uphold and exceed standards of product quality and GMP within their area that are appropriate to an industry-leading quality food manufacturer. To play an active role in the shift and be the go more »

in place to meet legal and statutory requirements. Keep records and provide reports in accordance with good engineering practices to external audit standards. Upholding GMP engineering standards across site, statutory inspections are compliant, and any non-conformances are closed out with root cause analysis to avoid repeat failure. Lead the 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 »

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 »

Compliance. Key responsibilities as our Technical & Quality Coordinator: Be a supportive member of the technical department by ensuring compliance with Food Safety, ACCP, Quality, GMP and H&S procedures. Develop and update technical documentation. Conduct internal audits, finished product traces, and support technical team during external audits. Collaborate with cross … Quality Coordinator: Food Technology/Science or equivalent degree Experience in a technical/quality role within food manufacturing Awareness, good understanding of HACCP, GMP, BRCGS standard and food legislation Be highly organised with the ability to work well under pressure and to tight deadlines Have competent IT skills and more »

the company’s procedures relating to your area of work Deliver a right first time quality product Embrace the company initiatives (Right First Time, GMP) Ensure break-downs and requests for engineering assistance are addressed within a timely manner Ensure work is managed in a professional manner and relevant parties more »

and supply chain as well as external partners like CDMOs to achieve objectives and ensure adequate product availability for launch. Ensure compliance with regulatory & GMP/GDP requirements for generic & specialty drug launches in relevant markets. Establish key performance indicators (KPIs) to track launch performance and evaluate post launch success more »

activities. What you'll need to succeed Our client is looking for an individual with strong experience as a Quality Assurance Officer within a GMP Pharmaceutical/Cleanroom environment. Other key desirables include: Quality Management System activities and maintenance. Experience in participating in internal/external audits. Be able to more »