76 to 100 of 110 GMP Jobs in England

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 »

Assist in coaching and developing other members of the team Main Tasks and Responsibilities n Follows approved methods and procedures in accordance with cGLP & GMP requirements. n Plan and prioritises own work with guidance from QC Senior Analyst/QC Manager n Report analytical results accurately and in a timely … Environmental requirements are met including (but not limited to) workplace organisation, work instructions, risk assessments, COSHH assessments, housekeeping standards in accordance with GLP and GMP n Demonstrable evidence of understanding the importance creating a safe environment n Working in a safe manner n Follow appropriate and relevant practices and procedures … 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 Key Skills Attention to detail Ability to Plan and organize workload Ability to think creatively and 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 »

product investigations Coordinate and resolve immediate/urgent customer complaints, ensuring prompt responses/resolution Participate in the internal audit programme to ensure continued GMP compliance of all site activities Utilise scientific resources in order to work on improving quality of products and services To maintain personal training folder in … Controls CAPAs Deviations Complaints Recalls OOS/OOT The Person: Will have a Degree in a relevant- Scientific discipline Will have good knowledge of GMP & experience in steriles is essential! Experience in CAPA, Deviations, OOS, OOT, Internal auditing (preferred), Customer Complaints handling would be very advantageous Strong IT skills (Microsoft more »

Maintaining and developing the Quality Management System. Maintaining and improving the accreditation standards of the site. Ensuring good hygiene, housekeeping and Good Manufacturing Practice (GMP) standards across the site. Delivering and reporting of key performance indicators (KPI) for food safety, quality, legal and integrity in a timely manner. Liaising with more »

Maintaining and developing the Quality Management System. Maintaining and improving the accreditation standards of the site. Ensuring good hygiene, housekeeping and Good Manufacturing Practice (GMP) standards across the site. Delivering and reporting of key performance indicators (KPI) for food safety, quality, legal and integrity in a timely manner. Liasing with more »

the position proactively contributes to the provision, continuous improvement, and delivery of a World Class service to the site, all ensuring statutory, regulatory and GMP Compliance requirements are met, to ensure stable and reliable UK operations. What you'll do: Take ownership of, and be responsible for, all actions undertaken … Engineers/stakeholders – providing Project Management oversight of all change activities subject to CDM regulations. Essential Skills . Strong project management experience within a GMP/Regulated industry is essential with good GMP experience in a regulated manufacturing industry. Strong project management of change programme across facilities/engineering service more »

Comfortable operating autonomously once goals and objectives are set. Excellent interpersonal, written and verbal communication skills. Confidence and ambition to provide pragmatic and considered GMP advice. Having current and up to date professional knowledge, expertise and best practice. Proven ability to engage constructively with colleagues at all levels across different more »

are under control Check compliance to Food Safety and Quality Management System procedures (QMS) including control measures for Allergens Conduct Good Manufacturing Practice audits (GMP) audits/Compliance Observation Process (COP) checklist Complaint investigation Check products against factory product specifications to ensure compliance with specifications, legality, and consistency in quality 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 »

they are met. • Oversees and performs complex ǪA activities involving evaluating and reviewing processes to ensure manufacturing, testing and clinical trials activities comply with GMP, GCP, HTA and other regulatory requirements relating to manufacture and clinical trials for cellular therapies and AT(I)MPs including. • Identifies and communicates significant quality … and batch records prior to ǪP review) to ensure good documentation, data integrity, essential GxP, quality and regulatory requirements are met. • Expert knowledge of GMP relating to sterile production, cleanrooms, aseptic technique, and hygienic requirements for sterile products • Extensive knowledge of regulatory requirements or processes that specifically apply for the more »

a Quality Director to head up a Quality department. The Quality Director will promote and integrate quality into every aspect of the business ensuring GMP compliance and meeting the authority's expectation. The role holder will perform all duties required of a Quality Director, provide leadership to the Quality Teams … the business and provide support to sister company for regulatory inspections and conduct self-inspection program Oversee the Pharmaceutical Management System. Implement the current GMP regulations and industry best practices, where applicable Support and develop the QA team Support/lead manufacturing deviation or testing out-of-specification/out … of-trend investigations Audit the contract manufacturing organisation and laboratory against EU GMP and relevant regulations and guideline Qualifications and Skills: Qualified Person (QP) Knowledge and experience in manufacturing and testing of oral dosage forms and topical products Experience in releasing medicinal products in a fast-paced environment Experience in more »

company (part of a large Pharmaceutical group); is looking to strengthen their QA team and recruit a Snr QA Release Officer. This is a GMP focused position and this person will play a key part in the growth and development of the team. Duties will include releasing batches of manufactured … change controls, unplanned deviations). The Person: Will have a Degree in a relevant- Scientific discipline A minimum of 3+ years experience working to GMP in a Pharmaceutical setting Candidates with experience in Laboratory, Production or Pharmacy who are looking to move into a QA role full time are also more »

can bring you in and support you at the right level. Key experience: Experience and/or understanding or quality assurance documentation Understanding of GMP – although you may have worked with other compliance systems Transferable experience to demonstrate accuracy and the ability to work in an administrative capacity with highly … skills with the capability to work in a small team Please apply below or contact Mark Bux-Ryan for further information. Quality, assurance, qa, GMP, manufacturing, pharmaceutical, QMS, system, operational, manager, supervisor, team, leader, specialist, compliance, regulatory, audit, lead, complaints, documentation, training, files, administration, admin, controller more »

This is a fantastic opportunity to work alongside our industry leading scientists in our GMP accredited laboratories, at our Sandwich facilities (Kent). You will gain a wide range of practical laboratory skills which are supported by our in-house training. Within the Analytical Sciences department in Sandwich, Kent we … of which used to support batch release, and regulatory packages. As such, you will be trained in all these techniques and general AMS and GMP procedures. There will also be a chance to undertake research for Solid Form Screening using some of the abovementioned methodologies. You will be trained to 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 »

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 Hannah more »

very thorough. Any experience of working in the pharmaceutical or medical device manufacturing sector would be a benefit, including working to Good Manufacturing Practice (GMP) standards. The Benefits - Field Service Engineer, Water Treatment Systems This is an excellent opportunity to join a world class water treatment equipment organisation. You will more »

reference for complex containment solutions for pharmaceutical chemical and biologics manufacturing projects. You'll be responsible for the selection, design, and startup of effective GMP containment technology and its performance, delivered to cost and schedule targets. You will have a direct impact selecting and integrating future containment technologies to enable … quality requirements. Supporting procurement’s strategic supplier management efforts, including establishing qualified suppliers and driving bid evaluations. Providing construction phase technical audits and leading GMP equipment testing and FAT’s, including authorization to release equipment from supplier to AZ site. Providing technical support to GMP equipment commissioning and validation, including … project delivery from business case development through project execution, including the specification, procurement, installation, start up and commissioning of containment equipment in a licensed GMP commercial plant. Knowledge of risk assessment methodology and the effectiveness of maintenance and cleaning methods, and how they may mitigate potential exposure. Ability to collaborate 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 »

has taken strides towards strengthening future project pipeline and therefore this position has a great prospect. Key experience: · Strong pharmaceutical validation experience in a GMP setting · Hands on experience in equipment and cleaning validations – CSV experience would be advantageous but knowledge of this area could also work · Experienced in direct … medium sized manufacturing unit Keywords: Validation, IQ, OQ, PQ, DQ, installation, commissioning, equipment, cleaning, engineer, specialist, lead, supervisor, csv, computer, systems, quality, assurance, manufacturing, GMP, protocol, master, plan more »

is ideal. 2. Proven industry experience in HPLC/LCMS as well as a background of maintenance and troubleshooting skills in a GLP/GMP environment. 3. Experience with other Analytical Instrumentation such as MALDI, Prep LC and SFC is beneficial but not essential. Key Words: Field Service Engineer | HPLC … LCMS | MALDI | Prep LC | SFC | Maintenance | GMP | GLP | Service Schedules | Installation | Validation | Instrumentation | IQOQ | SAP | Troubleshooting | Hyper Recruitment Solutions Ltd (HRS) is an Equal Opportunities employer who are certified by Investors in People for talent development. We therefore welcome applications for any interested parties who fulfil the role requirements for more »

GMP Pensions Specialist (Split with other specialist area) London Reputable and well known consultancy seeking a GMP consultant to work in a split role across GMP and another specialist area of their choosing | National role which can be based completely remotely or from any of their UK offices. Company client … pleased to be working with a reputable and well known consultancy seeking a GMP consultant to work in a split role across GMP and another specialist area of their choosing (risk settlement, member options, pension scheme wind-up). You will work as part of a well established projects team … with a focus on delivering GMP Equalisation projects for clients. You will also be given the opportunity to work in a split role, spending half of your week in another specialist team of your choosing. This is a crucial role to the business in a booming area of the market more »

implementation of processes and procedures to allow routine operation, maintenance and calibration strategies. • These processes and procedures will include but are not limited to GMP documentation, H&S documentation and Risk assessments, designing of layout fit for operational use, maintenance and calibration. Ownership of project related activities and tasks as … post you will need to have the following experience - • Relevant prior experience is required to be successful in this role. • Working knowledge of pharmaceutical GMP production is required to fulfil this role. Experience and competency in working with maintaining and calibrating production equipment used to manufacture sterile product is required … these may include, working in GMP classified clean rooms, Vial washer, Sterilising Tunnel, Isolators, Filling lines, Freeze Dryers. • Process Equipment knowledge mentioned, contamination control processes and procedures understanding. • Understanding Facility design, Equipment required and new technologies for implementation is highly desirable. • Good understanding of Validation requirements of new equipment and more »