41 GMP Jobs in the North of England

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 »

and equipment automationsystems at our Holmes Chapel site. You'll provide hardware and softwaresupport, resolve breakdowns, implement preventative maintenance, and ensurecompliance with GMP (Good Manufacturing Practice), EHS, and company standards.Your role also involves supporting computer system validation, qualityimprovement initiatives, and training other team members. This is a hands-onrole where … support to maintain system performance. Provide hardware,software, and coding support to maintain system performance. Resolve equipmentbreakdowns and conduct root cause analysis. Ensure compliancewith GMP, EHS, and company standards. Support computersystem validation and lifecycle management. Contribute toengineering best practices and project execution. Train team memberson equipment, systems, and procedures. Automation more »

and equipment automationsystems at our Holmes Chapel site. You'll provide hardware and softwaresupport, resolve breakdowns, implement preventative maintenance, and ensurecompliance with GMP (Good Manufacturing Practice), EHS, and company standards.Your role also involves supporting computer system validation, qualityimprovement initiatives, and training other team members. This is a hands-onrole where … support to maintain system performance. Provide hardware,software, and coding support to maintain system performance. Resolve equipmentbreakdowns and conduct root cause analysis. Ensure compliancewith GMP, EHS, and company standards. Support computersystem validation and lifecycle management. Contribute toengineering best practices and project execution. Train team memberson equipment, systems, and procedures. Automation 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 »

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 »

global pharmaceutical company who require a QA Production Support Supervisor/RP to join their well-established Quality and Operations team, focusing on the GMP and GDP requirements. This role involves the supervision and mentoring of a team of very capable Quality Assurance Production Support Officers. Responsibilities: Qualified RP/… systems (including, but not limited to the complaints and batch release processes) Write, implement, review and maintain SOPs, policies and other documentation for QA GMP and GDP activities. Act as Quality GMP and GDP advisor on site projects such as new product introductions or CAPEX projects. Host training sessions on … GMP and GDP QA related topics. Requirements Extensive GMP Quality Assurance experience, preferably in production support Experience of line management and leadership Qualified RP/RPi SRG is UK’s number 1 recruitment company specialising in the science, engineering, clinical, pharmaceutical, food/FMCG, renewable, biotech, chemicals and medical devices 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 »

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 »

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: It is essential that applicants hold entitlement to work in the UK. Please quote job 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 »

through both written and verbal channels are essential aspects of the role. Your ability to thrive in both regulated and agile environments, such as GMP and ISO 17025, will be crucial for success. Hours of Work: 40 hrs. Monday – Friday 8-hour days. 30 min lunch break. Development Scientist Requirements … user of standard ‘office' applications Desirable: Experience of method development/validation in a regulated environment Understanding of regulatory requirements such as ICH guidelines, GMP etc Able to troubleshoot problematic separations Experience with statistics packages E&L knowledge Development Scientist Benefits: Salary £27,820 - £40,660 Broughton Day Option of more »

of QA activities for your assigned portfolio of projects. Your role will involve providing advice to support the development, implementation and continuous improvement of GMP quality systems across the development functions and support implementation of agreed global standards. You will interpret, trend and report compliance data, to measure and improve … Quality Assurance input to business improvement projects. Essential Skills/Experience: - Appropriate scientific degree with significant years of experience of working within a pharmaceutical GMP environment, preferably within a pharmaceutical development organisation - A broad understanding of Quality Systems and GMP is essential - An understanding of the pharmaceutical/drug development more »

The Role - Development/GC MS/HPLC Scientist The Salary - Competitive The Location - Yorkshire Russell Taylor group has a brand-new opportunity for a chromatography scientist. If you think this role would be of interest, apply now to avoid more »

Be part of our journey As a global leader in speciality chemicals, we continue to succeed and strengthen our delivery of innovative, sustainable and high-performance solutions. We are passionate and excited about how we can develop and utilise new more »

Fixed term contract. Introduction to Role: Join our operations team and contribute to the completion of basic manufacturing support processes in compliance with AZ, GMP & SHE standards. Be part of shaping the future of Operations here at AstraZeneca. Accountabilities: As a Process Operator, you will promote an environment of safety … performance, proactively use STOP cards to identify SHE hazards and take appropriate actions. Essential Skills/Experience: - Basic knowledge of procedures and compliance with GMP & SHE requirements - Operational knowledge of specific equipment within the local plant area. This could include a requirement for a Fork lift truck driving licence - Capability more »