126 to 150 of 168 GMP Jobs

time-served Mechanical Engineer in a manufacturing/engineering . Experience ideally gained over a period of 3+ years in FMCG and/or GMP environment Health and Safety knowledge If this position sounds as if it could be of interest, then please apply here and Jamie Lunn from D more »

also oversee the work of junior QC staff, assist in managing the QC laboratory, and participate in assay transfer activities. This role requires maintaining GMP compliance in the QC laboratory. Key Responsibilities Establish, revise, and maintain procedures for QC testing. Maintain QC systems related to in-process, final drug product … and review of reports. Requirements A BA or BS in Chemistry/Biochemistry/Microbiology or other related science. Experience in a GLP/GMP environment. Computer literacy (including MS Word and Excel). Ability to work well with others. Effective communication skills. Good organizational skills. If you are having more »

Qualified Person (QP) Pharmaceuticals GMP NE England/London Our NE based pharmaceutical client is actively looking for a Qualified Person to join their successful operations. The successful candidate will be responsible for performing final and legal sign-off of batch records for imported and repackaged pharmaceutical products. This position … as a Qualified Person (articles 48-51, Directive 2001/83/EC , with previous operational QP experience. Additional responsibilities will include : Acting as GMP Subject Matter Expert for QMS site compliance Maintaining QMS systems, leading by example to implement and coordinate updates accordingly. Leading and coaching QA Team Ensuring … all activities are completed in line with GMP and GDP compliance and implementing CAPAs to manage and resolve any Quality issues Leading by example on all Compliance and Quality matters Completing both internal and external audits Communicating with onsite and offsite technical staff and liaising with customers and contract QPs more »

in industry? Or do you already have a background in an industrial chemistry lab but would like to develop your skills further in a GMP environment? SRG Synergy are currently working with a world-leading pharmaceutical organisation located in Ware with a vacancy for a QC Analyst – Level 1 Synergy … instruments, software packages and other analytical techniques (E.g. Empower 3). Is proficient in problem solving and may have expertise in troubleshooting analytical equipment. GMP experience would be desirable. more »

its capabilities. This will include ensuring activities associated with manufacturing and lab equipment, facilities, utilities, laboratory, and computer systems are completed, in accordance with GMP requirements Responsibilities : Manage a team and ensure validation master plans (VMPs), protocols and procedures are established To prepare and maintain validation plans (VPs) and identifying … protocols for equipment, facilities and utilities Your Background: Degree (or equivalent) in a Science or related discipline Qualifications related to validation and quality compliance (GMP/ICH/FDA/USP/EP policies). Experience of validating manufacturing/laboratory equipment, facilities/utilities and processes, including the generation more »

and relevant experience within a food/drink or pharmaceutical industry, including experience working within a quality function. A thorough knowledge of FDA, MHRA, GMP requirements, auditing and legislation is desirable. Other essential behaviours are the ability to work independently, good communication, facilitation skills and attention to detail. This is more »

Lab Analyst/Senior Lab Analyst Serving Society through Science, Tata Chemicals Europe (TCE) is one of Europes leading producers of sodium carbonate, salt and sodium bicarbonate and other products, from our plants in Cheshire, UK. British Salt has been more »

Global Category Specialist for Cleanroom and EI&C (w/m/d) - GMP/cold room/management/SAP/English,German, French Project : For our customer a big pharmaceutical company in Visp we are looking for a highly qualified Global Category Specialist for Cleanroom and EI&C. … semiconductors for clean rooms) * At least 2 years' experience doing tendering of complex and large E&IC, clean room or cold room packages in GMP environment for the relevant industry * At least 7 years of experience in plant construction as well as in the areas of purchasing, sales, contract management more »

Technical QA Manager (m/f/d) - Quality Management/Qualification/Validation/CSV of Small Molecules/Data Integrity/GMP/IMP/English & German Project : For our customer a big pharmaceutical company in Basel we are looking for a highly qualified Technical QA Manager (m … Operations is the Quality partner for all Manufacturing Units and Clinical Packaging in Pharmaceutical Technical Development in Switzerland and responsible for the Quality and GMP-compliance oversight of all Investigational Medicinal Products (IMPs) manufactured and packed for clinical studies in Switzerland. The candidate supports the end to end cGMP activities … in Qualification/Validation and CSV of Small Molecules, Analytics and/or Biologics. Tasks & Responsibilities: * QA supervision of qualification- and validation-activities for GMP-relevant equipment (including CSV), Analytics, infrastructure, critical utilities (WFI, PW, Gas) and processes within TR&D in Basel * Support of implementation of DI requirements * Review more »

of the highest standard. Main duties of the job To be responsible for supporting the delivery of the PMU Clinical Trials service within the GMP and GCP legislative framework. To provide expert input into all aspects of the Clinical Trial process from liaising with Sponsors, set up and manufacture of … of Clinical Trial medicines to ensure a safe and efficient service. To ensure that all IMP activities undertaken within the Production Unit comply with GMP/GDP/GCP, Health and Safety and COSHH legislation and that all work documentation and procedure manuals meet these regulations. To support senior staff … in the tasks they undertake. Clinical trials To lead on the set-up and implementation of Clinical Trials requiring preparation or manufacture to ensure GMP, GCP, full protocol, CTA, and IMPD compliance. To generate quality technical agreements, commercial and supply agreements in response to acceptance of a clinical trial, liaising more »

you will be responsible for testing and reporting laboratory activities to enable compliant, on time delivery of products to the customer whilst adhering to GMP standards. Your contribution will be the regular completion of on the bench testing of Asthma Inhalers (MDIs). You will be part of a quality more »

Ensures that there are robust processes in place for the review and release product for GLP and GCP studies. Ensures appropriate quality oversight of GMP activities performed by the Product Development teams at Dechra or CDMOs and contract laboratories. This may include review and approval of protocols, reports, methods, master more »

be key. You will be energetic, punctual, proactive, and reliable with the ability to lead, guide, and motivate others towards achievement whilst maintaining good GMP Standards. What you can expect from us: When joining us you can expect a highly competitive rewards package including group pension and other flexible benefits 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 »

of working within a Quality Assurance Officer role within a fast-paced environment. You should have at least 2 years' experience of working under GMP or have a degree within a science discipline. Knowledge and understanding of GMP with excellent communication and organisation skills are essential for this role. To … Society, Royal Society of Chemistry or Institute of Biology, GPhC, Science Council. Your duties & responsibilities The final review of pre-manufacture batch documentation, following GMP guidelines. The Approval for Use (final release) of all products manufactured or repackaged according to licensing requirements, GMP and professional discretion Being the primary point … attend any suitable training and update courses as deemed necessary and ensure a high level of competency is achieved. Ensuring that staff comply with GMP, COSHH and Health and Safety regulations and departmental SOP's. Participating in any rota system that may operate within the product release team in order 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 »

to detail and flexibility. Strong communication skills. Ability to handle stressful situations and controversial issues. Willingness to learn and develop new skills. Knowledge of GMP, GDPR, LSAS, and ethical trade issues. Key Tasks: Prepare and submit regulatory documentation for market registration. Support root cause identification and solution resolution. Conduct and more »

Creating & managing spreadsheets Answering and receiving phone calls Organising logistics, transportation, parcels & pallets Additional opportunity to learn Laboratory & manufacturing methods Be additionally trained in GMP standards Training Level 3 Apprenticeship in Business Administration consisting of: Level 3 Apprenticeship in Business Administration Level 2 Functional Skills in mathematics (if applicable) Level more »

addition, this role may develop into encompassing the following: Promoting HACCP principles throughout the Group; Carrying out Internal Audits including UKAS (ISO 17025) and GMP audits as required; Assisting with the development and understanding of Food Hygiene Standards and Practices and GMP throughout the Group. Assisting with the development and more »

aseptic and non-sterile products for Portsmouth Hospitals University NHS Trust (PHU), and its external customers. You will be working in accordance with Good Manufacturing Practice in order to maintain the standards required by the Medicines and Healthcare products Regulatory Agency (MHRA), and keep the department's manufacturing licence and … local work instructions Proactive attitude to ongoing training and assessment Desirable Previous experience working with aseptics/pharmaceuticals Knowledge of principles of GMP (good manufacturing practice) and Quality Management Systems Good understanding of principles of aseptic manufacturing Customer care skills Additional criteria Essential Punctual and reliable Self-motivated Desirable Willingness more »

within the Centre for Cell, Gene & Tissue Therapeutics. The post holder will be responsible for establishing a process development team that will support a GMP-compliant lentiviral manufacturing process. They will design and implement novel intermediate scale lentiviral manufacturing techniques in suspension cell bioreactors. The post holder will also develop … new downstream purificiation and packaging systems for the delivery of GMP-compliant lentiviral vectors to the cell manufacturing teams in the CCGTT. The post requires exceptional attention to detail and the ability to work in a systematic manner whilst keeping detailed records and managing junior staff. Main duties of the more »

be considered, to be clear we are looking for someone who has commercial lab experience working to QMS like UKAS 17025 or GLP/GMP/BRC) or GC/MS experience Strong interpersonal, organisation skills Able to work towards deadlines Good IT skills Important Information: We endeavour to process more »

which will include some weekend working as set by the rota. Day to day duties will be: To audit compliance against Quality Management Systems, GMP and HACCP controls, raising all non-conformances against relevant standards with objective evidence. Effectively communicating to enable the operational teams to take the appropriate and more »

service, we will do our best to make it work for you. Person Specification KNOWLEDGE Essential Up to date knowledge and understanding of GCP,GMP and its application Evidence of preparing worksheets/procedures Knowledge and understanding of the Law and Ethics relating to the dispensing of medicines. Working knowledge more »

Desirable JAC computer system knowledge Qualifications Essential GCSE grade 4-9 Math and English or equivalent Desirable NVQ2 in Pharmacy Services or evidence meeting GMP standards Other Essential Upholds and models Trust Values Desirable Willing to be flexible to service needs Disclosure and Barring Service Check This post is subject more »