1 to 18 of 18 GMP Jobs in the East of England

QA role in Pharma R&D, Infrastructure and Validation team, you will perform the quality assurance activities and quality oversight of the Validation and GMP facilities management activities performed within Pharma R&D across the UK sites. In this role you will be key in the following areas… • Providing review 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 »

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 »

standards and key performance indicators. Support sensory activities: taste panels, sample preparation, sample collection, sample submissions, processing of results. Adhere to good manufacturing practices (GMP), good laboratory practices (GLP) and master cleaning schedules (MCS). Comply with Company, third party and Customer standards demonstrated by successful completion of Inter-lab more »

URS, DRR/VRA, IOQ, OCD, C&QR, RTM, and VR. Execution and approval of the corresponding protocols to release the required equipment for GMP production Weekly Validation Report Draft, execution, and approval CSV/CQV validation protocols Qualifications & Requirements: Applicants will have experience of general validation on multiple projects more »

defining system architect and high-level product specifications to create robust, scalable, and secure solutions with familiarity with OPC-UA, GAMP5, and software for GMP applications Have identified requirements and worked with connectivity to 3rd party systems, both local and cloud based, for manufacturing control systems. Utilised appropriate tools and more »

defining system architect and high-level product specifications to create robust, scalable, and secure solutions with familiarity with OPC-UA, GAMP5, and software for GMP applications Have identified requirements and worked with connectivity to 3rd party systems, both local and cloud based, for manufacturing control systems. Utilised appropriate tools and 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 »

least 3 years industrial experience and be able to work on a number of product development projects. Previous industrial experience within a regulated environment GMP environment, pharmaceuticals, food, electronics . Demonstrate project control, with evidence on how you achieved the business goal. Provide support to design operatives to aid in more »

work environment and that all tools are maintained and accounted for. Liaise with the SHEQ team to resolve H&S issues, environmental, internal audits, GMP, COSHH and ISO quality issues, and ensure all compliance checks are complete and correctly filled. Attend all nominated training modules as necessary. Undertaking any other more »

on a permanent basis. The Validation Manager will be leading the validation function to be able to execute report activities within the framework of GMP - Annex 11 & 15 in compliance with QMS requirements. In addition, they will be supporting multiple validation projects, liaising with the project departments and the associated more »

Manager in the Process Engineering department. You will ensure that operations are performed in accordance with the requirements of company standards, industry standards, and GMP/GDP guidelines. Whats on offer? Excellent Salary & Benefits: You will receive compelling salary DOE, along with an exceptional benefits package. Innovative Leadership in Automation more »

and improvement of the Quality Management System (QMS). Assure the compliance of all activities with Good Distribution Practice (GDP) and Good Manufacturing practice (GMP) requirements. Responding to medical information enquiries from healthcare professionals, community pharmacies, patients, and wholesalers. Ensuring the completion of checks for new products; having the appropriate more »

services and ensure that all products are appropriately, efficiently and cost effectively prepared within the unit, according to the Guide to Good Manufacturing Practice (GMP) and that pharmaceutical guidelines relevant to aseptic dispensing (production) and departmental procedures are followed To provide pharmaceutical advice to patients/carers/ward staff … training in Technical Services Registered with the GPhC or relevant professional body Up to date CPD portfolio Knowledge: Essential Understanding of the principles of GMP and QA in Aseptics/Production manufacturing environment Understanding of Pharmaceutical Quality Systems Knowledge of Audit and validation Computer and IT competent COSHH Regulations and … Cato aseptic workflow system Experience: Essential Post qualification experience (at least 2 of which have been in hospital preparative services)Working in a Pharmaceutical GMP manufacturing facility or in a manufacturing environment that employs a quality system (Previous Production/Aseptic experience). Demonstrate ability to deliver induction and competency more »

related to the instruments You will produce timely and detailed reports for equipment Follow the companys procedures and policies as well as ISO and GMP standards on customer sites You will work closely with the technical team such as Field Application Specialist, Technical Sales Specialist, Technical Support Engineer and Sales … in a regulated environment, however training will be provided You may have field service experience working in the pharmaceutical, biological, or chemical industry following GMP or ISO standards in a similar role though candidates from other industries will also be considered (manufacturing, electronics etc.) Ability to work autonomously and unsupervised 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 »

to manage/adjust timelines and priorities; escalate issues and concerns as they arise. Ensure all activities are delivered compliant to defined processes and GMP; concerns/risks are identified. Ensure appropriate and complete records arising through operational activities are maintained and TPCs in compliance with GMP and that meet … commitments meet agreed timelines and quality KPIs. Interim Packaging Project Coordinator - The Skills You'll Need to Succeed: Experience working in an R&D GMP environment. Experience working in an operational Packaging Labelling Distribution (PLD) role within Clinical Trial Supplies. Knowledge of Clinical Trial Supply CMOs and their capabilities Knowledge … of the pharmaceutical and clinical development processes and their relationship to the clinical supplies delivery processes; aware of clinical supply GMP requirements and standards. Lean Sigma training/experience Project Management training/experience Experience demonstrating organizational and planning skills coupled with strong written and oral communication skills Demonstrated capability more »

growing portfolio of its own products? Working on a SME facility, you will have the perfect opportunity to gain fantastic exposure in an industry GMP setting that will provide development and advancement opportunities. Whilst the duties may seem routine – testing pharmaceutical and personal care products using GC, HPLC and various … two hires will be made in this round of recruitment. Key experience: Previous QC or analytical chemistry experience essential Must have worked within a GMP or GLP setting An understanding of raw materials and finished product testing Experience in some of the following will be important – HPLC, GC, UV, FTIR … Ryan. Quality, control, qc, analytical, chemistry, HPLC, chromatography, GC, gas, high, performance, liquid, testing, product, raw, materials, pharmacopoeia, FTIR, UV, bench, laboratory, analyst, technician, GMP, GLP, manufacturing, pharmaceutical more »