76 to 100 of 123 Permanent GMP Jobs

systems for various manufacturing companies. Experienced Required: Proven experience with the design and development of control systems e.g. PLC, SCADA, DCS, MES, etc. Ideally person would be from a GMP environment (e.g. Pharma, Food, FMCG, Chem, etc.) Experienced with Siemens Products Carbon60, Lorien & SRG - The Impellam Group STEM Portfolio are acting as an Employment Business in relation to this vacancy. More ❯

time and to a high quality In addition, you’ll also: Have experience in Paid Search Hands on experience with Google Ads and Microsoft Ads Possess an understanding of GMP stack, in particular Search Ads 360 Strong Excel skills Experience with running Performance Max/Shopping campaigns for retail clients Paid Social experience is desirable but not a requirement Our More ❯

time and to a high quality In addition, you’ll also: Have experience in Paid Search Hands on experience with Google Ads and Microsoft Ads Possess an understanding of GMP stack, in particular Search Ads 360 Strong Excel skills Experience with running Performance Max/Shopping campaigns for retail clients Paid Social experience is desirable but not a requirement Our More ❯

an award-winning and growing business In addition, you'll also: Have experience in Paid Search Hands on experience with Google Ads and Microsoft Ads Possess an understanding of GMP stack, in particular Search Ads 360 Strong Excel skills Experience with running Performance Max/Shopping campaigns for retail clients Paid Social experience is desirable but not a requirement The More ❯

that the relevant documents have been completed, e.g., hold log, non-conformance log. Reporting any complex issues to QA Supervisor. Hygiene Audits, micro swabbing, and micro sampling product Formal GMP and Process Control document completion About the shift pattern: This Monday - Friday QA role is based in our technical department but working in all areas of the factory as required More ❯

toxicological assessment, extractable and leachable analysis, medical device manufacturing processes, and biocompatibility assessment methodology Basic knowledge of FDA and international medical device regulations/directives and working knowledge of GMP/ISO/GLP guidelines as applied to medical device testing and documentation. Have the ability to work with people and teams in a complex, changing environment and be able More ❯

and deliver administration projects without the need to divert resources from existing day-to-day operations, you will see yourself gain experience working on a variety of projects including GMP reconciliation and equalisation, benefit analysis and rectification work, new scheme implementations and scheme events; and support etc. With the ability to prioritise projects and scheme work to ensure delivery in More ❯

and deliver administration projects without the need to divert resources from existing day-to-day operations, you will see yourself gain experience working on a variety of projects including GMP reconciliation and equalisation, benefit analysis and rectification work, new scheme implementations and scheme events; and support etc. With the ability to prioritise projects and scheme work to ensure delivery in More ❯

and deliver administration projects without the need to divert resources from existing day-to-day operations, you will see yourself gain experience working on a variety of projects including GMP reconciliation and equalisation, benefit analysis and rectification work, new scheme implementations and scheme events; and support etc. With the ability to prioritise projects and scheme work to ensure delivery in More ❯

and deliver administration projects without the need to divert resources from existing day-to-day operations, you will see yourself gain experience working on a variety of projects including GMP reconciliation and equalisation, benefit analysis and rectification work, new scheme implementations and scheme events; and support etc. With the ability to prioritise projects and scheme work to ensure delivery in More ❯

and deliver administration projects without the need to divert resources from existing day-to-day operations, you will see yourself gain experience working on a variety of projects including GMP reconciliation and equalisation, benefit analysis and rectification work, new scheme implementations and scheme events; and support etc. With the ability to prioritise projects and scheme work to ensure delivery in More ❯

and deliver administration projects without the need to divert resources from existing day-to-day operations, you will see yourself gain experience working on a variety of projects including GMP reconciliation and equalisation, benefit analysis and rectification work, new scheme implementations and scheme events; and support etc. With the ability to prioritise projects and scheme work to ensure delivery in More ❯

Developing specifications and leading multidisciplinary teams to clearly communicate the requirements for the Store and capture client requirements. The industries we serve have growing requirements for regulatory quality control (GMP, Medical Devices, ISO etc). The System Engineering role provides opportunity to develop the fully documented lifecycle to support adherence to these standards. What You'll Be Doing Designs, defines More ❯

plans that can be presented clearly at every level WHAT WE ARE LOOKING FOR Have extensive, relevant programmatic experience (Google Ads (Display/Video), DSPs (e.g. Adform, Tradedesk, DV360), GMP and Analytics Have experience with, and gain a lot of energy from, guiding other people Have experience with the Dutch and/or Nordic publisher landscape Are analytical, flexible and More ❯

in process control skills, including some of the following: PLC (AB Rockwell, Siemens), SCADA systems (Rockwell Historian), CAD, Trend BMS/Set, Lighthouse EMS, JDEdwards. Experience: Good Manufacturing Practice (GMP) experience. Attributes: Proactive, methodical, and a strong problem solver. Why You Should Join Catalent: Competitive Salary - Reflecting your experience and skills. Bonus & Benefits - Includes an annual performance bonus, a pension More ❯

and delivers solutions for wide-ranging issues and a varied customer base. Project & Data Solutions delivers the right, cost-effective strategies and solutions for the following: Guaranteed Minimum Pension (GMP) projects Auditing data, benefits and calculations Bulk data rectification and benefit (re-)construction Data cleansing and improving electronic data Supervising the data workstreams for de-risking projects so data is More ❯

Protective Security Officer - Police Staff - Protective Security Unit - Counter Terrorism Policing NW Location: GMP Force Headquarters, Central Park Complex, Northampton Road, Manchester, M40 5BP Contract type: Full Time, Permanent Grade: G Information about the role: We are seeking a dedicated individual to support CTPNW in achieving its mission. The role involves working as part of the Protective Security Team responsible More ❯

these projects might include; IT infrastructure changes Business process enhancement Administration system software upgrades Web site (member self-service) development Communication exercises on changes to pension benefits/arrangements GMP equalisation Changes to internal control framework (including compliance with the new General Code) To effectively build strong relationships with the different teams and successfully complete any required projects, it is More ❯

Data Scientist - Police Staff - Data Science Unit - Counter Terrorism Policing NW Location: GMP Force Headquarters, Central Park Complex, Northampton Road, Manchester, M40 5BP Contract type: Full Time, Permanent Grade: H/J About the role: This role offers an exciting opportunity for the successful candidate to help shape a new department dedicated to delivering innovative services to the counter terrorism More ❯

and experience ideally across all digital media channels but in particular paid search. You will have excellent knowledge of bid management and core technology platforms such as Google Analytics, GMP Platform, SA360 for example. Data analysis and an understanding of the strategic application of digital marketing channels will be a strength. More ❯

topics. Key Experience & Skills Required: Proven success in building effective digital solutions within an agency environment. Ability to consider digital and data across the entire customer journey. Experience with GMP stack. Strong proficiency in Excel. Desired: Experience managing international clients. Understanding of ad tech platforms. Contract Type : Permanent Agency : Havas Media Group Our Commitment: Here at Havas, we pride ourselves More ❯

Set Proven leadership in digital performance, measurement and data strategy roles. Hands-on experience with MMM, incrementality testing and advanced attribution. Strong understanding of ad tech and martech ecosystems (GMP, GA4/BigQuery , Meta CAPI, server-side GTM etc.). Fluent in using data to tell compelling stories and influence both internal teams and C-suite clients. Success Indicators (First More ❯

Manager is responsible for the qualification, oversight, and auditing of third-party suppliers and vendors supporting GxP activities, including pharmaceutical manufacturing, distribution, and clinical operations. This includes providers across GMP, GDP, GCP, GLP, and GVP domains. The role ensures partners meet regulatory requirements and internal standards to support the safe and compliant delivery of key service lines, such as Expanded … Own and lead global compliance monitoring programs for all GxP third parties, ensuring timely qualification, requalification, or disqualification. Design and manage a global, risk-based GxP audit program covering GMP, GDP, GCP, GLP, and GVP audits, both remote and on-site. Oversee third-party audits, ensuring findings are risk assessed, reported, and closed with appropriate CAPAs; follow up on CAPA … party audits and qualifications, maintaining audit readiness. What You'll Need: Bachelor's or Master's degree in Life Sciences, Pharmacy, Chemistry, or a related field. Extensive knowledge of GMP, GDP, and GCP activities, including qualification, requalification, and auditing best practices. Formal lead auditor certification required (e.g., IRCA/CQI, ISO 9001 or equivalent). Minimum 6-7 years of More ❯

responsible for the validation and transfer of novel and established test methods for the analysis of gene therapy products and associated materials used for manufacturing the EU and FDA GMP requirements at both the Meiragtx UK and Ireland sites. The role involves life cycle management of assays, equipment and materials/products. Job Description MajorActivities • Lead the development and validation … qualification/validation projects and associated documentation in support of the analytical activities performed ensuring compliance requirements are maintained. • Ensure all methods are validated and performed in the QC GMP labs in compliance to regulatory standards and adheres to data integrity requirements. Support Validation of Methods for raw Materials testing & sampling booth activities. Responsible for the project management of test … method implementation to required timescales to ensure seamless launch of new products. Responsible for ensuring any external testing activities meet GMP requirements. Maintain the flow of information to key stakeholders, ensure appropriate communications are passed forward and information folders are maintained with most recent versions/communications Ensure the development and rollout of training on new technology/methodology introduced More ❯

. Manage contractors to ensure work is carried out safely, efficiently, to the highest quality standards with minimal disruption to the process. Support and expertise in the application of GMP and Sanitary design standards across the sites is provided, developing and sharing best practices across the MEU network Work with Cluster, Regional and global teams to align Capital plans across … . Manage contractors to ensure work is carried out safely, efficiently, to the highest quality standards with minimal disruption to the process. Support and expertise in the application of GMP and Sanitary design standards across the sites is provided, developing and sharing best practices across the MEU network Work with Cluster, Regional and global teams to align Capital plans across More ❯