111 GMP Jobs in England

if required), considering safety, quality, integrity and legality. Ensure all procedures/process deviations are analysed and actioned in a safe & legal manner. Hygiene & GMP: Ensure that the company has up to date, consistent and appropriate cleaning and GMP procedures that meet the requirements of BRC/Customers. Ensure that more »

safety guidelines and protocols. Continuous Improvement: Driving factory process improvements through techniques like root cause analysis and downtime analysis. Contributing to plant housekeeping and GMP audits and managing logistics team standard tasks. Measures of Success: Clear logistics strategy and plans. Adherence to logistics budget. Decrease in logistic complaints. On-time 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 »

PhD or relevant degree in any chemistry or life science related subject. The ideal candidate will have previous experience of working to GLP/GMP Must be IT literate with competent use of the Microsoft systems. The ideal candidate will have previous experience of using LC-MS/MS. Previous 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 »

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 »

out by all departments. ·Conduct shelf-life trials and record results accurately. ·To ensure equipment is calibrated and checked as per schedule. ·To complete GMP, glass and internal audits as required. ·To work closely with the intake team on raw material, packaging and label receipt and ensure any non-conformances more »

most understandable to technology professionals. Key Responsibilities: To maintain consistent and documented compliance with all relevant Safety, Health and Environmental (SHE), Good Manufacturing Practice (GMP), Data Integrity (DI), quality and best practice requirements. To be responsible for the product planning and execution throughout the product lifecycle in line with PMO more »

skills in previous positions. Worked as an engineer or come from an analytical background carrying out on site support. Experience working in GLP/GMP environment. Be prepared to travel and stay away as required. Package: Salary up to £43,000 D.O.E Bonus Scheme (£6.5k) Company Car + Expenses Covered more »

promoted internally. We need someone who has experience working in a Pharma/life science environment who has good knowledge of working in a GMP/GxP environment. This is a strategic role and requires someone who has previous regional experience with some auditing experience. The role is based from more »

developing products used in hazardous environments (i.e. ATEX, nuclear or chemical industries) is preferred but not essential, as would experience of Good Manufacturing Practices (GMP) for the pharmaceutical industry, although neither are essential. Hybrid and flexible working can be discussed. More information available upon application. When applying for this role more »