51 to 75 of 146 GMP Jobs in England

policies. To be proactive in identifying and eliminating faulty processes by implementing long-term fixes. To uphold and exceed standards of product quality and GMP within their area that are appropriate to an industry-leading quality food manufacturer. To play an active role in the shift and be the go more »

level Project Engineer/Project Manager with experience in managing cross functional teams, delivering complex Manufacturing Facility and processing projects, in a highly automated GMP production environment Demonstrated capacity to effectively manage and execute projects from initiation to completion Equipment & Utility experience Understands project management process; programming, scope development, design more »

retrieve information from the Council’s various computer systems. Knowledge of current LGPS issues and legislation including but not limited to the McCloud judgement, GMP Rectification, reporting requirements and dispute resolution procedures Minorities, women, LGBTQ+ candidates, and individuals with disabilities are encouraged to apply. Interviews will commence next week, so more »

in a multi-talented and compliance orientated team. You have · A background in a scientific discipline (MSc is a plus) · Experience working within a GMP environment, preferably in a CDMO · Strong experience of QC environment and organisation · Experience of reagent preparations and material handling Touchlight Benefits Touchlight is a successful more »

background and come from a manufacturing of process background with strong leadership and management skills- in return you will work in a highly technical GMP environment where there will be huge amounts of personal development and career progression available. Skills required for the Senior Engineer: Multi-skilled Electrical qualification Previous more »

to our customers through timely response and effective communication. * Ensuring Engineering standards are maintained, compliant with all legal requirements and factory standards and procedures (GMP, HSE and Process, etc.) are adhered to. * Liaise with department streams through meetings, understanding issues and setting plans to resolve. * Drive PPM's completion to more »

and on into production phase 1 to 3 to ensure competent technology transfer of drug products Experience in completing manufacturing documentation in accordance with GMP Desirable Criteria (The following criteria may be applied if a large pool of applicants exist) Previous experience within a technical role in the pharmaceutical industry more »

fixed weekly rotation. Responsibilities: Perform routine quality control examinations. Conduct routine analysis of raw materials and products using various techniques. Ensure all work is GMP compliant. Use a variety of instrumental and wet chemistry techniques to ensure analysis is accurate. Ensure consistent production of high-quality self-care products. Key more »

probes, ph probes, etc.). Label verifications. Verify finished product labels and crate/case end labels to ensure correct Use By Dates. Complete GMP & Hygiene Audits. Completing of Daily/Monthly/Quarterly Glass & Hard Plastic Audits. Micro sampling to site schedule and manage an ongoing shelf-life library 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 »

corrective actions Collecting micro-samples as per schedule Traceability Investigations into complaints Daily auditing of CCPs Daily label checks Calibration Auditing of processing records GMP/fabric audits Temperature checks Quality checks The nature of this role requires a flexible approach to working hours. Core working hours are: Monday to more »

to respond to change environments and high growth, high pressure environments. Experience in managing stakeholders. Ability to track and report issues. Experience & understanding of GMP, FDA & TGA Quality requirements. Culture & Benefits We are fuelled by our commitment to sustainability, quality, efficiency, and an unwavering passion for our customers. Championing solutions 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 »

manner. • Ensure all technical systems and documentation is up to date and maintained. • Work closely with site QA team and where necessary do internal, GMP and Customer audits and visits. • Maintain up to date technical risk assessments. • Deputise and support others across the technical and quality function in all tasks more »

in using industry-standard software lifecycle management tools such as Jira, Confluence, and AHA! Previous exposure to applying industry compliance and quality standards (GLP, GMP, 21CFRPart11) in software products. Effective communication and stakeholder management skills to facilitate seamless collaboration and alignment across diverse stakeholders. If you possess a passion for more »

Search knowledge and experience with up-to-date certifications (Google and Microsoft ads). Understanding of bid management and core PPC platforms (Google Analytics, GMP platform, SA360 or Skai). Analytic mindset and an affinity for numbers. At least one year of PPC experience (ideally from an agency background). 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 »

background and ideally Team Leading people working on similar projects as listed below:- Skills and experience:- - Pensions Data Transfer - Client Onboarding - Implementation - System Configuration - GMP - BIBO - Buy in - Buy out - Pension projects Unique culture, fully diverse and inclusive, very supportive, with ability to grow and become senior manager. Responsibilities: Takes more »

the team's size and operational scope. Key qualifications: Extensive experience in Quality Assurance across diverse responsibilities Preferably, a background in pharmaceuticals, though other GMP environments will be considered Bachelor's degree or equivalent in a relevant technical field Strong proficiency across various quality functions such as batch review, investigations … into a senior leadership role within a fast-paced pharmaceutical environment, apply now to become part of a dedicated team. Keywords: Quality, QA, assurance, GMP, manufacturing, distribution, packaging, CDMO, pharmaceutical, batch release, systems, compliance, regulatory, specialist, investigations, CAPA, deviation, change control, operations, senior, leader, supervisor, manager, coach, mentor. 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 »

criteria outlined in personal specification Disposition, attitude and motivation Essential Demonstrates criteria outlined in personal specification KNOWLEDGE & EXPERIENCE Essential Interest in Science Understanding of GMP Understanding of environmental monitoring techniques Desirable Demonstrable experience in a medical or health related environment or clean room environment. Previous demonstrable aseptic experience Computer literate more »

and on occasions as required If you would like to discuss this further, please contact Mark Bux-Ryan for further information. QP, qualified, person, GMP, manufacturing, sterile, terminally, sterility, aseptic, quality, assurance, manager, leader, MHRA, audit, release more »

and on occasions as required If you would like to discuss this further, please contact Mark Bux-Ryan for further information. QP, qualified, person, GMP, manufacturing, sterile, terminally, sterility, aseptic, quality, assurance, manager, leader, MHRA, audit, release more »

and on occasions as required If you would like to discuss this further, please contact Mark Bux-Ryan for further information. QP, qualified, person, GMP, manufacturing, sterile, terminally, sterility, aseptic, quality, assurance, manager, leader, MHRA, audit, release more »

and provide corrective action Use root cause analysis to understand and deliver optimal cost maintenance Delivery of the required standards in relation to Engineering GMP and food safety standards Escalate potential consequences to line manager where work may impact on product quality or safety Key skills & experience: Strong engineering qualifications more »