Bishop's Stortford, England, United Kingdom Hybrid / WFH Options
HR GO Recruitment
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 »
organisational skills and ability to multitask. Keywords: Planner, service, equipment, coordinator, administrator, administration, planning, scheduler, CMMS, GMP. GLP, GXP, GDP, Good Laboratory Practice, GoodManufacturingPractice, Good Documentation Practices, Manchester, Northwest, Macclesfield. VRS8731MP. Follow VRS Recruitment on LinkedIn to view all our latest vacancies! Please note that by submitting your more »
of your role ensuring that all areas of the factory site are maintained to exceptional standards of hygiene process improvements, working to KPI's, GMP standards, food safety and health and safety standards. The overall focus of the role will be to manage and develop the hygiene standards, your team … food manufacturing sector although this is not essential A can-do attitude, able to communicate effectively at all levels A comprehensive understanding of modern GMP Experience operating to BRC standards The ability to multi task and balance multiple priorities Proficient in MS Office Knowledge of CIP systems Excellent Problem-solving more »
at a high level. What are we looking for? Essential Degree Qualified in an area related to an Engineering discipline. Experience gained within a GMP environment (or closely related regulatory environment) from an equipment, facilities, and engineering perspective. Demonstrated working knowledge of BMS, EMS & HVAC systems. Strong interpersonal and communication 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 »
naturally a flexible mindset is needed for this type of position. As such, I am interested in speaking with people from Production and QC GMP settings, as well as fresh graduates looking to get that key break. This team is very open to your background – it is all about your … experience would be advantageous but is not essential Experience and/or understanding of chromatography techniques including HPLC and GC. A solid understanding of GMP principles – or at least the ability to work to strict regulated procedures Flexible to work shifts Must have own transport to access the site due … to shift work QC, quality, control, analyst, analytical, laboratory, radiopharmaceutical, GMP, entry, graduate, science, pharmaceutical, biotechnology, manufacturing, shift more »
Loughborough, England, United Kingdom Hybrid / WFH Options
ECS Resource Group
pharmaceutical environment/Medical Device industry required Technical experience within the Manufacturing functions of a pharmaceutical company. Technical knowledge of Pharmaceutical Packaging. Vendor Audits (GMP, Technical and EHS) Knowledge in Supply Chain Risk management, GMP, Quality System requirements, the ‘Orange Guide’, equivalent FDA regulations and systems, procedures, products and organisation. more »
in Chemistry/Biochemistry/other related science or equivalent experience in a similar setup. - Competent analytical skills, attention to detail, and understanding of GMP requirements. - Ability to work independently and in a team, with strong computer literacy and communication skills. - 1 year of lab based experience is necessary. Are more »
products reach every corner of the globe with precision and efficiency. Be the guardian of quality, ensuring every launch meets the gold standard of GMP and GDP regulations. Tackle challenges head-on, turning obstacles into opportunities for innovation and growth. Keep stakeholders in the loop with your expert communication skills … Business, Life Sciences, Engineering). Strong experience in the pharmaceutical realm, where you've honed your project management skills. A deep-seated understanding of GMP and GDP guidelines. A proven track record of launching products would be advantageous. Great communication skills, coupled with the ability to navigate complex challenges with more »
in GCP Quality Assurance within the Pharmaceutical Industry. Strong knowledge of Quality Management Systems within the Pharmaceutical industry. Strong knowledge of ICH-GCP and GMP guidelines. Experience hosting, supporting and preparing MHRA inspections and auditing IT systems. Experience organising and performing internal and/or vendor audits. Experience working in more »
+ 8 Bank Holiday Cycle to Work Scheme Skills and Qualifications Required for Analyst BSc or higher in Chemistry or related field Experience within GMP environment Physical characterisation including; particle sizing (image and laser diffraction), specific surface area, XRD, thermal analysis, water content Chemical ID analysis including; UV-vis, FTIR 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 »
site and related functions are in compliance with GxP regulations and applicable quality guidelines, including, but not limited to UK/EU/US GMP/GDP, ICH and other region specific guidance. The individual will have ownership for key quality system elements and will support and execute site quality more »
team members on best practices and ensure compliance with regulatory standards. Conduct gap analysis, review change controls, and develop revalidation strategies as needed. Ensure GMP, Data Integrity, and GDP compliance, including timely training. Key Competencies: Proven track record in delivering regulatory-compliant validation strategies. Strong understanding of GxP compliance requirements. more »
global pharmaceutical company who require a QA Production Support Supervisor/RP to join their well-established Quality and Operations team, focusing on the GMP and GDP requirements. This role involves the supervision and mentoring of a team of very capable Quality Assurance Production Support Officers. Responsibilities: Qualified RP/… systems (including, but not limited to the complaints and batch release processes) Write, implement, review and maintain SOPs, policies and other documentation for QA GMP and GDP activities. Act as Quality GMP and GDP advisor on site projects such as new product introductions or CAPEX projects. Host training sessions on … GMP and GDP QA related topics. Requirements Extensive GMP Quality Assurance experience, preferably in production support Experience of line management and leadership Qualified RP/RPi SRG is UK’s number 1 recruitment company specialising in the science, engineering, clinical, pharmaceutical, food/FMCG, renewable, biotech, chemicals and medical devices more »
Responsibilities: - Perform environmental monitoring of the aseptic manufacturing facility and ensure all testing aligns with the Environmental Monitoring programme. - Maintain QC facilities to meet GMP requirements and conduct necessary checks to support health authority visits. - Operate and maintain laboratory equipment, ensuring all equipment is calibrated and suitable for use. Requirements … Microbiology or equivalent relevant work experience in a regulated industry (i.e. pharmaceuticals, biologics, or medical devices). - Proficiency in Microsoft Office and knowledge of GMP/GLP regulations, FDA regulations, etc. - Strong problem-solving skills, analytical abilities, and a keen eye for aseptic behaviour. If you are interested in learning more »
want you to join a leading food company dedicated to delivering excellence in every way! You will be responsible for delivering high levels of GMP, food safety and integrity standards. Responsibilities Include: • Supporting the overall technical strategy, tactics, policy & plans • Responsible for the company’s quality management system to ensure … Responsible for the internal audit programme of the business • Lead the site HACCP programme • Manage non-conformance investigation and resolution • Effective management of the GMP auditing system • To provide leadership to the technical team. Ensuring personal objectives are met. • To ensure a positive working environment • Working alongside all the other more »
proactive and timely manner which includes Quality Control testing and reporting of raw materials, in process, bulk drug substance, final products andstability products to GMP and in accordance with Annex 11 Computerised Systems and 21CFRpart11 Good Documentation Practices for Electronic Data. Perform stability study programme activities, storage of in process … timely manner of any failure of calibration Maintain Quality Control information systems Maintain a technical ability, knowledge and understanding of relevant regulatory requirements for GMP, safety and environmental policies required in order to perform role as QC Analyst Assist in investigation of quality incidents and other problem solving forums and … and conferences where appropriate Carry out general maintenance and house keeping of equipment and laboratories Essential Experience Experience within a QC laboratory working to GMP within a recognised quality system. Ability to organise work within a busy laboratory with experience of writing and working to SOP documentation. Knowledge of GMPmore »
naturally a flexible mindset is needed for this type of position. As such, I am interested in speaking with people from Production and QC GMP settings, as well as fresh graduates looking to get that key break. This team is very open to your background – it is all about your … experience would be advantageous but is not essential Experience and/or understanding of chromatography techniques including HPLC and GC. A solid understanding of GMP principles – or at least the ability to work to strict regulated procedures Flexible to work shifts Must have own transport to access the site due … to shift work QC, quality, control, analyst, analytical, laboratory, radiopharmaceutical, GMP, entry, graduate, science, pharmaceutical, biotechnology, manufacturing, shift 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 »
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 »
focus on compliance within a specific bakery, working with the teams to identify non-compliance and full engagement and support to ensure company processes. GMP and procedures are fully understood. Work with the bakeries to ensure compliance with relevant customer standards and codes of practice. Conduct physical factory audits (outside … safety and quality. Ensure that the Quality Management System internal audit schedule is completed, and all actions closed out in a timely manner. Ensure GMP & QA CCP audits are conducted to schedule and any non-conformances raised to bakery management. Verify that close out actions are robust and complete. Communicate more »
you a skilled technical assistant with a passion for food manufacturing? Do you have a keen eye for systems and specifications, and experience in GMP and supplier approval? If so, we have an exciting opportunity for you! About the Role: We are seeking a Technical Assistant for our esteemed client … maintaining high standards and ensuring compliance with industry regulations. Key Responsibilities: Manage and maintain technical systems and specifications. Ensure compliance with GoodManufacturing Practices (GMP). Conduct supplier approval processes and audits. Collaborate with various departments to ensure seamless production and quality control. Provide technical support and expertise where needed. … Requirements: Proven experience in a technical role within food manufacturing. Strong understanding of systems and specifications. Knowledge of GMP and experience in supplier approval processes. Excellent attention to detail and organizational skills. Must have an indefinite right to work in the UK. Why Join Us? Competitive salary up to more »
area highlighting any stock issues to the engineering team manager To maintain standards of hygiene and good housekeeping appropriate to a quality food manufacturer. GMP standard of workshops and engineers tool boxes is maintained at a high level Be the Engineering point of contact during & out of hours Respond to more »
