1 to 11 of 11 Permanent GMP Jobs in the South West

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 »

providing excellent service to clients and third parties with a desire to succeed at accomplishing challenging objectives. Desirable Criteria Knowledge of and experience with GMP Reconciliation/Equalisation calculations Practical knowledge of the Pension Protection Fund (PPF) The 3173 Culture Our primary aim is to provide interesting, worthwhile and healthy 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 »

a capable and robust/stable process. Adhere to Quality Management System (QMS) requirements in line with Corin’s ISO13485 QMS & Good Manufacturing Practice (GMP) FDA21 CFR Part 820. Support brainstorming and problem-solving as required activities for inspection processes and assist in resolving engineering/manufacturing problems, as well more »

factory. * Monitoring customers returns and give daily the report to finance team. * To ensure that all operatives and staff within the factory comply with GMP and hygiene procedures and to advise and give training when this is not the case. * To work effectively within the departmental rota, ensuring all aspects … company procedures and policies. * To monitoring, verify and report any issues daily on Day & Night Shifts check list Compliance Audit. * To carry out Internal GMP/Glass and Hard Plastic Audit within the factory. * Weekly monitoring of all PPE request orders. * To ensure that all operatives and staff within the … factory comply with GMP and hygiene procedures and to advise when this is not the case. * To actively partake in the resolution of quality related issues. * To support training all members of staff in food hygiene, health & safety, manual handling, fire safety, chemical safety, and allergen awareness training. * To assist 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 »

planning, resource and cost management and progress reporting. Your background - experience gained within the pharmaceutical industry - experience of ensuring compliance with all EHS and GMP requirements - experience of writing SOP's - formal engineering qualification - preparation of pre-qualification document for new and retrospective projects - flexibility to travel to alternative sites more »

processes Conduct investigations and root cause analysis for deviations and complaints Participate in continuous professional development to maintain a high level of competency Uphold GMP, COSHH, and health and safety regulations Contribute to ongoing improvement of the Quality Management SystemWho you are: Previous experience in a similar position A relevant … degree would be advantageous Possess at least 2 years of experience in a GMP or similarly regulated environment. Demonstrate a strong attention to detail and commitment to Quality Assurance principles Enjoy working collaboratively and possess excellent communication skills Be adaptable, self-motivated, and able to work effectively in a fast more »

QA Auditors in monitoring and evaluating product and processing systems. Duties To participate and direct QA team to observe and audit production processes and GMP ensuring products are made to specification and within customer codes of practice and Bakkavor standards, reporting findings to managers as appropriate To ensure products and … Line Manager, manage QA activities required to deliver improvement of Technical KPIs e.g. audit of non-conforming processes, complaint investigations, update of swab schedules, GMP audits, glass and plastic audits. Lead, motivate and inspire QA team to achieve personal development and continuous improvement To promote a quality culture and help 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 »

with our long standing client in Bristol at an exciting time in their business where they will be commissioning a new Good Manufacturing Practice (GMP) facility. This will be in a new building and be a blank canvas for the new Quality Assurance and Validation Engineer to work on! You … will be working with colleagues both internal and external on commissioning and qualification of this new GMP facility. This will include equipment IQ/OQ/PQ activities, as well as validation and qualification of the ISO 7 and ISO 8 cleanrooms. You will be responsible broadly for all systems … self motivated with a can-do approach. Your background: Bachelors Degree in science or engineering with experience in facilities and equipment validation. Experience of GMP manufacturing, facilities, equipment qualifications and process validations, including cleanrooms. Knowledge of cGMP manufacturing regulations for the MHRA, FDA and other countries as required. Experience in more »