17 GMP Jobs in the North West

Ensures that there are robust processes in place for the review and release product for GLP and GCP studies. Ensures appropriate quality oversight of GMP activities performed by the Product Development teams at Dechra or CDMOs and contract laboratories. This may include review and approval of protocols, reports, methods, master more »

providing direction and leadership to staff to ensure a quality mindset is embedded in the business Requirements: Expert in GCP with working knowledge of GMP 5 years experience in a QA Manager role within a CRO, Biotech or Pharma company Contract: Hours: 3 days a week - can worked across more »

have requirements: 2-5 years’ experience working with MES/EBR or similar systems in the life sciences industries. Experience deploying MES in a GMP environment, configuring Recipes, MBR’s, Materials, BOMs, Order Management, Equipment management, Batch Review/Approval and other typical components. A background in one or more more »

knowledge of material design such as solid state science, material science, structural informatics, data sciences, and work experience from a regulated environment (GLP/GMP). A habit of driving continuous improvement and Lean culture. Cultural awareness. Desirable requirements Scientific leadership skills, the ability to deliver robust scientific contributions to 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 »

archiving and ensure document control. Assist the team with technical issue resolution and continuous development of food safety & quality Complete site internal audits (CCP, GMP, Glass and plastic, hygiene etc) Collect and coordinate samples for routine micro/analytical analysis Actively reinforce the company's good manufacturing practices and hygiene more »

a relevant engineering discipline Pharmaceutical/BioPharma Projects experience Full lifecycle Project Management Cost Control Scheduling and achieving schedules Delivery of projects within a GMP environment Thorough understanding of engineering principles, concepts, industry practices and standards 16 hours (2/3 days onsite) Outside IR35 Till October more »

focus on DeltaV-controlled systems. Collaborate with engineering, operations, and quality assurance teams to define validation requirements, ensuring alignment with regulatory standards (e.g., FDA, GMP). Perform risk assessments and gap analyses to identify potential areas of concern in the validation process, proposing and implementing mitigation strategies as needed. Generate … DeltaV-controlled systems . Proficiency in validation principles and methodologies, with hands-on experience in executing validation protocols in a regulated environment (e.g., FDA, GMP). In-depth knowledge of DeltaV automation platform , including configuration, programming, and troubleshooting capabilities. Familiarity with regulatory requirements and standards governing automated process manufacturing, such more »

ABOUT YOU Are you a Quality professional with experience in a GMP laboratory, looking for a role that will challenge you, and help you develop new skills? You will possess rigorous attention to detail and be hungry for a challenge out of the lab. We need you to have: BSc …/MSc/PhD in Chemistry (or related scientific discipline) A sound working knowledge of relevant quality standards; GMP, GLP, GCP and other analytical related quality standards Good working knowledge of Quality Assurance in the Chemical and Pharmaceutical Industry Quality Assurance background which includes some specialist knowledge within a defined … Excellent attention to detail Impressive written and verbal communication ABOUT THE OPPORTUNITY You will provide general support to Quality Assurance activities relating to GLP, GMP, GCP, and other similar Quality Systems established to ensure that the appropriate standards and effective working systems and relationships are maintained and where necessary improved. 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 »

Clinical Supply Quality projects with expertise and delivery. This may include all Quality aspects of projects including IT projects. Support Clinical Supply functions in GMP inspections and input to GCP inspections where required Approve Clinical Supply GMP documentation Contribute to release and other routine activities required in the clinical supply … lean culture that promotes standardisation, simplification and continuous improvement Essential Requirements – Education and Experience Functional & Business Knowledge Extensive experience of working within a pharmaceutical GMP environment, preferably within a pharmaceutical development organisation Extensive experience from working in a Quality Assurance function is essential; A broad and comprehensive understanding of Quality … Systems and GMP A comprehensive understanding of the pharmaceutical/drug development process Good knowledge and reputation in the QA arena and specifically in GMP matters Understanding of Project Management and Supply Chain processes Skills and Capabilities Excellent team working, networking skills and encouragement of team efficiency Demonstrates independent judgement more »

a Quality Director to head up a Quality department. The Quality Director will promote and integrate quality into every aspect of the business ensuring GMP compliance and meeting the authority's expectation. The role holder will perform all duties required of a Quality Director, provide leadership to the Quality Teams … the business and provide support to sister company for regulatory inspections and conduct self-inspection program Oversee the Pharmaceutical Management System. Implement the current GMP regulations and industry best practices, where applicable Support and develop the QA team Support/lead manufacturing deviation or testing out-of-specification/out … of-trend investigations Audit the contract manufacturing organisation and laboratory against EU GMP and relevant regulations and guideline Qualifications and Skills: Qualified Person (QP) Knowledge and experience in manufacturing and testing of oral dosage forms and topical products Experience in releasing medicinal products in a fast-paced environment Experience in more »

company (part of a large Pharmaceutical group); is looking to strengthen their QA team and recruit a Snr QA Release Officer. This is a GMP focused position and this person will play a key part in the growth and development of the team. Duties will include releasing batches of manufactured … change controls, unplanned deviations). The Person: Will have a Degree in a relevant- Scientific discipline A minimum of 3+ years experience working to GMP in a Pharmaceutical setting Candidates with experience in Laboratory, Production or Pharmacy who are looking to move into a QA role full time are also more »

is ideal. 2. Proven industry experience in HPLC/LCMS as well as a background of maintenance and troubleshooting skills in a GLP/GMP environment. 3. Experience with other Analytical Instrumentation such as MALDI, Prep LC and SFC is beneficial but not essential. Key Words: Field Service Engineer | HPLC … LCMS | MALDI | Prep LC | SFC | Maintenance | GMP | GLP | Service Schedules | Installation | Validation | Instrumentation | IQOQ | SAP | Troubleshooting | Hyper Recruitment Solutions Ltd (HRS) is an Equal Opportunities employer who are certified by Investors in People for talent development. We therefore welcome applications for any interested parties who fulfil the role requirements for more »

through both written and verbal channels are essential aspects of the role. Your ability to thrive in both regulated and agile environments, such as GMP and ISO 17025, will be crucial for success. Hours of Work: 40 hrs. Monday – Friday 8-hour days. 30 min lunch break. Development Scientist Requirements … user of standard ‘office' applications Desirable: Experience of method development/validation in a regulated environment Understanding of regulatory requirements such as ICH guidelines, GMP etc Able to troubleshoot problematic separations Experience with statistics packages E&L knowledge Development Scientist Benefits: Salary £27,820 - £40,660 Broughton Day Option of more »

of QA activities for your assigned portfolio of projects. Your role will involve providing advice to support the development, implementation and continuous improvement of GMP quality systems across the development functions and support implementation of agreed global standards. You will interpret, trend and report compliance data, to measure and improve … Quality Assurance input to business improvement projects. Essential Skills/Experience: - Appropriate scientific degree with significant years of experience of working within a pharmaceutical GMP environment, preferably within a pharmaceutical development organisation - A broad understanding of Quality Systems and GMP is essential - An understanding of the pharmaceutical/drug development more »

Be part of our journey As a global leader in speciality chemicals, we continue to succeed and strengthen our delivery of innovative, sustainable and high-performance solutions. We are passionate and excited about how we can develop and utilise new more »