1 to 25 of 35 GMP Jobs in the North of England

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 »

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 »

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 »

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 »

values, promoting an ethical, positive company culture 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 Preparation and approval of validation documentation or management of the process (fulfilling the Quality Assurance role) in 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 »

focus: Actively participate in the implementation of site quality improvement projects, where necessary providing support to train operation teams and monitor project effectiveness. Complete GMP and Hygiene audits to required schedules. Assist in the investigation of consumer complaints and non-confirming items determining root cause and corrective action necessary to more »

in place to meet legal and statutory requirements. Keep records and provide reports in accordance with good engineering practices to external audit standards. Upholding GMP engineering standards across site, statutory inspections are compliant, and any non-conformances are closed out with root cause analysis to avoid repeat failure. Lead the more »

and supply chain as well as external partners like CDMOs to achieve objectives and ensure adequate product availability for launch. Ensure compliance with regulatory & GMP/GDP requirements for generic & specialty drug launches in relevant markets. Establish key performance indicators (KPIs) to track launch performance and evaluate post launch success 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 »

positions involve shift work, including nights, so flexibility is key. We welcome candidates from diverse backgrounds, whether you have experience in production and QC GMP settings or you're a fresh analytical graduate eager to kick-start your career. Key requirements: A degree in a Life Sciences discipline or equivalent … Previous QC chemistry or production experience is advantageous but not essential Familiarity with chromatography techniques such as HPLC and GC Understanding of GMP principles or willingness to adhere to regulated procedures Flexibility to work shifts If you're ready to join a supportive team and make your mark in the … pharmaceutical industry, apply below or contact Jolie Trahar for more information. Keywords: QC, quality control, analyst, analytical, laboratory, radiopharmaceutical, GMP, entry level, graduate, science, pharmaceutical, biotechnology, manufacturing, shift work. 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 »

has taken strides towards strengthening future project pipeline and therefore this position has a great prospect. Key experience: · Strong pharmaceutical validation experience in a GMP setting · Hands on experience in equipment and cleaning validations – CSV experience would be advantageous but knowledge of this area could also work · Experienced in direct … medium sized manufacturing unit Keywords: Validation, IQ, OQ, PQ, DQ, installation, commissioning, equipment, cleaning, engineer, specialist, lead, supervisor, csv, computer, systems, quality, assurance, manufacturing, GMP, protocol, master, plan 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 »

skills Qualifications Maths, English and Science GCSE or equivalent, grade A* - C (9 - 4) (Desired) About the Employer Cormica Cormica Bradford Ltd is a GMP/GLP accredited specialist contract research laboratory (CRO), with over 25 years’ experience in delivering high quality analytical and laboratory support to the pharmaceutical, medical more »

Governance Team, you will contribute to the provision, continuous improvement, and delivery of a World Class service to the site, ensuring statutory, regulatory and GMP Compliance requirements are met. Accountabilities: As an Accountable Engineer, you will establish collaborative ways of working to build and manage strong internal customer & supplier relationships. 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 »

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 »

be accountable for all commercial elements of the Small Molecule and Protein Delivery strategy comprising of M&A, licensing, innovation product promotion and wider GMP manufacturing strategy to deliver double digit organic and inorganic growth in line with business expectations. Who we're looking for: Degree qualified (ideally MBA) with 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 »

the company’s procedures relating to your area of work Deliver a right first time quality product Embrace the company initiatives (Right First Time, GMP) Ensure break-downs and requests for engineering assistance are addressed within a timely manner Ensure work is managed in a professional manner and relevant parties 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 »

with all company policies and procedures. Employee works in accordance with the installed ISO 9001 quality system and, if applicable, works in accordance with GMP-API. Your Profile BSc with previous working experience in a peptide lab is essential, MSc preferred Previous experience in a similar role would be desirable more »