1 to 25 of 39 GMP Jobs in the North of England

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 »

Team Leader, you will be responsible for up-keep and compliance of the QMS, overseeing internal company processes to ensure the business is always GMP and GDP complaint and lead a team of 3 QA Officers working directly with the Head Of Quality. Responsibilities for the Quality Assurance Team Leader 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 developing injectable dosage forms for preclinical & clinical use, this will include formulation development and product characterisation Appreciation of the regulatory environment, ideally GMP/GLP You will be able to coordinate multiple projects simultaneously You will be an effective team player and have strong interpersonal skills to enable 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 »

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 »

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 »

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 »

Durham area. Salary and Benefits of QC Analyst Salary up to £28,000 Permanent Role Skills and Qualifications needed for QC Analyst Awareness of GMP Standards Chemistry Degree 2 Years Experience in a relevant role Fine Chemistry/Pharmaceutical Experience HPLC and GC Experience Responsibilities of the QC Analyst The more »

and GC is desirable For more information please call Chris on 0161 526 1898. Keywords: quality control, laboratory, lab, pharmaceutical, QC, analytical, sample, chemical, GMP, science, QC inspection, testing, materials, ingredients, analysis, GC, wet chemistry, titrate, titration, HPLC, raw materials, intermediates, in-process, finished products. 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 »

all levels - work under own initiative 2+ Years QA experience within Food Manufacturing, ideally with both private label and branded product experience. Proficient in GMP and Quality Standards. Level 3 HACCP Level 3 Food Safety Auditor qualification Recognised allergen qualification Recognised microbiology qualification Working hours: 18:00/ 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 »

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 »

good stead: Experience with HPLC testing (desirable) Experience within a manufacturing environment (ideally within pharmaceutical, food, chemical etc) Understanding of data integrity (ALCOA principles GMP) Strong attention to detail Ambition and drive, not afraid to challenge the status quo 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 »

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 »

at our Manchester HQ located at Manchester Science Park. The Validation Scientist will be responsible for SOP writing and validation under ISO 13485/GMP environment and to drive validation of new processes and improvements in our manufacturing and operations teams. Key areas of responsibility: Validation of changes to Manufacturing … equivalency testing on hardware and software Health & Safety Improvements Qualifications, Skills and Abilities HND/Degree in an appropriate Biological Science. QC experience in GMP/ISO13485 laboratory environment. Experience of the use of ABI thermal cyclers and genetic analysers. Good analytical approach to investigating operations & product quality issues. Experience 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 »

s products. Provide US and European regulatory intelligence, train Subject Matter Experts and provide internal consultancy for quality compliance implementation and FDA/EU GMP/GDP remediation projects in the Dechra Internal Manufacturing network. Frequent global travel is required with this role, and you will need to travel to … manufacturing network (as required) across the product's registered lifecycle in compliance with all applicable ISO, ICH, FDA, EU, and national regulatory requirements for GMP/GDP. Lead GMP/GDP audits for Dechra DPMS based on specific expertise, criticality, and complexity. Periodically assess the liability, regulatory and/or … networks are all being adequately monitored. Recruit, lead, train and develop, as required, the team of quality and compliance experts (specialised in auditing different GMP/GDP areas) across the business, to keep the business abreast of ongoing developments through benchmarking activities, whilst proactively identifying and addressing any gaps relating more »

most understandable to technology professionals. Key Responsibilities: 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. To be responsible for the product planning and execution throughout the product lifecycle in line with PMO 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 »

Assist in coaching and developing other members of the team Main Tasks and Responsibilities n Follows approved methods and procedures in accordance with cGLP & GMP requirements. n Plan and prioritises own work with guidance from QC Senior Analyst/QC Manager n Report analytical results accurately and in a timely … Environmental requirements are met including (but not limited to) workplace organisation, work instructions, risk assessments, COSHH assessments, housekeeping standards in accordance with GLP and GMP n Demonstrable evidence of understanding the importance creating a safe environment n Working in a safe manner n Follow appropriate and relevant practices and procedures … subject) degree with experience as an analyst in a fine chemical or pharmaceutical industry role. HPLC and GC experience Experience of working in a GMP environment/method development experience/cleaning validation experience Key Skills Attention to detail Ability to Plan and organize workload Ability to think creatively and 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 »