1 to 13 of 13 GMP Jobs in Yorkshire

changes). This will require close collaboration with Product Development, Production and QA groups on NPIs using product lifecycle approach, preparation and approval of GMP documentations to support such projects, scheduling, raw material acquisition, supervising engineering batch manufacture, etc. Identifying potential process improvements for existing commercial products including proposals for 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 »

facilitate change. The ability to present information coherently, accurately and persuasively. PC literate Experience within food manufacturing, advanced Food Hygiene Certificate & good understanding of GMP/hygiene standards What you'll receive. As an equal opportunity employer, we're committed to providing a safe and rewarding environment for you to more »

Middlesbrough area. Salary and Benefits of QC Analyst Salary up to £27,000 Permanent Role Skills and Qualifications needed for QC Analyst Awareness of GMP/GLP Standards Pharmaceutical or Chemistry Degree 2 Years Experience in a relevant role Fine Chemistry/Pharmaceutical Experience 2 years of HPLC and GC more »

Middlesbrough area. Salary and Benefits of QC Analyst Salary up to £27,000 Permanent Role Skills and Qualifications needed for QC Analyst Awareness of GMP/GLP Standards Pharmaceutical or Chemistry Degree 2 Years Experience in a relevant role Fine Chemistry/Pharmaceutical Experience 2 years of HPLC and GC more »

background and ideally Team Leading people working on similar projects as listed below:- Skills and experience:- - Pensions Data Transfer - Client Onboarding - Implementation - System Configuration - GMP - BIBO - Buy in - Buy out - Pension projects Unique culture, fully diverse and inclusive, very supportive, with ability to grow and become senior manager. Responsibilities: Takes 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 »

and maintenance of the company's Quality Management System (QMS) in accordance with regulatory requirements. Assist in conducting internal audits to assess compliance with GMP/GDP standards and company policies. Participate in the review and approval of GMP documentation, including batch records, SOPs, and change controls. Assist in deviation … Bachelor's degree in Pharmacy, Chemistry, or related field. Some experience or internship in a pharmaceutical quality assurance role is preferred. Basic knowledge of GMP/GDP regulations and quality management systems. Strong analytical and problem-solving skills, with attention to detail. Effective communication and interpersonal skills. Ability to work more »

searching for a Lead Qualified Person (QP) to join a leading Pharmaceutical manufacturer in Northern England. As the Lead Qualified Person, you will ensure GMP compliance for the site and focus on the release of small molecule batches. Your responsibilities as the Qualified Person will be: The batch certification and … on manufacturing floor GEMBA walks. To provide support, guidance and advice on Quality matters to all departments within the company, contributing to the company GMP strategy. The successful candidate for the Qualified Person position will demonstrate the following: Extensive experience in Quality Assurance roles within the Pharmaceutical industry, with on … agile and flexible to enable them to adapt to situations when required. Quality Assurance | QA | QP | Qualified Person | Deviations | OOS | OOT | GEMBA | GMP | Good Manufacturing Practice | Orange Guide | Small molecule more »

instruments to identify profiles of 'unknown' organic compounds and mixtures, ensuring safe and compliant disposal. Follow approved methods and procedures in accordance with cGLP & GMP requirements. Ensure all Health, Safety, and Environmental standards are met, including workplace organization, work instructions, risk assessments, COSHH assessments, and housekeeping. Participate in method development … Analyst . Skills and Qualifications: Education: Degree in Chemistry. Experience: Minimum 2 years as a QC Analyst in the Fine Chemical or Pharmaceutical industry (GMP/GLP environment). Technical Skills: Proficiency in forensic investigation techniques such as HPLC, GC, GC-HS, LC-MS, GC-MS, FT-IR, XRF, RAMAN more »

and released in compliance with the relevant regulatory standards and our high-quality benchmarks. Key Responsibilities: Certify batches for release, ensuring compliance with EU GMP and relevant regulatory requirements. Conduct audits, both internally and externally, to ensure adherence to quality standards. Collaborate with various departments (eg, Manufacturing, Quality Control, Regulatory … Affairs) to ensure quality assurance throughout the product life cycle. Provide expert guidance on GMP and regulatory compliance issues. Lead and support continuous improvement initiatives in quality systems and processes. Handle deviations, investigations, and CAPAs effectively, ensuring root cause analysis and implementation of corrective actions. Requirements: A valid QP status more »

Desirable) Time served Engineer. NVQ Level 3 Qualification or above Electrical Bias The Role Carry out duties ensuring the site achieves and maintains required GMP standards. Ensure all work conforms to statutory & safety requirements. Ensure that risk assessments are completed and actioned. Carry out site maintenance activities and ensure GMP more »

addition, this role may develop into encompassing the following: Promoting HACCP principles throughout the Group; Carrying out Internal Audits including UKAS (ISO 17025) and GMP audits as required; Assisting with the development and understanding of Food Hygiene Standards and Practices and GMP throughout the Group. Assisting with the development and more »