1 to 8 of 8 GMP Jobs in the North East

Proactively address stakeholder concerns, resolve conflicts, and facilitate effective communication channels throughout the project lifecycle. Quality Assurance and Compliance Ensure compliance with regulatory requirements, GMP, and other relevant standards within the pharmaceutical industry. Implement robust quality assurance processes to monitor and evaluate project deliverables, ensuring adherence to specified quality standards. 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 »

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 »

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 »

qualified), with practical QP experience in a UK pharmaceutical setting, certifying product to market Knowledge of relevant EU legislation, particularly around good manufacturing practice (GMP), with experience working in a fast-paced, high volume environment Certifying multiple dosage forms would be beneficial, but solid dose and steriles experience would be more »

Job summary Are you looking for a new challenge and passionate about developing pharmaceutical quality control services? We have an exciting and rare opportunity available for a registered scientist professional to join our team and specialise in this area. This 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 »