1 to 25 of 35 GLP Jobs

Bux-Ryan for further information quality, assurance, QA, QC, control, analytical, chromatography, HPLC, laboratory, documentation, analyst, officer, specialist, executive, administrator, good, manufacturing, practice, GMP, GLP, audit, SOP, training, complaints, batch, review, release, CAPA, deviation, change, control more »

Educated to degree level or above in life sciences, chemistry or a related file with experience of working in a regulated laboratory environment (e.g. GLP or GMP) • Experience in using and troubleshooting ELISA analytical systems as well as the ability to develop and validate analytical methods using ELISA. • The ability more »

molecule bioanalytical studies. 3. A working knowledge and practical experience using LC-MS/MS. Key Words: Small Molecule | Study Manager | Team Lead | Bioanalysis | GLP | GCP | Method Development | Validation | Sample Analysis | Regulatory Compliance | LC-MS/MS Hyper Recruitment Solutions Ltd (HRS) is an Equal Opportunities employer who are certified more »

The Quality Control Supervisor is responsible for ensuring adherence to Good Manufacturing Practices (GMP) in all the manufacturing work cells and Good Laboratory Practices (GLP) in all the manufacturing and Quality Control laboratories. It will include applying tactical skills in a collaborative environment with cross-functional departments. A successful candidate more »

is a critical part of an innovative team that supports the company's drug discovery/development effort. Conceptualizes, develops, revises, and finalizes toxicology (GLP and non-GLP) study designs and reports; drafts nonclinical sections for IND/CTA and NDA/BLA submissions and other regulatory documents (e.g., IB … DSUR, PSUR, etc.) to ensure regulatory compliance. Manages and monitors nonclinical studies (GLP and non-GLP) at external CROs per Jazz standards and ensures that global regulatory/compliance requirements are met/exceeded. Critically reviews and edits CRO nonclinical toxicology study reports, analyzes and interprets data, defines PK/… to synthesize and communicate complex information. Capacity to propose practical mitigation (de-risking) strategies. Strong knowledge of FDA, EMA, and ICH guidance documents and GLP regulations. Required experience in authoring non-clinical elements of major regulatory submissions (INDs, CTAs, BLA/NDAs or sNDAs) and other regulatory documents (e.g., IB more »

The Quality Control Supervisor is responsible for ensuring adherence to Good Manufacturing Practices (GMP) in all the manufacturing work cells and Good Laboratory Practices (GLP) in all the manufacturing and Quality Control laboratories. It will include applying tactical skills in a collaborative environment with cross-functional departments. A successful candidate more »

delivery. Good 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 more »

within Immunoassay. You will build close relationships with a number of our customers and be responsible for delivering high quality results in compliance with GLP/GCP. Key responsibilities include: Line management of Senior Scientists and Scientists within your team Overall financial responsibility for the revenues generated within your team more »

their team. If you have a proven track record of implementing quality management systems, alongside an extensive background operating within the QA GC/GLP environment, I’d love to hear from you. This opportunity will offer you: ability to work within an extremely cutting edge area of the life … regulatory inspections within the GCP remit. You will bring the following: extensive number of years working at a senior manage level within GCP/GLP function. track record of establishing and harmonising QMS. leading regulatory inspections. If this role is for you or someone that you know then then please more »

office. Effective time management, and prioritization skills Ideally knowledge of one or more of Python, Webservices, Statistics, Scientific Software (bioinformatics, cheminformatics etc) Experience with GLP, GMP etc requirements a plus Ideally a second language (German, French, Japanese, Korean) Benefits And Other Perks • Quarterly team commission plan • Competitive medical, dental, vision more »

and execution of audits, including those conducted internally, at vendor sites, clinical sites, external laboratories, and suppliers. Providing guidance on GCP/GCLP/GLP practices to clinical project teams and identifying/mitigating operational risks and deviations. Overseeing Change Controls, Deviations, and Corrective and Preventive Actions (CAPAs) related to more »

hosting GCP Inspections Experience in IT Systems validation desirable Experience in implementation of general data protection regulations desirable Operational knowledge of GMP, knowledge of GLP and GCLP desirable Northreach is an equal-opportunity employer and we do not discriminate against any employee or applicant for employment based on race, colour more »

responsibility Experience with data privacy regulations preferred Experience with Medicines & Healthcare products Regulatory Agency (MHRA), Food & Drug Administration (FDA); knowledge of Good Laboratory Practice (GLP) and Good Clinical Practice (GCP) strongly preferred. RESPONSIBILITIES: Leadership. Strategic partnership with Global Quality Assurance team and Global Leadership Team Regional oversight of Quality Assurance … of a working knowledge of industry and regulatory standards and requirements Provision of guidance and leadership on Good Clinical Practice (GCP), Good Laboratory Practice (GLP), MHRA, FDA, data privacy, and other relevant regulatory standards Responsive escalation point for Clinical Trials quality issues and concerns Process Improvement. Development and execution of more »

teams and eQMS users Plan and conduct of audits, including internal, vendors, clinical sites, and external laboratories Provide guidance on GCP/GCLP/GLP to clinical project teams You will bring the following: Previous experience in GCP QA role, as well as working in Clinical laboratories Experience in Biologics more »

today to be considered Keywords: analyst, analytical scientist, senior scientist, analytical chemistry, pharmaceutical, pharmacy, pharmaceutical chemistry, biopharmaceutical, , GMP, cGMP, Good Manufacturing Practice, GLP, Good Laboratory Practice, GxP, HPLC, UPLC, Gas chromatography, GC, high performance liquid chromatography, NMR, liquid-state, Nuclear Magnetic Resonance Spectroscopy, method development, validation, North West, Manchester, Liverpool more »

pivotal role in fostering a culture of audit readiness within the Quality team. Responsible for overseeing Good Clinical Practice (GCP) and Good Laboratory Practice (GLP) activities within the BioA department, this specialist is dedicated to developing, implementing, and continuously improving the site's Audit program. Interfacing with business and functional … management. Act as Deputy Archivist, responsible for maintaining the archive and its contents in compliance with relevant regulations. Introduce systems to comply with revised GLP, GCP, EMA, FDA, and OECD guidelines or regulations. Provide support/host customer-initiated audits, mock regulatory inspections, and regulatory facility inspections. Participate in the … internal, 3rd party, and vendor audits. Process Improvement Responsibilities: Lead the development, improvement, implementation, and maintenance of new/modified quality systems to ensure GLP and GCP compliance. Recommend systems for audit, write audit plans, and coordinate scheduling and closure of internal audits. Training and Mentoring: Provide training and mentoring more »

Experience in aseptic technique and controlled environments with prevention of cross-contamination. Experience working within a Good Manufacturing Practice ( cGMP ) or Good Laboratory Practice ( GLP ) environment is highly advantageous but not essential. Strong interpersonal and communication skills. Touchlight Benefits Touchlight is a successful scale-up business with a record of more »

physical test methods within a laboratory such as tensile and absorption testing. Writing up of completed testing in a laboratory bench book complying with GLP and GDP. Logging in of test samples. Preparing testing plans and data template ready for testing. Working within a controlled ISO13485 and ISO9001 Laboratory quality … system and in accordance with GLP/GMP procedures. Design, plan and execute Physical testing in support of R&D activities and base business projects in accordance with applicable and procedures and guidelines. Involvement in the development and validation of new physical testing methods. Requirements: Bachelor's Degree in a more »

equivalent relevant work experience in a regulated industry (i.e. pharmaceuticals, biologics, or medical devices). - Proficiency in Microsoft Office and knowledge of GMP/GLP regulations, FDA regulations, etc. - Strong problem-solving skills, analytical abilities, and a keen eye for aseptic behaviour. If you are interested in learning more or more »

Change Control and Risk Management processes. Knowledge and experience of EXCiPACT and/or ISO 9001 requirements is highly advantageous. ISO/GMP/GLP/COSHH/H&S awareness This is a hybrid opportunity with the added benefit of a flexi-time scheme. more »

Proficient in using industry-standard software lifecycle management tools such as Jira, Confluence, and AHA! Previous exposure to applying industry compliance and quality standards (GLP, GMP, 21CFRPart11) in software products. Effective communication and stakeholder management skills to facilitate seamless collaboration and alignment across diverse stakeholders. If you possess a passion more »

The Quality Control Supervisor is responsible for ensuring adherence to Good Manufacturing Practices (GMP) in all the manufacturing work cells and Good Laboratory Practices (GLP) in all the manufacturing and Quality Control laboratories. It will include applying tactical skills in a collaborative environment with cross-functional departments. A successful candidate more »

The Quality Control Supervisor is responsible for ensuring adherence to Good Manufacturing Practices (GMP) in all the manufacturing work cells and Good Laboratory Practices (GLP) in all the manufacturing and Quality Control laboratories. It will include applying tactical skills in a collaborative environment with cross-functional departments. A successful candidate more »

The Quality Control Supervisor is responsible for ensuring adherence to Good Manufacturing Practices (GMP) in all the manufacturing work cells and Good Laboratory Practices (GLP) in all the manufacturing and Quality Control laboratories. It will include applying tactical skills in a collaborative environment with cross-functional departments. A successful candidate more »

The Quality Control Supervisor is responsible for ensuring adherence to Good Manufacturing Practices (GMP) in all the manufacturing work cells and Good Laboratory Practices (GLP) in all the manufacturing and Quality Control laboratories. It will include applying tactical skills in a collaborative environment with cross-functional departments. A successful candidate more »