1 to 25 of 32 GLP Jobs

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 »

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 »

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 »

experience will be considered, to be clear we are looking for someone who has commercial lab experience working to QMS like UKAS 17025 or GLP/GMP/BRC) or GC/MS experience Strong interpersonal, organisation skills Able to work towards deadlines Good IT skills Important Information: We endeavour 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 »

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 device, agrochemical more »

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 »

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 »

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 »

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 »

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 »

and troubleshooting 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 + 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 »

priorities A team player who is adaptable, can show initiative and pick up lots of new skills quickly Good general laboratory experience, ideally with GLP and/or GMP certification For the chance to join an exciting company on their journey to change the world for the better, please apply 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 »

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 »

Lead and mentor a growing team of formulation chemists, fostering an effective and collaborative team culture Maintain standards in the laboratory, with adherence to GLP (General Laboratory Practices) and utilisation of the 5S method Manufacturing Support: Offer scale-up support to the manufacturing team, working closely with the Technical Manager more »

will have responsibility for duties including: Designs and oversees the implementation quality management systems for CMC development activities including the release of product for GLP and GCP studies. Provides quality expertise in accordance with the global quality requirements in the creation of product characterisation, product specifications, method validation, stability and … process, including in the collaboration with C(D)MOs. 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 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 »