1 to 25 of 29 Permanent GLP Jobs

Environmental Science or a similar scientific subject. Do you have 10+ years of experience in Residue Analysis Or Environmental Fate and Metabolism in a GLP-regulated laboratory? Have you also worked within a CRO company and are looking for a change? You could play a crucial role in various research … study protocols and applicable regulatory guidelines. Manage and oversee study activities including sample preparation, analysis, and data interpretation. Ensure compliance with study protocols, SOPs, GLP regulations, and other applicable guidelines. Manage project timelines and budgets. Conduct field residue, method development, method validation and analytical phases of ecotoxicological studies. Benefits: Competitive 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 »

protection and biocidal products and technical compliance of their fertilisers within the UK and EU. This wide-ranging role includes ongoing liaison with consultants, GLP laboratories and efficacy testing organisations alongside participation in various industry taskforces to ensure compliance with relevant UK and EU regulations. Location: This role is located … in Leicestershire Key Responsibilities: Manage the registration/renewal processes for the plant protection and biocidal products, coordinating with consultants and external GLP laboratories as well as overseeing product labelling and compliance. Conduct liaison with GLP laboratories to address data gaps and stay updated with changes to regulatory guidance. Support more »

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 Experience Responsibilities 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 »

addition, it is one of the leading global emerging players in esoteric and molecular clinical diagnostic testing. Essential Duties and Responsibilities: • Applies GMP/GLP in all areas of responsibility, as appropriate. • Performs any combination of sample preparation tasks to ensure sample homogeneity which includes but is not limited to 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 »

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 … projects 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. Responsible for auditing GLP, GCP and GMP plans, raw data, study procedures and related facilities to ensure compliance with current relevant regulatory requirements and internal consistency, Identify and report any areas of non-compliance to both study and facility management. Liaise with key stakeholders, providing them with accurate information more »

that were ran overnight. They will be looking at backlogs and be assigned up to 10 assays. They will also: Adhere to GMP/GLP Conduct routine analyses independently and in compliance with applicable methods, protocols, SOP's and regulatory agency guidelines Document work and maintains study documentation and laboratory … review of data Plan assigned workload on a daily basis and effectively schedule multiple assignments Skills: UPLC, HPLC, pipetting, gmp, ph meter, wet chemistry, glp Top Skills Details: UPLC,HPLC,pipetting Additional Skills & Qualifications: Bachelor's Degree is Sciences (Chemistry, Biochemistry, Biology, etc.) preferred. Working in a lab setting - 6+ 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 »

in a quality assurance role within the pharmaceutical industry. Deep understanding of Good Clinical Practice guidelines, regulations, and standards. Relevant certifications such as RQAP-GLP, RQAP-GCP are desirable. Leadership experience along with excellent communication, collaboration, and interpersonal skills. Detail-oriented with strong analytical and problem-solving abilities. Proven ability 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 »

Quality Business Analyst BA in charge of being the link with business stakeholders and the Quality/BA Team. Experience as a BA - circa 5+ years to work independently. Experience with Veeva and other quality systems. Must understand GXP. Order 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 »

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 »

to detail, strong organisational skills and ability to multitask. Keywords: Planner, service, equipment, coordinator, administrator, administration, planning, scheduler, CMMS, GMP. GLP, GXP, GDP, Good Laboratory Practice, Good Manufacturing Practice, Good Documentation Practices, Manchester, Northwest, Macclesfield. VRS8731MP. Follow VRS Recruitment on LinkedIn to view all our latest vacancies! Please note that more »

teams • Maintain training and compliance in areas of health and safety, security, environmental and operational aspects of daily activities in the working environment Skills: GLP, GXP, Glassware, PPE, Stock, inventory management, inventory, distiller, descaling, laboratory, gmp Top Skills Details: GLP,GXP,Glassware,PPE,Stock,inventory management Additional Skills & Qualifications: Skills … role within a scientific environment. • Professional Certification/Associates degree in relevant field (Project Management, 6-Sigma, Business Administration, Supply Chain) • Basic understanding of GLP/GxP and/or experience working in a compliance driven environment. • Experience with 5S (Sort, Set in Order, Shine, Standardize, Sustain) principles • Sufficient knowledge more »

with provision and review of reports. Requirements A BA or BS in Chemistry/Biochemistry/Microbiology or other related science. Experience in a GLP/GMP environment. Computer literacy (including MS Word and Excel). Ability to work well with others. Effective communication skills. Good organizational skills. If you more »

or other plans Team player Review and sign of study data Responsible for regulatory compliance as assigned Ensure all processes are following GCP/GLP Liaising with clients regarding within agreed timescales Qualifications At least 3 years experience working in a regulatory bioanalytical laboratory. A degree in life sciences or … chemistry-related subject A good communicator with strong interpersonal skills. Experience working within a GLP/GCP accredited facility. Flexible and adaptable with an eye for detail Hand-on experience of LC-MS/MS, Sciex and Waters LC-MS/MS systems is an advantage Experience in Bioanalytical method more »

good work history in a repetitive work environment Be able to lift 40-50 lbs Attention to detail (documentation is a must)- working under GLP regulations Comfortable working independently Reliable 1+ years experience working with Microsoft Word and Excel programs Experience Level: Entry Level About Actalent Actalent is a global 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 »

Experience of managing a Quality management software system Experience working with database information. Experience of accreditation procedures and standards (e.g. CPA, UKAS, EFI, FDA, GLP) Disclosure and Barring Service Check This post is subject to the Rehabilitation of Offenders Act (Exceptions Order) 1975 and as such it will be necessary more »

identification and quantification and HPLC - Assist with training and qualification of new QC Techs - Lead investigations of corrective actions or out of spec results - GLP Skills: Quality control, Laboratory, Chemistry, microbiology, Wet chemistry, Physical testing, Gmp, Titration, Viscosity, fda, glp Top Skills Details: Quality control,Laboratory,Chemistry,microbiology Additional Skills more »

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 Experience Responsibilities more »