26 to 50 of 207 GMP Jobs

and adherence to Food Safety Standards for production. Check temperatures and calibrations of equipment with supporting documentation. Skills: Wet Chemistry, Aseptic Technique, Quality control, Gmp, line check, line inspection, Laboratory, Biology, Chemistry, Qc Additional Skills & Qualifications: EITHER: -2 Years of experience in Food Quality OR -AA or BA/BS more »

skills Qualifications 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 more »

in GCP Quality Assurance within the Pharmaceutical Industry. Strong knowledge of Quality Management Systems within the Pharmaceutical industry. Strong knowledge of ICH-GCP and GMP guidelines. Experience hosting, supporting and preparing MHRA inspections and auditing IT systems. Experience organising and performing internal and/or vendor audits. Experience working in more »

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 to document more »

other DSP, Facebook, Twitter Experience of managing vendor relationships Regularly contributes to platform best practices and campaign processes Experience with Google stack and have GMP & Adwords certifications (desirable) Experience with running campaigns across multiple countries/languages Experience with managing a mid- to large-sized team across a range of more »

the wider Quality group at Alba Bioscience, part of AliveDx, and its primary role is to ensure that all aspects of Good Manufacturing Practice (GMP) and Good Documentation Practice (GDP) compliance are met through effective control of the Quality Management System (QMS). The role is a full-time temporary … by the business . Participate in an 'in-house' programme of continuous training and assessment. Conduct all duties in compliance with Good Manufacturing Practice (GMP), Good Documentation Practice (GDP) and appropriate regulatory requirements including statutory Health & Safety legislation and internal practice. Perform any other duties as reasonably requested from the more »

be key. You will be energetic, punctual, proactive, and reliable with the ability to lead, guide, and motivate others towards achievement whilst maintaining good GMP Standards. What you can expect from us: When joining us you can expect a highly competitive rewards package including group pension and other flexible benefits more »

satisfy the requirements of external agencies. Responsible for timely and accurate reporting of internal Refresco KPIs to the management team. Be responsible for ensuring GMP and Hygiene standards are communicated to the operational teams and processes are in place to effectively monitor and manage them. Partake in site visits and more »

and at conventions. Mentoring and leadership Assist Quality Control in analysis of finished products and received goods when needed Skills: Chemistry, Formulation, Hplc, Laboratory, Gmp, Analytical chemistry, metallurgy Top Skills Details: Chemistry Additional Skills & Qualifications: Bachelor's degree in Chemistry • 10-15 years of formulation experience in a complex product more »

at a high level. What are we looking for? Essential Degree Qualified in an area related to an Engineering discipline. Experience gained within a GMP environment (or closely related regulatory environment) from an equipment, facilities, and engineering perspective. Demonstrated working knowledge of BMS, EMS & HVAC systems. Strong interpersonal and communication more »

duties as required for this position. Requirements: BS degree is a must. Biochem or Chemistry degree is preferred. 6 months+ of experience with in GMP environment. HPLC and/or GC experience are strongly preferred About Actalent Actalent is a global leader in engineering and sciences services and talent solutions. more »

Manage assigned inventory of raw materials and products. Percent (%) of time: 10 7. Review material inventory for disposition. Percent (%) of time: 5 Skills: Chemistry, Gmp, Process chemistry, Chemical, hplc, laboratory, analytical chemistry, wet chemistry, titration Additional Skills & Qualifications: Minimum requirement: Degree in Chemistry/Chemical Engineering/Materials Science or more »

site and related functions in maintaining compliance with GxP regulations and applicable quality guidelines, including, but not limited to UK/EU/US GMP/GDP, ICH and other region specific guidance. The individual will have support key quality system elements and compliance improvements, working closely with relevant stakeholders more »

time. Main responsibilities: Use a range of analytical chemistry techniques- predominantly HPLC Ensuring all analysis and documentation are conducted and recorded in compliance with GMP standards Perform stability study programme activities, storage of in process, and final products samples and retention sample management Working to set protocols within a busy more »

maintained and up to date. Education and experience : *Degree in chemistry, analytical chemistry or equivalent *Previous experience of HPLC, GC analysis with pharmaceutical/GMP regulated environment *Previous experience in analytical method transfer, cleaning validation *your previous experience could be QC analyst, stability analyst, development analyst, principal analyst and raw more »

in Chemistry/Biochemistry/other related science or equivalent experience in a similar setup. - Competent analytical skills, attention to detail, and understanding of GMP requirements. - Ability to work independently and in a team, with strong computer literacy and communication skills. - 1 year of lab based experience is necessary. Are more »

of GCP requirements as applied to biologics and related industry/regulatory guidelines governing clinical trials in the EU & USA.Basic understanding of GLP and GMP requirements for biologicsBasic Knowledge of GLP and cGMP and related industry/regulatory guidelines governing the manufacture of biologics in the UK, EU & US.Ability to 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 »

+ 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 »

method validation Additional Skills & Qualifications: Bachelors Degree in Chemistry 1-2 years of experience working within a pharma or medical device setting FDA and GMP Empower 3 experience nice to have HPLC Experience Level: Entry Level About Actalent Actalent is a global leader in engineering and sciences services and talent more »

will conduct, coordinate and support quality aspects of the Company business operation, ensuring quality compliance throughout the business with focus on WDA, MIA and GMP and GDP activities. Key Responsibilities: To ensure that a quality management system is implemented and maintained and appropriate to the activities at the Company inclusive … EU Guidelines on Good Distribution Practice of Medicinal Products for Human Use (2013/C343/01) and EudraLex – Volume 4 – Good Manufacturing Practice (GMP) guidelines. Providing compliance support and spreading the quality culture throughout the company. Maintain processes (GMP documentation lifecycle, Change Control, Deviation, CAPA, self-inspections, Complaints, GMP … the role of the enforcement group, the Inspection Action (IAG) and resulting actions that can be taken due to non-compliance. Good understanding of GMP/GDP. Excellent attention to detail. Effective time management. Self-motivated & highly target driven. more »

the management and improvement of quality systems processes to ensure both EU and US regulatory compliance to relevant company standards and Good Manufacturing Practice (GMP). • Implement and monitor established policies and procedures to ensure compliance with necessary regulatory bodies in the areas of: Corrective and Preventive Action (CAPA), Complaint … Work in accordance with Company Quality Standards, procedures and processes and comply with the requirements of Good Documentation Practice (GDP) and Good Manufacturing Practice (GMP). • Adhere to the standards of behaviours, policies and procedures as laid out in the employee handbook. • All other essential duties as directed more »

Assurance Supervisor • Assist in maintaining thorough, complete and timely documentation and recordkeeping as outlined in established SOP • Adhere to and models good manufacturing practices (GMP) and good laboratory practices (GLP) at all times Skills: Microbiology, environmental monitoring, Aseptic technique, microbiology testing, sample prep, food analysis testing, Food science Additional Skills more »

Job summary This position presents an exciting opportunity for an experienced radiochemist or radiopharmacist proficient in PET radiopharmaceutical production to GMP standards. As the Production Manager, you will lead our team of radiochemists at the Positron Emitting Radiopharmaceutical Laboratory (PERL), located within St Thomas Hospital. The ideal candidate must possess … expert knowledge in relevant regulatory governance areas, particularly Good Manufacturing Practice (GMP), as well as Health and Safety, Environmental Safety, and Radiation Protection Regulations (IRR2017 and IR(ME)R). This expertise will ensure adherence to these regulations within the PERL facility. Main duties of the job The role entails … managing radiochemists within PERL to ensure timely, safe, and efficient completion of production duties. Emphasis will be placed on compliance with GMP regulations, development of new procedures and radio tracers, and streamlining processes while maintaining safety standards. This includes supporting the installation and validation of new production equipment. The successful more »

focus: Actively participate in the implementation of site quality improvement projects, where necessary providing support to train operation teams and monitor project effectiveness. Complete GMP and Hygiene audits to required schedules. Assist in the investigation of consumer complaints and non-confirming items determining root cause and corrective action necessary to more »