Cheshire, Chester, North West Hybrid / WFH Options
Real Staffing
providing direction and leadership to staff to ensure a quality mindset is embedded in the business Requirements: Expert in GCP with working knowledge of GMP 5 years experience in a QA Manager role within a CRO, Biotech or Pharma company Contract: Hours: 3 days a week - can worked across more »
a Qualified Person to join our team at Harlow, UK. The successful person will perform the quality assurance activities and quality oversight of the GMP functions performed within Pharma R&D. As a Qualified Person, is personally accountable to conform to the legal regulatory requirements as stated in Clinical trials more »
Manchester Area, United Kingdom Hybrid / WFH Options
Factorytalk
have requirements: 2-5 years’ experience working with MES/EBR or similar systems in the life sciences industries. Experience deploying MES in a GMP environment, configuring Recipes, MBR’s, Materials, BOMs, Order Management, Equipment management, Batch Review/Approval and other typical components. A background in one or more more »
of Quality Assurance principles within the Pharmaceutical Industry. Strong understanding of Quality Management Systems in the pharmaceutical sector. Thorough familiarity with ICH-GCP and GMP guidelines. Experience in hosting Sponsor audits and/or Regulatory inspections. Demonstrated ability to organize and conduct internal and/or vendor audits. more »
main communication hub for all facets of your projects both internally amongst teams and externally with clients. - **Quality Assurance & Compliance**: Uphold unwavering adherence to GMP standards alongside other pharmaceutical-specific regulations ensuring quality assurance throughout every phase of each project - **Team Leadership & Development:** Lead by example instilling principles like accountability more »
main communication hub for all facets of your projects both internally amongst teams and externally with clients. - **Quality Assurance & Compliance**: Uphold unwavering adherence to GMP standards alongside other pharmaceutical-specific regulations ensuring quality assurance throughout every phase of each project - **Team Leadership & Development:** Lead by example instilling principles like accountability more »
SOF) Experience in 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 more »
Cambridge University Hospital NHS Foundation Trust
application of Standard Operating Procedures and Quality Assurance Systems. Health and Safety in the Workplace. Maintaining clean and hygienic work environments. GoodManufacturing Practise (GMP) and/or Good Distribution Practices (GDP). Knowledge of stock control systems. Desirable Aseptic dispensing and preparation. Pharmaceutical Science. Contamination Control Systems. Clinical trials more »
Huntingdon, Cambridgeshire, East Anglia, United Kingdom
MM Flowers Ltd
monitoring goodmanufacturing practices, applying HACCP principles and preventing reoccurrence of non-conformance against these standards. To audit compliance against Quality Management Systems and GMP, raising all non-conformances against relevant standards with objective evidence enabling the operational teams to take the appropriate and necessary corrective action, to follow up more »
experience leading IT at a senior management level • Track record of delivering results quickly • Experience in delivering IT services to customers • Work in a GMP or highly regulated environment Preferred Experience: • Experience of agile product development • Experience of Lean Six Sigma • Infrastructure delivery (networking, hardware) to customers • Experience with data more »
Royston, Hertfordshire, South East, United Kingdom Hybrid / WFH Options
Sartorius Corporate Administration GmbH
development with an understanding of the product life cycle ideally in laboratory automation, or pharmaceutical manufacturing environment following ISO/IEC and/or GMP standards though candidates from other industries will also be considered Hands on experience in electrical engineering in prototyping, engineering, design and testing Working knowledge of more »
Royston, England, United Kingdom Hybrid / WFH Options
Sartorius Corporate Administration GmbH
development with an understanding of the product life cycle ideally in laboratory automation, or pharmaceutical manufacturing environment following ISO/IEC and/or GMP standards though candidates from other industries will also be considered Hands on experience in electrical engineering in prototyping, engineering, design and testing Working knowledge of more »
record in Leading the HSE function across multiple companies in a Pharmaceutical environment. It is key that you have experience within a GXP/GMP environment. Purpose of the Job Health, Safety & Environment Lead and provide oversight and Global strategic leadership covering health, safety, and environment across the Pharmaceutical account. more »
Macclesfield, Cheshire, North West, United Kingdom
Russell Taylor Group Ltd
PhD or relevant degree in any chemistry or life science related subject. The ideal candidate will have previous experience of working to GLP/GMP Must be IT literate with competent use of the Microsoft systems. The ideal candidate will have previous experience of using LC-MS/MS. Previous more »
and vision systems integrated within packaging equipment including interfaces with enterprise systems. Responsible for providing cGMP compliant control systems as per GAMP5 and EU GMP Annex 11. Key Experience Essential - Practical experience working within manufacturing and packaging environments Experience of the automation project lifecycle including design, configuration, implementation, testing, commissioning 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 »
you will be responsible for testing and reporting laboratory activities to enable compliant, on time delivery of products to the customer whilst adhering to GMP standards. Your contribution will be the regular completion of on the bench testing of Asthma Inhalers (MDIs). You will be part of a quality more »
Unit 69, Listerhills Science Park, Bradford, England
Cormica
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 »
with a focus on Quality Assurance and Quality Control. Proven leadership skills with a track record of managing high-performing teams. Strong knowledge of GMP, GLP, and ISO standards. Excellent problem-solving skills and ability to make decisions under pressure. Exceptional communication and interpersonal skills. Please note that this role 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 »
equivalent, or relevant industry knowledge and experience. Good mathematical and reasoning ability. Ability to read and interpretate documentation. Knowledge of manufacturing and quality systems. GMP experience strongly preferred. Experience of quality documentation review advantageous. Good organisation/time management skills, ability to prioritize and ability to multi - task. Strong attention 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 »
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 »
